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Published online by Cambridge University Press:  23 September 2009

Mircea Steriade
Affiliation:
Université Laval, Québec
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Print publication year: 2003

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References

Abel, T., Nguyen, P. V., Barad, M., Deuel, T. A., Kandel, E. R. and Bourtchouladze, R. (1997) Genetic demonstration of a role for PKA in the late phase of LTP and in hippocampus-based long-term memory. Cell 88: 615–626CrossRefGoogle ScholarPubMed
Abramson, B. P. and Chalupa, L. M. (1985) The laminar distribution of cortical connections with the tecto- and cortico-recipient zones in the cat's lateral posterior nucleus. Neuroscience 15: 81–95CrossRefGoogle ScholarPubMed
Achermann, P. and Borbély, A. (1997) Low-frequency (< Hz) oscillations in the human sleep EEG. Neuroscience 81: 213–222CrossRefGoogle Scholar
Achermann, P. and Borbély, A. (1998a) Coherence analysis of the human sleep electroencephalogram. Neuroscience 85: 1195–1208CrossRefGoogle Scholar
Achermann, P. and Borbély, A. (1998b) Temporal evolution of coherence and power in the human sleep electroencephalogram. Journal of Sleep Research 7 (Suppl. 1): 36–41CrossRefGoogle Scholar
Adey, W. R. (1967) Hippocampal states and functional relations with corticosubcortical systems in attention and learning. Progress in Brain Research 27: 228–245CrossRefGoogle Scholar
Adolphs, R., Tranel, D., Damasio, H. and Damasio, A. (1994) Impaired recognition of emotion in facial expression following bilateral damage to the human amygdala. Nature 372: 669–672CrossRefGoogle ScholarPubMed
Adrian, E. D. and Matthews, B. H. C. (1934) The Berger rhythm: potential changes from the occipital lobes in man. Brain 57: 355–384CrossRefGoogle Scholar
Agmon, A. and Connors, B. W. (1991) Thalamocortical responses of mouse somatosensory (barrel) cortex in vitro. Neuroscience 41: 365–379CrossRefGoogle ScholarPubMed
Ajmone-Marsan, C. (1975) Focal electrical stimulation. In Experimental Models of Epilepsy, ed. D. P. Purpura, J. K. Penry, D. B. Tower, D. M. Woodbury and R. D. Walter, pp. 147–172, New York: Raven Press
Aladjalova, N. A. (1964) Slow Electrical Processes in the Brain. Progress in Brain Research (vol. 7). Amsterdam: Elsevier
Albe-Fessard, D. and Buser, P. (1955) Activités intracellulaires recueillies dans le cortex sigmoïde du chat: participation des neurones pyramidaux au “potential évoqué” somesthésique. Journal de Physiologie (Paris) 47: 67–69Google Scholar
Albowitz, B. and Kuhnt, U. (1993) The contribution of intracortical connections to horizontal spread of activity in the neocortex as revealed by voltage sensitive dyes and a fast optical recording method. European Journal of Neuroscience 5: 1349–1359CrossRefGoogle Scholar
Albowitz, B. and Kuhnt, U. (1995) Epileptiform activity in the guinea-pig neocortical slice spreads preferentially along supragranular layers – recordings with voltage-sensitive dyes. European Journal of Neuroscience 7: 1273–1284CrossRefGoogle ScholarPubMed
Albrecht, D., Royl, G. and Kaneoke, Y. (1998) Very slow oscillatory activities in lateral geniculate neurons of freely moving and anesthetized rats. Neuroscience Research 32: 209–220CrossRefGoogle ScholarPubMed
Alefeld, M., Sutor, B. and Luhmann, H. J. (1998) Pattern and pharmacology of propagating epileptiform activity in mouse cerebral cortex. Experimental Neurology 153: 113–122CrossRefGoogle ScholarPubMed
Alger, B. E. and Nicoll, R. A. (1982) Feed-forward dendritic inhibition in rat hippocampal pyramidal cells studied in vitro. Journal of Physiology (London) 328: 105–123CrossRefGoogle ScholarPubMed
Allen, P. J., Fish, D. R. and Smith, S. J. (1992) Very high-frequency rhythmic activity during SEEG suppression in frontal lobe epilepsy. Electroencephalography and Clinical Neurophysiology 82: 155–159CrossRefGoogle ScholarPubMed
Al-Noori, S. and Swann, J. (2000) A role for sodium and chloride in kainic acid-induced beading of inhibitory interneuron dendrites. Neuroscience 101: 337–348CrossRefGoogle ScholarPubMed
Alonso, A. and Klink, R. (1993) Differential electroresponsiveness of stellate and pyramidal-like cells of medial entorhinal cortex layer II. Journal of Neurophysiology 70: 128–143CrossRefGoogle ScholarPubMed
Alonso, A. and Köhler, C. (1984) A study of the reciprocal connection between the septum and the entorhinal area using anterograde and retrograde axonal transport methods in the rat brain. Journal of Comparative Neurology 225: 327–343CrossRefGoogle Scholar
Alonso, A. and Llinás, R. (1989) Subthreshold Na+-dependent theta-like rhythmicity in stellate cells of entorhinal cortex layer II. Nature 342: 175–177CrossRefGoogle ScholarPubMed
Alonso, A., Curtis, M. and Llinás, R. (1990) Postsynaptic Hebbian and non-Hebbian long-term potentiation of synaptic efficacy in the entorhinal cortex in slices and in isolated adult guinea pig brain. Proceedings of the National Academy of Sciences of the USA 87: 9280–9284CrossRefGoogle ScholarPubMed
Altman, J. and Bayer, S. A. (1979) Development of the diencephalons in the rat. V. Thymidine-radiographic observations on internuclear and intranuclear gradients in the thalamus. Journal of Comparative Neurology 188: 473–500CrossRefGoogle Scholar
Alvarez-Maubecin, V., Garcia-Hernandez, F., Williams, J. T. and Bockstaele, E. J. (2000) Functional coupling between neurons and glia. Journal of Neuroscience 20: 4091–4098CrossRefGoogle ScholarPubMed
Amadeo, M. and Shagass, C. (1973) Brief latency click-evoked potentials during waking and sleep in man. Psychophysiology 10: 244–250CrossRefGoogle ScholarPubMed
Amaral, D. G. and Price, J. L. (1984) Amygdalo-cortical projections in the monkey (Macaca fascicularis). Journal of Comparative Neurology 230: 465–496CrossRefGoogle Scholar
Amaral, D. G. and Witter, M. P. (1989) The three-dimensional organization of the hippocampal formation: a review of anatomical data. Neuroscience 31: 571–591CrossRefGoogle ScholarPubMed
Amaral, D. G., Price, J. L., Pitkänen, A. and Carmichael, S. T. (1992) Anatomical organization of the primate amygdaloid complex. In The Amygdala, ed. J. P. Aggleton, pp. 1–66, New York: Wiley-Liss
Amzica, F. and Massimini, M. (2000) Modulation of glia and neuronal activities by halothane. Society for Neuroscience Abstracts 26: 734Google Scholar
Amzica, F. and Massimini, M. (2002) Glia and neuronal interactions during slow wave and paroxysmal activities in the neocortex. Cerebral Cortex 12: 1101–1113CrossRefGoogle ScholarPubMed
Amzica, F. and Neckelmann, D. (1999) Membrane capacitance of cortical neurons and glia during sleep oscillations and spike-wave seizures. Journal of Neurophysiology 82: 2731–2746CrossRefGoogle ScholarPubMed
Amzica, F. and Steriade, M. (1995a) Disconnection of intracortical synaptic linkages disrupts synchronization of a slow oscillation. Journal of Neuroscience 15: 4658–4677CrossRefGoogle Scholar
Amzica, F. and Steriade, M. (1995b) Short- and long-range neuronal synchronization of the slow (< Hz) cortical oscillation. Journal of Neurophysiology 75: 20–38CrossRefGoogle Scholar
Amzica, F. and Steriade, M. (1996) Progressive cortical synchronization of ponto-geniculo-occipital potentials during rapid eye movement sleep. Neuroscience 72: 309–314CrossRefGoogle ScholarPubMed
Amzica, F. and Steriade, M. (1997) The K-complex: its slow (< Hz) rhythmicity and relation to delta waves. Neurology 49: 952–959CrossRefGoogle ScholarPubMed
Amzica, F. and Steriade, M. (1998a) Cellular substrates and laminar profile of sleep K-complex. Neuroscience 82: 671–686CrossRefGoogle Scholar
Amzica, F. and Steriade, M. (1998b) Electrophysiological correlates of sleep delta waves. Electroencephalography and Clinical Neurophysiology 107: 69–83CrossRefGoogle Scholar
Amzica, F. and Steriade, M. (1999) Spontaneous and artificial activation of neocortical seizures. Journal of Neurophysiology 82: 3123–3138CrossRefGoogle ScholarPubMed
Amzica, F. and Steriade, M. (2000) Neuronal and glial membrane potentials during sleep and paroxysmal oscillations in the cortex. Journal of Neuroscience 20: 6646–6665CrossRefGoogle Scholar
Amzica, F. and Steriade, M. (2002) The functional significance of K-complexes. Sleep Medicine Reviews 6: 139–149CrossRefGoogle ScholarPubMed
Amzica, F., Nuñez, A. and Steriade, M. (1992) Delta-frequency (1–4 Hz) oscillations of perigeniculate thalamic neurons and their modulation by light. Neuroscience 51: 285–294CrossRefGoogle Scholar
Amzica, F., Neckelmann, D. and Steriade, M. (1997) Instrumental conditioning of fast (20- to 50-Hz) oscillations in corticothalamic networks. Proceedings of the National Academy of Sciences of the USA 94: 1985–1989CrossRefGoogle ScholarPubMed
Amzica, F., Massimini, M. and Manfridi, A. (2002) Spatial buffering during slow and paroxysmal oscillations in cortical networks of glial cells in vivo. Journal of Neuroscience 22: 1042–1053CrossRefGoogle ScholarPubMed
Anderer, P., Klösch, G., Gruber, G., Trenker, E., Pascual-Marqui, R. D., Zeitlhofer, J., Barbanoj, M. J., Rappelsberger, P. and Saletu, B. (2001) Low-resolution brain electromagnetic tomography revealed simultaneously active frontal and parietal sleep spindle sources in the human cortex. Neuroscience 103: 581–592CrossRefGoogle ScholarPubMed
Andersen, P. and Andersson, S. A. (1968) Physiological Basis of the Alpha Rhythm. New York: Appleton-Century-Crofts
Andersen, P. and Sears, T. A. (1964) The role of inhibition in the phasing of spontaneous thalamocortical discharge. Journal of Physiology (London) 173: 459–480CrossRefGoogle Scholar
Andersen, P., Eccles, J. C. and Løyning, Y. (1964) Location of postsynaptic inhibitory synapses on hippocampal pyramids. Journal of Neurophysiology 27: 592–607CrossRefGoogle ScholarPubMed
Andersen, P., Blackstad, T. W. and Lømo, T. (1966) Location and identification of excitatory synapses on hippocampal pyramidal cells. Experimental Brain Research 1: 236–248CrossRefGoogle ScholarPubMed
Andersen, P., Gross, G. N., Lømo, T. and Sveen, O. (1969) Participation of inhibitory and excitatory interneurons in the control of hippocampal cortical output. In The Interneuron, ed. M. Brazier, pp. 415–465, Los Angeles: University of California Press
Andersen, P., Dingledine, R., Gjerstad, L., Langmoen, I. A. and Laursen, A. M. (1980a) Two different responses of hippocampal pyramidal cells to application of gamma-aminobutyric acid. Journal of Physiology (London) 305: 279–296CrossRefGoogle Scholar
Andersen, P., Silfvenius, H., Sundberg, S. H. and Sveen, O. (1980b) A comparison of distal and proximal dendritic synapses on CA1 pyramids in hippocampal slices in vitro. Journal of Physiology (London) 307: 273–299CrossRefGoogle Scholar
Andre, P. and Arrighi, P. (2001) Modulation of Purkinje cell response to glutamate during the sleep-waking cycle. Neuroscience 105: 731–746CrossRefGoogle ScholarPubMed
Andreasen, M. and Hablitz, J. J. (1993) Local anesthetics block transient outward potassium currents in rat neocortical neurons. Journal of Neurophysiology 69: 1966–1975CrossRefGoogle ScholarPubMed
Andrew, R. D. and Mac Vicar, B. A. (1994) Imaging cell volume changes and neuronal excitation in the hippocampal slice. Neuroscience 62: 371–383CrossRefGoogle ScholarPubMed
Annegers, J. W. (1994) The natural course of epilepsy: an epidemiologic perspective. In The Surgical Management of Epilepsy, ed. A. R. Wyler and B. P. Hermann, pp. 3–7, Boston: Butterworth-Heinemann
Araque, A., Sanzgiri, R. P., Parpura, V. and Haydon, P. G. (1998) Calcium elevation in astrocytes causes an NMDA receptor-dependent increase in the frequency of miniature synaptic currents in cultured hippocampal neurons. Journal of Neuroscience 18: 6822–6829CrossRefGoogle ScholarPubMed
Araque, A., Parpura, V., Sanzgiri, R. P. and Haydon, P. G. (1999) Tripartite synapses: glia, the unacknowledged partner. Trends in Neurosciences 22: 208–215CrossRefGoogle ScholarPubMed
Arduini, A. and Arduini, M. (1954) Effect of drugs and metabolic alterations on brainstem arousal mechanism. Journal of Pharmacology and Experimental Therapy 110: 76–85Google ScholarPubMed
Asanuma, C. (1989) Axonal arborizations of a magnocellular basal nucleus input, and their relation to the neurons in the thalamic reticular nucleus of rats. Proceedings of the National Academy of Sciences of the USA 86: 4746–4750CrossRefGoogle ScholarPubMed
Asanuma, C. (1997) Distribution of neuromodulatory inputs in the reticular and dorsal thalamic nuclei. In Thalamus, vol. 2 (Experimental and Clinical Aspects), ed. M. Steriade, E. G. Jones and D. A. McCormick, pp. 93–153, Oxford: Elsevier
Asanuma, C. and Porter, L. L. (1990) Light and electron microscopic evidence for a GABAergic projection from the caudal basal forebrain to the thalamic reticular nucleus in rats. Journal of Comparative Neurology 302: 159–172CrossRefGoogle ScholarPubMed
Aserinsky, E. and Kleitman, N. (1953) Regularly occurring periods of eye motility and concomitant phenomena during sleep. Science 118: 273–274CrossRefGoogle ScholarPubMed
Aserinsky, E. and Kleitman, N. (1955) Two types of ocular motility occurring in sleep. Journal of Applied Physiology 8: 11–18CrossRefGoogle ScholarPubMed
Aston-Jones, G. and Bloom, F. E. (1981) Activity of norepinephrine-containing locus coeruleus neurons in behaving rats anticipates fluctuations in the sleep-waking cycle. Journal of Neuroscience 1: 876–886CrossRefGoogle ScholarPubMed
Avanzini, G., Curtis, M., Panzica, F. and Spreafico, R. (1989) Intrinsic properties of nucleus reticularis thalami neurones of the rat studied in vitro. Journal of Physiology (London) 416: 111–122CrossRefGoogle ScholarPubMed
Avanzini, G., Curtis, M., Marescaux, C., Panzica, F., Spreafico, R. and Vergnes, M. (1992) Role of thalamic reticular nucleus in the generation of rhythmic thalamo-cortical activities subserving spike and waves. Journal of Neural Transmission 35 (Suppl.): 85–95Google ScholarPubMed
Avanzini, G., De Curtis, M., Pape, H. C. and Spreafico, R. (1999) Intrinsic properties of reticular thalamic neurons relevant to genetically determined spike-wave generation. In Jasper's Basic Mechanisms of the Epilepsies (3rd edn.), ed. A. V. Delgado-Escucta, W. A. Wilson, R. W. Olsen and R. J. Porter, pp. 297–309, Philadelphia: Lippincott – Williams & Wilkins
Avendaño, C., Rausell, E. and Reinoso-Suárez, F. (1985) Thalamic projections to areas 5a and 5b of the parietal cortex in the cat: a retrograde horseradish peroxidase study. Journal of Neuroscience 5: 1446–1470CrossRefGoogle ScholarPubMed
Avendaño, C., Rausell, E., Perez-Aguilar, D. and Isorna, S. (1988) Organization of the association cortical afferent connections of area 5: a retrograde tracer study in the cat. Journal of Comparative Neurology 278: 1–33CrossRefGoogle ScholarPubMed
Avoli, M. and Gloor, P. (1981) The effects of transient functional depression of the thalamus on spindles and on bilateral synchronous epileptic discharges of feline generalized penicillin epilepsy. Epilepsia 22: 443–452CrossRefGoogle ScholarPubMed
Avoli, M., Gloor, P., Kostopoulos, G. and Gotman, J. (1983) An analysis of penicillin-induced generalized spike and wave discharges using simultaneous recordings of cortical and thalamic single neurons. Journal of Neurophysiology 50: 819–837CrossRefGoogle ScholarPubMed
Avoli, M., Barbarosie, M., Lücke, A., Nagao, T., Lopantsev, V. and Köhling, R. (1996) Synchronous GABA-mediated potentials and epileptiform discharges in the rat limbic system in vitro. Journal of Neuroscience 16: 3912–3924CrossRefGoogle ScholarPubMed
Ayala, G. F., Dichter, M., Gumnit, R. J., Matsumoto, H. and Spencer, W. A. (1973) Genesis of epileptic spikes: new knowledge of cortical feedback systems suggests a neurophysiological explanation of brief paroxysms. Brain Research 52: 1–17CrossRefGoogle ScholarPubMed
Babb, T. L. (1999) Hippocampal neurophysiology in humans. In The Epilepsies – Etiologies and Prevention, ed. P. Kotagal and H. O. Lüders, pp. 167–170, San Diego: Academic Press
Babb, T. L., Pretorius, J. K., Kupfer, W. R. and Crandall, P. H. (1989) Glutamate decarboxylase-immunoreactive neurons are preserved in human epileptic hippocampus. Journal of Neuroscience 9: 2562–2574CrossRefGoogle ScholarPubMed
Bal, T. and McCormick, D. A. (1993) Mechanisms of oscillatory activity in guinea-pig nucleus reticularis thalami in vitro: a mammalian pacemaker. Journal of Physiology (London) 466: 669–691CrossRefGoogle Scholar
Bal, T. and McCormick, D. A. (1996) What stops synchronized thalamocortical oscillations?Neuron 17: 297–308CrossRefGoogle ScholarPubMed
Bal, T., Krosigk, M. and McCormick, D. A. (1995a) Synaptic and membrane mechanisms underlying synchronized oscillations in the ferret lateral geniculate nucleus in vitro. Journal of Physiology (London) 483: 641–663CrossRefGoogle Scholar
Bal, T., Krosigk, M. and McCormick, D. A. (1995b) Role of the ferret perigeniculate nucleus in the generation of synchronized oscillations in vitro. Journal of Physiology (London) 483: 665–685CrossRefGoogle Scholar
Bal, T., Debay, D. and Destexhe, A. (2000) Cortical feedback controls the frequency and synchrony of oscillations in the visual thalamus. Journal of Neuroscience 20: 7478–7488CrossRefGoogle ScholarPubMed
Baranyi, A., Szente, M. B. and Woody, C. D. (1991) Properties of associative long-lasting potentiation induced by cellular conditioning in the motor cortex of conscious cats. Neuroscience 42: 321–334CrossRefGoogle ScholarPubMed
Barnes, D. M. and Dichter, M. A. (1984) Effects of ethosuximide and tetramethylsuccinimide on cultured cortical neurons. Neurology 34: 620–625CrossRefGoogle ScholarPubMed
Barth, D. S., Sutherling, W., Engle, J. Jr. and Beatty, J. (1984) Neuromagnetic evidence of spatially distributed sources underlying epileptiform spikes in the human brain. Science 223: 293–296CrossRefGoogle ScholarPubMed
Bassetti, C., Mathis, J., Gugger, M., Lövblad, K. O. and Hess, C. W. (1996) Hypersomnia following paramedian thalamic stroke: a report of 12 patients. Annals of Neurology 39: 471–480CrossRefGoogle ScholarPubMed
Bazhenov, M., Timofeev, I., Steriade, M. and Sejnowski, T. J. (1998a) Cellular and network models for intrathalamic augmenting responses during 10-Hz stimulation. Journal of Neurophysiology 79: 2730–2748CrossRefGoogle Scholar
Bazhenov, M., Timofeev, I., Steriade, M. and Sejnowski, T. J. (1998b) Computational models of thalamocortical augmenting responses. Journal of Neuroscience 18: 6444–6465CrossRefGoogle Scholar
Bazhenov, M., Timofeev, I., Steriade, M. and Sejnowski, T. J. (1999) Self-sustained rhythmic activity in the thalamic reticular nucleus mediated by depolarizing GABAA receptor potentials. Nature Neuroscience 2: 168–174CrossRefGoogle ScholarPubMed
Bazhenov, M., Timofeev, I., Steriade, M. and Sejnowski, T. (2000) Spiking-bursting activity in the thalamic reticular nucleus initiates sequences of spindle oscillations in thalamic networks. Journal of Neurophysiology 84: 1076–1087CrossRefGoogle ScholarPubMed
Bazhenov, M., Timofeev, I., Steriade, M. and Sejnowski, T. J. (2002) Model of thalamocortical slow-wave sleep oscillations and transitions to activated states. Journal of Neuroscience 22: 8691–8704CrossRefGoogle ScholarPubMed
Beevor, C. E. and Horsley, V. (1890) A record of the results obtained by electrical excitation of the so-called motor cortex and internal capsule in an orang-outan (Simia satyrus). Philosophical Transactions of the Royal Society of London (B) 181: 129–158CrossRefGoogle Scholar
Bekisz, M. and Wróbel, A. (1993) 20 Hz rhythm of activity in visual system of perceiving cat. Acta Neurobiologiae Experimentalis (Warszaw) 53: 175–182Google ScholarPubMed
Ben-Ari, Y. (1985) Limbic seizures and brain damage produced by kainic acid: mechanisms and relevance to human temporal lobe epilepsy. Neuroscience 14: 375–403CrossRefGoogle ScholarPubMed
Ben-Ari, Y. and Represa, A. (1990) Brief seizure episodes induce long-term potentiation and mossy fibre sprouting in the hippocampus. Trends in Neurosciences 8: 312–318CrossRefGoogle Scholar
Ben-Ari, Y., Gal La Salle, G. and Champagnat, J. (1974) Lateral amygdala unit activity. I. Relationship between spontaneous and evoked activity. Electroencephalography and Clinical Neurophysiology 37: 449–461CrossRefGoogle ScholarPubMed
Ben-Ari, Y., Krnjeviæ, K., Reiffenstein, R. J. and Reinhardt, W. (1981) Inhibitory conductance changes and action of γ-aminobutyrate in rat hippocampus. Neuroscience 6: 2445–2463CrossRefGoogle ScholarPubMed
Benazzouz, A. and Hallett, M. (2000) Mechanism of action of deep brain stimulation. Neurology 55 (Suppl. 6): S13–S16Google ScholarPubMed
Benington, J. H. and Heller, H. C. (1995) Restoration of brain energy metabolism as the function of sleep. Progress of Neurobiology 45: 347–360CrossRefGoogle ScholarPubMed
Benson, D. L., Isackson, P. J., Hendry, S. H. C. and Jones, E. G. (1991) Differential gene expression for glutamic acid decarboxylase and type II calcium-calmodulin-dependent protein kinase in basal ganglia, thalamus and hypothalamus of the monkey. Journal of Neuroscience 11: 1540–1564CrossRefGoogle ScholarPubMed
Beranek, L., Obál, F. Jr., Taishi, P., Bodosi, B., Laczi, F. and Krueger, J. M. (1997) Changes in rat sleep after single and repeated injections of the long-acting somatostatin analog octreotide. American Journal of Physiology 273: R1484–1491Google ScholarPubMed
Berger, H. (1929) Uber das Elektroencephalogramm des Menschen. Archive für Psychiatrie und Nervenkrankheiten 87: 527–570CrossRefGoogle Scholar
Berger, H. (1937) Uber das Elektroencephalogramm des Menschen. Dreizehnte Mitteilung. Archive für Psychiatrie und Nervenkrankheiten 106: 577–584CrossRefGoogle Scholar
Bergmann, F., Costin, A. and Gutman, J. (1963) A low-threshold convulsive area in the rabbit's mesencephalon. Electroencephalography and Clinical Neurophysiology 15: 683–690CrossRefGoogle ScholarPubMed
Bernard, C., Hirsch, J. C. and Ben-Ari, Y. (1999) Excitation and inhibition in temporal lobe epilepsy: a close encounter. In Jasper's Basic Mechanisms of the Epilepsies (3rd edn.), ed. A. V. Delgado-Escueta, W. A. Wilson, R. W. Olsen and R. J. Porter, pp. 821–828, Philadelphia: Lippincott – Williams & Wilkins
Bernard, C., Cossart, R., Hirsch, J. C., Esclapez, M. and Ben-Ari, Y. (2000) What is GABAergic inhibition? How is it modified in epilepsy?Epilepsia 41 (Suppl. 6): S90–S95CrossRefGoogle Scholar
Bernusconi, R., Lauber, J., Marescaux, C., Vergnes, M., Martin, P., Rubio, V., Leonhardt, T., Reymann, N. and Bitiiger, H. (1992) Experimental absence seizures: potential role of gamma-hydroxybutyric acid and GABAB receptors. Journal of Neural Transmission 35 (Suppl.): 155–177Google Scholar
Bernusconi, R., Mathivet, P., Bischoff, S. and Marescaux, C. (1999) γ-Hydroxybutyric acid: an endogenous neuromodulator with abuse potential?Trends in Pharmacological Sciences 20: 135–141CrossRefGoogle Scholar
Berridge, M. J. (1998) Neuronal calcium signaling. Neuron 21: 13–26CrossRefGoogle ScholarPubMed
Berridge, M. J. (2000) Calcium signaling systems in neurons: synaptic plasticity and sleep. In The Regulation of Sleep, ed. A. A. Borbély, O. Hayaishi, T. J. Sejnowski and J. S. Altman, pp. 65–75, Strasbourg: Human Frontier Science Program
Bertram, E. H. and Scott, C. (2000) The pathological substrate of limbic epilepsy: neuronal loss in the medial dorsal thalamus nucleus as the consistent change. Epilepsia 41 (Suppl. 6): S3–S8CrossRefGoogle ScholarPubMed
Beurrier, C., Bioulac, B., Audin, J. and Hammond, C. (2001) High-frequency stimulation produces a transient blockade of voltage-gated currents in subthalamic neurons. Journal of Neurophysiology 85: 1351–1356CrossRefGoogle ScholarPubMed
Bezzi, P. and Volterra, A. (2001) A neuron-glia signaling network in the active brain. Current Opinion in Neurobiology 11: 387–394CrossRefGoogle ScholarPubMed
Bignall, K. E., Imbert, M. and Buser, P. (1966) Optic projections to non visual cortex in the cat. Journal of Neurophysiology 29: 396–409CrossRefGoogle Scholar
Bishop, P. O., Burke, W. and Hayhow, W. R. (1959) Repetitive stimulation of optic nerve and lateral geniculate synapses. Experimental Neurology 1: 534–555CrossRefGoogle ScholarPubMed
Bland, B. H. and Colom, L. V. (1993) Extrinsic and intrinsic properties underlying oscillation and synchrony in limbic cortex. Progress in Neurobiology 41: 157–208CrossRefGoogle ScholarPubMed
Blumenfeld, H. and McCormick, D. A. (2000) Corticothalamic inputs control the pattern of activity generated in thalamocortical networks. Journal of Neuroscience 20: 5153–5162CrossRefGoogle ScholarPubMed
Borbély, A. A. (1982) A two process model of sleep regulation. Human Neurobiology 1: 195–204Google ScholarPubMed
Borbély, A. A. (1984) Das Geheimnis der Schlafs. Stuttgart: Deutsche Verlags-Anstalt
Borbély, A. A. and Tobler, I. (1989) Endogenous sleep-promoting substances and sleep regulation. Physiological Reviews 69: 605–670CrossRefGoogle ScholarPubMed
Bormann, J. and Kettenmann, H. (1988) Patch clamp study of GABA receptor Cl- channels in cultured astrocytes. Proceedings of the National Academy of Sciences of the USA 85: 8336–8340CrossRefGoogle ScholarPubMed
Borst, J. G. and Sakmann, B. (1999) Depletion of calcium in the synaptic cleft of a calyx-type synapse in the rat brainstem. Journal of Physiology (London) 521: 123–133CrossRefGoogle ScholarPubMed
Bougousslavsky, J., Miklossy, J., Deruz, J. P., Regli, F. and Assai, G. (1986) Unilateral left paramedian infarction of the thalamus and midbrain: a clinico-pathological study. Journal of Neurology, Neurosurgery and Psychiatry 49: 686–694CrossRefGoogle Scholar
Bourassa, J., Pinault, D. and Deschênes, M. (1995) Corticothalamic projections from the cortical barrel field to the somatosensory thalamus in rats: a single-fiber study using biocytin as an anterograde tracer. European Journal of Neuroscience 7: 19–30CrossRefGoogle Scholar
Bouyer, J. J., Montaron, M. F., Vahnée, J. M., Albert, M. P. and Rougeul, A. (1987) Anatomical localization of cortical beta rhythm in cat. Neuroscience 22: 863–869CrossRefGoogle ScholarPubMed
Bragin, A., Engel, J. Jr., Wilson, C. L., Fried, I. and Mathern, G. W. (1999a) Hippocampal and entorhinal cortex high-frequency oscillations (100–500 Hz) in human epileptic brain and in kainic acid-treated rats with chronic seizures. Epilepsia 40: 127–137CrossRefGoogle Scholar
Bragin, A., Engel, J. Jr., Wilson, C. L., Vizentin, E. and Mathern, G. W. (1999b) Electrophysiologic analysis of a chronic seizure model after unilateral hippocampal KA injection. Epilepsia 40: 1210–1221CrossRefGoogle Scholar
Bragin, A., Wilson, C. L. and Engel, J. Jr. (2000) Chronic epileptogenesis requires development of a network of pathologically interconnected neuron clusters: a hypothesis. Epilepsia 41 (Suppl. 6): S144–S152CrossRefGoogle ScholarPubMed
Branch, C. L. and Martin, A. R. (1958) Inhibition of Betz cell activity by thalamic and cortical stimulation. Journal of Neurophysiology 21: 380–390CrossRefGoogle ScholarPubMed
Bratz, E. (1899) Ammonshornbefunde bei Epileptischen. Archives für Psychiatrie und Nervenkrankheiten 31: 820–835CrossRefGoogle Scholar
Braun, A. R., Balkin, T. J., Wesensten, N. J., Carson, R. E., Varga, M., Baldwin, P., Selbie, S., Belenky, G. and Herscovitch, P. (1997) Regional cerebral blood flow throughout the sleep-wake cycle. Brain 120: 1173–1197CrossRefGoogle ScholarPubMed
Brazier, M. A. B. (1961) A History of the Electrical Activity of the Brain. London: Pitman
Bremer, F. (1935) Cerveau “isolé” et physiologie du sommeil. Comptes Rendus de la Société de Biologie (Paris) 118: 1235–1241Google Scholar
Bremer, F. (1937) L'activité cérébrale au cours du sommeil et de la narcose. Contribution à l'étude du mécanisme du sommeil. Bulletin de l'Académie Royale de Médecine de Belgique 4: 68–86Google Scholar
Bremer, F. (1949) Considérations sur l'origine et la nature des “ondes” cérébrales. Electroencephalography and Clinical Neurophysiology 1: 177–193Google Scholar
Bremer, F. (1958a) Cerebral and cerebellar potentials. Physiological Reviews 38: 357–388CrossRefGoogle Scholar
Bremer, F. (1958b) Le processus d'excitation et d'inhibition dans les phénomènes épileptiques. In Bases Physiologiques et Aspects Cliniques de l'Épilepsie, ed. T. Alajouanine, pp. 1–35, Paris: Masson
Bremer, F. (1973) Preoptic hypnogenic area and reticular activating system. Archives Italiennes de Biologie 111: 85–111Google ScholarPubMed
Bremer, F. (1975) The isolated brain and its aftermath. In The Neurosciences: Paths of Discovery, ed. F. G. Worden, J. P. Swazey and G. A. Adelman, pp. 267–274. Cambridge, MA: The MIT Press
Bremer, F., Stoupel, N. and Reeth, P. C. (1960) Nouvelles recherches sur la facilitation et l'inhibition des potentiels évoqués corticaux dans l'éveil réticulaire. Archives Italiennes de Biologie 98: 229–247Google Scholar
Bringuier, V., Frégnac, Y., Baranyi, A., Debanne, D. and Shulz, D. E. (1997) Synaptic origin and stimulus dependency of neuronal oscillatory activity in the primary visual cortex of the cat. Journal of Physiology (London) 500: 751–774CrossRefGoogle ScholarPubMed
Brown, A. M., Schwindt, P. C. and Crill, W. E. (1993) Voltage dependence and activation kinetics of pharmacologically defined components of high-threshold calcium current in rat neocortical neurons. Journal of Neurophysiology 70: 1530–1543CrossRefGoogle ScholarPubMed
Brown, R. E., Sergeeva, O. A., Eriksson, K. S. and Haas, H. L. (2002) Convergent excitation of dorsal raphe serotonin neurons by multiple arousal systems (orexin/hypocretin, histamine and noradrenaline). Journal of Neuroscience 22: 8850–8859CrossRefGoogle Scholar
Browne, S. H., Kang, J., Akk, G., Chiang, L. W., Schulman, H., Huguenard, J. R. and Prince, D. A. (2001) Kinetic and pharmacological properties of GABAA receptors in single thalamic neurons and GABAA subunit expression. Journal of Neurophysiology 86: 2312–2322CrossRefGoogle Scholar
Browning, R. A. and Nelson, D. K. (1986) Modification of electroshock and pentylenetetrazol seizure patterns in rats after precollicular transections. Experimental Neurology 93: 546–556CrossRefGoogle ScholarPubMed
Browning, R., Maggio, R., Sahibzada, N. and Gale, K. (1993) Role of brainstem structures in seizures initiated from the deep prepiriform cortex of rats. Epilepsia 34: 393–407CrossRefGoogle ScholarPubMed
Brumberg, J. C., Nowak, L. G. and McCormick, D. A. (2000) Ionic mechanisms underlying repetitive high-frequency burst firing in supragranular cortical neurons. Journal of Neuroscience 20: 4829–4943CrossRefGoogle ScholarPubMed
Buchhalter, J. R. (1993) Animal models of inherited epilepsy. Epilepsia 34 (Suppl. 3): S31–S41CrossRefGoogle ScholarPubMed
Buckmaster, P. S., Jongen-Rêlo, A. L., Davari, S. B. and Wong, E. H. (2000) Testing the disinhibition hypothesis of epileptogenesis in vivo and during spontaneous seizures. Journal of Neuroscience 20: 6232–6240CrossRefGoogle ScholarPubMed
Budde, T., Mager, R. and Pape, H. C. (1992) Different types of potassium outward current in relay neurons acutely isolated from the lateral geniculate nucleus. European Journal of Neuroscience 4: 708–722CrossRefGoogle ScholarPubMed
Buhl, E. H., Otis, T. S. and Mody, I. (1996) Zinc-induced collapse of augmented inhibition by GABA in a temporal lobe epilepsy model. Science 271: 369–373CrossRefGoogle Scholar
Bullock, T. H. (1997) Signals and signs in the nervous system: the dynamic anatomy of electrical activity is probably information-rich. Proceedings of the National Academy of Sciences of the USA 94: 1–6CrossRefGoogle ScholarPubMed
Burns, B. D. (1951) Some properties of isolated cerebral cortex in the unanaesthetised cat. Journal of Physiology (London) 112: 156–175CrossRefGoogle Scholar
Burns, B. D. (1958) The Mammalian Cortex. London: Monographs of the Physiological Society
Burnstine, T. H., Vining, E. P., Uematsu, S. and Lesser, R. P. (1991) Multifocal independent epileptiform discharges in children: ictal correlates and surgical therapy. Neurology 41: 1223–1228CrossRefGoogle ScholarPubMed
Bush, P. C., Prince, D. A. and Miller, K. D. (1999) Increased pyramidal excitability and NMDA conductance can explain posttraumatic epileptogenesis without disinhibition: a model. Journal of Neurophysiology 82: 1748–1758CrossRefGoogle ScholarPubMed
Buzsáki, G. (1989) Two-stage model of memory trace formation: a role for “noisy” brain states. Neuroscience 31: 551–570CrossRefGoogle ScholarPubMed
Buzsáki, G. (1990) Petit-mal epilepsy and parkinsonian tremor: hypothesis of a common pacemaker. Neuroscience 36: 1–14CrossRefGoogle ScholarPubMed
Buzsáki, G. (1998) Memory consolidation during sleep: a neurophysiological perspective. Journal of Sleep Research 7 (Suppl. 1): 17–23CrossRefGoogle ScholarPubMed
Buzsáki, G. (2002) Theta oscillations in the hippocampus. Neuron, 33: 325–340CrossRefGoogle ScholarPubMed
Buzsáki, G. and Chrobak, J. J. (1995) Temporal structure in spatially organized neuronal ensembles: a role for interneuron networks. Current Opinion in Neurobiology 5: 504–510CrossRefGoogle Scholar
Buzsáki, G., Grastyan, E., Tveritskaya, I. and Czopf, J. (1979) Hippocampal evoked potentials and EEG changes during classical conditioning in the rat. Electroencephalography and Clinical Neurophysiology 47: 64–74CrossRefGoogle ScholarPubMed
Buzsáki, G., Leung, L. and Vanderwolf, C. H. (1983) Cellular bases of hippocampal EEG in the behaving rat. Brain Research Reviews 6: 139–171CrossRefGoogle Scholar
Buzsáki, G., Bickford, R. G., Armstrong, D. M., Ponomareff, G., Chen, K. S., Ruiz, R., Thal, L. G. and Gage, F. H. (1988a) Electrical activity in the neocortex of freely moving young and aged rats. Neuroscience 26: 735–744CrossRefGoogle Scholar
Buzsáki, G., Bickford, R. G., Ponomareff, G., Thal, L. J., Mandel, R. and Gage, F. H. (1988b) Nucleus basalis and thalamic control of neocortical activity in the freely moving rat. Journal of Neuroscience 8: 4007–4026CrossRefGoogle Scholar
Buzsáki, G., Kennedy, B., Solt, V. B. and Ziegler, M. (1991) Noradrenergic control of thalamic oscillations: the role of α-2 receptors. European Journal of Neuroscience 3: 222–229CrossRefGoogle Scholar
Buzsáki, G., Penttonen, M., Nádasdy, Z. and Bragin, A. (1996) Pattern and inhibition-dependent invasion of pyramidal cell dendrites by fast spikes in the hippocampus in vivo. Proceedings of the National Academy of Sciences of the USA 93: 9921–9925CrossRefGoogle ScholarPubMed
Cadilhac, J., Vlahovitch, B. and Delange, M. (1965) Considerations on the changes in epileptic discharges during the phase of eye movements. Electroencephalography and Clinical Neurophysiology 18: 96Google Scholar
Calvet, J., Calvet, M. C. and Scherrer, J. (1964) Etude stratigraphique corticale de l'activité EEG spontanée. Electroencephalography and Clinical Neurophysiology 17: 109–125CrossRefGoogle Scholar
Cannon, W. B. and Rosenblueth, A. (1949) The Supersensitivity of Denervated Structures: A Law of Denervation. New York: Macmillan
Canu, M. H. and Rougeul, A. (1992) Nucleus reticularis thalami participates in sleep spindles, not in beta rhythms concomitant with attention in cat. Comptes Rendus de l'Académie des Sciences (Paris) 315: 513–520Google Scholar
Cape, E. G. and Jones, B. E. (1998) Differential modulation of high-frequency γ-electroencephalogram activity and sleep-wake state by noradrenaline and serotonin microinjections into the region of cholinergic basalis neurons. Journal of Neuroscience 18: 2653–2666CrossRefGoogle ScholarPubMed
Cape, E. G. and Jones, B. E. (2000) Effects of glutamate versus procaine microinjections into the basal forebrain cholinergic cell area upon gamma and theta EEG activity and sleep-wake state. European Journal of Neuroscience 12: 2166–2184CrossRefGoogle ScholarPubMed
Carlen, P., Perez-Velazquez, J. L., Valiante, T. A., Jahromi, S. S. and Bardakjian, B. L. (1996) Electric coupling in epileptogenesis. In Gap Junctions in the Nervous System, ed. D. C. Spray and R. Dermietzel, pp. 289–299, Austin, TX: Landes Company
Carli, G., Diete-Spiff, K. and Pompeiano, O. (1967) Presynaptic and postsynaptic inhibition of transmission of somatic afferent volleys through the cuneate nucleus during sleep. Archives Italiennes de Biologie 105: 52–82Google ScholarPubMed
Carskadon, M. A. and Dement, W. C. (2000) Normal human sleep: an overview. In Principles and Practice of Sleep Medicine, ed. M. H. Kryger, T. Roth and W. C. Dement, pp. 15–25, Philadelphia: W. B. Saunders
Cassidi, R. M. and Gale, K. (1998) Mediodorsal thalamus plays a critical role in the development of limbic motor seizures. Journal of Neuroscience 18: 9002–9009CrossRefGoogle Scholar
Castaigne, P., Buge, A., Escourolle, R. and Mason, M. (1962) Ramollissement pédonculaire médian, tegmentothalamique avec ophtalmoplégie et hypersomnie. Revue Neurologique (Paris) 106: 357–367Google Scholar
Castro-Alamancos, M. (1999) Neocortical synchronized oscillations induced by thalamic disinhibition in vivo. Journal of Neuroscience (online) 19: RC27CrossRefGoogle ScholarPubMed
Castro-Alamancos, M. (2002a) Different temporal processing of sensory inputs in the rat thalamus during quiescent and information processing states in vivo. Journal of Physiology (London) 539: 567–578CrossRefGoogle Scholar
Castro-Alamancos, M. (2002b) Properties of primary sensory (lemniscal) synapses in the ventrobasal thalamus and the relay of high-frequency sensory inputs. Journal of Neurophysiology 87: 946–953CrossRefGoogle Scholar
Castro-Alamancos, M. and Calcagnotto, M. E. (2001) High-pass filtering of corticothalamic activity by neuromodulators released in the thalamus during arousal: in vitro and in vivo. Journal of Neurophysiology 85: 1489–1497CrossRefGoogle ScholarPubMed
Castro-Alamancos, M. A. and Connors, B. W. (1996a) Short-term plasticity of a thalamocortical pathway dynamically modulated by behavioral state. Science 272: 274–277CrossRefGoogle Scholar
Castro-Alamancos, M. A. and Connors, B. W. (1996b) Spatiotemporal properties of short-term plasticity in sensorimotor thalamocortical pathways of the rat. Journal of Neuroscience 16: 2767–2779CrossRefGoogle Scholar
Castro-Alamancos, M. A. and Connors, B. W. (1996c) Cellular mechanisms of the augmenting response: short-term plasticity in a thalamocortical pathway. Journal of Neuroscience 16: 7742–7756CrossRefGoogle Scholar
Caton, R. (1875) The electric currents of the brain. British Medical Journal 2: 278Google Scholar
Caton, R. (1887) Interim report on investigations of the electric currents of the brain. British Medical Journal (Suppl. 1): 62Google Scholar
Cauli, B., Audinat, E., Lambolez, B., Angulo, M. C., Ropert, N., Tauzuki, K., Hestrin, S. and Rossier, J. (1997) Molecular and physiological diversity of cortical nonpyramidal cells. Journal of Neuroscience 17: 3894–3906CrossRefGoogle ScholarPubMed
Cauller, L. J. and Connors, B. W. (1994) Synaptic physiology of horizontal afferents in layer I in slices of rat SI neocortex. Journal of Neuroscience 14: 751–762CrossRefGoogle ScholarPubMed
Cavazzuti, G. B., Ferrari, F., Galli, V. and Benatti, A. (1989) Epilepsy with typical absence seizures with onset during the first year of life. Epilepsia 30: 802–806CrossRefGoogle ScholarPubMed
Celio, M. R. (1986) Parvalbumin in most gamma-aminobutyric acid-containing neurons of rat cerebral cortex. Science 231: 995–997CrossRefGoogle ScholarPubMed
Cespuglio, R., Gomez, M. E., Walker, E. and Jouvet, M. (1979) Effets du refroidissement et de la stimulation des noyaux du système du raphé sur les états de vigilance chez le chat. Electroencephalography and Clinical Neurophysiology 47: 289–308CrossRefGoogle Scholar
Cespuglio, R., Faradji, H., Hahn, Z. and Jouvet, M. (1984) Voltammetric detection of brain 5-hydroxyindolamines by means of electrochemically treated carbon fibre electrodes: chronic recordings for up to one month with movable cerebral electrodes in the sleeping or waking rat. In Measurement of Neurotransmitter Release in Vivo (IBRO Handbook Series, vol. 6), ed. C. A. Marsden, pp. 173–191, New York: Wiley
Chagnac-Amitai, Y. and Connors, B. W. (1989) Synchronized excitation and inhibition driven by bursting neurons in neocortex. Journal of Neurophysiology 62: 1149–1162CrossRefGoogle ScholarPubMed
Chagnac-Amitai, Y., Luhmann, H. J. and Prince, D. A. (1990) Burst generating and regular spiking layer 5 pyramidal neurons of rat neocortex have different morphological features. Journal of Comparative Neurology 296: 598–613CrossRefGoogle ScholarPubMed
Chamberlin, N. L., Traub, R. D. and Dingledine, R. (1990) Role of EPSPs in initiation of spontaneous synchronized burst firing in rat hippocampal neurons bathed in high potassium. Journal of Neurophysiology 64: 1000–1008CrossRefGoogle ScholarPubMed
Chandler, S. H., Chase, M. H. and Nakamura, Y. (1980) Intracellular analysis of synaptic mechanisms controlling trigeminal motoneurons activity during sleep and wakefulness. Journal of Neurophysiology 44: 359–371CrossRefGoogle ScholarPubMed
Chang, H. T. (1950) The repetitive discharges of corticothalamic reverberating circuit. Journal of Neurophysiology 13: 235–257CrossRefGoogle Scholar
Charnay, Y., Bouras, C., Vallet, P. G., Golaz, J., Guntern, R. and Constantinidis, J. (1989) Immunohistochemical colocalization of delta-sleep-inducing peptide and luteinizing hormone-releasing hormone in rabbit brain neurons. Neuroscience 31: 495–505CrossRefGoogle ScholarPubMed
Charpier, S., Leresche, N., Deniau, J. M., Mahon, S., Hughes, S. W. and Crunelli, V. (1999) On the putative contribution of GABAB receptors to the electrical events occurring during spontaneous spike and wave discharges. Neuropharmacology 38: 1699–1706CrossRefGoogle Scholar
Chase, M. H. and Morales, F. R. (1983) Subthreshold excitatory activity and motoneuron discharge during REM periods of active sleep. Science 221: 1195–1198CrossRefGoogle ScholarPubMed
Chase, M. H., Chandler, S. H. and Nakamura, Y. (1980) Intracellular determination of membrane potential of trigeminal motoneurons during sleep and wakefulness. Journal of Neurophysiology 44: 349–358CrossRefGoogle ScholarPubMed
Chen, K., Baram, T. Z. and Soltesz, I. (1999) Febrile seizures in the developing brain result in persistent modifications of neuronal excitability in limbic circuits. Nature Medicine 5: 888–894CrossRefGoogle Scholar
Chen, W., Zhang, J. J., Hu, G. Y. and Wu, C. P. (1996) Electrophysiological and morphological properties of pyramidal and non-pyramidal neurons in the cat motor cortex in vitro. Neuroscience 73: 39–55CrossRefGoogle Scholar
Cherubini, E., Gaiarsa, J. L. and Ben-Ari, Y. (1991) GABA: an excitatory transmitter in early postnatal life. Trends in Neurosciences 14: 515–519CrossRefGoogle ScholarPubMed
Chervin, R. D., Pierce, P. A. and Connors, B. W. (1988) Periodicity and directionality in the propagation of epileptiform discharges across neocortex. Journal of Neurophysiology 60: 1695–1713CrossRefGoogle ScholarPubMed
Chou, T. C., Bjorkum, A. A., Gaus, S. E., Lu, J., Scammel, T. E. and Saper, C. B. (2002) Afferents to the ventrolateral preoptic nucleus. Journal of Neuroscience 22: 977–990CrossRefGoogle ScholarPubMed
Chow, A., Erisir, A., Farb, C., Nadal, M. S., Ozaita, A., Lau, D., Welker, E. and Rudy, B. (1999) K+ channel expression distinguishes subpopulations of parvalbumin- and somatostatin-containing neocortical interneurons. Journal of Neuroscience 19: 9332–9345CrossRefGoogle ScholarPubMed
Chrobak, J. J. and Buzsáki, G. (1996) High-frequency oscillations in the output networks of the hippocampal-entorhinal axis of the freely behaving rat. Journal of Neuroscience 16: 3056–3066CrossRefGoogle ScholarPubMed
Chronin, E. P. and Dudek, F. E. (1988) Chronic seizures and collateral sprouting of dentate mossy fibers after kainic acid treatment in rats. Brain Research 474: 181–184CrossRefGoogle Scholar
Chung, J. M., Huguenard, J. R. and Prince, D. A. (1993) Transient enhancement of low-threshold calcium current in thalamic relay neurons after corticectomy. Journal of Neurophysiology 70: 1–7CrossRefGoogle ScholarPubMed
Cirelli, C. and Tononi, G. (2000) Differential expression of plasticityr-elated genes in waking and sleep and their regulation by the noradrenergic system. Journal of Neuroscience 20: 9187–9194CrossRefGoogle ScholarPubMed
Cirelli, C., Pompeiano, M. and Tononi, G. (1996) Neuronal gene expression in the waking state: a role for locus coeruleus. Science 274: 1211–1215CrossRefGoogle ScholarPubMed
Cissé, Y., Timofeev, I., Grenier, F. and Steriade, M. (2001) Intracellular pairing with synaptic activation leads to neocortical plasticity. Society for Neuroscience Abstracts 27: 366Google Scholar
Cissé, Y., Grenier, F., Timofeev, I. and Steriade, M. (2003) Electrophysiological properties and input-output organization of callosal neurons in cat association cortex. Journal of Neurophysiology, in pressCrossRefGoogle ScholarPubMed
Claes, E. (1939) Contribution à l'étude physiologique de la fonction visuelle. I. Analyse oscillographique de l'activité spontanée et sensorielle de l'aire visuelle corticale chez le chat non anesthésié. Archives Internationales de Physiologie 48: 1181–1237Google Scholar
Claparède, E. (1905) Esquisse d'une théorie biologique du sommeil. Archives de Psychologie 4: 246–349Google Scholar
Clemens, B. and Majoros, E. (1987) Sleep studies in benign epilepsy of childhood with rolandic spikes. II. Analysis of discharge frequency and its relation to sleep dynamics. Epilepsia 28: 24–27CrossRefGoogle ScholarPubMed
Clements, J. R. and Grant, S. (1990) Glutamate-like immunoreactivity in neurons of the laterodorsal tegmental and pedunculopontine nuclei in the rat. Neuroscience Letters 120: 70–73CrossRefGoogle ScholarPubMed
Cobb, S. (1947) Photic driving as a cause of clinical seizures in epileptic patients. Archives of Neurology and Psychiatry (Chicago) 58: 70–71CrossRefGoogle ScholarPubMed
Cobb, S. R., Buhl, E. H., Halasy, K., Paulsen, O. and Somogyi, P. (1995) Synchronization of neuronal activity in hippocampus by individual GABAergic interneurons. Nature 378: 811–817CrossRefGoogle ScholarPubMed
Coenen, A. M. L. and Vendrik, A. J. H. (1972) Determination of the transfer ratio of cat's geniculate neurons through quasi-intracellular recordings and the relation with the level of alertness. Experimental Brain Research 14: 227–242CrossRefGoogle ScholarPubMed
Colder, B. W., Wilson, C. L., Frysinger, R. C., Chao, L. C., Harper, R. M. and Engel, J. Jr. (1996) Neuronal synchrony in relation to burst discharge in epileptic human temporal lobes. Journal of Neurophysiology 75: 2496–2508CrossRefGoogle ScholarPubMed
Collins, D. R., Lang, E. J. and Paré, D. (1999) Spontaneous activity of the perirhinal cortex in behaving cats. Neuroscience 89: 1025–1039CrossRefGoogle ScholarPubMed
Collins, D. R., Pelletier, J. G. and Paré, D. (2001) Slow and fast (gamma) neuronal oscillations in the perirhinal cortex and lateral amygdala. Journal of Neurophysiology 85: 1661–1672CrossRefGoogle ScholarPubMed
Collins, R. L. (1975) Audiogenic seizures. In Experimental Models of Epilepsy, ed. D. P. Purpura, J. K. Penry, D. B. Tower, D. M. Woodbury and R. D. Walter, pp. 347–372, New York: Raven Press
Colonnier, M. (1966) The structural design of the neocortex. In Brain and Conscious Experience, ed. J. C. Eccles, pp. 1–23, New York: Springer
Colonnier, M. (1968) Synaptic patterns on different cell types in the different laminae of the visual cortex. An electron microscope study. Brain Research 9: 268–287CrossRefGoogle ScholarPubMed
Coombs, S. J., Eccles, J. C. and Fatt, P. (1955) The electrical properties of the motoneurone membrane. Journal of Physiology (London) 130: 291–325CrossRefGoogle ScholarPubMed
Connors, B. W. (1984) Initiation of synchronized neuronal bursting in neocortex. Nature 310: 685–687CrossRefGoogle ScholarPubMed
Connors, B. W. and Amitai, Y. (1995) Functions of local circuits in neocortex: synchrony and laminae. In The Cortical Neuron, ed. M. J. Gutnick and I. Mody, pp. 123–140, New York: Oxford University Press
Connors, B. W. and Gutnick, M. J. (1990) Intrinsic firing patterns of diverse neocortical neurons. Trends in Neurosciences 13: 99–104CrossRefGoogle ScholarPubMed
Connors, B. W. and Prince, D. A. (1982) Effects of local anesthetic QX-314 on the membrane properties of hippocampal pyramidal neurons. Journal of Pharmacology and Experimental Therapy 220: 476–481Google ScholarPubMed
Connors, B. W., Gutnick, M. J. and Prince, D. A. (1982) Electrophysiological properties of neocortical neurons in vitro. Journal of Neurophysiology 48: 1302–1320CrossRefGoogle ScholarPubMed
Connors, B. W., Malenka, R. and Silva, L. R. (1988) Two inhibitory postsynaptic potentials, and GABAA and GABAB receptor-mediated responses in neocortex of rat and cat. Journal of Physiology (London) 406: 443–468CrossRefGoogle Scholar
Consolazione, A., Priestley, J. V. and Cuello, A. C. (1984) Serotonin-containing projections to the thalamus in the rat revealed by a horseradish peroxidase and peroxidase antiperoxidase double-staining technique. Brain Research 322: 233–243CrossRefGoogle ScholarPubMed
Contreras, D. and Llinás, R. (2001) Voltage-sensitive dye imaging of neocortical spatio-temporal dynamics to afferent activation frequency. Journal of Neuroscience 21: 9403–9413CrossRefGoogle Scholar
Contreras, D. and Steriade, M. (1995) Cellular basis of EEG slow rhythms: a study of dynamic corticothalamic relationships. Journal of Neuroscience 15: 604–622CrossRefGoogle ScholarPubMed
Contreras, D. and Steriade, M. (1996) Spindle oscillation: the role of corticothalamic feedback in a thalamically generated rhythm. Journal of Physiology (London) 490: 159–179CrossRefGoogle Scholar
Contreras, D., Curró Dossi, R. and Steriade, M. (1992) Bursting and tonic discharges in two classes of reticular thalamic neurons in vivo. Journal of Neurophysiology 68: 973–977CrossRefGoogle Scholar
Contreras, D., Curró Dossi, R. and Steriade, M. (1993) Electrophysiological properties of cat reticular neurones in vivo. Journal of Physiology (London) 470: 273–294CrossRefGoogle ScholarPubMed
Contreras, D., Destexhe, A., Sejnowski, T. J. and Steriade, M. (1996a) Control of spatiotemporal coherence of a thalamic oscillation by corticothalamic feedback. Science 274: 771–774CrossRefGoogle Scholar
Contreras, D., Timofeev, I. and Steriade, M. (1996b) Mechanisms of long-lasting hyperpolarizations underlying slow sleep oscillations in cat corticothalamic networks. Journal of Physiology (London) 494: 251–264CrossRefGoogle Scholar
Contreras, D., Destexhe, A., Sejnowski, T. J. and Steriade, M. (1997a) Spatiotemporal patterns of spindle oscillations in cortex and thalamus. Journal of Neuroscience 17: 1179–1196CrossRefGoogle Scholar
Contreras, D., Destexhe, A. and Steriade, M. (1997b) Spindle oscillations during cortical spreading depression in naturally sleeping cats. Neuroscience 77: 933–996Google Scholar
Contreras, D., Destexhe, A. and Steriade, M. (1997c) Intracellular and computational characterization of the intracortical inhibitory control of synchronized thalamic inputs in vivo. Journal of Neurophysiology 78: 335–350CrossRefGoogle Scholar
Contreras, D., Dürmüller, N. and Steriade, M. (1997d) Absence of a prevalent laminar distribution of IPSPs in association cortical neurons of cat. Journal of Neurophysiology 78: 2742–2753CrossRefGoogle Scholar
Corner, M. A., Pelt, J., Wolters, P. S., Baker, R. E. and Nuytinck, R. H. (2002) Physiological effects of sustained blockade of excitatory synaptic transmission on spontaneously active developing neuronal networks – an inquiry into the reciprocal linkage between intrinsic biorhythms and neuroplasticity in early ontogeny. Neuroscience and Behavioral Reviews 26: 127–185CrossRefGoogle ScholarPubMed
Cossart, R., Dinocourt, C., Hirsch, J., Merchan-Perez, A., Felipe, J., Ben-Ari, Y., Esclapez, M. and Bernard, C. (2001) Dendritic but not somatic GABAergic inhibition is decreased in experimental epilepsy. Nature Neuroscience 4: 52–62CrossRefGoogle Scholar
Coulter, D. A. (1999) Chronic epileptogenic cellular alterations in the limbic system after status epilepticus. Epilepsia 40 (Suppl. 1): S23–S33CrossRefGoogle ScholarPubMed
Coulter, D. A., Huguenard, J. R. and Prince, D. A. (1989) Characterization of ethosuximide reduction of low-threshold calcium current in thalamic neurons. Annals of Neurology 25: 582–593CrossRefGoogle ScholarPubMed
Cowan, R. L. and Wilson, C. J. (1994) Spontaneous firing patterns and axonal projections of single corticostriatal neurons in the rat medial agranular cortex. Journal of Neurophysiology 71: 17–32CrossRefGoogle ScholarPubMed
Cragg, B. G. (1975) The development of synapses in the visual system of the cat. Journal of Comparative Neurology 160: 147–166CrossRefGoogle ScholarPubMed
Creutzfeldt, O. D., Watanabe, S. and Lux, H. D. (1966) Relations between EEG phenomena and potentials of single cortical cells. I. Evoked responses after thalamic and epicortical stimulation. Electroencephalography and Clinical Neurophysiology 20: 1–18CrossRefGoogle Scholar
Crill, W. E. (1996) Persistent sodium current in mammalian central neurons. Annual Reviews of Physiology 58: 349–362CrossRefGoogle ScholarPubMed
Crochet, S. and Sakai, K. (1999) Effects of microdialysis application of monoamines on the EEG and behavioural states in the cat mesopontine tegmentum. European Journal of Neuroscience 11: 3738–3752CrossRefGoogle ScholarPubMed
Crowne, D. P. and Radcliffe, D. D. (1975) Some characteristics and functional relations of the electrical activity of the primate hippocampus and hypotheses of hippocampal function. In The Hippocampus, ed. R. L. Isaacson and J. H. Pribram, pp. 185–203, New York: Plenum
Crunelli, V. and Leresche, N. (1991) A role for GABAB receptors in excitation and inhibition of thalamocortical neurons. Trends in Neuroscience 14: 16–21CrossRefGoogle Scholar
Crunelli, V. and Leresche, N. (2002) Childhood absence epilepsy: genes, channels, neurons and networks. Nature Reviews Neuroscience 3: 371–382CrossRefGoogle ScholarPubMed
Crunelli, V., Kelly, J. S., Leresche, N. and Pirchio, M. (1987) The ventral and dorsal lateral geniculate nucleus of the rat: intracellular recordings in vitro. Journal of Physiology (London) 384: 587–601CrossRefGoogle ScholarPubMed
Crunelli, V., Haby, M., Jassik-Gerschenfeld, D., Leresche, N. and Pirchio, M. (1988) Cl- and K+-dependent inhibitory postsynaptic potentials evoked by interneurons of the rat lateral geniculate nucleus. Journal of Physiology (London) 399: 153–176CrossRefGoogle ScholarPubMed
Csicsvari, J., Hirase, H., Czurkó, A. and Buzsáki, G. (1998) Reliability and state dependence of pyramidal cell – interneuron synapses in the hippocampus: an ensemble approach in the behaving rat. Neuron 21: 179–189CrossRefGoogle ScholarPubMed
Csicsvari, J., Hirase, H., Czurkó, A., Mamiya, A. and Buzsáki, G. (1999) Fast network oscillations in the hippocampal CA1 region of the behaving rat. Journal of Neuroscience 19: RC20 (1–4), 1999CrossRefGoogle ScholarPubMed
Cunningham, E. T. and LeVay, S. (1986) Laminar and synaptic organization of the projection from the thalamic nucleus centralis to primary visual cortex in the cat. Journal of Comparative Neurology 254: 65–77CrossRefGoogle ScholarPubMed
Curró Dossi, R., Paré, D. and Steriade, M. (1991) Short-lasting nicotinic and long-lasting muscarinic depolarizing responses of thalamocortical neurons to stimulation of mesopontine cholinergic nuclei. Journal of Neurophysiology 65: 393–406CrossRefGoogle ScholarPubMed
Curró Dossi, R., Nuñez, A. and Steriade, M. (1992a) Electrophysiology of a slow (0.5–4 Hz) intrinsic oscillation of cat thalamocortical neurones in vivo. Journal of Physiology (London) 447: 215–234CrossRefGoogle Scholar
Curró Dossi, R., Paré, D. and Steriade, M. (1992b) Various types of inhibitory postsynaptic potentials in anterior thalamic cells are differentially altered by stimulation of laterodorsal tegmental cholinergic nucleus. Neuroscience 47: 279–289CrossRefGoogle Scholar
Curtis, D. R. and Eccles, J. C. (1960) Synaptic action during and after repetitive stimulation. Journal of Physiology (London) 150: 374–398CrossRefGoogle ScholarPubMed
Daikoku, S., Kawano, H., Noguchi, M., Nakanishi, J., Tokuzen, M., Chihara, K. and Nagatsu, I. (1986) GRF neurons in the rat hypothalamus. Brain Research 399: 250–261CrossRefGoogle ScholarPubMed
Dalla Bernardina, B. and Berghini, G. (1976) Rolandic spikes in children with or without epilepsy (20 subjects polygraphically studied during sleep). Epilepsia 17: 161–167CrossRefGoogle Scholar
Danober, L. and Pape, H. C. (1998) Strychnine-sensitive glycine responses in neurons of the lateral amygdala: an electrophysiological and immunocytochemical characterization. Neuroscience 85: 427–441CrossRefGoogle ScholarPubMed
Danober, L., Depaulis, A., Marescaux, C. and Vergnes, M. (1993) Effects of cholinergic drugs on genetic absence seizures in rats. European Journal of Pharmacology 234: 263–268CrossRefGoogle ScholarPubMed
Danober, L., Vergnes, M., Depaulis, A. and Marescaux, C. (1994) Nucleus basalis lesions suppress spike and wave discharges in rats with spontaneous absence epilepsy. Neuroscience 59: 531–539CrossRefGoogle ScholarPubMed
Danober, L., Depaulis, A., Vergnes, M. and Marescaux, C. (1995) Mesopontine cholinergic control over generalized non-convulsive seizures in a genetic model of absence epilepsy in the rat. Neuroscience 69: 1183–1193CrossRefGoogle Scholar
Danober, L., Deransart, C., Depaulis, A., Vergnes, M. and Marescaux, C. (1998) Pathophysiological mechanisms of genetic absence epilepsy in the rat. Progress in Neurobiology 55: 27–57CrossRefGoogle ScholarPubMed
Datta, S., Curró Dossi, R., Paré, D., Oakson, G. and Steriade, M. (1991) Substantia nigra reticulata neurons during sleep-waking states: relation with ponto-geniculo-occipital waves. Brain Research 566: 344–347CrossRefGoogle ScholarPubMed
Davenport, C. J., Brown, W. J. and Babb, T. L. (1990) Sprouting of GABAergic and mossy fibers axons in the dentate gyrus following intrahippocampal kainate in the rats. Experimental Neurology 109: 180–190CrossRefGoogle Scholar
Dawson, T. M., Bredt, D. S., Fotuhi, M., Hwang, P. M. and Snyder, S. H. (1991) Nitric oxide synthase and neuronal NADPH diaphorase are identical in brain and peripheral tissues. Proceedings of the National Academy of Sciences of the USA 88: 7797–7801CrossRefGoogle ScholarPubMed
Deans, M. R., Gibson, J. R., Sellitto, C., Connors, B. W. and Paul, D. L. (2001) Synchronous activity of inhibitory networks in neocortex requires electrical synapses containing connexin36. Neuron 31: 477–485CrossRefGoogle ScholarPubMed
Debarbieux, F., Brunton, J. and Charpak, S. (1998) Effect of bicuculline in thalamic activity: a direct blockade of IAHP in reticularis neurons. Journal of Neurophysiology 79: 2911–2918CrossRefGoogle ScholarPubMed
Curtis, M. and Avanzini, G. (2001) Interictal spikes in focal epileptogenesis. Progress in Neurobiology 63: 541–567CrossRefGoogle ScholarPubMed
DeFelipe, J. (1993) Neocortical neuronal diversity: chemical heterogeneity revealed by co-localization studies of classic transmitters, neuropeptides, calcium-binding proteins and cell surface molecules. Cerebral Cortex 3: 273–289CrossRefGoogle Scholar
DeFelipe, J. (1999) Chandelier cells and epilepsy. Brain 122: 1807–1822CrossRefGoogle ScholarPubMed
DeFelipe, J. and Farinas, I. (1992) The pyramidal neuron of the cerebral cortex: morphological and chemical characteristics of the synaptic inputs. Progress in Neurobiology 39: 563–607CrossRefGoogle ScholarPubMed
Dégenètais, E., Thierry, A. M., Glowinski, J. and Gioanni, Y. (2002) Electrophysiological properties of pyramidal neurons in the rat prefrontal cortex: an in vivo intracellular recording study. Cerebral Cortex 12: 1–16CrossRefGoogle Scholar
Gennaro, L., Ferrara, M. and Bertini, M. (2001) The boundary between wakefulness and sleep: quantitative electroencephalographic changes during the sleep onset period. Neuroscience 107: 1–11CrossRefGoogle ScholarPubMed
Deiber, M. P., Ibanez, V., Bastuji, H., Fischer, C. and Mauguière, F. (1988) Changes of middle latency auditory evoked potentials during natural sleep in humans. Neurology 39: 806–813CrossRefGoogle Scholar
Deisz, R. A., Billard, J. M. and Zieglgänsberger, W. (1997) Presynaptic and postsynaptic GABAB receptors of neocortical neurons of the rat in vitro: differences in pharmacology and ionic mechanisms. Synapse 25: 62–723.0.CO;2-D>CrossRefGoogle ScholarPubMed
DeLanerolle, N., Kim, J., Robbins, R. and Spencer, D. (1989) Hippocampal interneuron loss and plasticity in human temporal lobe epilepsy. Brain Research 495: 387–395CrossRefGoogle Scholar
Dell, P. and Padel, Y. (1965) Rapid falling asleep provoked by selective stimulation of vagal afferents in the cat. Electroencephalography and Clinical Neurophysiology 18: 725Google Scholar
Delphs, J. R. and Dichter, M. A. (1983) Effects of somatostatin on mammalian cortical neurons in culture: physiological actions and unusual dose response characteristics. Journal of Neuroscience 3: 1176–1188CrossRefGoogle Scholar
Dement, W. C. (2001) Remembering Nathaniel Kleitman. Archives Italiennes de Biologie 139: 11–17Google ScholarPubMed
Dement, W. C. and Kleitman, N. (1957) Cyclic variations in EEG during sleep and their relation to eye movements, body motility, and dreaming. Electroencephalography and Clinical Neurophysiology 9: 673–690CrossRefGoogle ScholarPubMed
Dement, W. C., Hendricksen, S., Jacobs, B. L. and Mitler, M. M. (1973) Biogenic amines, phasic events, and behavior. In Pharmacology and the Future of Man, ed. F. E. Bloom and G. H. Acheson, pp. 74–89, New York: Karger
Dempsey, E. W. and Morison, R. S. (1942) The production of rhythmically recurrent cortical potentials after localized thalamic stimulation. American Journal of Physiology 135: 293–300Google Scholar
Denti, A., McGaugh, J. L., Landfield, P. W. and Shinkman, P. G. (1970) Effects of posttrial electrical stimulation of the mesencephalic reticular formation on avoidance learning in rats. Physiology and Behavior 5: 659–662CrossRefGoogle ScholarPubMed
Deransart, C., Lé-Pham, B. T., Hirsch, E., Marescaux, C. and Depaulis, A. (2001) Inhibition of the substantia nigra suppresses absences and clonic seizures in audiogenic rats, but not tonic seizures: evidence for seizure specificity of the nigral control. Neuroscience 105: 203–211CrossRefGoogle Scholar
Dermietzel, R. and Spray, D. C. (1993) Gap junctions in the brain: where, what type, how many and why?Trends in Neurosciences 16: 186–192CrossRefGoogle Scholar
Descarries, L., Gisiger, V. and Steriade, M. (1997) Diffuse transmission by acetylcholine in the CNS. Progress in Neurobiology 53: 603–625CrossRefGoogle ScholarPubMed
Deschênes, M. and Hu, B. (1990) Electrophysiology and pharmacology of the corticothalamic input to lateral thalamic nuclei: an intracellular study in the cat. European Journal of Neuroscience 2: 140–152CrossRefGoogle Scholar
Deschênes, M., Paradis, M., Roy, J. P. and Steriade, M. (1984) Electrophysiology of neurons of lateral thalamic nuclei in cat: resting properties and burst discharges. Journal of Neurophysiology 51: 1196–1219CrossRefGoogle ScholarPubMed
Deschênes, M., Madariaga-Domich, A. and Steriade, M. (1985) Dendrodendritic synapses in cat reticularis thalami nucleus, a structural basis for thalamic spindle synchronization. Brain Research 334: 169–171Google ScholarPubMed
Desmedt, J. E. (1981) Scalp-recorded cerebral event-related potentials in man as point of entry into the analysis of cognitive processing. In The Organization of the Cerebral Cortex, ed. F. O. Schmitt, F. G. Worden, G. Adelman and S. G. Dennis, pp. 441–473, Cambridge, MA: The MIT Press
Desmedt, J. E. and Tomberg, C. (1994) Transient phase-locking of 40 Hz electrical oscillations in prefrontal and parietal human cortex reflects the process of conscious somatic perception. Neuroscience Letters 168: 126–129CrossRefGoogle ScholarPubMed
Destexhe, A. (1998) Spike-and-wave oscillations based on the properties of GABAB receptors. Journal of Neuroscience 18: 9099–9111CrossRefGoogle ScholarPubMed
Destexhe, A. and Paré, D. (1999) Impact of network activity on the integrative properties of neocortical pyramidal neurons in vivo. Journal of Neurophysiology 81: 1531–1547CrossRefGoogle ScholarPubMed
Destexhe, A. and Sejnowski, T. J. (2001) Thalamocortical Assembly. Oxford: Oxford University Press
Destexhe, A., Contreras, D., Sejnowski, T. J. and Steriade, M. (1994a) A model of spindle rhythmicity in the isolated thalamic reticular nucleus. Journal of Neurophysiology 72: 803–818CrossRefGoogle Scholar
Destexhe, A., Contreras, D., Sejnowski, T. J. and Steriade, M. (1994b) Modeling the control of reticular thalamic oscillations by neuromodulators. NeuroReport 5: 2217–2220CrossRefGoogle Scholar
Destexhe, A., Contreras, D.Steriade, M., Sejnowski, T. J. and Huguenard, J. R. (1996) In vivo, in vitro and computational analysis of dendritic calcium currents in thalamic reticular neurons. Journal of Neuroscience 16: 169–185CrossRefGoogle ScholarPubMed
Destexhe, A., Contreras, D., and Steriade, M. (1998) Mechanisms underlying the synchronizing action of corticothalamic feedback through inhibition of thalamic relay cells. Journal of Neurophysiology 79: 999–1016CrossRefGoogle ScholarPubMed
Destexhe, A., Contreras, D. and Steriade, M. (1999a) Neocortical excitability controls the coherence of thalamic-generated oscillations through corticothalamic feedback. Neuroscience 92: 427–443CrossRefGoogle Scholar
Destexhe, A., Contreras, D. and Steriade, M. (1999b) Spatiotemporal analysis of local field potentials and unit discharges in cat cerebral cortex during natural wake and sleep states. Journal of Neuroscience 19: 4595–4608CrossRefGoogle Scholar
Destexhe, A., McCormick, D. A. and Sejnowski, T. J. (1999c) Thalamic and thalamocortical mechanisms underlying 3 Hz spike-and-wave discharges. Progress in Brain Research 121: 289–307CrossRefGoogle Scholar
Destexhe, A., Contreras, D. and Steriade, M. (2001) LTS cells in cerebral cortex and their role in generating spike-and-wave oscillations. Neurocomputing 38–40: 555–563CrossRefGoogle Scholar
Détári, L. and Vanderwolf, C. H. (1987) Activity of identified cortically projecting neurones during large slow waves and cortical activation in anaesthetized rats. Brain Research 437: 1–8CrossRefGoogle ScholarPubMed
Détári, L., Juhasz, G. and Kukorelli, T. (1984) Firing properties of cat basal forebrain neurones during sleep-wakefulness cycle. Electroencephalography and Clinical Neurophysiology 58: 362–368CrossRefGoogle ScholarPubMed
Détári, L., Rasmusson, D. D. and Semba, K. (1997) Phasic relationship between the activity of basal forebrain neurons and cortical EEG in urethane-anesthetized rat. Brain Research 759: 112–121CrossRefGoogle ScholarPubMed
Devinsky, O., Ehremberg, B., Barthlen, G. M., Abramson, H. S. and Luciano, D. (1994) Epilepsy and sleep apnea syndrome. Neurology 44: 2060–2064CrossRefGoogle ScholarPubMed
Dichter, M. A. and Spencer, W. A. (1969a) Penicillin-induced interictal discharges from the cat hippocampus. I. Characteristics and topographical features. Journal of Neurophysiology 32: 649–662CrossRefGoogle Scholar
Dichter, M. A. and Spencer, W. A. (1969b) Penicllin-induced interictal discharges from the cat hippocampus. II. Mechanisms underlying origin and restriction. Journal of Neurophysiology 32: 663–687CrossRefGoogle Scholar
Dichter, M. A., Herman, C. J. and Selzer, M. (1972) Silent cells during interictal discharges and seizures in hippocampal penicillin foci. Evidence for the role of extracellular K+ in the transition from the interictal state to seizures. Brain Research 48: 173–183CrossRefGoogle Scholar
Dickson, C. T. and Alonso, A. (1997) Muscarinic induction of synchronous population activity in the entorhinal cortex. Journal of Neuroscience 17: 6729–6744CrossRefGoogle ScholarPubMed
Dickson, C. T., Kirk, I. J., Oddie, S. D. and Bland, B. H. (1995) Classification of theta-related cells in the entorhinal cortex: cell discharges are controlled by the ascending brainstem synchronizing pathway in parallel with hippocampal theta-related cells. Hippocampus 5: 306–319CrossRefGoogle ScholarPubMed
Dickson, C. T., Mena, A. R. and Alonso, A. (1997) Electroresponsiveness of medial entorhinal cortex layer III neurons in vitro. Neuroscience 81: 937–950CrossRefGoogle ScholarPubMed
Dijk, D. J. and Czeisler, C. A. (1995) Contribution of the circadian pacemaker and sleep homeostat to sleep propensity, sleep structure, electroencephalographic slow waves, and sleep spindle activity. Journal of Neuroscience 15: 3526–3538CrossRefGoogle ScholarPubMed
Dijk, D. J., Hayes, B. and Czeisler, C. A. (1993) Dynamics of electroencephalographic sleep spindles and slow wave activity in men: effect of sleep deprivation. Brain Research 626: 190–199CrossRefGoogle ScholarPubMed
Dinner, D. S. (1993) Posttraumatic epilepsy. In The Treatment of Epilepsy: Principles, ed. E. Wyllie, pp. 654–658, Philadelphia: Lea & Fibinger
Do, K. Q., Binns, K. E. and Salt, T. E. (1994) Release of the nitric oxide precursor, arginine, from the thalamus upon sensory afferent stimulation, and its effect on thalamic neurons in vivo. Neuroscience 60: 581–586CrossRefGoogle ScholarPubMed
Dolmetsch, R. E., Pajvani, U., Fife, K., Spotts, J. M. and Greenberg, M. E. (2001) Signaling to the nucleus by an L-type calcium channel-calmodulin complex through the MPA kinase pathway. Science 294: 333–339CrossRefGoogle Scholar
Domich, L., Oakson, G. and Steriade, M. (1986) Thalamic burst patterns in the naturally sleeping cat: a comparison between cortically projecting and reticularis neurones. Journal of Physiology (London) 379: 429–449CrossRefGoogle ScholarPubMed
Domich, L., Oakson, G. and Steriade, M. (1987) Thalamic and cortical spindles during early ontogenesis in kittens. Developmental Brain Research 31: 140–142CrossRefGoogle Scholar
Douglas, R. and Martin, K. (1991) A functional microcircuit for cat visual cortex. Journal of Physiology (London) 440: 735–769CrossRefGoogle ScholarPubMed
Draguhn, A., Traub, R. D., Schmitz, D. and Jefferys, J. G. (1998) Electrical coupling underlies high-frequency oscillations in the hippocampus in vitro. Nature 394: 189–192CrossRefGoogle ScholarPubMed
Drake, M. E., Weate, S. J., Newell, S. A., Padamadan, H. and Pakalnis, A. (1994) Multiple sleep latency tests in epilepsy. Clinical Electroencephalography 25: 59–62CrossRefGoogle ScholarPubMed
Dreifuss, F. E. (1997) Classification of epileptic seizures. In Epilepsy: A Comprehensive Textbook, ed. J. Engel Jr. and T. A. Pedley, pp. 517–524, Philadelphia: Lippincott-Raven
Dudek, F. E., Snow, R. S. and Taylor, C. P. (1986) Role of electrical interactions in synchronization of epileptiform bursts. Advances in Neurology 44: 593–617Google ScholarPubMed
Dulac, O. and N'Guyen, T. (1993) The Lennox-Gastaut syndrome. Epilepsia 34 (Suppl. 7): S7–S17CrossRefGoogle ScholarPubMed
Dunwiddie, T. V. (1985) The physiological role of adenosine in the central nervous system. International Review of Neurobiology 27: 63–139CrossRefGoogle ScholarPubMed
Dusser de Barenne, J. G. and McCulloch, W. S. (1938) The direct functional interrelation of sensory cortex and optic thalamus. Journal of Neurophysiology 1: 176–186CrossRefGoogle Scholar
Dzubay, J. A. and Jahr, C. E. (1999) The concentration of synaptically released glutamate outside of the climbing fiber – Purkinje cell synaptic cleft. Journal of Neuroscience 19: 5265–5274CrossRefGoogle ScholarPubMed
Eccles, J. C. (1961) Chairman's opening remarks. In The Nature of Sleep, ed. G. E. W. Wolstenholme and M. O'Connor, pp. 1–3, London: Churchill
Eccles, J. C., Libet, B. and Young, R. R. (1958) The behavior of chromatolysed motoneurones studied by intracellular recording. Journal of Physiology (London) 143: 11–40CrossRefGoogle ScholarPubMed
Eccles, J. C., Ito, M. and Szentágothai, J. (1967) The Cerebellum as a Neuronal Machine. New York: Springer
Echlin, F. A., Arnett, V. and Zoll, J. (1952) Paroxysmal high voltage discharges from isolated and partially isolated cerebral cortex as a mechanism in focal cortical epilepsy. Electroencephalography and Clinical Neurophysiology 4: 147–164CrossRefGoogle Scholar
Eckhorn, R., Bauer, R., Jordan, W., Brosch, M., Kruse, W., Munk, M. and Reitboeck, H. J. (1988) Coherent oscillations: a mechanism of feature linking in the visual cortex?Biological Cybernetics 60: 121–130CrossRefGoogle ScholarPubMed
Economo, C. von (1918) Die Encephalitis Lethargica. Vienna: Deuticke
Economo, C. (1929) Schlaftheorie. Ergebnisse der Physiologie 28: 312–339CrossRefGoogle Scholar
Egan, T. M. and North, R. A. (1985) Acetylcholine acts on m2-muscarinic receptors to excite rat locus coeruleus neurones. British Journal of Pharmacology 85: 733–735CrossRefGoogle ScholarPubMed
Eisenman, J. S. (1982) Electrophysiology of the anterior hypothalamus: thermoregulation and fever. In Pyretics and Antipyretics, ed. G. Milton, pp. 187–217, Berlin: Springer
Elton, M., Winter, O., Heslenfeld, D., Loewy, D., Campbell, K. and Kok, A. (1997) Event-related potentials to tones in the absence and presence of sleep spindles. Journal of Sleep Research 6: 78–83CrossRefGoogle ScholarPubMed
Engel, A., König, P., Kreiter, A. and Singer, W. (1991) Interhemispheric synchronization of oscillatory neuronal responses in cat visual cortex. Science 252: 1177–1179CrossRefGoogle ScholarPubMed
Engel, J. (1995) Inhibitory mechanisms of epileptic seizure generation. Advances in Neurology 67: 157–171Google ScholarPubMed
Engel, J. Jr., Henry, T. R., Risinger, M. W., Mazziotta, J. C., Sutherling, W. W., Levesque, M. F. and Phelps, M. E. (1990) Presurgical evaluation for partial epilepsy: relative contributions of chronic depth electrode recordings versus FDG-PET and scalp-sphenoidal ictal EEG. Electroencephalography and Clinical Neurophysiology 40: 1670–1677Google ScholarPubMed
Esclapez, M., Hirsch, J., Khazipov, R., Ben-Ari, Y. and Bernard, C. (1997) Operative GABAergic inhibition in hippocampal CA1 pyramidal neurons in experimental epilepsy. Proceedings of the National Academy of Sciences of the USA 94: 12151–12156CrossRefGoogle ScholarPubMed
Evarts, E. V. (1964) Temporal patterns of discharge of pyramidal tract neurons during sleep and waking. Journal of Neurophysiology 27: 152–171CrossRefGoogle ScholarPubMed
Everson, C. A., Smith, C. B. and Sokoloff, L. (1994) Effects of prolonged sleep deprivation on local rates of cerebral energy metabolism in freely moving rats. Journal of Neuroscience 14: 6769–6778CrossRefGoogle ScholarPubMed
Façon, E., Steriade, M. and Wertheimer, N. (1958) Hypersomnie prolongée engendrée par des lésions bilatérales du système activateur médial: le syndrome thrombotique de la bifurcation du tronc basilaire. Revue Neurologique (Paris) 98: 117–133Google Scholar
Faingold, C. L. and Meldrum, B. S. (1990) Excitant amino acids in epilepsy. In Generalized Epilepsy, ed. M. Avoli, P. Gloor, G. Kostopoulos and R. Naquet, pp. 102–117, Boston: Birkhäuser
Farid, H. and Adelson, E. H. (2001) Synchrony does not promote grouping in temporally structured displays. Nature Neuroscience 4: 875–876CrossRefGoogle Scholar
Farmer, S. F. (1998) Rhythmicity, synchronization and binding in human and primate motor cortex. Journal of Physiology (London) 509: 3–14CrossRefGoogle Scholar
Federico, P. and MacVicar, B. A. (1996) Imaging the induction and spread of seizure activity in the isolated brain of guinea pig: the roles of GABA and glutamate receptors. Journal of Neurophysiology 76: 3471–3492CrossRefGoogle ScholarPubMed
Feinberg, I. and Campbell, I. G. (1993) Ketamine administration during waking increases delta EEG intensity in rat sleep. Neuropharmacology 9: 41–48Google ScholarPubMed
Feindel, W. and Penfield, W. (1954) Localization of discharge in temporal lobe automatism. Archives of Neurology and Psychiatry (Chicago) 72: 605–630CrossRefGoogle ScholarPubMed
Feindel, W. and Rasmussen, T. (1991) Temporal lobectomy with amygdalectomy and minimal hippocampal resection: review of 100 cases. Canadian Journal of Neurological Sciences 18: 603–605CrossRefGoogle ScholarPubMed
Feldberg, L. A. and Sherwood, P. D. (1954) Injections of drugs into the lateral ventricle of the cat. Journal of Physiology (London) 123: 148–167CrossRefGoogle ScholarPubMed
Fencl, V., Koski, G. and Pappenheimer, J. R. (1971) Factors in cerebrospinal fluid from goats that affect sleep and activity in rats. Journal of Physiology (London) 216: 565–589CrossRefGoogle ScholarPubMed
Ferencz, I., Kokaia, M., Keep, M., Elmér, E., Metsis, M., Kokaia, Z. and Lindvall, O. (1997) Effects of cholinergic denervation on seizure development and neurotrophin messenger RNA regulation in rapid hippocampal kindling. Neuroscience 80: 389–399CrossRefGoogle ScholarPubMed
Ferencz, I., Leanza, G., Nanobashvili, A., Kokaia, M. and Lindvall, O. (2000) Basal forebrain neurons suppress amygdala kindling via cortical but not hippocampal cholinergic projections in rats. European Journal of Neuroscience 12: 2107–2116CrossRefGoogle Scholar
Ferrara, M., Gennaro, L., Curcio, G., Cristiani, R., Corvasce, C. and Bertino, M. (2002) Regional differences of the human sleep electroencephalogram in response to selective slow-wave sleep deprivation. Cerebral Cortex 12: 737–748CrossRefGoogle ScholarPubMed
Ferrier, D. (1876) The Functions of the Brain. London: Smith, Elder & Co
Ferster, D. and Lindström, S. (1985) Augmenting responses evoked in area 17 of the cat by intracortical axonal collaterals of cortico-geniculate cells. Journal of Physiology (London) 367: 217–232CrossRefGoogle Scholar
Fetz, E. E., Chen, D., Murphy, V. N. and Matsumara, M. (2000) Synaptic interactions mediating synchrony and oscillations in primate sensorimotor cortex. Journal de Physiologie (Paris) 94: 323–331CrossRefGoogle ScholarPubMed
Feucht, M., Möller, U., Witte, H., Schmidt, K., Arnold, M., Benninger, F., Steinberger, K. and Friedrich, M. H. (1998) Nonlinear dynamics of 3 Hz spike-and-wave discharges recorded during typical absence seizures in children. Cerebral Cortex 8: 524–533CrossRefGoogle ScholarPubMed
Finnerty, G. T. and Jefferys, J. G. R. (2000) 9–16 Hz oscillation precedes secondary generalization of seizures in the rat tetanus toxin model of epilepsy. Journal of Neurophysiology 83: 2217–2226CrossRefGoogle ScholarPubMed
Fischer-Perroudon, C., Mouret, J. and Jouvet, M. (1974) Sur un cas d'agrypnie (4 mois sans sommeil) au cours d'une maladie de Morvan: effet favorable du 5–hydroxytryptophane. Electroencephalography and Clinical Neurophysiology 36: 1–18CrossRefGoogle Scholar
Fiset, P., Paus, T., Daloze, T., Plourde, G., Meuret, P., Bonhomme, V., Hajj-Ali, N., Backman, S. B. and Evans, A. C. (1999) Brain mechanisms of propofol-induced loss of consciousness in humans: a positron emission tomography study. Journal of Neuroscience 19: 5506–5513CrossRefGoogle Scholar
Fish, D. R., Gloor, P., Quesney, L. F. and Olivier, A. O. (1993) Clinical responses to electrical brain stimulation of the temporal and frontal lobes in patients with epilepsy. Brain 116: 397–414CrossRefGoogle ScholarPubMed
Fisher, R. S. and Prince, D. A. (1977) Spike-wave rhythms in cat cortex induced by parenteral penicillin. I. Electroencephalographic patterns. Electroencephalography and Clinical Neurophysiology 42: 608–624CrossRefGoogle Scholar
Fisher, R. S., Buchwald, N. A., Hull, C. D. and Levine, M. S. (1988) GABAergic basal forebrain neurons project to the neocortex: the localization of glutamic acid decarboxylase and choline acetyltransferase in feline corticopetal neurons. Journal of Comparative Neurology 272: 489–502CrossRefGoogle ScholarPubMed
Fisher, R. S., Webber, W. R., Lesser, R. P., Arroyo, S. and Uematsu, S. (1992) High-frequency EEG activity at the start of seizures. Journal of Clinical Neurophysiology 9: 441–448Google ScholarPubMed
Fleidervish, I. A. and Gutnick, M. J. (1996) Kinetics of slow inactivation of persistent sodium current in layer V neurons of mouse neocortical slices. Journal of Neurophysiology 76: 2125–2130CrossRefGoogle Scholar
Foehring, R. C., Schwindt, P. C. and Crill, W. E. (1989) Norepinephrine selectively reduces slow Ca2+- and Na+-mediated currents in cat neocortical neurons. Journal of Neurophysiology 61: 245–256CrossRefGoogle ScholarPubMed
Foldvary, N. (2001) Sleep disorders in epilepsy. In Epilepsy and Sleep, ed. D. S. Dinner and H. O. Lüders, pp. 191–201, San Diego: Academic Press
Ford, B., Holmes, C. J., Mainville, L. and Jones, B. E. (1995) GABAergic neurons in the rat pontomesencephalic tegmentum: codistribution with cholinergic and other tegmental neurons projecting to the posterior lateral hypothalamus. Journal of Comparative Neurology 363: 177–196CrossRefGoogle ScholarPubMed
Foulkes, D. (1967) Nonrapid eye movement mentation. Experimental Neurology 19: 28–38CrossRefGoogle Scholar
Franck, J. E. and Schwartzkroin, P. A. (1985) Do kainite-lesioned hippocampi become epileptogenic?Brain Research 329: 309–313CrossRefGoogle ScholarPubMed
Frank, G. (1969) A study of the inter-relations of spike discharge density and sleep stages in epileptic patients. Electroencephalography and Clinical Neurophysiology 26: 238Google ScholarPubMed
Frank, M. G., Issa, N. P. and Stryker, M. P. (2001) Sleep enhances plasticity in the developing visual cortex. Neuron 30: 275–287CrossRefGoogle ScholarPubMed
Frantseva, M. V., Kokarovtseva, L., Naus, C. G., Carlen, P. L., MacFabe, D. and Perez Velazquez, J. L. (2002) Specific gap junctions enhance the neuronal vulnerability to brain traumatic injury. Journal of Neuroscience 22: 644–653CrossRefGoogle ScholarPubMed
Freeman, W. J. (1975) Mass Action in the Nervous System. New York: Academic Press
Freeman, W. J. and Dijk, B. W. (1988) Spatial patterns of visual cortical fast EEG during conditioned reflex in a rhesus monkey. Brain Research 422: 267–276CrossRefGoogle Scholar
French, C. R., Sah, P., Buckett, K. J. and Gage, P. W. (1990) A voltage-dependent persistent sodium current in mammalian hippocampal neurons. Journal of General Physiology 95: 1139–1157CrossRefGoogle ScholarPubMed
Freund, T. F. (1993) Anterograde PHAL-tracing combined with pre- and postembedding immunocytochemistry. In Immunohistochemistry, ed. A. C. Cuello, pp. 329–348, New York: Wiley
Freund, T. F. and Buzsáki, G. (1988) Alterations in excitatory and GABA-ergic inhibitory connections in hippocampal transplants. Neuroscience 27: 373–385CrossRefGoogle Scholar
Freund, T. F. and Buzsáki, G. (1996) Interneurons of the hippocampus. Hippocampus 6: 347–4703.0.CO;2-I>CrossRefGoogle ScholarPubMed
Fries, P., Neuenschwander, S., Engel, A. K., Goebel, R. and Singer, W. (2001a) Rapid feature selective neuronal synchronization through correlated latency shifting. Nature Neuroscience 4: 194–200CrossRefGoogle Scholar
Fries, P., Reynolds, J. H., Rorie, A. E. and Desimone, R. (2001b) Modulation of oscillatory neuronal synchronization by selective visual attention. Science 291: 1560–1563CrossRefGoogle Scholar
Fritsch, G. and Hitzig, E. (1870) Uber die elektrische Erregbarkeit des Grosshirns. Archive für Anatomie, Physiologie und wissenschaftliche Medizin 37: 300–332Google Scholar
Fromm, G. H. (1986) Role of inhibitory mechanisms in staring spells. Journal of Clinical Neurophysiology 3: 297–311CrossRefGoogle ScholarPubMed
Futamachi, K. J., Mutani, R. and Prince, D. A. (1974) Potassium activity in rabbit cortex. Brain Research 75: 5–25CrossRefGoogle ScholarPubMed
Gabor, A. J. and Ajmone-Marsan, C. (1968) Coexistence of focal bilateral diffuse paroxysmal discharges in epileptics. Epilepsia 10: 453–472CrossRefGoogle Scholar
Gais, S., Plihal, W., Wagner, U. and Born, J. (2000) Early sleep triggers memory for early visual discrimination skills. Nature Neuroscience 3: 1335–1339CrossRefGoogle ScholarPubMed
Gais, S., Mölle, M., Helms, K. and Born, J. (2002) Learning-dependent increases in sleep density. Journal of Neuroscience 22: 6830–6834CrossRefGoogle Scholar
Galarreta, M. and Hestrin, S. (1998) Frequency-dependent synaptic depression and the balance of excitation and inhibition in the neocortex. Nature Neuroscience 1: 587–594CrossRefGoogle ScholarPubMed
Galarreta, M. and Hestrin, S. (1999) A network of fast-spiking cells in the neocortex connected by electrical synapses. Nature 402: 72–75CrossRefGoogle ScholarPubMed
Gallopin, T., Fort, P., Eggerman, E., Cauli, B., Luppi, P. H., Rossier, J., Audinat, E., Mühlethaler, , and Serafin, M. (2000) Identification of sleep-promoting neurons in vitro. Nature 404: 992–995CrossRefGoogle ScholarPubMed
Garcia-Cairasco, N., Terra, V. C. and Doretto, M. C. (1993) Midbrain substrates of audiogenic seizures in rats. Behavioral and Brain Research 58: 57–67CrossRefGoogle ScholarPubMed
Garcia-Rill, E., Skinner, R. D., Miyazato, H. and Homma, Y. (2001) Pedunculopontine stimulation induces prolonged activation of pontine reticular neurons. Neuroscience 104: 455–465CrossRefGoogle ScholarPubMed
Gastaut, H. (1950) Combined photic and metrazol activation of the brain. Electroencephalography and Clinical Neurophysiology 2: 263–275CrossRefGoogle Scholar
Gastaut, H. (1968) Clinical and electroencephalographic correlates of generalized spike and wave bursts occurring spontaneously in man. Epilepsia 9: 179–184CrossRefGoogle ScholarPubMed
Gastaut, H. and Broughton, R. (1972) Epileptic Seizures. Clinical and Electrographic Features, Diagnosis and Treatment. Springfield, ILL: Charles C. Thomas
Gastaut, H., Roger, J. and Gastaut, Y. (1948) Les formes expérimentales de l'épilepsie humaine. I. L'épilepsie induite par la stimulation lumineuse intermittente rythmée, ou épilepsie photogénique. Revue Neurologique (Paris) 80: 161–183Google Scholar
Gastaut, H., Roger, J., Soulayrol, R., Tassinari, C. T., Régis, H., Dravet, C., Bernard, R., Pinsard, N. and Saint-Jean, M. (1966) Childhood epileptic encephalopathy with diffuse slow spike-waves (otherwise known as “petit mal variant”) or Lennox syndrome. Epilepsia 7: 139–179CrossRefGoogle Scholar
Gaudin-Chazal, G., Portalier, P., Barrit, M. C. and Puizillout, J. J. (1982) Serotonin-like immunoreactivity in paraffin-sections of the nodose ganglia of the cat. Neuroscience Letters 33: 169–172CrossRefGoogle ScholarPubMed
Gean, P. W., Shinnick-Gallagher, P. and Anderson, C. (1989) Spontaneous epileptiform activity and alterations of GABA- and NMDA-mediated neurotransmission in amygdala neurons kindled in vivo. Brain Research 494: 177–181CrossRefGoogle Scholar
Gevins, A., Smith, E. M., McEvoy, L. and Yu, D. (1997) High-resolution EEG mapping of cortical activation related to working memory: effects of task difficulty, type of processing, and practice. Cerebral Cortex 7: 374–385CrossRefGoogle ScholarPubMed
Giaretta, D., Avoli, M. and Gloor, P. (1987) Intracellular recordings in precruciate neurons during spike and wave discharges of feline generalized penicillin epilepsy. Brain Research 405: 68–79CrossRefGoogle Scholar
Gibbs, E. L. and Gibbs, F. A. (1947) Diagnostic and localizing value of electroencephalographic studies in sleep. Research Publications of the Association for the Research of Nervous and Mental Diseases 26: 366–376Google Scholar
Gibbs, F. A. and Gibbs, E. L. (1952) Atlas of Electroencephalography, 2nd edn. Cambridge, MA: Addison-Wesley
Gibbs, F. A., Gibbs, E. L. and Lennox, W. G. (1937) Epilepsy: a paroxysmal cerebral dysrhythmia. Brain 60: 377–388CrossRefGoogle Scholar
Gibbs, F. A., Gibbs, E. L. and Lennox, W. G. (1938) Cerebral dysrhythmias of epilepsy: measures for their control. Archives of Neurology and Psychiatry (Chicago) 39: 298CrossRefGoogle Scholar
Gibbs, F. A., Gibbs, E. L. and Lennox, W. G. (1939) The influence of the blood sugar level on the wave and spike formation in petit mal epilepsy. Archives of Neurology and Psychiatry (Chicago) 47: 1111–1116CrossRefGoogle Scholar
Gibbs, J. W., Berkow-Schroeder, G. and Coulter, D. A. (1996) GABAA receptor function in developing rat thalamic reticular neurons: whole cell recordings of GABA-mediated currents and modulation by clonazepam. Journal of Neurophysiology 76: 2568–2579CrossRefGoogle ScholarPubMed
Gibbs, J. W., Shumate, M. D. and Coulter, D. A. (1997) Differential epilepsy-associated alterations in postsynaptic GABAA receptor function in dentate granule cells and CA1 neurons. Journal of Neurophysiology 77: 1924–1938CrossRefGoogle Scholar
Gibson, J. R., Beierlein, M. and Connors, B. W. (1999) Two networks of electrically coupled inhibitory neurons in neocortex. Nature 402: 75–79CrossRefGoogle ScholarPubMed
Gilbert, C. D. (1992) Horizontal integration and cortical dynamics. Neuron 9: 1–13CrossRefGoogle ScholarPubMed
Gilbert, C. D. and Wiesel, T. N. (1983) Clustered intrinsic connections in cat visual cortex. Journal of Neuroscience 3: 1116–1133CrossRefGoogle ScholarPubMed
Gilliland, M. A., Bergmann, B. M. and Rechtschaffen, A. (1989) Sleep deprivation in the rat. VIII. High EEG amplitude sleep deprivation. Sleep 12: 53–59CrossRefGoogle ScholarPubMed
Girgis, M. (1980) Participation of muscarinic cholinergic receptors may be an important requirement of the kindling process. Experimental Neurology 70: 458–461CrossRefGoogle ScholarPubMed
Glenn, L. L. and Dement, W. C. (1981) Membrane potential, synaptic activity and excitability of hindlimb motoneurons during wakefulness and sleep. Journal of Neurophysiology 46: 839–854CrossRefGoogle ScholarPubMed
Glenn, L. L. and Steriade, M. (1982) Discharge rate and excitability of cortically projecting intralaminar thalamic neurons during waking and sleep states. Journal of Neuroscience 2: 1287–1404CrossRefGoogle ScholarPubMed
Glenn, L. L., Hada, J., Roy, J. P., Deschênes, M. and Steriade, M. (1982) Anterograde tracer and field potential analysis of the neocortical layer I projection from the nucleus ventralis medialis of the thalamus in cat. Neuroscience 7: 1861–1877CrossRefGoogle ScholarPubMed
Gloor, P. (1969) Hans Berger on the Electroencephalogram of Man. Amsterdam: Elsevier (Suppl. no. 28 of Electroencephalography and Clinical Neurophysiology)
Gloor, P. (1976) Generalized and widespread bilateral paroxysmal abnormalities. In Handbook of Electroencephalography and Clinical Neurophysiology, vol. 11/B, ed. A. Rémond, pp. 11B52–11B87, Amsterdam: Elsevier
Gloor, P. (1987) Volume conductor principles: their application to the surface and depth electroencephalogram. In Presurgical Evaluation of Epileptics, ed. H. G. Wieser and C. E. Elger, pp. 59–68, Berlin: Springer
Gloor, P. (1991) Mesial temporal sclerosis: historical background and an overview from a modern perspective. In Epilepsy Surgery, ed. H. Lüders, pp. 689–703, New York: Raven Press
Gloor, P. (1992) Role of the amygdala in temporal lobe epilepsy. In The Amygdala: Neurobiological Aspects of Emotion, Memory, and Mental Dysfunction, ed. J. P. Aggleton, pp. 505–538, New York: Wiley-Liss
Gloor, P. (1997) The Temporal Lobe and Limbic System. New York: Oxford University Press
Gloor, P. and Fariello, R. G. (1988) Generalized epilepsy: some of its cellular mechanisms differ from those of focal epilepsy. Trends in Neuroscience 11: 63–68CrossRefGoogle ScholarPubMed
Gloor, P., Ball, G. and Schaul, N. (1977) Brain lesions that produce delta waves. Neurology 27: 326–333CrossRefGoogle ScholarPubMed
Gloor, P., Olivier, A., Quesney, L. F., Anderman, F. and Horowitz, S. (1982) The role of the limbic system in experiential phenomena of temporal lobe epilepsy. Annals of Neurology 12: 129–144CrossRefGoogle ScholarPubMed
Gloor, P., Avoli, M. and Kostopoulos, G. (1990) Thalamocortical relationships in generalized epilepsy with bilaterally synchronous spike-and-wave discharges. In Generalized Epilepsies, ed. M. Avoli, P. Gloor, G. Kostopoulos and R. Naquet, pp. 190–212, Boston: Birkhäuser
Goff, W. R., Allison, T., Shapiro, A. and Rosner, B. S. (1966) Cerebral somatosensory responses evoked during sleep in man. Electroencephalography and Clinical Neurophysiology 21: 1–9CrossRefGoogle ScholarPubMed
Gökyigit, A. and Caliskan, A. (1995) Diffuse spike-wave seizures of 9–year duration without behavioral change or intellectual decline. Epilepsia 36: 210–213CrossRefGoogle ScholarPubMed
Goldensohn, E. S. and Purpura, D. P. (1963) Intracellular potentials of cortical neurons during focal epileptogenic discharges. Science 139: 840–842CrossRefGoogle ScholarPubMed
Goldman-Rakic, P. S. (1987) Circuitry of the prefrontal cortex and the regulation of behavior by representational memory. In Handbook of Physiology (vol. V, The Nervous System), ed. F. Plum and V. B. Mountcastle, pp. 373–417, Bethesda: American Physiological Society
Goldman-Rakic, P. S. (1988) Changing concepts of cortical connectivity: parallel distributed cortical networks. In Neurobiology of Neocortex, ed. P. Kakic and W. Singer, pp. 177–202, New York: Wiley
Goldring, N. L., Jung, H. Y., Mickus, T. and Spruston, N. (1999) Dendritic calcium spikes initiation and repolarization are controlled by distinct potassium channel subtypes in CA1 pyramidal neurons. Journal of Neuroscience 19: 8789–8798CrossRefGoogle Scholar
Goldring, S., Edwards, I., Harding, G. W. and Bernardo, K. L. (1992) Results of anterior temporal lobectomy that spares the amygdala in patients with complex partial seizures. Journal of Neurosurgery 77: 185–193CrossRefGoogle ScholarPubMed
Golomb, D., Wang, X. J. and Rinzel, J. (1994) Synchronization properties of spindle oscillations in a thalamic reticular nucleus model. Journal of Neurophysiology 72: 1109–1126CrossRefGoogle Scholar
Golshani, P. and Jones, E. G. (1999) Synchronized paroxysmal activity in the developing thalamocortical network mediated by corticothalamic projections and “silent” synapses. Journal of Neuroscience 19: 2865–2875CrossRefGoogle ScholarPubMed
Golshani, P., Liu, X. B. and Jones, E. G. (2001) Differences in quantal amplitude reflect GluR4–subunit number at corticothalamic synapses on two populations of thalamic neurons. Proceedings of the National Academy of Sciences of the USA 98: 4172–4177CrossRefGoogle ScholarPubMed
Gomez, M. R. and Westmoreland, B. F. (1987) Absence seizures. In Clinical Medicine and the Nervous System: Epilepsy – Electroclinical Syndromes, ed. H. Lüders and R. P. Lesser, pp. 105–129, New York: Springer
Gonchar, Y. and Burkhalter, A. (1997) Three distinct families of GABAergic neurons in rat visual cortex. Cerebral Cortex 7: 347–358CrossRefGoogle ScholarPubMed
Gotman, J. and Marciani, M. G. (1985) Electroencephalographic spiking activity, drug levels and seizure occurrence in epileptic patients. Annals of Neurology 17: 597–603CrossRefGoogle ScholarPubMed
Gottselig, J. M., Bassetti, C. L. and Achermann, P. (2002) Power and coherence of sleep spindle frequency activity following hemispheric strokes. Brain 125: 373–383CrossRefGoogle Scholar
Gowers, W. R. (1885) Epilepsy and Other Chronic Convulsive Disorders. New York: William Wood
Grace, A. A. and Bunney, B. S. (1979) Paradoxical GABA excitation of nigral dopaminergic cells: indirect mediation through reticulata inhibitory neurons. European Journal of Pharmacology 59: 211–218CrossRefGoogle ScholarPubMed
Grace, A. A. and Bunney, B. S. (1985) Opposing effects of striatonigral feed-back pathways on midbrain dopamine cell activity. Brain Research 333: 271–284CrossRefGoogle Scholar
Gray, C. M. and McCormick, D. A. (1996) Chattering cells: superficial pyramidal neurons contributing to the generation of synchronous oscillations in the visual cortex. Science 274: 109–113CrossRefGoogle ScholarPubMed
Gray, C. M., König, P., Engel, A. K. and Singer, W. (1989) Stimulus-specific neuronal oscillations in cat visual cortex exhibit inter-columnar synchronization which reflects global stimulus properties. Nature 338: 334–337CrossRefGoogle Scholar
Gray, C. M., Engel, A. K., König, P. and Singer, W. (1990) Stimulus-dependent neuronal oscillations in cat visual cortex: receptive field properties and feature dependence. European Journal of Neuroscience 2: 607–619CrossRefGoogle ScholarPubMed
Gray, E. G. (1959) Axo-somatic and axo-dendritic synapses of the cerebral cortex: an electron microscope study. Journal of Anatomy 93: 420–433Google Scholar
Graybiel, A. M. and Elde, R. P. (1983) Somatostatin-like immunoreactivity characterizes neurons of the nucleus reticularis thalami in the cat and monkey. Journal of Neuroscience 3: 1303–1321CrossRefGoogle ScholarPubMed
Graybiel, A. M. and Ragsdale, C. W. (1979) Fiber connections of the basal ganglia. In Development and Chemical Specificity of Neurons, ed. M. Cuénod, G. W. Kreutzberg and F. E. Bloom, pp. 239–283, Amsterdam: Elsevier
Green, J. D. (1969) The hippocampus. Physiological Reviews 44: 561–608CrossRefGoogle Scholar
Greene, R. W., Haas, H. L. and McCarley, R. W. (1986) A low-threshold calcium spike mediates firing pattern alterations in pontine reticular neurons. Science 234: 738–740CrossRefGoogle ScholarPubMed
Grenier, F., Timofeev, I. and Steriade, M. (1998) Leading role of thalamic over cortical neurons during postinhibitory rebound excitation. Proceedings of National Academy of Sciences of the USA 95: 13929–13934CrossRefGoogle ScholarPubMed
Grenier, F., Timofeev, I. and Steriade, M. (2001) Focal synchronization of ripples (80–200 Hz) in neocortex and their neuronal correlates. Journal of Neurophysiology 86: 1884–1898CrossRefGoogle ScholarPubMed
Grenier, F., Timofeev, I. and Steriade, M. (2002) Thalamic short-term plasticity and its impact on the neocortex. Thalamus and Related Systems 1: 331–340Google Scholar
Grenier, F., Timofeev, I. and Steriade, M. (2003) Neocortical ripples (80–200 Hz) and their role in initiation of electrical seizures. Journal of Neurophysiology, in pressGoogle Scholar
Grill, W. M. and McIntyre, C. C. (2001) Extracellular excitation of central neurons: implications for the mechanisms of deep brain stimulation. Thalamus and Related Systems 1: 269–277Google Scholar
Gritti, I., Mainville, L. and Jones, B. E. (1994) Projections of GABAergic and cholinergic basal forebrain and GABAergic preoptic-anterior hypothalamic neurons to the posterior lateral hypothalamus of the rat. Journal of Comparative Neurology 339: 251–268CrossRefGoogle ScholarPubMed
Grossman, R. G. and Hampton, T. (1968) Depolarization of cortical glial cells during electrical activity. Brain Research 11: 316–324CrossRefGoogle Scholar
Grüner, J. E., Hirsch, J. C. and Sotelo, C. (1974) Ultrastructural features of the isolated suprasylvian gyrus in the cat. Journal of Comparative Neurology 154: 1–28CrossRefGoogle ScholarPubMed
Guberman, A., Gloor, P. and Sherwin, A. L. (1975) Response of generalized epilepsy in the cat to ethosuximide and diphenylhydantoin. Neurology 25: 758–764CrossRefGoogle ScholarPubMed
Gulyas, A. I., Miles, R., Sok, A., Toth, K., Tamamaki, N. and Freund, T. F. (1993) Hippocampal pyramidal cells excite inhibitory neurons through a single release site. Nature 366: 683–687CrossRefGoogle ScholarPubMed
Gupta, A., Wang, Y. and Markram, H. (2000) Organizing principles for a diversity of GABAergic interneurons and synapses in the neocortex. Science 287: 273–278CrossRefGoogle ScholarPubMed
Gutfreund, Y., Yarom, Y. and Segev, I. (1995) Subthreshold oscillations and resonant frequency in guinea-pig cortical neurons: physiology and modelling. Journal of Physiology (London) 483: 621–640CrossRefGoogle ScholarPubMed
Gutnick, M. J. and Mody, I. (eds.) (1995) The Cortical Neuron. Oxford: Oxford University Press
Gutnick, M. J., Heinemann, U. and Prince, D. A. (1979) Stimulus induced and seizure related changes in extracellular potassium concentration in cat thalamus (VPL). Electroencephalography and Clinical Neurophysiology 47: 329–344CrossRefGoogle Scholar
Gutnick, M. J., Connors, B. W. and Prince, D. A. (1982) Mechanisms of neocortical epileptogenesis in vitro. Journal of Neurophysiology 48: 1321–1335CrossRefGoogle ScholarPubMed
Gutnick, M. J., Amitai, Y. and Barkai, E. (1992) Chronic models of cortical epilepsy: experimental manipulations leading to long-term reorganization of local neocortical circuitry. In Molecular Neurobiology of Epilepsy, ed. J. Engel Jr., C. Wasterlain, E. A. Cavalheiro, U. Heinemann and G. Avanzini, pp. 221–229, Amsterdam: Elsevier
Haas, H. L. and Greene, R. W. (1986) Effects of histamine on hippocampal pyramidal cells of the rat in vitro. Experimental Brain Research 62: 123–130CrossRefGoogle ScholarPubMed
Halasz, P. (1991) Runs of rapid spikes in sleep: a characteristic EEG expression of generalized malignant epileptic encephalopathies. A conceptual review with new pharmacological data. Epilepsy Research (Suppl.) 2: 49–71Google ScholarPubMed
Halgren, E., Smith, M. E. and Stapleton, J. M. (1985) Hippocampal field potentials evoked by repeated vs nonrepeated words. In Electrical Activity of the Archicortex, ed. G. Buzsáki and C. H. Vanderwolf, pp. 67–81, Budapest: Akademiai Kiadó
Hallanger, A. E. and Wainer, B. H. (1988) Ultrastructure of ChAT-immunoreactive synaptic terminals in the thalamic reticular nucleus of the rat. Journal of Comparative Neurology 278: 486–497CrossRefGoogle ScholarPubMed
Hallanger, A. E., Levey, A. I., Lee, H. J., Rye, D. B. and Wainer, B. H. (1987) The origins of cholinergic and other subcortical afferents to the thalamus in the rat. Journal of Comparative Neurology 262: 105–124CrossRefGoogle ScholarPubMed
Halliwell, J. V. (1986) M-current in human neocortical neurones. Neuroscience Letters 67: 1–6CrossRefGoogle ScholarPubMed
Halpern, L. M. (1972) Chronically isolated aggregates of mammalian cerebral cortical neurons studied in situ. In Experimental Models of Epilepsy, ed. D. P. Purpura, J. F. Penry, D. B. Tower, D. M. Woodbury and R. D. Walter, pp. 197–221, New York: Raven
Han, Z. S., Buhl, E. H., Lorinczi, Z. and Somogyi, P. (1993) A high degree of spatial selectivity in the axonal and dendritic domains of physiologically identified local-circuit neurons in the dentate gyrus of the rat hippocampus. European Journal of Neuroscience 5: 395–410CrossRefGoogle ScholarPubMed
Hansen, J. C. and Hillyard, S. (1980) Endogenous brain potentials associated with auditory selective attention. Electroencephalography and Clinical Neurophysiology 49: 277–290CrossRefGoogle Scholar
Harding, B. N. and Powell, T. P. S. (1972) An electron microscopic study of afferent fibre connexions to the monkey thalamus from motor cortex and basal ganglia. Journal of Anatomy 111: 503–504Google ScholarPubMed
Haulica, I., Ababei, L., Branisteanu, D. and Topoliceanu, F. (1973) Preliminary data on the possible hypnogenic role of adenosine. Journal of Neurochemistry 21: 1019–1020CrossRefGoogle ScholarPubMed
Hayaishi, O. (1988) Sleep-wake regulation by prostaglandin D2 and E2. Journal of Biological Chemistry 263: 14593–14596Google ScholarPubMed
Heath, R. (1954) Studies in Schizophrenia: A Multidisciplinary Approach to Mind-Brain Relationships. Cambridge, MA: Harvard University Press
Heilman, K. M., Bowers, D., Coslett, H. B., Whelan, H. and Watson, R. T. (1985) Direction hypokinesia: prolonged reaction times for leftward movements in patients with right hemisphere lesions and neglect. Neurology 35: 855–860CrossRefGoogle Scholar
Heinemann, U. and Pumain, R. (1981) Effects of tetrodotoxin on changes in extracellular free calcium induced by repetitive electrical stimulation and iontophoretic application of excitatory amino acids in the sensorimotor cortex of cats. Neuroscience Letters 21: 87–91CrossRefGoogle Scholar
Heinemann, U., Gabriel, S., Jauch, R., Schulze, K., Kivi, A., Eilers, A., Kovacs, R. and Lehmann, T. N. (2000) Alterations of glial cell function in temporal lobe epilepsy. Epilepsia 41: S185–S189CrossRefGoogle ScholarPubMed
Heller, H. C., Glotzbach, S., Grahn, D. and Radeke, C. (1988) Sleep-dependent changes in the thermoregulatory system. In Clinical Physiology of Sleep, ed. R. Lydic and J. F. Biebuyck, pp. 145–169, Bethesda: American Physiological Society
Hennevin, E., Hars, B., Maho, C. and Bloch, V. (1995) Processing of learned information in paradoxical sleep: relevance for memory. Behavioral and Brain Research 69: 125–135CrossRefGoogle ScholarPubMed
Herculano-Houzel, S., Munk, M. H. J., Neuenschwander, S. and Singer, W. (1999) Precisely synchronized oscillatory firing patterns require electroencephalographic activation. Journal of Neuroscience 19: 3992–4010CrossRefGoogle ScholarPubMed
Herkenham, M. (1987) Mismatches between neurotransmitter and receptor localization in brain: observations and implications. Neuroscience 23: 1–38CrossRefGoogle Scholar
Hernández-Cruz, A. and Pape, H. C. (1989) Identification of two calcium currents in acutely dissociated neurons from the rat lateral geniculate nucleus. Journal of Neurophysiology 61: 1270–1283CrossRefGoogle ScholarPubMed
Hess, G. and Gustafsson, B. (1990) Changes in field excitatory postsynaptic potential shape induced by tetanization in the CA1 region of the guinea-pig hippocampal slice. Neuroscience 37: 61–69CrossRefGoogle ScholarPubMed
Hess, W. R. (1944) Das Schlafsyndrom als Folge dienzephaler Reizung. Helvetica Physiologica et Pharmacologica Acta 2: 305–344Google Scholar
Hestrin, S. and Armstrong, W. E. (1996) Morphology and physiology of cortical neurons in layer I. Journal of Neuroscience 16: 5290–5300CrossRefGoogle ScholarPubMed
Hikosaka, O. and Wurtz, R. H. (1983) Visual and oculomotor function of monkey substantia nigra pars reticulata. IV: relation of substantia nigra to superior colliculus. Journal of Neurophysiology 49: 1285–1301CrossRefGoogle ScholarPubMed
Hille, B. (1992) Ionic Channels of Excitable Membranes. Sunderland, MA: Sinauer
Hirsch, J. C. and Burnod, Y. (1987) A synaptically evoked late hyperpolarization in the rat dorsolateral geniculate neurons in vitro. Neuroscience 23: 457–468CrossRefGoogle ScholarPubMed
Hirsch, J. C., Fourment, A. and Marc, M. E. (1983) Sleep-related variations of membrane potential in the lateral geniculate body relay neurons of the cat. Brain Research 259: 308–312CrossRefGoogle ScholarPubMed
Hirsch, J. C., Quesada, O., Esclapez, M., Gozlan, H., Ben-Ari, Y. and Bernard, C. L. (1996) Enhanced NMDAR-dependent epileptiform activity is controlled by oxidizing agents in a chronic model of temporal lobe epilepsy. Journal of Neurophysiology 76: 4185–4189CrossRefGoogle Scholar
Hobson, J. A. and Pace-Schott, E. F. (2002) The cognitive neuroscience of sleep: neuronal systems, consciousness and learning. Nature Reviews Neuroscience 3: 679–693CrossRefGoogle Scholar
Hobson, J. A., McCarley, R. W. and Wyzinski, P. W. (1975) Sleep cycle oscillation: reciprocal discharge by two brain stem neuronal groups. Science 189: 55–58CrossRefGoogle ScholarPubMed
Hobson, J. A., Pace-Schott, E. and Stickgold, R. (2000) Dreaming and the brain: toward a cognitive neuroscience of conscious states. Brain and Behavioral Sciences 23: 793–842CrossRefGoogle Scholar
Hoffman, D. A., Magee, J. C., Colbert, C. M. and Johnston, D. (1997) K+ channel regulation of signal propagation in dendrites of hippocampal pyramidal neurons. Nature 387: 869–875CrossRefGoogle ScholarPubMed
Hoffman, S. N., Salin, P. A. and Prince, D. A. (1994) Chronic neocortical epileptogenesis in vitro. Journal of Neurophysiology 71: 1762–1772CrossRefGoogle ScholarPubMed
Hoffman, W. H. and Haberly, L. B. (1991) Bursting induced epileptiform EPSPs in slices of piriform cortex are generated by deep cells. Journal of Neuroscience 11: 2021–2031CrossRefGoogle ScholarPubMed
Hofle, N., Paus, T., Reutens, D., Fiset, P., Gotman, J., Evans, A. C. and Jones, B. E. (1997) Regional cerebral blood flow changes as a function of delta and spindle activity during slow wave sleep in humans. Journal of Neuroscience 17: 4800–4808CrossRefGoogle ScholarPubMed
Homma, Y., Skinner, R. D. and Garcia-Rill, E. (2002) Effects of pedunculopontine nucleus (PPN) stimulation on caudal pontine reticular formation (PnC) neurons in vitro. Journal of Neurophysiology 87: 3033–3047CrossRefGoogle ScholarPubMed
Honda, T. and Semba, K. (1995) An ultrastructural study of cholinergic and non-cholinergic neurons in the laterodorsal and pedunculopontine tegmental nuclei in the rat. Neuroscience 68: 837–853CrossRefGoogle ScholarPubMed
Hoogland, P. V., Wouterlood, F. G., Welker, E. and Loos, H. (1991) Ultrastructure of giant and small thalamic terminals of cortical origin: a study of the projections from the barrel cortex in mice using Phaseolus vulgaris-leucoagglutinin (PHA-L). Experimental Brain Research 87: 159–172CrossRefGoogle Scholar
Horne, J. (1988) Why We Sleep. Oxford: Oxford University Press
Hosford, D. A., Clark, S., Cao, Z., Wilson, W. A. Jr., Lin, F. H., Morrisett, R. A. and Huin, A. (1992) The role of GABAB receptor activation in absence seizures of lethargic (Ih/Ih) mice. Science 257: 398–401CrossRefGoogle Scholar
Hosford, D. A., Caddick, S. J. and Lin, F. H. (1997) Generalized epilepsies: emerging insights into cellular and genetic mechanisms. Current Opinion in Neurology 10: 115–120CrossRefGoogle ScholarPubMed
Houser, C. R. and Esclapez, M. (1996) Vulnerability and plasticity of the GABA system in the pilocarpine model of spontaneous recurrent seizures. Epilepsy Research 26: 207–218CrossRefGoogle ScholarPubMed
Houser, C. R., Vaughan, J. E., Barber, R. P. and Roberts, E. (1980) GABA neurons are the major cell type of the nucleus reticularis thalami. Brain Research 200: 341–354CrossRefGoogle ScholarPubMed
Houser, C. R., Miyashiro, J. E., Swartz, B. E., Walsh, G. O., Rich, J. R. and Delgado-Escueta, A. V. (1990) Altered patterns of dynorphin immunoreactivity suggest mossy fiber reorganization in human hippocampal epilepsy. Journal of Neuroscience 10: 267–282CrossRefGoogle ScholarPubMed
Houweling, A., Bazhenov, M., Timofeev, I., Steriade, M. and Sejnowski, T. J. (1999) Cortical and thalamic components of augmenting responses: a modelling study. Neurocomputing 26–27: 735–742CrossRefGoogle Scholar
Houweling, A. R., Bazhenov, M., Timofeev, I., Grenier, F., Steriade, M. and Sejnowski, T. J. (2002) Frequency-selective augmenting responses by short-term synaptic depression in cat neocortex. Journal of Physiology (London) 542: 599–617CrossRefGoogle ScholarPubMed
Hu, B., Bouhassira, D., Steriade, M. and Deschênes, M. (1988) The blockage of ponto-geniculo-occipital waves in the cat lateral geniculate nucleus by nicotinic antagonists. Brain Research 473: 394–397CrossRefGoogle ScholarPubMed
Hu, B., Steriade, M. and Deschênes, M. (1989a) The effects of peribrachial stimulation on reticular thalamic neurons: the blockage of spindle waves. Neuroscience 31: 1–12CrossRefGoogle Scholar
Hu, B., Steriade, M. and Deschênes, M. (1989b) The effects of brainstem peribrachial stimulation on neurons of the lateral geniculate nucleus. Neuroscience 31: 13–24CrossRefGoogle Scholar
Hu, B., Steriade, M. and Deschênes, M. (1989c) The cellular mechanism of thalamic ponto-geniculo-occipital waves. Neuroscience 31: 25–35CrossRefGoogle Scholar
Hubel, D. H. (1960) Single unit activity in lateral geniculate body and optic tract of unrestrained cats. Journal of Physiology (London) 150: 91–104CrossRefGoogle ScholarPubMed
Hudson, L. P., Munoz, D. G., Miller, L., McLahlan, R. S., Girvin, J. P. and Blume, W. T. (1993) Amygdaloid sclerosis in temporal lobe epilepsy. Annals of Neurology 33: 622–631CrossRefGoogle ScholarPubMed
Hughes, J. R. (1980) Two forms of the 6/sec spike and wave complex. Electroencephalography and Clinical Neurophysiology 48: 535–550CrossRefGoogle ScholarPubMed
Huguenard, J. R. (1996) Low-threshold calcium currents in central nervous system neurons. Annual Review of Physiology 58: 329–348CrossRefGoogle ScholarPubMed
Huguenard, J. R. (1999) Neuronal circuitry of thalamocortical epilepsy and mechanisms of antiabsence drug action. Advances in Neurology 79: 991–999Google ScholarPubMed
Huguenard, J. R. and Prince, D. A. (1992) A novel T-type current underlies prolonged Ca2+-dependent burst firing in GABAergic neurons of rat thalamic reticular nucleus. Journal of Neuroscience 12: 3804–3817CrossRefGoogle Scholar
Huguenard, J. R. and Prince, D. A. (1994a) Clonazepam suppresses GABAB-mediated inhibition in thalamic relay neurons through effects in nucleus reticularis. Journal of Neurophysiology 71: 2576–2581CrossRefGoogle Scholar
Huguenard, J. R. and Prince, D. A. (1994b) Intrathalamic rhythmicity studied in vitro: nominal T current modulation causes robust anti-oscillatory effects. Journal of Neuroscience 14: 5485–5502CrossRefGoogle Scholar
Huguenard, J. R., Chung, J. M. and Prince, D. A. (1996) Excitability changes in thalamic and neocortical neurons after injury. In Progressive Nature of Epileptogenesis (Epilepsy Research, Suppl. 12), ed. U. Heinemann, pp. 129–135, Amsterdam: Elsevier
Huntsman, M. M. and Huguenard, J. R. (2000) Nucleus-specific differences in GABAA receptor mediated inhibition are enhanced during thalamic development. Journal of Neurophysiology 83: 350–358CrossRefGoogle Scholar
Huntsman, M. M., Porcello, D. M., Homanics, G. E., DeLorey, T. M. and Huguenard, J. R. (1999) Reciprocal inhibitory connections and network synchrony in the mammalian thalamus. Science 283: 541–543CrossRefGoogle ScholarPubMed
IFSECN (1974) A glossary of terms most commonly used by clinical electroencephalographers. Electroencephalography and Clinical Neurophysiology 37: 538–548CrossRef
Imig, T. J. and Reale, R. A. (1981) Ipsilateral corticocortical projections related to binaural columns in cat primary auditory cortex. Journal of Comparative Neurology 203: 1–14CrossRefGoogle ScholarPubMed
Immon, H., Ito, K., Dauphin, L. and McCarley, R. W. (1996) Electrical stimulation of the cholinergic laterodorsal tegmental nucleus elicits scopolamine-sensitive excitatory postsynaptic potentials in medial pontine reticular formation neurons. Neuroscience 74: 393–401CrossRefGoogle Scholar
Inglis, W. L. and Semba, K. (1996) Colocalization of ionotropic glutamate receptor subunits with NADPH-diaphorase-containing neurons in the rat mesopontine tegmentum. Journal of Comparative Neurology 368: 17–323.0.CO;2-N>CrossRefGoogle ScholarPubMed
Ingvar, D. H., Sjölund, B. and Ardo, A. (1976) Correlation between ECG frequency, cerebral oxygen uptake and blood flow. Electroencephalography and Clinical Neurophysiology 41: 268–276CrossRefGoogle Scholar
Innocenti, B., Parpura, V. and Haydon, P. G. (2000) Imaging extracellular waves of glutamate during calcium signaling in cultured astrocytes. Journal of Neuroscience 20: 1800–1808CrossRefGoogle ScholarPubMed
Isokawa, M. and Levesque, M. F. (1991) Increased NMDA responses and dendritic degeneration in human epileptic hippocampal neurons in slices. Neuroscience Letters 132: 212–216CrossRefGoogle ScholarPubMed
Ito, H., Halldin, C. and Farde, L. (1999) Localization of 5–HT1A receptors in the living human brain using [carbonyl-11C]WAY-100635: PET with anatomic standardization technique. Journal of Nuclear Medicine 40: 102–109Google Scholar
Ito, K. and McCarley, R. W. (1984) Alterations in membrane potential and excitability of cat medial pontine reticular formation neurons during changes in naturally occurring sleep-wake states. Brain Research 292: 169–175CrossRefGoogle ScholarPubMed
Ito, K., Yanagihara, M., Imon, L., Dauphin, L. and McCarley, R. W. (2002) Intracellular recordings of pontine medial gigantocellular tegmental field neurons in the naturally sleeping cat: behavioral state-related activity and soma size difference in order of recruitment. Neuroscience, 114: 23–37CrossRefGoogle ScholarPubMed
Iyer, K. S. and McCann, S. M. (1987) Delta sleep inducing peptide (DSIP) stimulates growth hormone (GH) release in the rat by hypothalamic and pituitary actions. Peptides 8: 45–48CrossRefGoogle ScholarPubMed
Jackson, J. H. (1864) Illustrations of diseases of the nervous system: clinical lectures and reports by the medical staff of the London hospital. London Hospital Reports 1: 337–387Google Scholar
Jackson, J. H. (1931) Selected Writings of John Hughlings Jackson (vol. 1, On Epilepsy and Epileptiform Convulsions), ed. J. Taylor, London: Hodder and Stroughton
Jacobs, K. M., Graber, K. D., Kharazia, V. N., Parada, I. and Prince, D. A. (2000) Postlesional epilepsy: the ultimate brain plasticity. Epilepsia 41 (Suppl. 6): S153–S161CrossRefGoogle ScholarPubMed
Jacobsen, R. B., Uhlrich, D. and Huguenard, J. R. (2001) GABAB and NMDA receptors contribute to spindle-like oscillations in rat thalamus in vitro. Journal of Neurophysiology 86: 1365–1375CrossRefGoogle Scholar
Jahnsen, H. and Llinás, R. (1984a) Electrophysiological properties of guinea-pig thalamic neurones: an in vitro study. Journal of Physiology (London) 349: 205–226CrossRefGoogle Scholar
Jahnsen, H. and Llinás, R. (1984b) Ionic basis for electroresponsiveness and oscillatory properties of guinea-pig thalamic neurones in vitro. Journal of Physiology (London) 349: 227–247CrossRefGoogle Scholar
Jandó, G., Carpi, D., Kandel, A., Urioste, R., Horvath, Z., Pierre, E., Vati, D., Vadasz, C. and Buzsáki, G. (1995) Spike-and-wave epilepsy in rats: sex differences and inheritance of physiological traits. Neuroscience 64: 301–317CrossRefGoogle ScholarPubMed
Jasper, H. H. (1949) Diffuse projection systems: the integrative action of the thalamic reticular system. Electroencephalography and Clinical Neurophysiology 1: 405–420CrossRefGoogle ScholarPubMed
Jasper, H. H. (1969) Mechanism of propagation. In Brain Mechanisms of the Epilepsies, ed. H. H. Jasper, A. A. Ward and A. Pope, pp. 421–438, Boston: Little, Brown
Jasper, H. H. (1975) Application of experimental models to human epilepsy. In Experimental Models of Epilepsy, ed. D. P. Purpura, J. K. Penry, D. B. Tower, D. M. Woodbury and R. D. Walter, pp. 585–601, New York: Raven Press
Jasper, H. H. (1981) Problems relating cellular or modular specificity to cognitive functions: importance of state-dependent reactions. In The Organization of the Cerebral Cortex, ed. F. O. Schmitt, F. G. Worden, G. Adelman and S. G. Dennis, pp. 375–393, Cambridge, MA: The MIT Press
Jasper, H. H. (1990) Historical introduction. In Generalized Epilepsies, ed. M. Avoli, P. Gloor, G. Kostopoulos and R. Naquet, pp. 1–15, Boston: Birkhäuser
Jasper, H. H. and Droogleever-Fortuyn, J. (1949) Experimental studies on the functional anatomy of petit-mal epilepsy. Research Publications of the Association of Nervous and Mental Diseases 26: 272–298Google Scholar
Jasper, H. H. and Hawkes, W. A. (1938) Electroencephalography. IV. Localization of seizure waves in epilepsy. Archives of Neurology (Chicago) 39: 885–901CrossRefGoogle Scholar
Jasper, H. H. and Kershman, J. (1941) Electroencephalographic classification of the epilepsies. Archives of Neurology and Psychiatry 45: 903–943CrossRefGoogle Scholar
Jasper, H. H. and Shagass, C. (1941) Conscious time judgments related to conditioned time intervals and voluntary control of the alpha rhythm. Journal of Experimental Psychology 28: 503–508CrossRefGoogle Scholar
Jasper, H. H. and Tessier, J. (1971) Acetylcholine liberation from cerebral cortex during paradoxical (REM) sleep. Science 172: 601–602CrossRefGoogle ScholarPubMed
Jasper, H. H., Pertuiset, B. and Flaniginn, H. (1951) EEG and cortical electrogram in patients with temporal lobe epilepsy. Archives of Neurology and Psychiatry (Chicago) 65: 272–290CrossRefGoogle Scholar
Jasper, H. H., Ward, A. A. Jr. and Pope, A. (eds) (1969) Basic Mechanisms of the Epilepsies. Boston: Little, Brown
Jeanmonod, D., Magnin, M., Morel, A., Siegemund, M., Cancro, A., Lanz, M., Llinás, R., Ribary, U., Kronberg, E., Schulman, J. and Zonenshayn, M. (2001) Thalamocortical dysrhythmia. II. Clinical and surgical aspects. Thalamus and Related Systems 1: 245–254Google Scholar
Jefferson, G. (1958) Reticular formation and clinical neurology. In Reticular Formation of the Brain, ed. H. H. Jasper, L. D. Proctor, R. S. Knighton, W. C. Noshay and R. T. Costello, pp. 729–738, Boston: Little, Brown
Jefferys, J. G. R. (1995) Nonsynaptic modulation of neuronal activity in the brain: electric currents and extracellular ions. Physiological Reviews 75: 689–723CrossRefGoogle ScholarPubMed
Jefferys, J. G. R. and Haas, H. L. (1982) Synchronized bursting of CA1 pyramidal cells in absence of synaptic transmission. Nature 300: 448–450CrossRefGoogle ScholarPubMed
Jensen, F. E., Holmes, G. L., Lombroso, C. T., Blume, H. K. and Firkusny, I. R. (1992) Age-dependent changes in long-term seizures susceptibility and behavior after hypoxia in rats. Epilepsia 33: 971–980CrossRefGoogle ScholarPubMed
Jensen, M. S. and Yaari, Y. (1997) Role of intrinsic burst firing, potassium accumulation, and electrical coupling in the elevated postassium model of hippocampal epilepsy. Journal of Neurophysiology 77: 1224–1233CrossRefGoogle Scholar
Jensen, M. S., Cherubini, E. and Yaari, Y. (1993) Opponent effects of potassium on GABAA-mediated postsynaptic inhibition in the rat hippocampus. Journal of Neurophysiology 69: 764–771CrossRefGoogle ScholarPubMed
Jensen, M. S., Azouz, R. and Yaari, Y. (1994) Variant firing patterns in rat hippocampal pyramidal cells modulated by extracellular potassium. Journal of Neurophysiology 71: 831–839CrossRefGoogle ScholarPubMed
Jensen, M. S., Azouz, R. and Yaari, Y. (1996) Spike afterdepolarization and burst generation in adult rat hippocampal CA1 pyramidal cells. Journal of Physiology (London) 492: 199–210CrossRefGoogle Scholar
Jobert, M., Poiseau, E., Jähnig, P., Schulz, H. and Kubicki, S. (1992) Topographical analysis of sleep spindle activity. Neuropsychobiology 26: 210–217CrossRefGoogle ScholarPubMed
Johnston, D. and Brown, T. H. (1981) Giant spike potential hypothesis for epileptiform activity. Science 211: 294–297CrossRefGoogle ScholarPubMed
Johnston, D. and Brown, T. H. (1984) The synaptic nature of the paroxysmal depolarizing shift in hippocampal neurons. Annals of Neurology 16 (Suppl.): S65–S75CrossRefGoogle ScholarPubMed
Johnston, D., Magee, J. C., Colbert, C. M. and Cristie, B. R. (1996) Active properties of neuronal dendrites. Annual Reviews of Neuroscience 19: 165–186CrossRefGoogle ScholarPubMed
Johnston, D., Hoffman, D. A., Magee, J. C., Poolos, N. P., Watanabe, S., Colbert, C. M. and Migliore, M. (2000) Dendritic potassium channels in hippocampal pyramidal neurons. Journal of Physiology (London) 525: 75–81CrossRefGoogle ScholarPubMed
Jones, B. E. (1995) Reticular formation: cytoarchitecture, transmitters, and projections. In The Rat Nervous System, 2nd edn., ed. G. Paxinos, pp. 155–171, New York: Academic
Jones, B. E. (2000) Basic mechanisms of sleep-wake states. In Principles and Practice of Sleep Medicine, ed. M. H. Kryger, T. Toth and W. C. Dement, pp. 134–154, Philadelphia: Saunders
Jones, E. G. (1975) Varieties and distribution of non-pyramidal cells in the somatic sensory cortex of the squirrel monkey. Journal of Comparative Neurology 160: 205–268CrossRefGoogle ScholarPubMed
Jones, E. G. (1985) The Thalamus. New York: Plenum
Jones, E. G. (1995) Overview: basic elements of the cortical network. In The Cortical Neuron, ed. M. J. Gutnick and I. Mody, pp. 111–122, New York: Oxford University Press
Jones, E. G. (1998) What are local circuits? In Neurobiology of Neocortex, ed. P. Rakic and W. Singer, pp. 137–152, New York: Wiley
Jones, E. G. (2000) Cortical and subcortical contributions to activity-dependent plasticity in primate somatosensory cortex. Annual Reviews of Neuroscience 23: 1–37CrossRefGoogle ScholarPubMed
Jones, E. G. (2001) The thalamic matrix and thalamocortical synchrony. Trends in Neurosciences 24: 595–601CrossRefGoogle ScholarPubMed
Jones, E. G. and Powell, T. P. S. (1969) An electron microscopic study of the mode of transmission of cortico-thalamic fibres within the sensory relay nuclei of the thalamus. Proceedings of the Royal Society of London (Series B) 172: 173–185CrossRefGoogle Scholar
Jones, E. G., Coulter, J. D. and Hendry, S. H. C. (1978) Intracortical connectivity of architectonic fields in somatic sensory, motor and parietal cortex of monkeys. Journal of Comparative Neurology 181: 291–348CrossRefGoogle ScholarPubMed
Jones, M. S. and Barth, D. S. (1999) Spatiotemporal organization of fast (>200 Hz) electrical oscillations in rat vibrissa/barrel cortex. Journal of Neurophysiology 82: 1599–1609CrossRefGoogle ScholarPubMed
Jones, M. S., MacDonald, K. D., Choi, B., Dudek, F. E. and Barth, D. S. (2000) Intracellular correlates of fast (>200 Hz) electrical oscillations in rat somatosensory cortex. Journal of Neurophysiology 84: 1505–1518CrossRefGoogle ScholarPubMed
Jones, R. S. and Heinemann, V. (1988) Synaptic and intrinsic responses of medial entorhinal cortical cells in normal and magnesium-free medium in vitro. Journal of Neurophysiology 59: 1476–1496CrossRefGoogle ScholarPubMed
Jouvet, M. (1962) Recherches sur les structures nerveuses et les mécanismes responsables des différentes phases du sommeil physiologique. Archives Italiennes de Biologie 100: 125–206Google Scholar
Jouvet, M. (1965) Paradoxical sleep – a study of its nature and mechanisms. Progress in Brain Research 18: 20–57CrossRefGoogle ScholarPubMed
Jouvet, M. (1972) The role of monoamines and acetylcholine-containing neurons in the regulation of the sleep-waking cycle. Ergebnisse der Physiologie 64: 166–307Google ScholarPubMed
Jouvet, M. (1986) Programmation génétique itérative et sommeil paradoxal. Confrontations Psychiatriques 27: 153–181Google Scholar
Jouvet, M. (1988) The regulation of paradoxical sleep by the hypothalamo-hypophysis. Archives Italiennes de Biologie 126: 259–274Google ScholarPubMed
Jouvet, M. (1992) Le Château des Songes. Paris: Odile Jacob
Jouvet, M. (1999) The Paradox of Sleep. Cambridge, MA: The MIT Press
Jouvet, M. and Michel, F. (1959) Corrélations électromyographiques du sommeil chez le chat décortiqué et mésencéphalique chronique. Comptes Rendus de la Société de Biologie (Paris) 153: 422–425Google Scholar
Jouvet, M., Michel, F. and Courjon, J. (1959) Sur un stade d'activité électrique cérébrale rapide au cours du sommeil physiologique. Comptes Rendus de la Société de Biologie (Paris) 153: 1024–1028Google Scholar
Jouvet-Mounier, D., Astic, L. and Lacote, D. (1970) Ontogenesis of the states of sleep in rat, cat, and guinea-pig during the first postnatal month. Developmental Psychobiology 2: 216–239CrossRefGoogle ScholarPubMed
Jung, R. (1962) Blocking of petit-mal attacks by sensory arousal and inhibition of attacks by an active change in attention during the epileptic aura. Epilepsia 3: 435–437CrossRefGoogle Scholar
Kammermeier, P. J. and Jones, S. W. (1997) High-voltage-activated calcium currents in neurons acutely isolated from the ventrobasal nucleus of the rat thalamus. Journal of Neurophysiology 77: 465–475CrossRefGoogle ScholarPubMed
Kamondi, A., Williams, J. A., Hutcheon, B. and Reiner, P. B. (1992) Membrane properties of mesopontine cholinergic neurons studied with the whole-cell patch-clamp technique: implications for behavioral state control. Journal of Neurophysiology 68: 1359–1372CrossRefGoogle ScholarPubMed
Kamondi, A., Acsády, L. and Buzsáki, G. (1998) Dendritic spikes are enhanced by cooperative network activity in the intact hippocampus. Journal of Neuroscience 18: 3919–3928CrossRefGoogle ScholarPubMed
Kamphuis, W., Huisman, E., Dreijer, A. M., Ghijsen, W. E., Verhage, M. and Lopes da Silva, F. H. (1990) Kindling increases the K+-evoked Ca2+-dependent release of endogenous GABA in area CA1 of rat hippocampus. Brain Research 511: 63–70CrossRefGoogle ScholarPubMed
Kandel, A. and Buzsáki, G. (1997) Cellular-synaptic generation of sleep spindles, spike-and-wave discharges, and evoked thalamocortical responses in the neocortex of rat. Journal of Neuroscience 17: 6783–6797CrossRefGoogle ScholarPubMed
Kandel, E. R. and Spencer, W. A. (1961) Electrophysiology of hippocampal neurons. I. After-potentials and repetitive firing. Journal of Neurophysiology 24: 243–259CrossRefGoogle ScholarPubMed
Kandel, E. R., Spencer, W. A. and Brinley, F. J. Jr. (1961) Electrophysiology of hippocampal neurons. I. Sequential invasion and synaptic organization. Journal of Neurophysiology 24: 225–242CrossRefGoogle ScholarPubMed
Kang, J., Jiang, L., Goldman, S. A. and Nedergaard, M. (1998) Astrocyte-mediated potentiation of inhibitory synaptic transmission. Nature Neuroscience 1: 683–692CrossRefGoogle ScholarPubMed
Kang, Y. and Kayano, F. (1994) Electrophysiological and morphological characteristics of layer VI pyramidal cells in the cat motor cortex. Journal of Neurophysiology 72: 578–591CrossRefGoogle ScholarPubMed
Kang, Y. and Kitai, S. T. (1990) Electrophysiological properties of pedunculopontine neurons and their postsynaptic responses following stimulation of substantia nigra reticulata. Brain Research 535: 79–95CrossRefGoogle ScholarPubMed
Kao, C. Q. and Coulter, D. A. (1997) Physiology and pharmacology of corticothalamic stimulation-evoked responses in rat somatosensory thalamic neurons in vitro. Journal of Neurophysiology 77: 2661–2676CrossRefGoogle ScholarPubMed
Kapas, L., Obal, F. Jr. and Krueger, J. M. (1993) Humoral regulation of sleep. International Reviews of Neurobiology 35: 131–160CrossRefGoogle Scholar
Karni, A., Tanne, D., Rubenstein, B. S., Askenasy, J. J. M. and Sagi, D. (1994) Dependence on REM sleep of overnight improvement of a perceptual skill. Science 265: 679–682CrossRefGoogle ScholarPubMed
Kato, N. (1990) Cortico-thalamo-cortical projection between visual cortices. Brain Research 509: 150–152CrossRefGoogle ScholarPubMed
Kawaguchi, Y. (1993) Groupings of nonpyramidal and pyramidal cells with specific physiological and morphological characteristics in rat frontal cortex. Journal of Neurophysiology 69: 416–431CrossRefGoogle ScholarPubMed
Kawaguchi, Y. (1995) Physiological subgroups of nonpyramidal cells with specific morphological characteristics in layers II/III of rat frontal cortex. Journal of Neuroscience 15: 2638–2655CrossRefGoogle Scholar
Kawaguchi, Y. and Kubota, Y. (1993) Correlation of physiological subgroups of nonpyramidal cells with parvalbumin- and calbindinD28k-immunoreactive neurons in layer V of rat frontal cortex. Journal of Neurophysiology 70: 387–396CrossRefGoogle Scholar
Kawaguchi, Y. and Kubota, Y. (1996) Physiological and morphological identification of somatostatin- or vasoactive intestinal polypeptide-containing cells among GABAergic cell subtypes in rat frontal cortex. Journal of Neuroscience 16: 2701–2715CrossRefGoogle ScholarPubMed
Kawaguchi, Y. and Kubota, Y. (1997) GABAergic cell subtypes and their synaptic connections in rat frontal cortex. Cerebral Cortex 7: 476–486CrossRefGoogle ScholarPubMed
Kayama, Y., Sugitani, M. and Iwama, K. (1982) Effects of locus coeruleus stimulation on neuronal activities of dorsal lateral geniculate nucleus and perigeniculate reticular nucleus of the rat. Neuroscience 7: 655–666CrossRefGoogle ScholarPubMed
Keifer, J. C., Baghdoyan, H. A., Becker, L. and Lydic, R. (1994) Halothane decreases pontine acetylcholine release and increases spindles. NeuroReport 5: 577–580CrossRefGoogle ScholarPubMed
Kellaway, P. (1985) Sleep and epilepsy. Epilepsia 26 (Suppl. 1): 15–30CrossRefGoogle ScholarPubMed
Kellaway, P. and Frost, J. D. Jr. (1983) Biorhythmic modulation of epileptic events. In Recent Advances in Epilepsy (vol. 1), ed. T. A. Pedley and B. S. Meldrum, pp. 139–154, London: Churchill-Livingstone
Kellaway, P., Crawley, J. W. and Kagawa, N. (1960) Paroxysmal pain and autonomic disturbances of cerebral origin: a specific electroclinical syndrome. Epilepsia 1: 466–483CrossRefGoogle Scholar
Kellaway, P., Hrachovy, R. A., Frost, J. D. Jr. and Zion, T. (1979) Precise characterization and quantification of infantile spasms. Annals of Neurology 6: 214–218CrossRefGoogle ScholarPubMed
Kellaway, P., Frost, J. D. Jr. and Crawley, J. W. (1980) Time modulation of spike-and-wave activity in generalized epilepsy. Annals of Neurology 8: 491–500CrossRefGoogle ScholarPubMed
Kellaway, P., Frost, J. D. Jr. and Crawley, J. W. (1990) The relations between sleep spindles and spike-and-wave bursts in human epilepsy. In Generalized Epilepsy, ed. M. Avoli, P. Gloor, G. Kostopoulos and R. Naquet, pp. 36–48, Boston: Birkhäuser
Keller, A. (1993) Intrinsic synaptic organization of the motor cortex. Cerebral Cortex 3: 43–51CrossRefGoogle ScholarPubMed
Kennedy, C., Gillin, J. C., Mendelson, W., Suda, S., Miyaoka, M., Ito, M., Nakamura, R. K., Storch, F. I., Pettigrew, K., Mishkin, M. and Sokoloff, L. (1982) Local cerebral glucose utilization in non-rapid eye movement sleep. Nature 297: 325–327CrossRefGoogle ScholarPubMed
Kettenmann, H. and Schachner, M. (1985) Pharmacological properties of γ-aminobutyric acid-, glutamate-, and aspartate-induced depolarizations in cultured astrocytes. Journal of Neuroscience 5: 3295–3301CrossRefGoogle ScholarPubMed
Khateb, A., Serafin, M. and Mühlethaler, M. (1989) Midbrain reticular neurones in vitro are sensitive to amines and opiates. Society of Neuroscience Abstracts 15: 451Google Scholar
Khateb, A., Serafin, M., Jones, B. E., Alonso, A. and Mühlethaler, M. (1991) Pharmacological study of basal forebrain neurons in guinea pig brain slices. Society for Neuroscience Abstracts 17: 881Google Scholar
Khateb, A., Fort, P., Alonso, A., Jones, B. E. and Mühlethaler, M. (1993) Pharmacological and immunohistochemical evidence for serotonergic modulation of cholinergic nucleus basalis neurons. European Journal of Neuroscience 5: 541–547CrossRefGoogle ScholarPubMed
Khazipov, R., Esclapez, M., Caillard, O., Bernard, C., Khalikov, I., Tyzio, R., Hirsch, J., Dzhala, V., Berger, B. and Ben-Ari, Y. (2001) Early development of neuronal activity in the primate hippocampus in utero. Journal of Neuroscience 21: 9770–9781CrossRefGoogle ScholarPubMed
Kia, H. K., Miquel, M. C., Brisorgeuil, M. J., Daval, G., Riad, M., Mestikawy, S., Hamon, M. and Verge, D. (1996) Immunocytochemical localization of serotonin 1A receptors in the rat central nervous system. Journal of Comparative Neurology 365: 289–3053.0.CO;2-1>CrossRefGoogle Scholar
Killam, K. F., Killam, E. K. and Naquet, R. (1967) An animal model of light sensitive epilepsy. Electroencephalography and Clinical Neurophysiology 22: 497–513CrossRefGoogle ScholarPubMed
Kim, D., Song, I., Keum, S., Lee, T., Jeong, M. J., Kim, S. S., McEnery, M. W. and Shin, H. S. (2001) Lack of the burst firing of thalamocortical relay neurons and resistance to absence seizures in mice lacking α1G T-type Ca2+ channels. Neuron 31: 35–45CrossRefGoogle Scholar
Kim, U. and McCormick, D. A. (1998) Functional and ionic properties of a slow afterhyperpolarization in ferret perigeniculate neurons in vitro. Journal of Neurophysiology 80: 1222–1235CrossRefGoogle ScholarPubMed
Kim, U., Bal, T. and McCormick, D. A. (1995) Spindle waves are propagating synchronized oscillations in the ferret LGNd in vitro. Journal of Neurophysiology 74: 1301–1323CrossRefGoogle ScholarPubMed
Kim, U., Sanchez-Vives, M. V. and McCormick, D. A. (1997) Functional dynamics of GABAergic inhibition in the thalamus. Science 278: 130–134CrossRefGoogle ScholarPubMed
Kinomura, S., Larsson, J., Gulyás, B. and Roland, P. (1996) Activation by attention of the human reticular formation and thalamic intralaminar nuclei. Science 271: 512–515CrossRefGoogle ScholarPubMed
Kita, Y. and Kitai, S. T. (1990) Electrophysiological properties of pedunculopontine neurons and their postsynaptic responses following stimulation of substantia nigra pars reticulata. Brain Research 535: 79–95Google Scholar
Kitsikis, A. and Steriade, M. (1981) Immediate behavioral effects of kainic acid injections into the midbrain reticular core. Behavioral Brain Research 3: 361–380CrossRefGoogle ScholarPubMed
Kleitman, N. (1963) Sleep and Wakefulness. Chicago: University of Chicago Press
Kleitman, N. (1993) Basic rest-activity cycle. In Encyclopedia of Sleep and Dreaming, ed. M. A. Carskadon, pp. 65–66, New York: Macmillan
Klink, R. and Alonso, A. (1997a) Muscarinic modulation of the oscillatory and repetitive firing properties of entorhinal cortex layer II neurons. Journal of Neurophysiology 77: 1813–1828CrossRefGoogle Scholar
Klink, R. and Alonso, A. (1997b) Ionic mechanisms of muscarinic depolarization in entorhinal cortex layer II neurons. Journal of Neurophysiology 77: 1829–1843CrossRefGoogle Scholar
Klüver, H. and Bucy, P. C. (1937) An analysis of certain effects of bilateral lobectomy in the rhesus monkey, with special reference to “psychic blindness”. Journal of Psychology 5: 33–54CrossRefGoogle Scholar
Knight, A. R. and Bowery, N. G. (1992) GABA receptors in rats with spontaneous generalized nonconvulsive epilepsy. Journal of Neural Transmission 35 (Suppl.): 189–196Google ScholarPubMed
Knowles, W. D. and Schwartzkroin, P. A. (1981) Local circuit synaptic interactions in hippocampal brain slices. Journal of Neuroscience 1: 318–322CrossRefGoogle ScholarPubMed
Kobayashi, K., Nishibayashi, N., Ohtsuka, Y., Oka, E. and Ohtahara, S. (1994) Epilepsy with electrical status epilepticus during slow sleep and secondary bilateral synchrony. Epilepsia 35: 1097–1103CrossRefGoogle ScholarPubMed
Konorski, J. (1967) Integrative Activity of the Brain. Chicago: University of Chicago Press
Kosaka, T., Kosaka, K., Hataguchi, Y., Nagatsu, I., Wu, J. Y., Ottersen, O. P., Storm-Mathisen, J. and Hama, K. (1987) Catecholaminergic neurons containing GABA-like and/or glutamic acid decarboxylase-like immunoreactivities in various brain regions of the rat. Experimental Brain Research 66: 191–201CrossRefGoogle ScholarPubMed
Kostopoulos, G. (1992) The tottering mouse: a critical review of its usefulness in the study of neuronal mechanisms underlying epilepsy. Journal of Neural Transmission 35 (Suppl.): 21–36Google Scholar
Kostopoulos, G. (2000) Spike-and-wave discharges of absence seizures as a transformation of sleep spindles: the continuing development of a hypothesis. Clinical Neurophysiology 111 (Suppl. 2): S27–S38CrossRefGoogle ScholarPubMed
Kotagal, P. (1995) Multifocal independent spike syndrome: relationship to hypsarrhthymia and the slow spike-wave (Lennox-Gastaut) syndrome. Clinical Electroencephalography 26: 23–29CrossRefGoogle ScholarPubMed
Kotila, M. and Waltimo, O. (1992) Epilepsy after stroke. Epilepsia 33: 495–498CrossRefGoogle ScholarPubMed
Koukkou, M. and Lehmann, D. (1968) EEG and memory storage in sleep experiments with humans. Electroencephalography and Clinical Neurophysiology 25: 455–462CrossRefGoogle ScholarPubMed
Kreindler, A. (1965) Experimental Epilepsy. Progress in Brain Research (vol. 19), Amsterdam: Elsevier
Kreindler, A. and Steriade, M. (1963) Functional differentiation within the amygdaloid complex inferred from peculiarities of afterdischarges. Electroencephalography and Clinical Neurophysiology 15: 811–826CrossRefGoogle Scholar
Kreindler, A. and Steriade, M. (1964) EEG patterns of arousal and sleep induced by stimulating various amygdaloid levels in the cat. Archives Italiennes de Biologie 102: 576–586Google ScholarPubMed
Kreindler, A., Zuckermann, E., Steriade, M. and Chimion, D. (1958) Electroclinical features of the convulsive fit induced experimentally through stimulation of the brain stem. Journal of Neurophysiology 21: 430–436CrossRefGoogle Scholar
Krnjević, K., Pumain, R. and Renaud, L. (1971) The mechanisms of excitation by acetylcholine in the cerebral cortex. Journal of Physiology (London) 215: 247–268CrossRefGoogle Scholar
Krueger, J. M. and Toth, L. A. (1994) Cytokines as regulators of sleep. Annals of New York Academy of Sciences 739: 299–310CrossRefGoogle Scholar
Krueger, J. M., Pappenheimer, J. R. and Karnovsky, M. L. (1982) Sleep-promoting effects of muramyl peptides. Proceedings of the National Academy of Sciences of the USA 79: 6102–6106CrossRefGoogle ScholarPubMed
Krueger, J. M., Walter, J., Karnovsky, M. L., Chedid, L., Choay, J. P., Lefrancier, P. and Lederer, E. (1984) Muramyl peptides. Variation of somnogenic activity with structure. Journal of Experimental Medicine 159: 68–76CrossRefGoogle ScholarPubMed
Krueger, J. M., Obal, F. Jr. and Fang, J. (1999) Humoral regulation of physiological sleep: cytokines and GHRH. Journal of Sleep Research 8 (Suppl. 1): 53–59CrossRefGoogle ScholarPubMed
Krushinsky, L. V. (1962) Study of pathophysiological mechanism of cerebral haemorrhages provoked by reflex epileptic seizures in rats. Epilepsia 3: 363–380CrossRefGoogle Scholar
Kudrimoti, H. S., Barnes, C. A. and McNaughton, B. L. (1999) Reactivation of hippocampal cell assemblies: effects of behavioral state, experience, and EEG dynamics. Journal of Neuroscience 19: 4090–4101CrossRefGoogle ScholarPubMed
Lacaille, J. C. and Schwartzkroin, P. A. (1988a) Stratum lacunosum-moleculare interneurons of hippocampal CA1 region. I. Intracellular response characteristics, synaptic responses and morphology. Neuroscience 8: 1400–1410CrossRefGoogle Scholar
Lacaille, J. C. and Schwartzkroin, P. A. (1988b) Stratum lacunosum-moleculare interneurons of hippocampal CA1 region. II. Intrasomatic and intradendritic recordings of local circuit synaptic interactions. Neuroscience 8: 1411–1424CrossRefGoogle Scholar
Lai, Y. Y., Clements, J. R. and Siegel, J. M. (1993) Glutamatergic and cholinergic projections to the pontine inhibitory area identified with horseradish peroxidase retrograde transport and immunohistochemistry. Journal of Comparative Neurology 336: 321–330CrossRefGoogle ScholarPubMed
Lampl, I., Reichova, I. and Ferster, D. (1999) Synchronous membrane potential fluctuations in neurons of the cat visual cortex. Neuron 22: 361–374CrossRefGoogle ScholarPubMed
Lancel, M., Riezen, H. and Glatt, A. (1992) The time course of σ activity and slow-wave activity during NREMS in cortical and thalamic EEG of the cat during baseline and after 12 hours of wakefulness. Brain Research 596: 285–295CrossRefGoogle ScholarPubMed
Landisman, C. E., Long, M. A., Beierlein, M., Deans, M. R., Paul, D. L. and Connors, B. W. (2002) Electrical synapses in the thalamic reticular nucleus. Journal of Neuroscienc 22: 1002–1009Google ScholarPubMed
Lang, E. J. and Paré, D. (1997) Synaptic and synaptically activated intrinsic conductances underlie inhibitory potentials in cat lateral amygdaloid projection neurons in vivo. Journal of Neurophysiology 77: 353–363CrossRefGoogle ScholarPubMed
Lang, E. J. and Paré, D. (1998) Synaptic responses of interneurons of the cat lateral amygdaloid nucleus. Neuroscience 83: 877–889CrossRefGoogle ScholarPubMed
Laureys, S., Peigneux, P., Phillips, C., Fuchs, S., Degueldre, C., Aerts, J., Del Fiore, G., Petiau, C., Luxen, A., Linden, M., Cleeremans, A., Smith, C. and Maquet, P. (2001) Experience-dependent changes in cerebral functional connectivity during human rapid eye movement sleep. Neuroscience 105: 521–525CrossRefGoogle ScholarPubMed
Lavoie, B. and Parent, A. (1994) Pedunculopontine nucleus in the squirrel monkey: distribution of cholinergic and monoaminergic neurons in the mesopontine tegmentum with evidence for the presence of glutamate in cholinergic neurons. Journal of Comparative Neurology 344: 190–209CrossRefGoogle ScholarPubMed
LeDoux, J. E. (1996) The Emotional Brain. New York: Simon and Schuster
LeDoux, J. E., Cicchetti, P., Xagoraris, A. and Romanski, L. M. (1990) The lateral amygdaloid nucleus: sensory interface of the amygdala in fear conditioning. Journal of Neuroscience 10: 1062–1069CrossRefGoogle ScholarPubMed
Lee, K. and McCormick, D. A. (1996) Abolition of spindle oscillations by serotonin and norepinephrine in the ferret lateral geniculate and perigeniculate nuclei in vitro. Neuron 17: 309–321CrossRefGoogle ScholarPubMed
Lehmann, T. N., Gabriel, S., Kovacs, R., Eilers, A., Kivi, A., Schulze, K., Lanksch, W. R., Meencke, H. J. and Heinemann, U. (2000) Alterations in neuronal connectivity in area CA1 of hippocampal slices from temporal lobe epilepsy patients and pilocarpine-treated epileptic rats. Epilepsia 41 (Suppl. 6): S190–S194CrossRefGoogle ScholarPubMed
Lemieux, J. F. and Blume, W. T. (1986) Topographical evolution of spike-wave complexes. Brain Research 373: 275–287CrossRefGoogle ScholarPubMed
Lennox, W. G. (1951) Phenomena and correlates of the psychomotor triad. Archives of Neurology 1: 357–371CrossRefGoogle ScholarPubMed
Lennox, W. G. and Lennox, M. A. (1960) Epilepsy and Related Disorders. London: Churchill
Leonard, C. S. and Llinás, R. R. (1990) Electrophysiology of mammalian pedunculopontine and laterodorsal tegmental neurons in vitro: implications for the control of REM sleep. In Brain Cholinergic Systems, ed. M. Steriade and D. Biesold, pp. 205–223, Oxford: Oxford University Press
Leonard, C. S. and Llinás, R. R. (1994) Serotonergic and cholinergic inhibition of mesopontine cholinergic neurons controlling REM sleep: an in vitro electrophysiological study. Neuroscience 59: 309–330CrossRefGoogle Scholar
Leonard, C. S., Rao, S. and Sanchez, R. M. (1995) Patterns of neuromodulation and the nitric oxide signaling pathway in mesopontine cholinergic neurons. Seminars in the Neurosciences, ed. M. Steriade, 7: 319–328CrossRefGoogle Scholar
Leonard, C. S., Michaelis, E. K. and Mitchell, K. M. (2001) Activity-dependent nitric oxide concentration dynamics in the laterodorsal tegmental nucleus in vitro. Journal of Neurophysiology 86: 2159–2172CrossRefGoogle ScholarPubMed
Leresche, N., Jassik-Gerschenfeld, D., Haby, M., Soltesz, I. and Crunelli, V. (1990) Pacemaker-like and other types of spontaneous membrane potential oscillations of thalamocortical cells. Neuroscience Letters 113: 72–77CrossRefGoogle ScholarPubMed
Leresche, N., Lightowler, S., Soltesz, I., Jassik-Gerschenfeld, D. and Crunelli, V. (1991) Low-frequency oscillatory activities intrinsic to rat and cat thalamocortical cells. Journal of Physiology (London) 441: 155–174CrossRefGoogle ScholarPubMed
Leresche, N., Parri, H. R., Erdemli, G., Guyon, A., Turner, J. P., Williams, S. R., Asprodini, E. and Crunelli, V. (1998) On the action of the anti-absence drug ethosuximide in the rat and cat thalamus. Journal of Neuroscience 18: 4842–4853CrossRefGoogle ScholarPubMed
Leresche, N., Asprodini, E., Emri, Z., Cope, D. W. and Crunelli, V. (2000) Somatostatin inhibits GABAergic transmission in the sensory thalamus via presynaptic receptors. Neuroscience 98: 513–522CrossRefGoogle ScholarPubMed
Leschinger, A., Stabel, J., Igelmund, P. and Heinemann, U. (1993) Pharmacological and electrographic properties of epileptiform activity induced by elevated K+ and lowered Ca2+ and Mg2+ concentration in rat hippocampal slices. Experimental Brain Research 96: 230–240CrossRefGoogle ScholarPubMed
Letinic, K. and Rakic, P. (2001) Telencephalic origin of human thalamic GABAergic neurons. Nature Neuroscience 4: 931–936CrossRefGoogle ScholarPubMed
Lévesque, M., Charara, A., Gagnon, S., Parent, A. and Deschênes, M. (1996) Corticostriatal projections from layer V cells in rat are collaterals of long-range corticofugal axons. Brain Research 709: 311–315CrossRefGoogle Scholar
Levi, G. and Gallo, V. (1995) Release of neuroactive amino acids from glia. In Neuroglia, ed. H. Kettenmann and B. R. Ransom, pp. 815–826, New York: Oxford University Press
Li, C. L. and McIlwain, H. (1957) Maintenance of resting membrane potentials in slices of mammalian cerebral cortex and other tissues in vitro. Journal of Physiology (London) 139: 178–190CrossRefGoogle ScholarPubMed
Li, X. G., Somogyi, P., Ylinen, A. and Buzsáki, G. (1994) The hippocampal CA3 network: an in vivo intracellular labeling study. Journal of Comparative Neurology 339: 181–208CrossRefGoogle Scholar
Lin, J. S., Sakai, K. and Jouvet, M. (1988) Evidence for histaminergic arousal mechanisms in the hypothalamus of cats. Neuropharmacology 27: 111–122CrossRefGoogle Scholar
Lin, J. S., Sakai, K., Vanni-Mercier, G. and Jouvet, M. (1989) A critical role of the posterior hypothalamus in the mechanisms of wakefulness determined by microinjections of muscimol in freely moving cats. Brain Research 479: 225–240CrossRefGoogle ScholarPubMed
Lingenhoehl, K., Brom, R., Heid, J., Beck, P., Froestl, W., Kaupmann, K., Bettler, B. and Mosbacher, J. (1999) γ-hydroxybutyrate is a weak agonist at recombinant GABAB receptors. Neuropharmacology 38: 1667–1674CrossRefGoogle Scholar
Lipman, I. J. and Hughes, J. R. (1968) Rhythmic mid-temporal discharges. Electroencephalography and Clinical Neurophysiology 27: 43–47CrossRefGoogle Scholar
Lisman, J. E. (1997) Bursts as a unit of neural information: making unreliable synapses reliable. Trends in Neurosciences 20: 38–43CrossRefGoogle ScholarPubMed
Litt, B., Esteller, R., Echauz, J., D'Alessandro, M., Shor, R., Henry, T., Pennell, P., Epstein, C., Bakay, R., Dichter, M. and Vachtsevanos, G. (2001) Epileptic seizures may begin hours in advance of clinical onset: a report of five patients. Neuron 30: 51–64CrossRefGoogle ScholarPubMed
Liu, X. B. and Jones, E. G. (1999) Predominance of corticothalamic synaptic inputs to thalamic reticular nucleus neurons in the rat. Journal of Comparative Neurology 414: 67–793.0.CO;2-Z>CrossRefGoogle ScholarPubMed
Liu, X. B., Warren, R. A. and Jones, E. G. (1995) Synaptic distribution of afferents from reticular nucleus in ventroposterior nucleus of cat thalamus. Journal of Comparative Neurology 352: 187–202CrossRefGoogle ScholarPubMed
Liu, X. B., Bolea, S., Golshani, P. and Jones, E. G. (2001) Differentiation of corticothalamic and collateral thalamocortical synapses on mouse reticular nucleus by EPSC amplitude and AMPA receptor subunit composition. Thalamus and Related Systems 1: 15–29Google Scholar
Liu, Z., Vergnes, M., Depaulis, A. and Marescaux, C. (1992) Involvement of intrathalamic GABAB neurotransmission in the control of absence seizures in the rat. Neuroscience 48: 87–93CrossRefGoogle ScholarPubMed
Livingstone, M. S. and Hubel, D. H. (1981) Effects of sleep and arousal on the processing of visual information in the cat. Nature 291: 554–561CrossRefGoogle ScholarPubMed
Llinás, R. R. (1964) Mechanisms of supraspinal action upon spinal cord activities. Differences between reticular and cerebellar inhibitory action upon alpha extensor motorneurones. Journal of Neurophysiology 27: 1117–1126CrossRefGoogle Scholar
Llinás, R. R. (1985) Electrotonic transmission in the mammalian central nervous system. In Gap Junctions, ed. M. V. L. Bennett, pp. 337–353, New York: Cold Harbor Spring
Llinás, R. R. (1988) The intrinsic electrophysiological properties of mammalian neurons: insights into central nervous system function. Science 242: 1654–1664CrossRefGoogle ScholarPubMed
Llinás, R. R. and Paré, D. (1991) Of dreaming and wakefulness. Neuroscience 44: 521–535CrossRefGoogle ScholarPubMed
Llinás, R. R. and Ribary, U. (1993) Coherent 40-Hz oscillation characterizes dream state in humans. Proceedings of the National Academy of Sciences of the USA 90: 2078–2081CrossRefGoogle ScholarPubMed
Llinás, R. R. and Terzuolo, C. A. (1964) Mechanisms of supraspinal actions upon spinal cord activities. Reticular inhibitory mechanisms on alpha-extensor motoneurons. Journal of Neurophysiology 27: 579–591CrossRefGoogle ScholarPubMed
Llinás, R., Grace, A. A. and Yarom, Y. (1991) In vitro neurons in mammalian cortical layer 4 exhibit intrinsic oscillatory activity in the 10- to 50-Hz frequency range. Proceedings of the National Academy of Sciences of the USA 88: 897–901CrossRefGoogle ScholarPubMed
Llinás, R., Ribary, U., Jeanmonod, D., Kronberg, E. and Mitra, P. P. (1999) Thalamocortical dysrhythmia: a neurological and neuropsychiatric syndrome characterized by magneto-encephalography. Proceedings of the National Academy of Sciences of the USA 96: 15222–15227CrossRefGoogle Scholar
Llinás, R., Ribary, U., Jenamonod, D., Cancro, R., Kronberg, E., Schulman, J., Zonenshayn, M., Magnin, M., Morel, A. and Siegemund, M. (2001) Thalamocortical dysrhythmia. I. Functional and imaging aspects. Thalamus and Related Systems 1: 237–244Google Scholar
Loiseau, P. (1992) Human absence epilepsies. Journal of Neural Transmission 35 (Suppl.): 1–6Google ScholarPubMed
Loomis, A. L., Harvey, N. and Hobart, G. A. (1938) Distribution of disturbance patterns in the human electroencephalogram, with special reference to sleep. Journal of Neurophysiology 1: 413–430CrossRefGoogle Scholar
Lopantsev, V. and Avoli, M. (1998) Participation of GABAA-mediated inhibition in ictal-like discharges in the rat entorhinal cortex. Journal of Neurophysiology 79: 352–360CrossRefGoogle Scholar
Lopes da Silva, F. H., Rotterdam, A., Storm van Leeuwen, W. and Tielen, A. M. (1970) Dynamic characteristics of visual evoked potentials in the dog. II. Beta frequency selectivity in evoked potentials and background activity. Electroencephalography and Clinical Neurophysiology 29: 260–268CrossRefGoogle ScholarPubMed
Lopes da Silva, F. H., Witter, M. P., Boeijinga, P. H. and Lohman, A. H. M. (1990) Anatomic organization and physiology of the limbic system. Physiological Reviews 70: 453–511CrossRefGoogle Scholar
Lopes da Silva, F. H., Kamphuis, W., Titulaer, M., Vreugdenhil, M. and Wadman, W. J. (1995) An experimental model of progressive epilepsy: the development of kindling of the hippocampus of the rat. Italian Journal of Neurological Sciences 16: 45–57CrossRefGoogle ScholarPubMed
LoPiccolo, M. A. (1977) Behavioral and Neuronal Effects of EEG Synchronizing Stimuli in the Cat. Ph.D. Thesis, McMaster University, Hamilton (Ontario)
Lorente de Nó, R. (1933) Studies on the structure of the cerebral cortex. I. The area entorhinalis. Journal of Psychology and Neurology 45: 381–438Google Scholar
Loszádi, D. A. (1995) Organization of connections between the thalamic reticular and the anterior thalamic nuclei in the rat. Journal of Comparative Neurology 358: 233–246CrossRefGoogle Scholar
Lothman, E. W., Bertram, E. H. and Stringer, J. L. (1991) Functional anatomy of hippocampal seizures. Progress in Neurobiology 37: 1–82CrossRefGoogle ScholarPubMed
Loup, F., Wieser, H. G., Yonekawa, Y., Aguzzi, A. and Fritschy, J. M. (2000) Selective alterations in GABAA receptor subtypes in human temporal lobe epilepsy. Journal of Neuroscience 20: 5401–5419CrossRefGoogle ScholarPubMed
Lübke, J. I., Greene, R. W., Semba, K., Kamondi, A., McCarley, R. W. and Reiner, P. B. (1992) Serotonin hyperpolarizes cholinergic low-threshold burst neurons in the rat laterodorsal tegmental nucleus in vitro. Proceedings of the National Academy of Sciences of the USA 89: 743–747CrossRefGoogle Scholar
Luciani, L. (1911) Fisiologia dell'uomo. Milano: Societa Editrice Libraria
Lucretius, T. C. (1988) On the Nature of the Universe (translated by R. E. Latham). London: Penguin Books
Lüders, H. O., Engel, J. Jr. and Munari, C. (1993) General principles. In Surgical Treatment of the Epilepsies, ed. J. Engel Jr., pp. 137–153, New York: Raven
Luhmann, H. J., Mittmann, T., Schmidt-Kastner, R., Eysel, U. T., Mudrick-Donnon, L. A. and Heinemann, U. (1999) Hyperexcitability after focal lesions and transient ischemia in rat neocortex. In Progressive Nature of Epileptogenesis (Epilepsy Research, Suppl. 12), ed. U. Heinemann, pp. 119–128, Amsterdam: Elsevier
Lüthi, A. and McCormick, D. A. (1998) Periodicity of thalamic synchronized oscillations: the role of Ca2+-mediated upregulation of IH. Neuron 20: 553–63CrossRefGoogle ScholarPubMed
Lux, H. D. and Neher, E. (1973) The equilibrium time course of [K+]o in cat cortex. Experimental Brain Research 17: 190–205CrossRefGoogle Scholar
Lydic, R., McCarley, R. W. and Hobson, J. A. (1987) Serotonin neurons and sleep. II. Time course of dorsal raphe discharge frequency, PGO waves, and behavioral states. Archives Italiennes de Biologie 126: 1–28Google Scholar
Lytton, W. W. and Sejnowski, T. J. (1991) Simulation of cortical pyramidal neurons synchronized by inhibitory interneurons. Journal of Neurophysiology 66: 1059–1079CrossRefGoogle ScholarPubMed
Lytton, W. W., Contreras, D., Destexhe, A. and Steriade, M. (1997) Dynamic interactions determine partial thalamic quiescence in a computer network model of spike-and-wave seizures. Journal of Neurophysiology 77: 1679–1696CrossRefGoogle Scholar
MacDonald, K. D., Fifkova, E., Jones, M. S. and Barth, D. S. (1998) Focal stimulation of the thalamic reticular nucleus induces focal gamma waves in cortex. Journal of Neurophysiology 79: 474–477CrossRefGoogle ScholarPubMed
Macnish, R. (1830) The Philosophy of Sleep. Glasgow: M'Phun
MacVicar, B. A. (1985) Depolarizing prepotentials are Na+-dependent in CA1 pyramidal neurons. Brain Research 333: 378–381CrossRefGoogle ScholarPubMed
MacVicar, B. A. and Dudek, F. E. (1981) Electrotonic coupling between pyramidal cells: a direct demonstration in rat hippocampal slices. Science 213: 782–785CrossRefGoogle ScholarPubMed
MacVicar, B. A. and Dudek, F. E. (1982) Electrotonic coupling between granule cells of rat dentate gyrus. Physiological and anatomical evidence. Journal of Neurophysiology 47: 579–592CrossRefGoogle ScholarPubMed
MacVicar, B. A., Tse, F. W., Crichton, S. A. and Kettenmann, H. (1989) GABA-activated Cl- channels in astrocytes of hippocampal slices. Journal of Neuroscience 9: 3577–3583CrossRefGoogle ScholarPubMed
Maffei, L., Moruzzi, G. and Rizzolatti, G. (1965) Influence of sleep and wakefulness on the response of lateral geniculate units to sinewave photic stimulation. Archives Italiennes de Biologie 103: 596–608Google ScholarPubMed
Magee, J., Hoffman, D., Colbert, C. and Johnston, D. (1998) Electrical and calcium signaling in dendrites of hippocampal pyramidal neurons. Annual Reviews of Physiology 60: 327–346CrossRefGoogle ScholarPubMed
Magill, P. J., Bolam, P. and Bevan, M. D. (2000) Relationship of activity in the subthalamic nucleus – globus pallidus network to cortical EEG. Journal of Neuroscience 20: 820–833CrossRefGoogle Scholar
Magill, P. J., Bolam, J. P. and Bevan, M. D. (2001) Dopamine regulates the impact of the cerebral cortex on the subthalamic nucleus-globus pallidus network. Neuroscience 106: 313–330CrossRefGoogle ScholarPubMed
Magistris, M. R., Mouradian, M. S. and Gloor, P. (1988) Generalized convulsions induced by pentylenetetrazol in the cat: participation of forebrain, brainstem, and spinal cord. Epilepsia 29: 379–388CrossRefGoogle ScholarPubMed
Mahon, S., Deniau, J. M. and Charpier, S. (2001) Relationship between EEG potentials and intracellular activity of striatal and cortico-striatal neurons: an in vivo study under different anesthetics. Cerebral Cortex 11: 360–373CrossRefGoogle Scholar
Mahowald, M. K. and Schenck, C. H. (1997) Sleep disorders. In Epilepsy: A Comprehensive Textbook, ed. J. Engel Jr. and T. A. Pedley, pp. 2705–2715, Philadelphia: Lippincot-Raven
Malow, B. A., Fromes, G. A. and Aldrich, M. S. (1997) Usefulness of polysomnography in epilepsy patients. Neurology 48: 1389–1394CrossRefGoogle ScholarPubMed
Manaye, K. F., Zweig, R., Wu, D., Hersh, L. B., Lacalle, S., Saper, C. B. and German, D. C. (1999) Quantification of cholinergic and select non-cholinergic mesopontine neuronal populations in the human brain. Neuroscience 89: 759–770CrossRefGoogle ScholarPubMed
Mangan, P. S., Scott, C. A., Williamson, J. M. and Bertram, E. H. III (2000) Aberrant neuronal physiology in the basal nucleus of the amygdala in a model of chronic limbic epilepsy. Neuroscience 101: 377–391CrossRefGoogle Scholar
Manganotti, P., Zanette, G., Beltramello, A., Puppini, G., Miniussi, C., Maravita, A., Santorum, E., Marzi, C. A., Fiaschi, A. and Dalla Bernardina, B. (1999) Spike topography and fMRI in benign rolandic epilepsy with spikes evoked by tapping stimulation. Electroencephalography and Clinical Neurophysiology 107: 88–92CrossRefGoogle Scholar
Manor, Y., Koch, C. and Segev, I. (1991) Effect of geometrical irregularities on propagation delay in axonal trees. Biophysical Journal 60: 1424–1437CrossRefGoogle ScholarPubMed
Mao, B. Q., Hamzei-Sichani, F., Aronov, D., Froemke, R. C. and Yuste, R. (2001) Dynamics of spontaneous activity in neocortical slices. Neuron 32: 883–898CrossRefGoogle ScholarPubMed
Maquet, P. (2000) Functional neuroimaging of normal human sleep by positron emission tomography. Journal of Sleep Research 9: 207–231CrossRefGoogle ScholarPubMed
Maquet, P. and Phillips, C. (1998) Functional imaging of human sleep. Journal of Sleep Research 7 (Suppl. 1): 42–47CrossRefGoogle ScholarPubMed
Maquet, P., Dive, D., Salmon, E., Sadzot, B., Franco, G., Poirrier, R. and Franck, G. (1992) Cerebral glucose utilization during stage 2 sleep in man. Brain Research 571: 149–153CrossRefGoogle ScholarPubMed
Maquet, P., Péters, J. M., Aerts, J., Delfiore, G., Degueldre, C., Luxen, A. and Franck, G. (1996) Functional neuro-anatomy of human rapid-eye-movement sleep and dreaming. Nature 383: 163–166CrossRefGoogle Scholar
Maquet, P., Degueldre, C., Delfiore, G., Aerts, J., Péters, J. P., Luxen, A. and Franck, G. (1997) Functional neuroanatomy of human slow wave sleep. Journal of Neuroscience 17: 2807–2812CrossRefGoogle ScholarPubMed
Maquet, P., Laureys, S., Peigneux, P., Fuchs, S., Petiau, C., Phillips, C., Aerts, J., Del Fiore, G., Degueldre, C., Meulemans, T., Luxen, A., Franck, G., Van der Linden, M., Smith, C. and Cleeremans, A. (2000) Experience-dependent changes in cerebral activation during human REM sleep
Marco, P. and DeFelipe, J. (1997) Altered synaptic circuitry in the human temporal neocortex removed from epileptic patients. Experimental Brain Research 114: 1–10CrossRefGoogle ScholarPubMed
Marcus, E. M. and Watson, C. W. (1966) Bilateral synchronous spike-wave electrographic patterns in the cat. Archives of Neurology (Chicago) 14: 601–610CrossRefGoogle ScholarPubMed
Marcus, E. M., Watson, C. W. and Simon, S. A. (1968a) An experimental model of some varieties of petit mal epilepsy. Electrical-behavioral correlations of acute bilateral epileptogenic foci in cerebral cortex. Epilepsia 9: 233–248CrossRefGoogle Scholar
Marcus, E. M., Watson, C. W. and Simon, S. A. (1968b) Behavioral correlates of acute bilateral symmetrical epileptogenic foci in monkey cerebral cortex. Brain Research 9: 370–373CrossRefGoogle Scholar
Marescaux, C., Vergnes, M. and Bernusconi, R. (1992a) GABAB receptor antagonists: potential new anti-absence drugs. Journal of Neural Transmission 35 (Suppl.): 179–188Google Scholar
Marescaux, C., Vergnes, M. and Depaulis, A. (1992b) Genetic absence epilepsy in rats from Strasbourg – a review. Journal of Neural Transmission 35 (Suppl.): 37–69Google Scholar
Margerison, J. H. and Corsellis, J. A. N. (1966) Epilepsy and the temporal lobe: a clinical, electroencephalographic and neuropathological study of the brain in epilepsy, with particular reference to the temporal lobes. Brain 89: 499–530CrossRefGoogle ScholarPubMed
Marini, G., Macchi, G. and Mancia, M. (1992) Potentiation of electroencephalographic spindles by ibotenate microinjections into nucleus reticularis thalami of cats. Neuroscience 51: 759–762CrossRefGoogle ScholarPubMed
Mariño, J., Canedo, A. and Aguilar, J. (2000) Sensorimotor cortical influences on cuneate nucleus rhythmic activity in the anesthetized cat. Neuroscience 95: 657–673CrossRefGoogle ScholarPubMed
Markram, H. (1997) A network of tufted layer 5 pyramidal neurons. Cerebral Cortex 7: 523–533CrossRefGoogle ScholarPubMed
Markram, H. and Sakmann, B. (1994) Calcium transients in dendrites of neocortical neurons evoked by single subthreshold excitatory postsynaptic potentials via low-voltage-activated calcium channels. Proceedings of the National Academy of Sciences of the USA 91: 5207–5211CrossRefGoogle ScholarPubMed
Markram, H., Lübke, J., Frötscher, M., Roth, A. and Sakmann, B. (1997a) Physiology and anatomy of synaptic connections between thick tufted pyramidal neurones in the developing rat neocortex. Journal of Physiology (London) 500: 409–440CrossRefGoogle Scholar
Markram, H., Lübke, J., Frötscher, M. and Sakmann, B. (1997b) Regulation of synaptic efficacy by coincidence of postsynaptic APs and EPSPs. Science 275: 213–215CrossRefGoogle Scholar
Markram, H., Wang, M. and Tsodycs, M. (1998) Differential signaling via the same axon of neocortical pyramidal neurons. Proceedings of the National Academy of Sciences of the USA 95: 5323–5328CrossRefGoogle ScholarPubMed
Marshall, L. H. (1987) An annotated interview with Giuseppe Moruzzi, 1910–1986. Experimental Neurology 97: 225–242CrossRefGoogle Scholar
Marshall, L. H. and Magoun, H. W. (1998) Discoveries in the Human Brain – Neuroscience Prehistory, Brain Structure, and Function. Totowa, NJ: Humana Press
Marshall, L., Mölle, M., Fehm, H. L. and Born, J. (1998) Scalp recorded direct current brain potentials during human sleep. European Journal of Neuroscience 10: 1167–1178CrossRefGoogle ScholarPubMed
Martin, J. H. (1991) Autoradiographic estimation of the extent of reversible inactivation produced by microinjections of lidocaine and muscimol in the rat. Neuroscience Letters 127: 160–164CrossRefGoogle ScholarPubMed
Martin, J. H. and Ghez, C. (1988) Red nucleus and motor cortex: parallel motor systems for the initiation and control of skilled movement. Behavioral Brain Research 28: 217–223CrossRefGoogle ScholarPubMed
Martin, S. J., Grimwood, P. D. and Morris, R. G. M. (2000) Synaptic plasticity and memory: an evaluation of the hypothesis. Annual Reviews of Neuroscience 23: 649–711CrossRefGoogle ScholarPubMed
Martina, M., Royer, S. and Paré, D. (1999) Physiological properties of central medial and central lateral amygdala neurons. Journal of Neurophysiology 82: 1843–1854CrossRefGoogle ScholarPubMed
Martina, M., Vida, I. and Jonas, P. (2000) Distal initiation and active propagation of action potentials in interneuron dendrites. Science 287: 295–300CrossRefGoogle ScholarPubMed
Mason, A. and Larkman, A. (1990) Correlations between morphology and electrophysiology of pyramidal neurons in slices of rat visual cortex. II. Electrophysiology. Journal of Neuroscience 10: 1415–1428CrossRefGoogle ScholarPubMed
Masselmo, M. E. (1999) Neuromodulation: acetylcholine and memory consolidation. Trends in Cognitive Sciences 3: 351–359CrossRefGoogle Scholar
Massimini, M. and Amzica, F. (2001) Extracellular calcium fluctuations and intracellular potentials in the cortex during the slow sleep oscillation. Journal of Neurophysiology 85: 1346–1350CrossRefGoogle ScholarPubMed
Mathern, G. W., Babb, T. L., Pretorius, J. K. and Leite, J. P. (1995) Reactive synaptogenesis and neuron densities for neuropeptide Y, somatostatin, and glutamate decarboxylase immunoreactivity in the epileptogenic human fascia dentate. Journal of Neuroscience 15: 3990–4004CrossRefGoogle Scholar
Matsumoto, H. and Ajmone-Marsan, C. (1964) Cortical cellular phenomena in experimental epilepsy. Experimental Neurology 9: 286–304CrossRefGoogle ScholarPubMed
Matsumoto, H., Ayala, G. F. and Gumnit, R. J. (1969) Neuronal behavior and triggering mechanism in cortical epileptic focus. Journal of Neurophysiology 32: 688–703CrossRefGoogle ScholarPubMed
Mauguière, P. (1992) A consensus statement on relative merits of EEG and MEG. Electroencephalography and Clinical Neurophysiology 82: 317–319Google ScholarPubMed
McAllister, A. K., Katz, L. C. and Lo, D. C. (1999) Neurotrophins and synaptic plasticity. Annual Reviews of Neuroscience 22: 295–318CrossRefGoogle ScholarPubMed
McCarley, R. W. and Hobson, J. A. (1975) Neuronal excitability modulation over the sleep cycle: a structural and mathematical model. Science 189: 58–60CrossRefGoogle ScholarPubMed
McCarley, R. W. and Massequoi, S. G. (1986) A limit cycle mathematical model of the REM sleep oscillator system. American Journal of Physiology 251: R1033–R1036Google ScholarPubMed
McCarley, R. W., Benoit, O. and Barrionuevo, G. (1983) Lateral geniculate nucleus unitary discharge in sleep and waking: state- and rate-specific aspects. Journal of Neurophysiology 50: 798–818CrossRefGoogle ScholarPubMed
McCormick, D. A. (1989) GABA as an inhibitory neurotransmitter in the human cerebral cortex. Journal of Neurophysiology 62: 1018–1027CrossRefGoogle ScholarPubMed
McCormick, D. A. (1991) Functional properties of a slowly inactivating potassium current IAs in guinea pig dorsal lateral geniculate relay neurons. Journal of Neurophysiology 66: 1176–1189CrossRefGoogle ScholarPubMed
McCormick, D. A. (1992) Neurotransmitter actions in the thalamus and cerebral cortex and their role in neuromodulation of thalamocortical activity. Progress in Neurobiology 39: 337–388CrossRefGoogle ScholarPubMed
McCormick, D. A. and Contreras, D. (2001) On the cellular and network bases of epileptic seizures. Annual Reviews of Physiology 63: 815–846CrossRefGoogle ScholarPubMed
McCormick, D. A. and Krosigk, M. (1992) Corticothalamic activation modulates thalamic firing through glutamate metabotropic receptors. Proceedings of the National Academy of Sciences of the USA 89: 2774–2778CrossRefGoogle ScholarPubMed
McCormick, D. A. and Pape, H. C. (1988) Acetylcholine inhibits identified interneurons in the cat lateral geniculate nucleus. Nature 334: 246–248CrossRefGoogle ScholarPubMed
McCormick, D. A. and Pape, H. C. (1990a) Properties of a hyperpolarization-activated cation current and its role in rhythmic oscillation in thalamic relay neurones. Journal of Physiology (London) 431: 291–318CrossRefGoogle Scholar
McCormick, D. A. and Pape, H. C. (1990b) Noradrenergic and serotonergic modulation of a hyperpolarization-activated cation current in thalamic relay cells. Journal of Physiology (London) 431: 319–342CrossRefGoogle Scholar
McCormick, D. A. and Prince, D. A. (1986) Acetylcholine induces burst firing in thalamic reticular neurones by activating a K+ conductance. Nature 319: 147–165CrossRefGoogle Scholar
McCormick, D. A. and Prince, D. A. (1987) Actions of acetylcholine in the guinea pig and cat medial and lateral geniculate nuclei, in vitro. Journal of Physiology (London) 392: 147–165CrossRefGoogle ScholarPubMed
McCormick, D. A. and Prince, D. A. (1988) Noradrenergic modulation of firing pattern in guinea pig and cat thalamic neurones, in vitro. Journal of Neurophysiology 59: 978–996CrossRefGoogle Scholar
McCormick, D. A. and Wang, Z. (1991) Serotonin and noradrenaline excite GABAergic neurones of the guinea-pig and cat nucleus reticularis thalami. Journal of Physiology (London) 442: 235–255CrossRefGoogle ScholarPubMed
McCormick, D. A. and Williamson, A. (1991) Modulation of neuronal firing mode in cat and guinea-pig LGNd by histamine: possible cellular mechanisms of histaminergic control of arousal. Journal of Neuroscience 11: 3188–3199CrossRefGoogle ScholarPubMed
McCormick, D. A., Connors, B. W., Lighthall, J. W. and Prince, D. A. (1985) Comparative electrophysiology of pyramidal and sparsely spiny stellate neurons of the neocortex. Journal of Neurophysiology 54: 782–806CrossRefGoogle ScholarPubMed
McDonald, A. J. (1994) Calretinin immunoreactive neurons in the basolateral amygdala of the rat and monkey. Brain Research 667: 238–242CrossRefGoogle ScholarPubMed
McDonald, A. J. and Augustine, J. R. (1993) Localization of GABA-like immunoreactivity in the monkey amygdala. Neuroscience 52: 281–294CrossRefGoogle ScholarPubMed
McGinty, D. J. and Harper, R. M. (1976) Dorsal raphe neurons: depression of firing during sleep in cats. Brain Research 101: 569–575CrossRefGoogle ScholarPubMed
McGinty, D. J. and Sterman, M. B. (1968) Sleep suppression after basal forebrain lesions in the cat. Science 160: 1253–1255CrossRefGoogle ScholarPubMed
McKeown, M. J. and McNamara, J. O. (2001) When do epileptic seizures really begin?Neuron 30: 1–3CrossRefGoogle ScholarPubMed
McKeown, M. J., Humphries, C., Iragui, V. and Sejnowski, T. J. (1999) Spatially fixed patterns account for the spike and wave features in absence seizures. Brain Tomography 12: 107–116CrossRefGoogle ScholarPubMed
McNaughton, B. L., Barnes, C. A. and Andersen, P. (1981) Synaptic efficacy and EPSP summation in granule cells of rat fascia dentata studied in vitro. Journal of Neurophysiology 46: 952–966CrossRefGoogle ScholarPubMed
Meeren, H. K. M., Pijn, J. P. M., Luijtelaar, E. J. L. M., Coenen, A. M. L. and Lopes da Silva, F. H. (2002) Cortical focus drives widespread corticothalamic networks during spontaneous absence seizures in rats. Journal of Neuroscience 22: 1480–1495CrossRefGoogle ScholarPubMed
Meis, S., Munsch, T. and Pape, H. C. (2002) Antioscillatory effects of nociceptin/orphanin FQ in synaptic networks of the rat thalamus. Journal of Neuroscience 22: 718–727CrossRefGoogle ScholarPubMed
Merica, H., Blois, R., Fortune, R. D. and Gaillard, J. M. (1997) Evolution of delta activity within the nonREM sleep episode: a biphasic hypothesis. Physiology and Behavior 62: 213–219CrossRefGoogle ScholarPubMed
Merlet, I., Garcia-Larrea, L., Grégoire, M. C., Lavenne, F. and Mauguière, F. (1996) Source propagation of interictal spikes in temporal lobe epilepsy. Brain 119: 377–392CrossRefGoogle ScholarPubMed
Metherate, R., Cox, C. L. and Ashe, J. H. (1992) Cellular bases of neocortical activation: modulation of neural oscillations by the nucleus basalis and endogenous acetylcholine. Journal of Neuroscience 12: 4701–4711CrossRefGoogle ScholarPubMed
Miles, R. and Wong, R. K. S. (1983) Single neurones can initiate synchronized population discharges in the hippocampus. Nature 306: 371–373CrossRefGoogle ScholarPubMed
Miles, R. and Wong, R. K. S. (1987) Latent synaptic pathways revealed after titanic stimulation in the hippocampus. Nature 329: 724–726CrossRefGoogle Scholar
Miles, R., Toth, K., Gulyas, A. I., Hajos, N. and Freund, T. F. (1996) Differences between somatic and dendritic inhibition in the hippocampus. Neuron 16: 815–823CrossRefGoogle ScholarPubMed
Miller, L. A., McLachlan, R. S., Bouwer, M. S., Hudson, L. P. and Munoz, M. G. (1994) Amygdalar sclerosis: preoperative indicators and outcome after temporal lobe lobectomy. Journal of Neurology, Neurosurgery and Psychiatry 57: 1099–1105CrossRefGoogle Scholar
Minamimoto, T. and Kimura, M. (2002) Participation of the thalamic CM-Pf complex in attentional orienting. Journal of Neurophysiology 87: 3090–3101CrossRefGoogle ScholarPubMed
Mineff, E. M. and Weinberg, R. J. (2000) Differential synaptic distribution of AMPA receptor subunits in the ventral posterior and reticular thalamic nuclei of the rat. Neuroscience 101: 969–982CrossRefGoogle ScholarPubMed
Mitchell, S. J. and Ranck, J. B. J. (1980) Generation of theta rhythm in medial entorhinal cortex of freely moving rats. Brain Research 189: 49–66CrossRefGoogle ScholarPubMed
Miyauchi, T., Nomura, Y., Ohno, S., Kishimoto, H. and Matsushita, M. (1988) Positron emission tomography in three cases of Lennox-Gastaut syndrome. Japanese Journal of Psychiatry Neurology 42: 795–804Google ScholarPubMed
Mody, I. (1998) Ion channels in epilepsy. International Review of Neurobiology 42: 199–226CrossRefGoogle ScholarPubMed
Mogilner, A. I., Benabid, A. L. and Rezai, A. (2001) Brain stimulation: current applications and future prospects. Thalamus and Related Systems 1: 255–267Google Scholar
Mölle, M., Marshall, L., Gais, S. and Born, J. (2003) Grouping of spindle activity during slow oscillations in human non-REM sleep. Journal of Neuroscience 22: 10941–10947CrossRefGoogle Scholar
Monckton, J. E. and McCormick, D. A. (2002) The neuromodulatory role of serotonin in the ferret thalamus. Journal of Neurophysiology, in pressCrossRefGoogle ScholarPubMed
Montero, V. M. (1987) Ultrastructural identification of synaptic terminals from the axon of type 3 interneurons in the cat lateral geniculate nucleus. Journal of Comparative Neurology 264: 268–283CrossRefGoogle ScholarPubMed
Montero, V. M. (1991) A quantitative study of synaptic contacts on interneurons and relay cells of the cat lateral geniculate nucleus. Experimental Brain Research 86: 257–270CrossRefGoogle ScholarPubMed
Montero, V. M. and Singer, W. (1985) Ultrastructural identification of somata and neural processes immunoreactive to antibodies against glutamic acid decarboxylase (GAD) in the dorsal lateral geniculate nucleus of the cat. Experimental Brain Research 59: 151–165CrossRefGoogle ScholarPubMed
Moody, W. J. Jr., Futamachi, K. J. and Prince, D. A. (1974) Extracellular potassium activity during epileptogenesis. Experimental Neurology 42: 248–263CrossRefGoogle ScholarPubMed
Morales, F. R. and Chase, M. H. (1978) Intracellular recording of lumbar motoneuron membrane potential during sleep and wakefulness. Experimental Neurology 62: 821–827CrossRefGoogle ScholarPubMed
Morimoto, K., Dragunow, M. and Goddard, G. V. (1986) Deep prepyriform cortex kindling and its relation to amygdala kindling in the rat. Experimental Neurology 94: 637–648CrossRefGoogle ScholarPubMed
Morin, D. and Steriade, M. (1981) Development from primary to augmenting responses in the somatosensory system. Brain Research 205: 49–66CrossRefGoogle ScholarPubMed
Morin, F., Beaulieu, C. and Lacaille, J. C. (1998) Selective loss of GABA neurons in area CA1 of the rat hippocampus after intraventricular kainate. Epilepsy Research 32: 363–369CrossRefGoogle ScholarPubMed
Morison, R. S. and Bassett, D. L. (1945) Electrical activity of the thalamus and basal ganglia in decorticated cats. Journal of Neurophysiology 8: 309–314CrossRefGoogle Scholar
Morison, R. S. and Dempsey, E. W. (1942) Mechanism of thalamocortical augmentation and repetition. American Journal of Physiology 138: 297–308Google Scholar
Morrell, F. (1960) Secondary epileptogenic lesions. Epilepsia 1: 538–560CrossRefGoogle ScholarPubMed
Morrison, J. H. and Foote, S L. (1986) Noradrenergic and serotoninergic innervation of cortical, thalamic and tectal visual structures in old and new world monkeys. Journal of Comparative Neurology 243: 117–138CrossRefGoogle ScholarPubMed
Moruzzi, G. (1964) The historical development of the deafferentation hypothesis of sleep. Proceedings of the American Philosophical Society 108: 19–28Google Scholar
Moruzzi, G. (1966) The functional significance of sleep with particular regard to the brain mechanisms underlying consciousness. In Brain and Conscious Experience, ed. J. C. Eccles, pp. 345–379, New York: Springer
Moruzzi, G. (1969) Sleep and instinctive behavior. Archives Italiennes de Biologie 107: 175–216Google ScholarPubMed
Moruzzi, G. (1972) The sleep-waking cycle. Ergebnisse der Physiologie 64: 1–165Google ScholarPubMed
Moruzzi, G. and Magoun, H. W. (1949) Brain stem reticular formation and activation of the EEG. Electroencephalography and Clinical Neurophysiology 1: 455–473CrossRefGoogle ScholarPubMed
Mountcastle, V. B. (1997) The columnar organization of the neocortex. Brain 120: 701–722CrossRefGoogle ScholarPubMed
Mountcastle, V. B. (1998) Perceptual Neuroscience – The Cerebral Cortex. Cambridge, MA: Harvard University Press
Mouret, J. and Coindet, J. (1980) Polygraphic evidence against a critical role of the raphe nuclei in sleep in the rat. Brain Research 186: 273–287CrossRefGoogle ScholarPubMed
Mulle, C., Steriade, M. and Deschênes, M. (1985) Absence of spindle oscillations in the cat anterior thalamic nuclei. Brain Research 334: 169–171CrossRefGoogle ScholarPubMed
Mulle, C., Madariaga, A. and Deschênes, M. (1986) Morphology and electrophysiological properties of reticularis thalami neurons in cat: in vivo study of a thalamic pacemaker. Journal of Neuroscience 6: 2134–2145CrossRefGoogle ScholarPubMed
Munk, M. H. J., Roelfsema, P. R., König, P., Engel, A. K. and Singer, W. (1996) Role of reticular activation in the modulation of intracortical synchronization. Science 272: 271–274CrossRefGoogle ScholarPubMed
Murthy, V. N. and Fetz, E. E. (1992) Coherent 25- to 35-Hz oscillations in the sensorimotor cortex of awake behaving monkeys. Proceedings of National Academy of Sciences of the USA 89: 5670–5674CrossRefGoogle ScholarPubMed
Murthy, V. N. and Fetz, E. E. (1997a) Oscillatory activity in sensorimotor cortex of awake monkeys: synchronization of local field potentials and relation to behavior. Journal of Neurophysiology 76: 3949–3967CrossRefGoogle Scholar
Murthy, V. N. and Fetz, E. E. (1997b) Synchronization of neurons during local field potential oscillations in sensorimotor cortex of awake monkeys. Journal of Neurophysiology 76: 3968–3982CrossRefGoogle Scholar
Nadler, J. V., Perry, B. W. and Cotman, C. W. (1978) Preferential vulnerability of hippocampus to intraventricular kainic acid. In Kainic Acid as a Tool in Neurobiology, ed. E. G. McGeer, J. W. Olney and P. L. McGeer, pp. 219–237, New York: Raven Press
Nagao, T., Alonso, A. and Avoli, M. (1996) Epileptiform activity induced by pilocarpine in the rat hippocampal-entorhinal slice preparation. Neuroscience 72: 399–408CrossRefGoogle ScholarPubMed
Nagy, J. I., Yamamoto, T., Shiosaka, S., Dewar, K. M., Whittaker, M. E. and Hertzberg, E. L. (1988) Immunohistochemical localization of gap junction protein in rat CNS: a preliminary account. In Gap Junctions, ed. E. L. Hertzberg and R. G. Johnson, pp. 375–389, New York: A. R. Liss
Nakabayashi, T., Uchida, S., Maehara, T., Hirai, N., Nakamura, M., Arakaki, H., Shimisu, H. and Okubo, Y. (2001) Absence of sleep spindles in human medial and basal temporal lobes. Psychiatry and Clinical Neuroscience 55: 57–65CrossRefGoogle ScholarPubMed
Nakamura, A., Nakashima, M., Sugao, T., Kanemoto, H., Fukumura, Y. and Shiomi, H. (1988) Potent antinociceptive effect of centrally administered delta-sleep-inducing peptide (DSIP). European Journal of Pharmacology 155: 247–253CrossRefGoogle Scholar
Nakamura, A., Nakashima, M., Sakai, K., Niwa, M., Nozaki, M. and Shiomi, H. (1989) Delta-sleep-inducing peptide (DSIP) stimulates the release of immunoreactive Met-enkephalin from rat lower brainstem slices in vitro. Brain Research 481: 165–168CrossRefGoogle ScholarPubMed
Naquet, R. and Meldrum, B. S. (1975) In Experimental Models of Epilepsy, ed. D. P. Purpura, J. K. Penry, D. B. Tower, D. M. Woodbury and R. D. Walter, pp. 373–406, New York: Raven Press
Naquet, R. and Valin, A. (1990) Focal discharges in photosensitive generalized epilepsy. In Generalized Epilepsy, ed. M. Avoli, P. Gloor, G. Kostopoulos and R. Naquet, pp. 273–285, Boston: Birkhäuser
Nathan, T., Jensen, M. S. and Lambert, J. D. (1990) The slow inhibitory postsynaptic potential in rat hippocampal CA1 neurones is blocked by intracellular injection of QX-314. Neuroscience Letters 110: 309–313CrossRefGoogle ScholarPubMed
Nauta, W. J. H. (1946) Hypothalamic regulation of sleep in rats. Experimental study. Journal of Neurophysiology 9: 285–316CrossRefGoogle ScholarPubMed
Neckelmann, D., Amzica, F. and Steriade, M. (1998) Spike-wave complexes and fast components of cortically generated seizures. III. Synchronizing mechanisms. Journal of Neurophysiology 80: 1480–1494CrossRefGoogle ScholarPubMed
Neckelmann, D., Amzica, F. and Steriade, M. (2000) Changes in neuronal conductance during different components of cortically generated spike-wave seizures. Neuroscience 96: 475–485CrossRefGoogle ScholarPubMed
Nelson, J. P., McCarley, R. W. and Hobson, J. A. (1983) REM sleep burst neurons, PGO waves, and eye movement information. Journal of Neurophysiology 50: 784–797CrossRefGoogle ScholarPubMed
Neugebauer, V., Keele, N. B. and Shinnick-Gallagher, P. (1997) Epileptogenesis in vivo enhances the sensitivity of inhibitory presynaptic metabotropic glutamate receptors in basolateral amygdala neurons in vitro. Journal of Neuroscience 17: 983–995CrossRefGoogle ScholarPubMed
Nicholson, C. (1980) Modulation of extracellular calcium and its functional implications. Federation Proceedings 39: 1519–1523Google ScholarPubMed
Nicoll, R. A., Malenka, R. C. and Kauer, J. A. (1990) Functional comparison of neurotransmitter receptor subtypes in mammalian central nervous system. Physiological Reviews 70: 513–565CrossRefGoogle ScholarPubMed
Niedermeyer, E. (1965) Sleep electroencephalograms in petit mal. Archives of Neurology 12: 625–630CrossRefGoogle ScholarPubMed
Niedermeyer, E. (1969) The Lennox-Gastaut syndrome: a severe type of childhood epilepsy. Deutsche Zeitschrift für Nervenheilkrankheiten 195: 263–282Google ScholarPubMed
Niedermeyer, E. (1993) Historical aspects. In Electroencephalography: Basic Principles, Clinical Applications and Related Field, 3rd edn., ed. E. Niedermeyer and F. Lopes da Silva, pp. 1–14, Baltimore: Williams & Wilkins
Niedermeyer, E. (1999a) Abnormal EEG patterns (epileptic and paroxysmal). In Electroencephalography: Basic Principles, Clinical Applications and Related Fields, 4th edn., ed. E. Niedermeyer and F. Lopes da Silva, pp. 235–260, Baltimore: Williams & Wilkins
Niedermeyer, E. (1999b) Epileptic seizure disorders. In Electroencephalography: Basic Principles, Clinical Applications and Related Fields, 4th edn., ed. E. Niedermeyer and F. Lopes da Silva, pp. 476–585, Baltimore: Williams & Wilkins
Nielsen, T. (2000) Cognition in REM and NREM sleep. Brain and Behavioral Sciences 23: 851–866CrossRefGoogle ScholarPubMed
Nishimura, Y., Kitagawa, H., Saitoh, K., Asahi, M., Itoh, K., Yoshioka, K., Asahara, T., Tanaka, T. and Yamamoto, T. (1996) The burst firing in the layer III and V pyramidal neurons of the cat sensorimotor cortex in vitro. Brain Research 727: 212–216CrossRefGoogle ScholarPubMed
Nishimura, Y., Asahi, M., Saitoh, K., Kitagawa, H., Kumazawa, Y., Itoh, K., Lin, M., Akamine, T., Shibuyam, H., Asahara, T. and Yamamoto, T. (2001) Ionic mechanisms underlying burst firing of layer III sensorimotor cortical neurons of the cat: and in vitro slice study. Journal of Neurophysiology 86: 771–781CrossRefGoogle ScholarPubMed
Nitecka, L., Tremblay, E., Charton, G., Bouillot, J. P., Berger, M. L. and Ben-Ari, Y. (1984) Maturation of kainic acid seizure-brain damage syndrome in the rat. II. Histopathological sequelae. Neuroscience 13: 1073–1094CrossRefGoogle ScholarPubMed
Nitz, D. and Siegel, J. M. (1997a) GABA release in the dorsal raphe nucleus: role in the control of REM sleep. American Journal of Physiology 273: R451–455Google Scholar
Nitz, D. and Siegel, J. M. (1997b) GABA release in the locus coeruleus as a function of sleep/wake state. Neuroscience 78: 795–801CrossRefGoogle Scholar
Noachtar, S. (2001) Generalized epilepsy and sleep. In Epilepsy and Sleep, ed. D. S. Dinner and H. O. Lüders, pp. 75–83, San Diego: Academic Press
Noebels, J. L. (1984) A single error of noradrenergic axon growth synchronizes central neurons. Nature 310: 409–411CrossRefGoogle Scholar
Noebels, J. L. (1999) Single-gene models of epilepsy. Advances in Neurology 79: 227–238Google ScholarPubMed
Nosjean, A., Arluison, M. and Laguzzi, R. F. (1987) Increase in paradoxical sleep after destruction of serotoninergic innervation in the nucleus tractus solitarius of the rat. Neuroscience 23: 469–481CrossRefGoogle ScholarPubMed
Nuñez, A. (1996) Unit activity of rat basal forebrain neurons: relationship to cortical activity. Neuroscience 72: 757–766CrossRefGoogle ScholarPubMed
Nuñez, A., Amzica, F. and Steriade, M. (1992a) Intrinsic and synaptically generated delta (1–4 Hz) rhythms in dorsal lateral geniculate neurons and their modulation by light-induced fast (30–70 Hz) events. Neuroscience 51: 269–284CrossRefGoogle Scholar
Nuñez, A., Amzica, F. and Steriade, M. (1992b) Intracellular evidence for incompatibility between spindle and delta oscillations in thalamocortical neurons of cat. Neuroscience 48: 75–85CrossRefGoogle Scholar
Nuñez, A., Amzica, F. and Steriade, M. (1992c) Voltage-dependent fast (20–40 Hz) oscillations in long-axoned neocortical neurons. Neuroscience 51: 7–10CrossRefGoogle Scholar
Nuñez, A., Amzica, F. and Steriade, M. (1993) Electrophysiology of cat association cortical neurons in vivo: intrinsic properties and synaptic responses. Journal of Neurophysiology 70: 418–430CrossRefGoogle ScholarPubMed
Obál, F. Jr., Alfoldi, P., Cady, A. B., Johannsen, L., Sary, G. and Krueger, J. M. (1988) Growth hormone-releasing factor enhances sleep in rats and rabbits. American Journal of Physiology 255: R310–316Google ScholarPubMed
Obál, F. Jr., Payne, L., Kapas, L., Opp, M. and Krueger, J. M. (1991) Inhibition of growth hormone-releasing factor suppresses both sleep and growth hormone secretion in the rat. Brain Research 557: 149–153CrossRefGoogle ScholarPubMed
O'Brien, J. L., Goldensohn, E. S. and Hoefer, R. T. (1959) Electroencephalographic abnormalities in addition to bilaterally synchronous 3 cycle per second spike and wave activity in petit mal. Electroencephalography and Clinical Neurophysiology 13: 747–761CrossRefGoogle Scholar
Oertel, W. H., Graybiel, A. M., Mugnaini, E., Elde, R. P., Schmechel, D. E. and Kopin, I. J. (1983) Coexistence of glutamic acid decarboxylase and somatostatin-like immunoreactivity in neurons of the feline nucleus reticularis thalami. Journal of Neuroscience 3: 1322–1332CrossRefGoogle ScholarPubMed
Ogawa, J. (1963) Midbrain reticular influences upon single neurons in lateral geniculate nucleus. Science 139: 343–344CrossRefGoogle ScholarPubMed
Ohara, P. T. and Lieberman, A. R. (1985) The thalamic reticular nucleus of the adult rat: experimental anatomical studies. Journal of Neurocytology 14: 365–411CrossRefGoogle ScholarPubMed
Ojima, H. (1994) Terminal morphology and distribution of corticothalamic fibers originating from layers 5 and 6 of cat primary auditory cortex. Cerebral Cortex 4: 646–663CrossRefGoogle ScholarPubMed
Okasaki, M. M., Evenson, D. A. and Nadler, J. V. (1995) Hippocampal mossy fiber sprouting and synapse formation after status epilepticus in rats: visualization after retrograde transport of biocytin. Journal of Comparative Neurology 352: 515–534CrossRefGoogle Scholar
O'Leary, J. L. and Goldring, S. (1976) Science and Epilepsy. New York: Raven Press
Orkand, R. K. (1969) Neuroglial-neuronal interactions. In Basic Mechanisms of the Epilepsies, ed. H. H. Jasper, A. A. Ward Jr. and A. Pope, pp. 737–746, Boston: Little, Brown
Otis, T. S., Koninck, Y. and Mody, I. (1994) Lasting potentiation of inhibition is associated with an increased number of γ-aminobutyric acid type A receptors activated during miniature inhibitory postsynaptic currents. Proceedings of the National Academy of Sciences of the USA 91: 7698–7702CrossRefGoogle ScholarPubMed
Pabst, M. J., Beranova-Giorgianni, S. and Krueger, J. M. (1999) Effects of muramyl peptides on macrophages, monokines and sleep. Neuroimmunomodulation 6: 261–283CrossRefGoogle ScholarPubMed
Pape, H. C. (1995) Nitric oxide: an adequate modulatory link between biological oscillators and control systems in the mammalian brain. Seminars in the Neurosciences 7: 329–340CrossRefGoogle Scholar
Pape, H. C. (1996) Queer current and pacemaker: the hyperpolarization-activated cation current in neurons. Annual Reviews of Physiology 58: 299–327CrossRefGoogle ScholarPubMed
Pape, H. C. and Eysel, U. T. (1987) Modulatory actions of the reticular transmitters norepinephrine and 5–hydroxytryptamine (serotonin) in the cat's visual thalamus. Society for Neuroscience Abstracts 13: 86Google Scholar
Pape, H. C. and Mager, R. (1992) Nitric oxide controls oscillatory activity in thalamocortical neurons. Neuron 9: 441–448CrossRefGoogle ScholarPubMed
Pape, H. C. and McCormick, D. A. (1989) Noradrenaline and serotonin selectively modulate thalamic burst firing by enhancing a hyperpolarization-activated cation current. Nature 340: 715–718CrossRefGoogle ScholarPubMed
Pape, H. C. and McCormick, D. A. (1995) Electrophysiological and pharmacological properties of interneurons in the cat dorsal lateral geniculate nucleus. Neuroscience 68: 1105–1125CrossRefGoogle ScholarPubMed
Pape, H. C., Budde, T., Mager, R. and Kisvrday, Z. F. (1994) Prevention of Ca2+-mediated action potentials in GABAergic local circuit neurones of rat thalamus by a transient K+ current. Journal of Physiology (London). 478: 403–422CrossRefGoogle Scholar
Pappenheimer, J. R., Miller, T. B. and Goodrich, C. A. (1967) Sleep-promoting effects of cerebrospinal fluid from sleep-deprived goats. Proceedings of the National Academy of Sciences of the USA 58: 513–517CrossRefGoogle ScholarPubMed
Paré, D. and Gaudreau, H. (1996) Projection cells and interneurons of the lateral and basolateral amygdala: distinct firing patterns and differential relation to theta and delta rhythms in conscious cats. Journal of Neuroscience 16: 3334–3350CrossRefGoogle ScholarPubMed
Paré, D. and Lang, E. J. (1998) Calcium electrogenesis in neocortical pyramidal neurons in vivo. European Journal of Neuroscience 10: 3164–3170CrossRefGoogle ScholarPubMed
Paré, D. and Llinás, R. (1995) Conscious and pre-conscious processes as seen from the standpoint of sleep-waking cycle neurophysiology. Neuropsychologia 33: 1155–1168CrossRefGoogle ScholarPubMed
Paré, D. and Smith, Y. (1993) Distribution of GABA immunoreactivity in the amygdaloid complex of the cat. Neuroscience 57: 1061–1076CrossRefGoogle ScholarPubMed
Paré, D. and Smith, Y. (1994) GABAergic projection from the intercalated cell masses of the amygdala to the basal forebrain in cats. Journal of Comparative Neurology 344: 33–49CrossRefGoogle ScholarPubMed
Paré, D. and Smith, Y. (1996) Thalamic collaterals of corticostriatal axons: their termination field and synaptic targets in cats. Journal of Comparative Neurology 372: 551–5673.0.CO;2-3>CrossRefGoogle ScholarPubMed
Paré, D. and Steriade, M. (1990) Control of mamillothalamic axis by brainstem cholinergic laterodorsal tegmental afferents: possible involvement in mnemonic processes. In Brain Cholinergic Systems, ed. M. Steriade and D. Biesold, pp. 337–354, Oxford: Oxford University Press
Paré, D., Steriade, M., Deschênes, M. and Oakson, G. (1987) Physiological properties of anterior thalamic nuclei, a group devoid of inputs from the reticular thalamic nucleus. Journal of Neurophysiology 57: 1669–1685CrossRefGoogle ScholarPubMed
Paré, D., Smith, Y., Parent, A. and Steriade, M. (1988) Projections of upper brainstem cholinergic and non-cholinergic neurons of cat to intralaminar and reticular thalamic nuclei. Neuroscience 25: 69–88CrossRefGoogle ScholarPubMed
Paré, D., Steriade, M., Deschênes, M. and Bouhassira, D. (1990) Prolonged enhancement of anterior thalamic synaptic responsiveness by stimulation of a brainstem cholinergic group. Journal of Neuroscience 10: 20–33CrossRefGoogle ScholarPubMed
Paré, D., Curró Dossi, R. and Steriade, M. (1991) Three types of inhibitory postsynaptic potentials generated by interneurons in the anterior thalamic complex of cat. Journal of Neurophysiology 66: 1190–1204CrossRefGoogle ScholarPubMed
Paré, D., Smith, Y. and Paré, J. F. (1995) Intra-amygdaloid projections of the basolateral and basomedial nuclei in the cat: Phaseolus vulgaris-leucoagglutinin anterograde tracing at the light electron microscopic level. Neuroscience 69: 567–583CrossRefGoogle ScholarPubMed
Paré, D., Shink, E., Gaudreau, H., Destexhe, A. and Lang, E. J. (1998) Impact of spontaneous synaptic activity on the resting properties of cat neocortical pyramidal neurons in vivo. Journal of Neurophysiology 79: 1450–1460CrossRefGoogle ScholarPubMed
Paré, D., Collins, D. R. and Pelletier, J. G. (2002) Amygdala oscillations and the consolidation of emotional memories. Trends in Cognitive Sciences 6: 306–314CrossRefGoogle ScholarPubMed
Parent, A. and Steriade, M. (1984) Midbrain tegmental projections of nucleus reticularis thalami of cat and monkey: a retrograde transport and antidromic identification study. Journal of Comparative Neurology 229: 548–558CrossRefGoogle Scholar
Parent, A., Paré, D., Smith, Y. and Steriade, M. (1988) Basal forebrain cholinergic and non-cholinergic projections to the thalamus and brainstem in cats and monkeys. Journal of Comparative Neurology 277: 281–301CrossRefGoogle Scholar
Parmeggiani, P. L. (1988) Thermoregulation during sleep from the view point of homeostasis. In Clinical Physiology of Sleep, ed. R. Lydic and J. F. Biebuyck, pp. 159–179, Bethesda: American Physiological Society
Parmeggiani, P. L., Azzaroni, A., Cevolani, D. and Ferrari, G. (1986) Polygraphic study of anterior hypothalamic-preoptic neuron thermosensitivity during sleep. Electroencephalography and Clinical Neurophysiology 63: 289–295CrossRefGoogle ScholarPubMed
Parmentier, R., Ohtsu, H., Djebarra-Hannas, Z., Valatx, J. L., Watanabe, T. and Lin, J. S. (2002) Anatomical, physiological, and pharmacological characteristics of histidine decarboxylase knock-out mice: evidence for the role of brain histamine in behavioral and sleep-wake control. Journal of Neuroscience 22: 7695–7711CrossRefGoogle ScholarPubMed
Parpura, V., Basarsky, T. A., Liu, F., Jeftinija, K. and Haydon, P. G. (1994) Glutamate-mediated astrocyte-neuron signaling. Nature 369: 744–747CrossRefGoogle Scholar
Parri, H. R. and Crunelli, V. (1998) Sodium current in rat and cat thalamocortical neurons: role of a non-inactivating component in tonic and burst firing. Journal of Neuroscience 18: 854–867CrossRefGoogle ScholarPubMed
Parri, H. R., Gould, T. M. and Crunelli, V. (2001) Spontaneous astrocytic Ca2+ oscillations in situ drive NMDAR-mediated neuronal excitation. Nature Neuroscience 4: 803–812CrossRefGoogle ScholarPubMed
Passouant, P. (1984) Historical aspects of sleep and epilepsy. In Epilepsy and Sleep Deprivation, ed. R. Degen and E. Niedermeyer, pp. 67–73, Amsterdam: Elsevier
Patry, F. L. (1931) The relation of time of day, sleep and other factors to the incidence of epileptic seizures. American Journal of Psychiatry 10: 789–813CrossRefGoogle Scholar
Pavlides, C. and Winson, J. (1989) Influences of hippocampal place cell firing in awake state on the activity of these cells during subsequent sleep episodes. Journal of Neuroscience 9: 2907–2918CrossRefGoogle ScholarPubMed
Pavlov, I. P. (1923) “Innere Hemmung” der bedingten Reflexe und der Schlaf – ein und derselbe Prozess. Skandinavische Archive für Physiologie 44: 42–58Google Scholar
Pedley, R. A. (1987) Epilepsy. In A Textbook of Clinical Neurology, ed. A. M. Halliday, S. R. Butler and R. Paul, pp. 231–268, New York: Wiley
Pedroarena, C. and Llinás, R. (1997) Dendritic calcium conductances generate high-frequency oscillation in thalamocortical neurons. Proceedings of the National Academy of Sciences of the USA 94: 24–28CrossRefGoogle ScholarPubMed
Pedroarena, C. and Llinás, R. (2001) Interactions of synaptic and intrinsic electroresponsiveness determine corticothalamic activation dynamics. Thalamus and Related Systems 1: 3–14Google Scholar
Pellegrini, A., Musgrave, J. and Gloor, P. (1979) Role of afferent input of subcortical origin in the genesis of bilaterally synchronous epileptic discharges of feline generalized penicillin epilepsy. Experimental Neurology 64: 155–173CrossRefGoogle ScholarPubMed
Pellegrini, A., Curró Dossi, R., Dal Pos, F., Ermani, M., Zanotto, I. and Testa, F. (1989) Ethosuximide alters intrathalamic and thalamocortical synchronizing mechanisms: a possible explanation of its antiabsence effect. Brain Research 497: 344–360CrossRefGoogle ScholarPubMed
Peña, E. and Geijo-Barrientos, E. (1996) Laminar localization, morphology, and physiological properties of pyramidal neurons that have low-threshold calcium current in the guinea-pig medial frontal cortex. Journal of Neuroscience 16: 5301–5311CrossRefGoogle ScholarPubMed
Penfield, W. and Jasper, H. H. (1954) Epilepsy and the Functional Anatomy of the Human Brain. Boston: Little, Brown
Penfield, W. and Rasmussen, T. (1950) The Cerebral Cortex of Man. A Clinical Study of Localization of Function. New York: Macmillan Co
Penry, J. K., Porter, R. J. and Dreifuss, F. E. (1971) Patterns of paroxysmal abnormal discharges in twelve-hour telemetered EEGs of untreated children with absence (petit mal) seizures. Neurology 21: 392Google Scholar
Perez-Velazquez, J. L. and Carlen, P. L. (1999) Synchronization of GABAergic interneuronal networks during seizure-like activity in the rat horizontal hippocampal slice. European Journal of Neuroscience 1111: 4110–4118CrossRefGoogle Scholar
Perez-Velazquez, J. L. and Carlen, P. L. (2000) Gap junctions, synchrony and seizures. Trends in Neurosciences 23: 68–74CrossRefGoogle ScholarPubMed
Perez-Velazquez, J. L., Valiante, T. A. and Carlen, P. L. (1994) Modulation of gap junctional mechanisms during calcium-free induced field burst activity: a possible role for electrotonic coupling in epileptogenesis. Journal of Neuroscience 14: 4308–4317CrossRefGoogle ScholarPubMed
Perkins, K. L. and Wong, R. K. S. (1995) Intracellular QX-314 blocks the hyperpolarization-activated inward current IQ in hippocampal CA1 pyramidal cells. Journal of Neurophysiology 73: 911–915CrossRefGoogle ScholarPubMed
Perreault, M. C., Qin, Y., Heggelund, P. and Zhu, J. J. (2003) Postsynaptic development of GABAergic signaling in the rat lateral geniculate nucleus: presynaptic dendritic mechanisms. Journal of Physiology (London) 546: 137–148CrossRefGoogle Scholar
Perreault, P. and Avoli, M. (1992) 4-Aminopyridine-induced epileptiform activity and a GABA-mediated long-lasting depolarization in the rat hippocampus. Journal of Neuroscience 12: 104–115CrossRefGoogle Scholar
Perrin, F., Garcia-Larrea, L., Mauguière, F. and Bastuji, H. (1999) A differential brain response to the subject's own name persists during sleep. Clinical Neurophysiology 110: 2153–2164CrossRefGoogle ScholarPubMed
Petsche, H. (1962) Pathophysiologie und Klinik des Petit-Mal. Wiener Zeitschrift für Nervenheilkrankheiten 19: 345–442Google Scholar
Petsche, H., Pockberger, H. and Rappelsberger, P. (1984) On the search for the sources of the electroencephalogram. Neuroscience 11: 1–27CrossRefGoogle ScholarPubMed
Piéron, H. (1913) Le Problème Physiologique du Sommeil. Paris: Masson
Pinault, D. (1996) A novel single-cell staining procedure performed in vivo under electrophysiological control: morpho-functional features of juxtacellularly labelled thalamic cells and other central neurons with biocytin or Neurobiotin. Journal of Neuroscience Methods 65: 113–136CrossRefGoogle ScholarPubMed
Pinault, D. and Deschênes, M. (1992a) Voltage-dependent 40-Hz oscillations in rat reticular thalamic neurons in vivo. Neuroscience 51: 245–258CrossRefGoogle Scholar
Pinault, D. and Deschênes, M. (1992b) Control of 40-Hz firing of reticular thalamic cells by neurotransmitters. Neuroscience 51: 259–268CrossRefGoogle Scholar
Pinault, D., Smith, Y. and Deschênes, M. (1997) Dendrodendritic and axoaxonic synapses in the thalamic reticular nucleus of the adult rat. Journal of Neuroscience 17: 3215–3233CrossRefGoogle ScholarPubMed
Pinault, D., Leresche, N., Charpier, S., Deniau, J. M., Marescaux, C., Vergnes, M. and Crunelli, V. (1998) Intracellular recordings in thalamic neurones during spontaneous spike and wave discharges in rats with absence epilepsy. Journal of Physiology (London) 509: 449–456CrossRefGoogle ScholarPubMed
Pinault, D., Vergnes, M. and Marescaux, C. (2001) Medium-voltage 5–9 Hz oscillations give rise to spike-and-wave discharges in a genetic model of absence epilepsy: in vivo dual extracellular recordings of thalamic relay and reticular neurons. Neuroscience 105: 181–201CrossRefGoogle Scholar
Pirchio, M., Turner, J. P., Williams, S. R., Asprodini, E. and Crunelli, V. (1997) Postnatal development of membrane properties and δ oscillations in thalamocortical neurons of the cat dorsal lateral geniculate nucleus. Journal of Neuroscience 17: 5428–5444CrossRefGoogle ScholarPubMed
Plihal, W. and Born, J. (1997) Effects of early and late nocturnal sleep on declarative and procedural memory. Journal of Cognitive Neuroscience 9: 534–547CrossRefGoogle ScholarPubMed
Plum, F. (1991) Coma and related global disturbances of the human conscious state. In Cerebral Cortex (vol. 9, Normal and Altered States of Function), ed. A. Peters and E. G. Jones, pp. 359–425, New York: Plenum
Pohlmann-Eden, B., Hoch, D. B., Cochius, J. I. and Chiappa, K. H. (1996) Periodic lateralized epileptiform discharges – a critical review. Journal of Clinical Neurophysiology 13: 519–530CrossRefGoogle ScholarPubMed
Pollen, D. A. (1964) Intracellular studies of cortical neurons during thalamic induced wave and spike. Electroencephalography and Clinical Neurophysiology 17: 398–404CrossRefGoogle ScholarPubMed
Pollen, D. and Lux, H. (1966) Conductance changes during inhibitory postsynaptic potentials in normal and strychninized cortical neurons. Journal of Neurophysiology 29: 367–381CrossRefGoogle ScholarPubMed
Pompeiano, O. (1967a) The neurophysiological mechanisms of the postural and motor events during desynchronized sleep. Proceedings of the Association for the Research of Nervous and Mental Diseases 45: 351–423Google Scholar
Pompeiano, O. (1967b) Sensory inhibition during motor activity in sleep. In Neurophysiological Basis of Normal and Abnormal Motor Activities, ed. M. D. Yahr and D. P. Purpura, pp. 323–375, New York: Raven Press
Pool, J. L. (1954) Psychosurgery in older people. Journal of American Geriatric Society 2: 456–465CrossRefGoogle ScholarPubMed
Porkka-Heiskanen, T., Strecker, R. E., Thakkar, M., Bjorkum, A. A., Greene, R. W. and McCarley, R. W. (1997) Adenosine: a mediator of the sleep-inducing effects of prolonged wakefulness. Science 276: 1265–1268CrossRefGoogle ScholarPubMed
Portas, C. M., Thakkar, M., Rainnie, D. G., Greene, R. W. and McCarley, R. W. (1997) Role of adenosine in behavioral state modulation: a microdialysis study in the freely moving cat. Neuroscience 79: 225–235CrossRefGoogle ScholarPubMed
Portas, C. M., Krakow, K., Allen, P., Josephs, O., Armony, J. L. and Frith, C. D. (2000) Auditory processing across the sleep-wake cycle: simultaneous EEG and fMRI monitoring in humans. Neuron 28: 991–999CrossRefGoogle ScholarPubMed
Porter, R. J. (1993) The absence epilepsies. Epilepsia 34 (Suppl. 3): S42–S48CrossRefGoogle ScholarPubMed
Preuss, T. M. and Goldman-Rakic, P. S. (1987) Crossed corticothalamic and thalamocortical connections of macaque prefrontal cortex. Journal of Comparative Neurology 257: 269–281CrossRefGoogle ScholarPubMed
Prevett, M. C., Duncan, J. S., Jones, T., Fish, D. R. and Brooks, D. J. (1995) Demonstration of thalamic activation during typical absence seizures during H215O and PET. Neurology 45: 1396–1402CrossRefGoogle Scholar
Price, J. L. and Amaral, D. (1981) An autoradiographic study of the projections of the central nucleus of the monkey amygdala. Journal of Neuroscience 1: 1242–1259CrossRefGoogle ScholarPubMed
Prince, D. A. (1968) Inhibition in “epileptic” neurons. Experimental Neurology 21: 467–485CrossRefGoogle ScholarPubMed
Prince, D. A. (1975) Topical convulsants drugs and metabolic antagonists. In Experimental Models of Epilepsy, ed. D. P. Purpura, J. K. Penry, D. B. Tower, D. M. Woodbury and R. D. Walter, pp. 51–83, New York: Raven Press
Prince, D. A. (1983) Ionic mechanisms in cortical and hippocampal epileptogenesis. In Basic Mechanisms of Neuronal Hyperexcitability, ed. H. H. Jasper and N. M. van Gelder, pp. 217–238, New York: Alan R. Liss
Prince, D. A. and Farrell, D. (1963) “Centrencephalic” spike-wave discharges following parenteral injection of penicillin in the cat. Neurology 19: 309–310Google Scholar
Prince, D. A. and Jacobs, K. (1998) Inhibitory function in two models of chronic epileptogenesis. Epilepsy Research 32: 83–92CrossRefGoogle ScholarPubMed
Prince, D. A. and Shanzer, S. (1966) Effects of anesthetics upon the EEG response to reticular stimulation of slow synchrony. Electroencephalography and Clinical Neurophysiology 21: 578–588CrossRefGoogle ScholarPubMed
Prince, D. A. and Tseng, G. F. (1993) Epileptogenesis in chronically injured cortex: in vitro studies. Journal of Neurophysiology 69: 1276–1291CrossRefGoogle ScholarPubMed
Puizillout, J. J. and Ternaux, J. (1974) Endormement vago-aortique après section sagittale médiane du tronc cérébral et après administration de p-chlophenylalanine or destruction des noyaux du raphé. Brain Research 70: 9–42CrossRefGoogle Scholar
Puizillout, J. J., Gaudin-Chazal, G., Daszuta, A., Seyfritz, N. and Ternaux, J. P. (1979) Release of endogenous serotonin from encéphale isolé cats. II. Correlations with raphe neuronal activity and sleep and wakefulness. Journal de Physiologie (Paris) 75: 531–537Google ScholarPubMed
Puizillout, J. J., Gaudin-Chazal, G. and Bras, H. (1984) Vagal mechanisms in sleep regulation. In Sleep Mechanisms, ed. A. Borbély and J. L. Valatx, pp. 19–38 (Suppl. 8 of Experimental Brain Research), Berlin: Springer
Pumain, R., Menini, C., Heinemann, U., Louvel, J. and Silva-Barrat, C. (1985) Chemical synaptic transmission is not necessary for epileptic seizures to persist in the baboon Papio papio. Experimental Neurology 89: 250–258CrossRefGoogle Scholar
Purpura, D. P. (1970) Operations and processes in thalamic and synaptically related neural subsystems. In The Neuroscience: Second Study Program, ed. F. O. Schmitt, pp. 458–470, New York: Rockefeller University Press
Purpura, D. P. and Cohen, B. (1962) Intracellular recording from thalamic neurons during recruiting responses. Journal of Neurophysiology 25: 621–635CrossRefGoogle ScholarPubMed
Purpura, D. P. and Shofer, R. J. (1963) Intracellular recording from thalamic neurons during reticulocortical activation. Journal of Neurophysiology 26: 494–505CrossRefGoogle ScholarPubMed
Purpura, D. P., McMurtry, J. G. and Maekawa, K. (1966) Synaptic events in ventrolateral thalamic neurons during suppression of recruiting responses by brain stem reticular stimulation. Brain Research 1: 63–76CrossRefGoogle ScholarPubMed
Purpura, D. P., Bodick, N., Suzuki, K., Rapin, I. and Wurtzelmann, S. (1982) Microtubule disarray in cortical dendrites and neurobehavioral failure. I. Golgi and electron microscope studies. Brain Research 281: 287–297CrossRefGoogle Scholar
Qin, Y. L., McNaughton, B. L., Skaggs, W. E. and Barnes, C. A. (1997) Memory reprocessing in corticocortical and hippocampocortical neurons ensembles. Philosophical Transactions of the Royal Society (London, Series B) 352: 1525–1533CrossRefGoogle ScholarPubMed
Quirk, G. J., Muller, R. U., Kubie, J. L. and Ranck, J. B. Jr. (1992) The positional firing properties of medial entorhinal neurons: description and comparison with hippocampal place cells. Journal of Neuroscience 12: 1945–1963CrossRefGoogle ScholarPubMed
Racine, R. J., Burnham, W. M., Gilbert, M. and Kairiss, E. W. (1986) Kindling mechanisms. I. Electrophysiological studies. In Kindling 3, ed. J. A. Wada, pp. 263–282, New York: Raven
Raczkowski, D. and Fitzpatrick, D. (1989) Organization of cholinergic synapses in the cat's dorsal lateral geniculate and perigeniculate nuclei. Journal of Comparative Neurology 288: 231–254Google ScholarPubMed
Radulovacki, M. (1985) Role of adenosine in sleep in rats. Review of Clinical and Basic Pharmacology 5: 327–339Google ScholarPubMed
Raichle, M. E. (1998) Behind the scenes of functional brain imaging: a historical and physiological perspective. Proceedings of the National Academy of Sciences of the USA 95: 765–772CrossRefGoogle ScholarPubMed
Rainey, W. T. and Jones, E. G. (1983) Spatial distribution of individual medial lemniscal axons in the thalamic ventrobasal complex of the cat. Experimental Brain Research 49: 229–246CrossRefGoogle ScholarPubMed
Rainnie, D. G., Holmes, K. H. and Shinnick-Gallagher, P. (1992) Kindling-induced long-lasting changes in synaptic transmission in the basolateral amygdala. Journal of Neurophysiology 67: 443–454CrossRefGoogle ScholarPubMed
Rainnie, D. G., Grünze, H. C. R., McCarley, R. W. and Greene, R. W. (1994) Adenosine inhibition of mesopontine cholinergic neurons: implications for EEG arousal. Science 263: 689–692CrossRefGoogle ScholarPubMed
Ralston, B. and Ajmone-Marsan, C. (1956) Thalamic control of certain normal and abnormal cortical rhythms. Electroencephalography and Clinical Neurophysiology 8: 559–582CrossRefGoogle Scholar
Ramm, P. and Frost, B. J. (1983) Regional metabolic activity in the rat brain during sleep-like activity. Sleep 6: 196–216CrossRefGoogle Scholar
Rámon y Cajal, S. (1911) Histologie du Système Nerveux de l'Homme et des Vertéés (2 vol.), translated by L. Azoulay. Paris: Maloine. Also the 1952 edition, Madrid: Consejo Superior de Investigaciones Scientificas, Instituto Rámon y Cajal
Rasmusson, D. D., Clow, K. and Szerb, J. C. (1994) Modification of neocortical acetylcholine release and electroencephalogram desynchronization due to brainstem stimulation by drugs applied to the basal forebrain. Neuroscience 60: 665–677CrossRefGoogle ScholarPubMed
Rasmusson, D. D., Szerb, J. C. and Jordan, J. L. (1996) Differential effects of α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid and N-methyl-d-aspartate receptor antagonists applied to the basal forebrain on cortical acetylcholine release and EEG desynchronization. Neuroscience 72: 419–427CrossRefGoogle Scholar
Rechtschaffen, A. (1998) Current perspectives on the function of sleep. Perspectives in Biology and Medicine 41: 359–390CrossRefGoogle ScholarPubMed
Rechtschaffen, A., Lovell, R. A., Freedman, D., Whitehead, W. E. and Aldrich, M. (1973) The effect of parachlorophenylalanine on sleep in the rat: some implications for the serotonin sleep hypothesis. In Serotonin and Behavior, ed. J. Barchas and E. Usdin, pp. 401–418, New York: Academic
Rechtschaffen, A., Bergmann, B. M., Everson, C. A., Kushida, C. A. and Gilliland, M. A. (1989a) Sleep deprivation in the rat. I. Conceptual issues. Sleep 12: 1–4CrossRefGoogle Scholar
Rechtschaffen, A., Bergmann, B. M., Everson, C. A., Kushida, C. A. and Gilliland, M. A. (1989b) Sleep deprivation in the rat. X. Integration and discussion of the findings. Sleep 12: 68–87Google Scholar
Reiher, J., Lebel, M. and Klass, D. W. (1977) Small sharp spikes (SSS): reassessment of electroencephalographic characteristics and clinical significance. Electroencephalography and Clinical Neurophysiology 43: 775Google Scholar
Rempe, D. A., Bertram, E. H., Williamson, J. M. and Lothman, E. W. (1997) Interneurons in area CA1, stratum radiatum and stratum oriens remain functionally connected to excitatory synaptic input in chronically epileptic animals. Journal of Neurophysiology 78: 1504–1515CrossRefGoogle ScholarPubMed
Renaud, L., Kelly, J. and Provini, L. (1974) Synaptic inhibition in pyramidal tract neurons: membrane potential and conductance changes evoked by pyramidal tract and cortical surface stimulation. Journal of Neurophysiology 37: 1144–1155CrossRefGoogle ScholarPubMed
Reutens, D. C., Bye, A. M., Hopkins, I. J., Danks, A., Somerville, E., Walsh, J., Bleasel, A., Ouvrier, R., McKenzie, R. A. and Manson, J. I. (1993) Corpus callosotomy for intractable epilepsy: seizure outcome and prognostic factors. Epilepsia 34: 904–909CrossRefGoogle ScholarPubMed
Ribak, C. E. and Peterson, G. M. (1991) Intragranular mossy fibers in rats and gerbils form synapses with the somata and proximal dendrites of basket cells in the dentate gyrus. Hippocampus 1: 355–364CrossRefGoogle ScholarPubMed
Riou, F., Cespuglio, R. and Jouvet, M. (1982) Endogenous peptides and sleep in the rat. III. The hypnogenic properties of vasoactive intestinal peptide. Neuropeptides 2: 265–277CrossRefGoogle Scholar
Rodin, E. (1999) Decomposition and mapping of generalized spike-wave complexes. Clinical Neurophysiology 110: 1868–1875CrossRefGoogle ScholarPubMed
Roffwarg, H. P., Muzio, J. N. and Dement, W. C. (1966) Ontogenetic development of the human sleep-dream cycle. Science 152: 604–619CrossRefGoogle ScholarPubMed
Roger, A., Rossi, G. F. and Zirondoli, A. (1956) Le rôle des afférences des nerfs craniens dans le maintien de l'etat vigile de la preparation “encéphale isolé”. Electroencephalography and Clinical Neurophysiology 8: 1–13CrossRefGoogle Scholar
Romanski, L. M. and LeDoux, J. E. (1992) Equipotentiality of thalamo-amygdala and thalamo-cortico-amygdala circuits in auditory fear conditioning. Journal of Neuroscience 12: 4501–4509CrossRefGoogle ScholarPubMed
Rosen, A. S. and Andrew, R. D. (1990) Osmotic effects upon excitability in rat neocortical slices. Neuroscience 38: 579–590CrossRefGoogle ScholarPubMed
Ross, J. J., Johnson, L. C. and Walter, R. D. (1966) Spike and wave discharges during stages of sleep. Annals of Neurology 14: 399–407Google Scholar
Roth, M., Shaw, J. and Green, J. (1956) The form, voltage distribution and physiological significance of the K-complex. Electroencephalography and Clinical Neurophysiology 8: 385–402CrossRefGoogle ScholarPubMed
Rougeul-Buser, A., Bouyer, J. J., Montaron, M. F. and Buser, P. (1983) Patterns of activities in the ventrobasal thalamus and somatic cortex SI during behavioural immobility in the awake cat: focal waking rhythms. Experimental Brain Research 7 (Suppl.): 69–87CrossRefGoogle Scholar
Roy, J. P., Clercq, M., Steriade, M. and Deschênes, M. (1984) Electrophysiology of neurons of the lateral thalamic nuclei in cat: mechanisms of long-lasting hyperpolarizations. Journal of Neurophysiology 51: 1220–1235CrossRefGoogle ScholarPubMed
Roy, S. A., Dear, S. P. and Alloway, K. D. (2001) Long-range cortical synchronization without concomitant oscillations in the somatosensory system of anesthetized cats. Journal of Neuroscience 21: 1795–1808CrossRefGoogle ScholarPubMed
Royer, S., Martina, M. and Paré, D. (1999) An inhibitory interface gates impulse traffic between the input and output stations of the amygdala. Journal of Neuroscience 19: 10575–10583CrossRefGoogle ScholarPubMed
Royer, S., Martina, M. and Paré, D. (2000a) Polarized synaptic interactions between intercalated neurons of the amygdala. Journal of Neurophysiology 83: 3509–3518CrossRefGoogle Scholar
Royer, S., Martina, M. and Paré, D. (2000b) Bistable behavior of inhibitory neurons controlling impulse traffic through amygdala: role of a slowly deinactivating K+ current. Journal of Neuroscience 20: 9034–9039CrossRefGoogle Scholar
Rubboli, G., Meletti, S., Gardella, E., Zaniboni, A., D'Orsi, G., Dravet, C. and Tassinari, C. A. (1999) Photic reflex myoclonus: a neuropphysiological study in progressive myoclonus epilepsies. Epilepsia 40 (Suppl. 4): 50–58CrossRefGoogle ScholarPubMed
Ruch-Monachon, M. A., Jaffre, M. and Haefely, W. (1976) Drugs and PGO waves in the lateral geniculate body of the curarized cat. IV. The effects of acetylcholine, GABA and benzodiazepines on PGO wave activity. Archives Internationales de Pharmacodynamie et Thérapie 219: 308–325Google ScholarPubMed
Rudy, B. and McBain, C. J. (2001) Kv3 channels: voltage-gated K+ channels designed for high-frequency repetitive firing. Trends in Neurosciences 24: 517–526CrossRefGoogle ScholarPubMed
Russchen, F. T., Amaral, D. G. and Price, J. L. (1985) The afferent connections of the substantia innominata in the monkey, Macaca fascicularis. Journal of Comparative Neurology 242: 1–27CrossRefGoogle ScholarPubMed
Sadler, R. M. and Blume, W. T. (1989) Significance of bisynchronous spike-wave in patients with temporal lobe spikes. Epilepsia 30: 143–146CrossRefGoogle ScholarPubMed
Sakai, K. and Crochet, S. (2000) Serotonergic dorsal raphe neurons cease firing by disfacilitation during paradoxical sleep. NeuroReport 11: 3237–3241CrossRefGoogle ScholarPubMed
Sakai, K. and Crochet, S. (2001a) Differentiation of presumed serotonergic dorsal raphe neurons in relation to behavior and wake-sleep states. Neuroscience 104: 1141–1155CrossRefGoogle Scholar
Sakai, K. and Crochet, S. (2001b) Role of dorsal raphe neurons in paradoxical sleep generation in the cat: no evidence for a serotonergic mechanisms. European Journal of Neuroscience 13: 103–112Google Scholar
Sakai, K. and Jouvet, M. (1980) Brain stem PGO-on cells projecting directly to the cat dorsal lateral geniculate nucleus. Brain Research 194: 500–505CrossRefGoogle ScholarPubMed
Sakai, K., El Mansari, M. and Jouvet, M. (1990) Inhibition by carbachol microinjections of presumptive cholinergic PGO-on neurons in freely moving cats. Brain Research 527: 213–223CrossRefGoogle ScholarPubMed
Sakai, K., Crochet, S. and Onoe, H. (2001) Pontine structures and mechanisms involved in the generation of paradoxical (REM) sleep. Archives Italiennes de Biologie 139: 93–107Google ScholarPubMed
Sakakura, H. (1968) Spontaneous and evoked unitary activities of cat lateral geniculate neurons in sleep and wakefulness. Japanese Journal of Physiology 18: 23–42CrossRefGoogle ScholarPubMed
Sallanon, M., Sakai, K., Buda, C., Puymartin, M. and Jouvet, M. (1986) Augmentation du sommeil paradoxal, induite par l'injection d'acide iboténique dans l'hypothalamus ventrolatéral postérieur, chez le chat. Comptes Rendus de l'Académie de Sciences (Paris) 303: 175–179Google Scholar
Sallanon, M., Denoyer, M., Kitahama, K., Aubert, C., Gay, N. and Jouvet, M. (1989) Long-lasting insomnia induced by preoptic lesions and its transient reversal by muscimol injection into the posterior hypothalamus in the cat. Neuroscience 32: 669–683CrossRefGoogle ScholarPubMed
Sammaritano, M., Gigli, G. L. and Gotman, J. (1991) Interictal spiking during wakefulness and sleep and the localization of foci in temporal lobe epilepsy. Neurology 41: 290–297CrossRefGoogle ScholarPubMed
Samoriski, G. M. and Applegate, C. D. (1997) Repeated generalized seizures induce time-dependent changes in the behavioral seizure response independent of continued seizure induction. Journal of Neuroscience 17: 5581–5590CrossRefGoogle ScholarPubMed
Sanchez, R. and Leonard, C. S. (1996) NMDA-receptor-mediated synaptic currents in guinea pig laterodorsal tegmental neurons in vitro. Journal of Neurophysiology 76: 1101–1111CrossRefGoogle ScholarPubMed
Sanchez-Vives, M. V. and McCormick, D. A. (1997a) Functional properties of perigeniculate inhibition of dorsal lateral geniculate nucleus thalamocortical neurons in vitro. Journal of Neuroscience 17: 8880–8893CrossRefGoogle Scholar
Sanchez-Vives, M. V. and McCormick, D. A. (1997b) Inhibitory interactions between perigeniculate GABAergic neurons. Journal of Neuroscience 17: 8894–8908CrossRefGoogle Scholar
Sanchez-Vives, M. V. and McCormick, D. A. (2000) Cellular and network mechanisms of rhythmic recurrent activity in neocortex. Nature Neuroscience 3: 1027–1034CrossRefGoogle ScholarPubMed
Sanchez-Vives, M. V., Bal, T. and McCormick, D. A. (1997) Inhibitory interactions between perigeniculate GABAergic neurons. Journal of Neuroscience 17: 8894–8908CrossRefGoogle ScholarPubMed
Saper, C. B., Chou, T. C. and Scammell, T. E. (2001) The sleep switch: hypothalamic control of sleep and wakefulness. Trends in Neurosciences 24: 726–731CrossRefGoogle ScholarPubMed
Sato, S., Dreifuss, F. E. and Penry, J. K. (1973) The effects of sleep on spike-wave discharges in absence seizures. Neurology 23: 1335–1345CrossRefGoogle Scholar
Sato, S., White, B. G., Penry, J. K., Dreifuss, F. E., Sackellares, J. C. and Kupferberg, H. J. (1982) Valproic acid versus ethosuximide in the treatment of absence seizures. Neurology 32: 157–163CrossRefGoogle ScholarPubMed
Saunders, M. G. and Westmoreland, B. F. (1979) The EEG in evaluation of disorders affecting the brain diffusely. In Current Practice of Clinical Electroencephalography, ed. D. W. Klass and D. D. Daly, pp. 343–379, New York: Raven Press
Sawyer, S. F., Tepper, J. M. and Groves, P. M. (1994) Cerebellar-responsive neurons in the thalamic ventroanterior-ventrolateral complex of rats: light and electron microscopy. Neuroscience 63: 725–745CrossRefGoogle ScholarPubMed
Scharfman, H. E., Goodman, J. H., Du, F. and Schwarcz, R. (1998) Chronic changes in synaptic responses of entorhinal and hippocampal neurons after amino-oxyacetic acid (AOAA)-induced entorhinal cortical neuron loss. Journal of Neurophysiology 80: 3031–3046CrossRefGoogle ScholarPubMed
Scheibel, M. E., Crandall, P. H. and Scheibel, A. B. (1974) The hippocampal-dentate complex in temporal lobe epilepsy. Epilepsia 15: 55–80CrossRefGoogle ScholarPubMed
Scherg, M., Bast, T. and Berg, P. (1999) Multiple source analysis of interictal spikes: goals, requirements and clinical value. Journal of Clinical Neurophysiology 16: 214–224CrossRefGoogle ScholarPubMed
Schiff, N. D., Labar, D. R. and Victor, J. D. (1999) Common dynamics in temporal lobe seizures and absence seizures. Neuroscience 91: 417–428CrossRefGoogle ScholarPubMed
Schwartzkroin, P. A. (1975) Characteristics of CA1 neurons recorded intracellularly in the hippocampal in vitro slice preparation. Brain Research 85: 423–432CrossRefGoogle ScholarPubMed
Schwartzkroin, P. A. (1977) Further characteristics of hippocampal CA1 cells in vitro. Brain Research 128: 53–68CrossRefGoogle ScholarPubMed
Schwartzkroin, P. A. (1983) Local circuit considerations and intrinsic neuronal properties involved in hyperexcitability and cell synchronization. In Basic Mechanisms of Neuronal Hyperexcitability, ed. H. H. Jasper and N. M. van Gelder, pp. 75–105, New York: Alan R. Liss
Schwartzkroin, P. A. and Mueller, A. L. (1987) Electrophysiology of hippocampal neurons. In Cerebral Cortex (vol. 6, Further Aspects of Cortical Function, Including Hippocampus), ed. E. G. Jones and A. Peters, pp. 295–343, New York: Plenum
Schwartzkroin, P. A. and Prince, D. A. (1978) Cellular and field potential properties of epileptogenic hippocampal slices. Brain Research 147: 117–130CrossRefGoogle ScholarPubMed
Schwartzkroin, P. A. and Prince, D. A. (1980) Changes in excitatory and inhibitory synaptic potentials leading to epileptogenic activity. Brain Research 183: 61–73CrossRefGoogle ScholarPubMed
Schwindt, P. C. and Crill, W. E. (1995) Amplification of synaptic currents by persistent sodium conductance in apical dendrite of neocortical neurons. Journal of Neurophysiology 74: 2220–2224CrossRefGoogle Scholar
Schwindt, P. C., Spain, W. J., Foehring, R. C., Stafstrom, C. E., Chubb, M. C. and Crill, W. E. (1988a) Multiple potassium conductances and their functions in neurons from cat sensorimotor cortex in vitro. Journal of Neurophysiology 59: 424–449CrossRefGoogle Scholar
Schwindt, P. C., Spain, W. J., Foehring, R. C., Chubb, M. C. and Crill, W. E. (1988b) Slow conductances in neurons from cat sensorimotor cortex in vitro and their role in slow excitability changes. Journal of Neurophysiology 59: 450–467CrossRefGoogle Scholar
Schwindt, P. C., Spain, W. J. and Crill, W. E. (1989) Long-lasting reduction of excitability by a sodium-dependent potassium current in cat neocortical neurons. Journal of Neurophysiology 61: 233–244CrossRefGoogle ScholarPubMed
Scott, D. E. (1993) The History of Epileptic Therapy: Account of How Medication was Discovered. Pearl River, NY: The Parthenon Publishing Group
Seidenbecher, T. and Pape, H. C. (2001) Contribution of intralaminar thalamic nuclei to spike-and-wave-discharges during spontaneous seizures in a genetic model of absence epilepsy. European Journal of Neuroscience 13: 1537–1546CrossRefGoogle Scholar
Seidenbecher, T., Staak, R. and Pape, H. T. (1998) Relations between cortical and thalamic cellular activities during absence seizures in rats. European Journal of Neuroscience 10: 1103–1112CrossRefGoogle ScholarPubMed
Sejnowski, T. J. and Destexhe, A. (2000) Why do we sleep?Brain Research 886: 208–223CrossRefGoogle ScholarPubMed
Semba, K. and Fibiger, H. (1992) Afferent connections of the laterodorsal and the pedunculopontine tegmental nuclei in the rat: a retro- and anterograde transport and immunohistochemical study. Journal of Comparative Neurology 323: 387–410CrossRefGoogle ScholarPubMed
Semba, K., Reiner, P. B., McGeer, E. G. and Fibiger, H. (1989) Brainstem projecting neurons in the rat basal forebrain: neurochemical, topographical, and physiological distinctions from cortically projecting cholinergic neurons. Brain Research Bulletin 22: 501–509CrossRefGoogle ScholarPubMed
Señaris, R. M., Humphrey, P. P. A. and Emson, P. C. (1994) Distribution of somatostatin receptors 1, 2 and 3 mRNA in rat brain and pituitary. European Journal of Neuroscience 6: 1883–1896CrossRefGoogle ScholarPubMed
Sernagor, E., Yarom, Y. and Werman, R. (1986) Sodium-dependent regenerative responses in dendrites of axotomized motoneurons in the cat. Proceedings of the National Academy of Sciences of the USA 83: 7966–7970CrossRefGoogle ScholarPubMed
Servit, Z. (1959) Audiogenic epilepsy in rats as a model of reflex mechanisms in the pathogenesis of epileptic seizures. Journal of Experimental Medical Sciences 3: 37–44Google Scholar
Seyfried, T. N. and Todorova, M. (1999) Experimental models of epilepsy. In The Epilepsies, ed. P. Kotagal and H. O. Lüders, pp. 527–542, San Diego: Academic Press
Shadlen, M. N. and Movshon, J. A. (1999) Synchrony unbound: a critical evaluation of the temporal binding hypothesis. Neuron 24: 67–77CrossRefGoogle ScholarPubMed
Shatz, C. J. (1983) The prenatal development of the cat's retinogeniculate pathway. Journal of Neuroscience 3: 482–499CrossRefGoogle ScholarPubMed
Shatz, C. J. and Rakic, P. (1981) The genesis of efferent connections from the visual cortex of fetal rhesus monkey. Journal of Comparative Neurology 196: 287–308CrossRefGoogle ScholarPubMed
Sheer, D. (1984) Focused arousal, 40 Hz, and dysfunction. In Selfregulation of the Brain and Behavior, ed. T. Ebert, pp. 64–84, Berlin: Springer
Sherin, J. E., Shiromani, P. J., McCarley, R. W. and Saper, C. B. (1996) Activation of preoptic neurons during sleep. Science 271: 216–219CrossRefGoogle ScholarPubMed
Sherrington, C. S. (1955) Man on his Nature. New York: Doubleday
Shibasaki, H. and Neshige, R. (1987) Photic cortical reflex myoclonus. Annals of Neurology 22: 252–257CrossRefGoogle ScholarPubMed
Shibata, M., Blatteis, C. M., Krueger, J. M., Obál, F. Jr. and Opp, M. (1989) Pyrogenic, inflammatory and somnogenic responses to cytokines: differential modes of action. In Thermoregulation Research and Clinical Applications, ed. P. Lomax and E. Schanbaun, pp. 69–73, Basel: Karger
Shima, K., Nakahama, H. and Yamamoto, M. (1986) Firing properties of two types of nucleus raphe dorsalis neurons during the sleep-waking cycle and their responses to sensory stimuli. Brain Research 399: 317–326CrossRefGoogle ScholarPubMed
Shoham, S. and Krueger, J. M. (1988) Muramyl dipeptide-induced sleep and fever: effects of ambient temperature and time of injections. American Journal of Physiology 255: R157–165Google ScholarPubMed
Shoham, S., Davenne, D., Cady, A. B., Dinarello, C. A. and Krueger, J. M. (1987) Recombinant tumor necrosis factor and interleukin 1 enhance slow-wave sleep. American Journal of Physiology 253: R142–149Google ScholarPubMed
Shouse, M. N. (2001) Physiology underlying relationship of epilepsy and sleep. In Epilepsy and Sleep, ed. D. S. Dinner and H. O. Lüders, pp. 43–62, San Diego: Academic Press
Shouse, M. N., Martins da Silva, A. and Sammaritano, M. (1996) Circadian rhythm, sleep, and epilepsy. Journal of Clinical Neurophysiology 13: 32–50CrossRefGoogle ScholarPubMed
Siapas, A. G. and Wilson, M. A. (1998) Coordinated interactions between hippocampal ripples and cortical spindles during slow-wave sleep. Neuron 21: 1123–1128CrossRefGoogle ScholarPubMed
Sik, A., Penttonen, M., Ylinen, A. and Buzsáki, G. (1995) Hippocampal CA1 interneurons: an in vivo intracellular study. Journal of Neuroscience 15: 6651–6665CrossRefGoogle Scholar
Silva, A. J., Kogan, J. H., Frankland, P. W. and Kida, S. (1998) CREB and memory. Annual Reviews of Neuroscience 21: 127–148CrossRefGoogle ScholarPubMed
Silva-Barrat, C., Champagnat, J., Leiva, J. and Pavlik, V. (1994) Noradrenaline mediates paradoxical effects on rat neocortical neurons after GABA withdrawal. Journal of Neurophysiology 71: 1139–1150CrossRefGoogle ScholarPubMed
Silveira, D. C., Holmes, G. L., Schachter, S. C., Geula, C. and Schomer, D. L. (2000) Increased susceptibility to generalized seizures after immunolesions of the basal forebrain cholinergic neurons in rats. Brain Research 878: 223–227CrossRefGoogle ScholarPubMed
Simon, N. R., Lopes da Silva, F. H. and Manshanden, I. (1999) Preliminary results from a whole-head MEG study of sleep. In Recent Advances in Biomagnetism, ed. T. Yoshimoto, pp. 373–376, Sendai: Tohoku University Press
Simon, N. R., Mandshanden, I. and Lopes da Silva, F. H. (2000) A MEG study of sleep. Brain Research 860: 64–76CrossRefGoogle Scholar
Singer, W. (1977) Control of thalamic transmission by corticofugal and ascending pathways in the visual system. Physiological Reviews 57: 386–420CrossRefGoogle ScholarPubMed
Singer, W. (1990a) Search for coherence: a basic principle of cortical self-organization. Concepts in Neuroscience 1: 1–26Google Scholar
Singer, W. (1990b) Role of acetylcholine in use-dependent plasticity of the visual cortex. In Brain Cholinergic Systems, ed. M. Steriade and D. Biesold, pp. 314–336, Oxford: Oxford University Press
Slaght, S., Charpier, S., Deniau, J. M., Leresche, N. and Crunelli, V. (2000) In vivo intracellular recordings in neurones of the nucleus reticularis thalami during spike and wave discharges in the GAERS genetic model of absence epilepsy. Society of Neuroscience Abstracts 26: 735Google Scholar
Slaght, S. J., Leresche, N., Deniau, J. M., Crunelli, V. and Charpier, S. (2002) Activity of thalamic reticular neurons during spontaneous genetically determined spike and wave discharges. Journal of Neuroscience 22: 2323–2334CrossRefGoogle ScholarPubMed
Sloviter, R. S. (1987) Decreased hippocampal inhibition and a selective loss of interneurons in experimental epilepsy. Science 235: 73–76CrossRefGoogle Scholar
Sloviter, R. S. (1992) Possible functional consequences of synaptic reorganization in the dentate gyrus of kainite-treated rats. Neuroscience Letters 137: 91–96CrossRefGoogle Scholar
Smart, T. G., Xie, X. and Krishek, B. J. (1994) Modulation of inhibitory and excitatory amino acid receptor ion channels by zinc. Progress in Neurobiology 42: 393–441CrossRefGoogle ScholarPubMed
Smith, K. A. and Fisher, R. S. (1996) The selective GABAB antagonist CGP-35348 blocks spike-wave bursts in the cholesterol synthesis rat absence epilepsy model. Brain Research 729: 147–150Google ScholarPubMed
Smith, T. G. and Purpura, D. P. (1960) Electrophysiological studies on epileptogenic lesions of cat cortex. Electroencephalography and Clinical Neurophysiology 12: 59–82CrossRefGoogle ScholarPubMed
Smith, Y., Paré, D., Deschênes, M., Parent, A. and Steriade, M. (1988) Cholinergic and non-cholinergic projections from the upper brainstem to the visual thalamus in the cat. Experimental Brain Research 70: 166–180Google ScholarPubMed
Snead, O. C. (1995) Basic mechanisms of generalized absence seizures. Annals of Neurology 37: 146–157CrossRefGoogle ScholarPubMed
Snead, O. C., Depaulis, A., Vergnes, M. and Marescaux, C. (1999) Absence epilepsy: advances in experimental animal models. In Jasper's Basic Mechanisms of the Epilepsies, ed. A. V. Delgado-Escueta, W. Wilson, R. W. Olsen and R. J. Porter, 253–278, New York: Raven
Snead, O. C., Banerjee, P. K., Burnham, M. and Hampson, D. (2000) Modulation of absence seizures by the GABAAreceptor: a critical role for metabotropic glutamate receptor (mGluR4). Journal of Neuroscience 20: 6218–6224CrossRefGoogle Scholar
Snyder, S. H. and Bredt, D. A. (1991) Nitric oxide as a neuronal messenger. Trends in Pharmacological Sciences 12: 125–128CrossRefGoogle ScholarPubMed
Soderling, T. R. and Derkach, V. A. (2000) Postsynaptic protein phosphorylation and LTP. Trends in Neurosciences 23: 75–80CrossRefGoogle ScholarPubMed
Sohal, V. S., Huntsman, M. M. and Huguenard, J. R. (2000) Reciprocal inhibitory connections regulate the spatiotemporal properties of intrathalamic oscillations. Journal of Neuroscience 20: 1735–1745CrossRefGoogle ScholarPubMed
Solomon, J. S., Doyle, J. F., Burkhalter, H. and Nerbonne, J. M. (1993) Differential expression of hyperpolarization-activated currents reveals distinct classes of visual cortical projection neurons. Journal of Neuroscience 13: 5082–5091CrossRefGoogle ScholarPubMed
Soltesz, I. and Crunelli, V. (1992) GABAA and pre- and post-synaptic GABAB receptor-mediated responses in the lateral geniculate nucleus. In Progress in Brain Research (vol. 90), ed. R. R. Mize, R. E. Marc and A. M. Sillito, pp. 151–169, Amsterdam: Elsevier
Soltesz, I., Lightowler, S., Leresche, N., Jassik-Gerschenfeld, D. and Crunelli, V. (1991) Two inward currents and the transformation of low-frequency oscillations of rat and cat thalamocortical cells. Journal of Physiology (London) 441: 175–197CrossRefGoogle ScholarPubMed
Somogyi, P. (1977) A specific “axo-axonal” interneuron in the visual cortex of the rat. Brain Research 136: 345–350CrossRefGoogle ScholarPubMed
Somogyi, P. (1989) Synaptic organisation of GABAergic neurons and GABAA receptors in the lateral geniculate nucleus and visual cortex. In Retina Research Foundation Symposium, vol. 2, Neural mechanisms of visual perception, ed. D. K. T. Lam and C. D. Gilbert, pp. 35–62, Woodlands, TX: Portfolio
Somogyi, P. and Cowey, A. (1981) Combined Golgi and electron microscopic study on the synapses formed by double bouquet cells in the visual cortex of the cat and monkey. Journal of Comparative Neurology 195: 547–566CrossRefGoogle ScholarPubMed
Somogyi, P. and Freund, T. F. (1989) Immunocytochemistry and synaptic relationships of physiologically characterized, HRP-filled neurons. In Neuroanatomical Tract-Tracing Methods (vol. 2), ed. L. Heimer and L. Zaborsky, pp. 239–264, New York: Plenum
Somogyi, P. and Soltesz, I. (1986) Immunogold demonstration of GABA synaptic terminals of intracellularly recorded, horseradish peroxidase-filled basket cells and clutch cells in the cat's visual cortex. Neuroscience 19: 1051–1065CrossRefGoogle ScholarPubMed
Somogyi, P., Hajdu, F. and Tömböl, T. (1978) Ultrastructure of the anterior ventral and anterior medial nuclei of the cat thalamus. Experimental Brain Research 31: 417–431CrossRefGoogle ScholarPubMed
Somogyi, P., Smith, A. D., Nunzi, M. G., Gorio, A., Takagi, H. and Wu, J. Y. (1983) Glutamate decarboxylase immunoreactivity in the hippocampus of the cat: distribution of immunoreactive synaptic terminals with special reference to the axon initial segment of pyramidal neurons. Journal of Neuroscience 3: 1450–1468CrossRefGoogle ScholarPubMed
Somogyi, P., Freund, T. F., Hodgson, A. J., Somogyi, J., Beroukas, D. and Chubb, I. W. (1985) Identified axo-axonic cells are immunoreactive for GABA in the hippocampus and visual cortex of cats. Brain Research 332: 143–149CrossRefGoogle Scholar
Somogyi, P., Tamás, G., Lujan, R. and Buhl, E. H. (1998) Salient features of synaptic organisation in the cerebral cortex. Brain Research Reviews 26: 113–135CrossRefGoogle ScholarPubMed
Sontheimer, H., Kettenmann, H., Backus, K. H. and Schachner, M. (1988) Glutamate opens Na+/K+ channels in cultured astrocytes. Glia 1: 328–336CrossRefGoogle ScholarPubMed
Spencer, S. S. and Spencer, D. D. (1994) Entorhinal-hippocampal interactions in medial temporal lobe epilepsy. Epilepsia 35: 721–727CrossRefGoogle ScholarPubMed
Spencer, S. S., Williamson, P. D., Spencer, D. D. and Mattson, R. H. (1987) Human hippocampal seizure spread studied by depth and subdural recording: the hippocampal commissure. Epilepsia 28: 479–489CrossRefGoogle ScholarPubMed
Spencer, S. S., Kim, J., DeLanerolle, N. and Spencer, D. D. (1999) Differential neuronal and glia relations with parameters of ictal discharge in mesial temporal lobe epilepsy. Epilepsia 40: 708–712CrossRefGoogle ScholarPubMed
Spencer, W. A. and Brookhart, J. M. (1961) Electrical patterns of augmenting and recruiting waves in the depths of the sensorimotor cortex of cat. Journal of Neurophysiology 24: 26–49CrossRefGoogle Scholar
Spencer, W. A. and Kandel, E. R. (1961) Electrophysiology of hippocampal neurons. IV. Fast pre-potentials. Journal of Neurophysiology 24: 272–285CrossRefGoogle Scholar
Spreafico, R., Curtis, M., Frassoni, C. and Avanzini, G. (1988) Electrophysiological characteristics of morphologically identified reticular thalamic neurons from rat slices. Neuroscience 27: 629–638CrossRefGoogle ScholarPubMed
Spreafico, R., Frassoni, C., Regondi, M. C., Arcelli, P. and De Biasi, S. (1993) Interneurons in the mammalian thalamus, a marker of species? In Thalamic Networks for Relay and Modulation, ed. D. Minciacchi, M. Molinari, G. Macchi and E. G. Jones, pp. 17–28, New York: Pergamon Press
Squire, L. R. (1987) Memory and Brain. New York: Oxford University Press
Squire, L. R., Cohen, N. J. and Nadel, L. (1984) The medial temporal region and memory consolidation: a new hypthesis. In Memory Consolidation, ed. H. Weingartner and E. Parker, pp. 185–201, Hillsdale: Erlbaum
Staak, R. and Pape, H. C. (2001) Contribution of GABAA and GABAB receptors to thalamic neuronal activity during spontaneous absence seizures in rats. Journal of Neuroscience 21: 1378–1384CrossRefGoogle Scholar
Staba, R. J., Wilson, C. L., Bragin, A., Fried, I. and Engel, J. Jr. (2002) Sleep states differentiate single neuron activity recorded from human epileptic hippocampus, entorhinal cortex, and subiculum. Journal of Neuroscience 22: 5694–5704CrossRefGoogle ScholarPubMed
Stafstrom, C. E., Schwindt, P. C., Chubb, M. C. and Crill, W. E. (1985) Properties of persistent sodium conductance and calcium conductance of layer V neurons from cat sensorimotor cortex in vitro. Journal of Neurophysiology 53: 153–170CrossRefGoogle Scholar
Staley, K. J., Soldo, B. L. and Proctor, W. R. (1995) Ionic mechanisms of neuronal excitation by inhibitory GABAA receptors. Science 269: 977–981CrossRefGoogle ScholarPubMed
Stefan, H. and Snead, O. C. Jr. (1997) Absence seizures. In Epilepsy: A Comprehensive Textbook, ed. J. Engel Jr. and T. A. Pedley, pp. 579–590, Philadelphia: Lippincot-Raven
Steinhäuser, C. and Gallo, V. (1996) News on glutamate receptors on glial cells. Trends in Neurosciences 19: 339–345CrossRefGoogle ScholarPubMed
Steininger, T. L., Rye, D. B. and Wainer, B. H. (1992) Afferent projections to the cholinergic pedunculopontine tegmental nucleus and adjacent midbrain extrapyramidal area in the albino rat. Journal of Comparative Neurology 321: 515–543CrossRefGoogle ScholarPubMed
Steininger, T. L., Gong, H., McGinty, D. and Szymusiak, R. (2001) Subregional organization of preoptic/anterior hypothalamic projections to arousal-related monoaminergic cell groups. Journal of Comparative Neurology 429: 638–6533.0.CO;2-Y>CrossRefGoogle ScholarPubMed
Steriade, M. (1960) Mechanisms of facilitation and inhibition in focal cortical epilepsy induced by penicillin. Studies and Research in Neurology 5: 463–471 (in Romanian)Google Scholar
Steriade, M. (1964) Development of evoked responses into self-sustained activity within amygdalo-hippocampal circuits. Electroencephalography and Clinical Neurophysiology 16: 221–236CrossRefGoogle Scholar
Steriade, M. (1970) Ascending control of thalamic and cortical responsiveness. International Review of Neurobiology 12: 87–144CrossRefGoogle ScholarPubMed
Steriade, M. (1974) Interneuronal epileptic discharges related to spike-and-wave cortical seizures in behaving monkeys. Electroencephalography and Clinical Neurophysiology 37: 247–263CrossRefGoogle ScholarPubMed
Steriade, M. (1976) Cortical inhibition during sleep and waking. In Mechanisms in Transmission of Signal for Conscious Behavior, ed. T. Desiraju, pp. 209–248, Amsterdam: Elsevier
Steriade, M. (1978) Cortical long-axoned cells and putative interneurons during the sleep-waking cycle. Behavioral and Brain Sciences 3: 465–514CrossRefGoogle Scholar
Steriade, M. (1981) Mechanisms underlying cortical activation: neuronal organization and properties of the midbrain reticular core and intralaminar thalamic nuclei. In Brain Mechanisms of Perceptual Awareness and Purposeful Behavior, ed. O. Pompeiano and C. Ajmone-Marsan, pp. 327–377, New York: Raven Press
Steriade, M. (1984) The excitatory-inhibitory sequence in thalamic and neocortical cells: state-related changes and regulatory systems. In Dynamic Aspects of Neocortical Function, ed. G. M. Edelman, W. E. Gall and W. M. Cowan, pp. 107–157, New York: Wiley
Steriade, M. (1990) Spindling, incremental thalamocortical responses, and spike-wave epilepsy. In Generalized Epilepsy, ed. M. Avoli, P. Gloor, G. Kostopoulos and R. Naquet, pp. 161–180, Boston: Birkäuser
Steriade, M. (1991) Alertness, quiet sleep, dreaming. In Cerebral Cortex (vol. 9, Normal and Altered States of Function), ed. A. Peters and E. G. Jones, pp. 279–357, New York: Plenum
Steriade, M. (1995) Two channels in the cerebellothalamocortical system. Journal of Comparative Neurology 354: 57–70CrossRefGoogle ScholarPubMed
Steriade, M. (1997a) Synchronized activities of coupled oscillators in the cerebral cortex and thalamus at different levels of vigilance. Cerebral Cortex 7: 583–604CrossRefGoogle Scholar
Steriade, M. (1997b) Thalamic substrates of disturbances in states of vigilance and consciousness in humans. In Thalamus (vol. 2, Experimental and Clinical aspects), ed. M. Steriade, E. G. Jones and D. A. McCormick, pp. 721–742, Oxford: Elsevier
Steriade, M. (1998) Corticothalamic networks, oscillations, and plasticity. In Consciousness: At the Frontiers of Neuroscience (vol. 77, Advances in Neurology), ed. H. H. Jasper, L. Descarries, V. F. Castellucci and S. Rossignol, pp. 105–134, Philadelphia: Lippincott-Raven
Steriade, M. (1999a) Cellular substrates of brain rhythms. In Electroencephalography: Basic Principles, Clinical Applications, and Related Fields, 4th edn., ed. E. Niedermeyer and F. Lopes Da Silva, pp. 28–75, Baltimore: Williams & Wilkins
Steriade, M. (1999b) Coherent oscillations and short-term plasticity in corticothalamic networks. Trends in Neurosciences 22: 337–345CrossRefGoogle Scholar
Steriade, M. (2000) Corticothalamic resonance, states of vigilance, and mentation. Neuroscience 101: 243–276CrossRefGoogle ScholarPubMed
Steriade, M. (2001a) Impact of network activities on neuronal properties in corticothalamic systems. Journal of Neurophysiology 86: 1–39CrossRefGoogle Scholar
Steriade, M. (2001b) The Intact and Sliced Brain. Cambridge, MA: The MIT Press
Steriade, M. (2001c) The GABAergic reticular nucleus: a preferential target of corticothalamic projections. Proceedings of the National Academy of Sciences of the USA 98: 3625–3627CrossRefGoogle Scholar
Steriade, M. (2003) Presynaptic dendrites of thalamic local-circuit neurons and sculpting inhibition during activated states. Journal of Physiology (London) 546: 1CrossRefGoogle ScholarPubMed
Steriade, M. and Amzica, F. (1994) Dynamic coupling among neocortical neurons during evoked and spontaneous spike-wave seizure activity. Journal of Neurophysiology 72: 2051–2069CrossRefGoogle ScholarPubMed
Steriade, M. and Amzica, F. (1996) Intracortical and corticothalamic coherency of fast spontaneous oscillations. Proceedings of National Academy of Sciences of the USA 93: 2533–2538CrossRefGoogle ScholarPubMed
Steriade, M. and Amzica, F. (1998) Coalescence of sleep rhythms and their chronology in corticothalamic networks. Sleep Research Online 1: 1–10Google ScholarPubMed
Steriade, M. and Amzica, F. (1999) Intracellular study of excitability in the seizure-prone neocortex in vivo. Journal of Neurophysiology 82: 3108–3122CrossRefGoogle ScholarPubMed
Steriade, M. and Buzsáki, G. (1990) Parallel activation of thalamic and cortical neurons by brainstem and basal forebrain cholinergic systems. In Brain Cholinergic Systems, ed. M. Steriade and D. Biesold, pp. 3–63, Oxford: Oxford University Press
Steriade, M. and Contreras, D. (1995) Relations between cortical and thalamic cellular events during transition from sleep pattern to paroxysmal activity. Journal of Neuroscience 15: 623–642CrossRefGoogle Scholar
Steriade, M. and Contreras, D. (1998) Spike-wave complexes and fast runs of cortically generated seizures. I. Role of neocortex and thalamus. Journal of Neurophysiology 80: 1439–1455CrossRefGoogle ScholarPubMed
Steriade, M. and Demetrescu, M. (1960) Unspecific systems of inhibition and facilitation of potentials evoked by intermittent light. Journal of Neurophysiology 23: 602–617CrossRefGoogle Scholar
Steriade, M. and Deschênes, M. (1974) Inhibitory processes and interneuronal apparatus in motor cortex during sleep and waking. II. Recurrent and afferent inhibition of pyramidal tract neurons. Journal of Neurophysiology 37: 1093–1113CrossRefGoogle ScholarPubMed
Steriade, M. and Deschênes, M. (1984) The thalamus as a neuronal oscillator. Brain Research Reviews 8: 1–63CrossRefGoogle Scholar
Steriade, M. and Deschênes, M. (1987) Inhibitory processes in the thalamus. Journal of Mind and Behavior 8: 559–572Google Scholar
Steriade, M. and Deschênes, M. (1988) Intrathalamic and brainstem-thalamic networks involved in resting and alert states. In Cellular Thalamic Mechanisms, ed. M. Bentivoglio and R. Spreafico, pp. 37–62, Amsterdam: Elsevier
Steriade, M. and Glenn, L. L. (1982) Neocortical and caudate projections of intralaminar thalamic neurons and their synaptic excitation from the midbrain reticular core. Journal of Neurophysiology 48: 352–371CrossRefGoogle ScholarPubMed
Steriade, M. and Llinás, R. R. (1988) The functional states of the thalamus and the associated neuronal interplay. Physiological Reviews 68: 649–742CrossRefGoogle ScholarPubMed
Steriade, M. and McCarley, R. W. (1990) Brainstem Control of Wakefulness and Sleep. New York: Plenum
Steriade, M. and Morin, D. (1981) Reticular influences on primary and augmenting responses in the somatosensory cortex. Brain Research 205: 67–80CrossRefGoogle ScholarPubMed
Steriade, M. and Timofeev, I. (1997) Short-term plasticity during intrathalamic augmenting responses in decorticated cats. Journal of Neuroscience 17: 3778–3795CrossRefGoogle ScholarPubMed
Steriade, M. and Timofeev, I. (2001) Corticothalamic operations through prevalent inhibition of thalamocortical neurons. Thalamus and Related Systems 1: 225–236Google Scholar
Steriade, M. and Timofeev, I. (2002a) Generators of ictal and interictal electroencephalograms associated with infantile spasms: intracellular studies of cortical and thalamic neurons. International Review of Neurobiology 49: 77–98CrossRefGoogle Scholar
Steriade, M. and Timofeev, I. (2002b) Neuronal plasticity during sleep oscillations in corticothalamic systems. In Sleep and Brain Plasticity, ed. P. Maquet, R. Stickgold and C. S. Smith, in press, Oxford: Oxford University Press
Steriade, M. and Wyzinski, P. (1972) Cortically elicited activities in thalamic reticularis neurons. Brain Research 42: 514–520CrossRefGoogle ScholarPubMed
Steriade, M. and Yossif, G. (1974) Spike-and-wave afterdischarges in cortical somatosensory neurons of cat. Electroencephalography and Clinical Neurophysiology 37: 633–648CrossRefGoogle ScholarPubMed
Steriade, M., Iosif, G. and Apostol, V. (1969) Responsiveness of thalamic and cortical motor relays during arousal and various stages of sleep. Journal of Neurophysiology 32: 251–265CrossRefGoogle Scholar
Steriade, M., Apostol, V. and Oakson, G. (1971) Control of unitary activities in cerebellothalamic pathway during wakefulness and synchronized sleep. Journal of Neurophysiology 34: 389–413CrossRefGoogle ScholarPubMed
Steriade, M., Wyzinski, P. and Apostol, V. (1972) Corticofugal projections governing rhythmic thalamic activity. In Corticothalamic Projections and Sensorimotor Activities, ed. T. L. Frigyesi, E. Rinvik and M. D. Yahr, pp. 221–272. New York: Raven Press
Steriade, M., Deschênes, M. and Oakson, G. (1974a) Inhibitory processes and interneuronal apparatus in motor cortex during sleep and waking. I. Background firing and synaptic responsiveness of pyramidal tract neurons and interneurons. Journal of Neurophysiology 37: 1065–1092CrossRefGoogle Scholar
Steriade, M., Deschênes, M., Wyzinski, P. and Hallé, J. P. (1974b) Input-output organization of the motor cortex during sleep and waking. In Basic Sleep Mechanisms, ed. O. Petre-Quadens and J. Schlag, pp. 144–200, New York: Academic Press
Steriade, M., Oakson, G. and Diallo, A. (1976) Cortically elicited spike-wave afterdischarges in thalamic neurons. Electroencephalography and Clinical Neurophysiology 41: 641–644CrossRefGoogle Scholar
Steriade, M., Diallo, A., Oakson, G. and White-Guay, B. (1977a) Some synaptic inputs and ascending projections of lateral posterior thalamic neurons. Brain Research 131: 39–53CrossRefGoogle Scholar
Steriade, M., Oakson, G. and Diallo, A. (1977b) Reticular influences on lateralis posterior thalamic neurons. Brain Research 131: 55–71CrossRefGoogle Scholar
Steriade, M., Kitsikis, A. and Oakson, G. (1979a) Excitatory-inhibitory processes in parietal association neurons during reticular activation and sleep-waking cycle. Sleep 1: 339–355CrossRefGoogle Scholar
Steriade, M., Kitsikis, A. and Oakson, G. (1979b) Selectively REM-related increased firing rates in association interneurons during sleep: possible implications for learning. In Brain Mechanisms in Memory and Learning, ed. M. A. Brazier, pp. 47–52, New York: Raven Press
Steriade, M., Parent, A. and Hada, J. (1984) Thalamic projections of nucleus reticularis thalami: a study using retrograde transport of horseradish peroxidase and double fluorescent tracers. Journal of Comparative Neurology 229: 531–547CrossRefGoogle ScholarPubMed
Steriade, M., Deschênes, M., Domich, L. and Mulle, C. (1985) Abolition of spindle oscillations in thalamic neurons disconnected from nucleus reticularis thalami. Journal of Neurophysiology 54: 1473–1497CrossRefGoogle ScholarPubMed
Steriade, M., Domich, L. and Oakson, G. (1986) Reticularis thalami neurons revisited: activity changes during shifts in states of vigilance. Journal of Neuroscience 6: 68–81CrossRefGoogle ScholarPubMed
Steriade, M., Domich, L., Oakson, G. and Deschênes, M. (1987a) The deafferented reticularis thalami nucleus generates spindle rhythmicity. Journal of Neurophysiology 57: 260–273CrossRefGoogle Scholar
Steriade, M., Parent, A., Paré, D. and Smith, Y. (1987b) Cholinergic and non-cholinergic neurons of cat basal forebrain project to reticular and mediodorsal thalamic nuclei. Brain Research 408: 372–376CrossRefGoogle Scholar
Steriade, M., Paré, D., Parent, A. and Smith, Y. (1988) Projections of cholinergic and non-cholinergic neurons of the brainstem core to relay and associational thalamic nuclei in the cat and macaque monkey. Neuroscience 25: 47–67CrossRefGoogle ScholarPubMed
Steriade, M., Datta, S., Paré, D., Oakson, G. and Curró Dossi, R. (1990a) Neuronal activities in brainstem cholinergic nuclei related to tonic activation processes in thalamocortical systems. Journal of Neuroscience 10: 2541–2559CrossRefGoogle Scholar
Steriade, M., Jones, E. G. and Llinás, R. R. (1990b) Thalamic Oscillations and Signaling. New York: Wiley-Interscience
Steriade, M., Paré, D., Datta, S., Oakson, G. and Curró Dossi, R. (1990c) Different cellular types in mesopontine cholinergic nuclei related to ponto-geniculo-occipital waves. Journal of Neuroscience 10: 2560–2579CrossRefGoogle Scholar
Steriade, M., Gloor, P., Llinás, R. R., Lopes da Silva, F. H. and Mesulam, M. M. (1990d) Basic mechanisms of cerebral rhythmic activities. Electroencephalography and Clinical Neurophysiology 76: 481–508CrossRefGoogle Scholar
Steriade, M., Curró Dossi, R. and Nuñez, A. (1991a) Network modulation of a slow intrinsic oscillation of cat thalamocortical neurons implicated in sleep delta waves: cortical potentiation and brainstem cholinergic suppression. Journal of Neuroscience 11: 3200–3217CrossRefGoogle Scholar
Steriade, M., Curró Dossi, R., Paré, D. and Oakson, G. (1991b) Fast oscillations (20–40 Hz) in thalamocortical systems and their potentiation by mesopontine cholinergic nuclei in the cat. Proceedings of the National Academy of Sciences of the USA 88: 4396–4400CrossRefGoogle Scholar
Steriade, M., Amzica, F. and Nuñez, A. (1993a) Cholinergic and noradrenergic modulation of the slow (∼0.3 Hz) oscillation in neocortical cells. Journal of Neurophysiology 70: 1384–1400CrossRefGoogle Scholar
Steriade, M., Contreras, D., Curró Dossi, R. and Nuñez, A. (1993b) The slow (<1 Hz) oscillation in reticular thalamic and thalamocortical neurons: scenario of sleep rhythm generation in interacting thalamic and neocortical networks. Journal of Neuroscience 13: 3284–3299CrossRefGoogle Scholar
Steriade, M., Curró Dossi, R. and Contreras, D. (1993c) Electrophysiological properties of intralaminar thalamocortical cells discharging rhythmic (∼40 Hz) spike-bursts at ∼1000 Hz during waking and rapid eye movement sleep. Neuroscience 56: 1–9CrossRefGoogle Scholar
Steriade, M., McCormick, D. A. and Sejnowski, T. J. (1993d) Thalamocortical oscillation in the sleeping and aroused brain. Science 262: 679–685CrossRefGoogle Scholar
Steriade, M., Nuñez, A. and Amzica, F. (1993e) A novel slow (<1 Hz) oscillation of neocortical neurons in vivo: depolarizing and hyperpolarizing components. Journal of Neuroscience 13: 3252–3265CrossRefGoogle Scholar
Steriade, M., Nuñez, A. and Amzica, F. (1993f) Intracellular analysis of relations between the slow (<1 Hz) neocortical oscillation and other sleep rhythms. Journal of Neuroscience 13: 3266–3283CrossRefGoogle Scholar
Steriade, M., Amzica, F. and Contreras, D. (1994a) Cortical and thalamic cellular correlates of electroencephalographic burst-suppression. Electroencephalography and Clinical Neurophysiology 90: 1–16CrossRefGoogle Scholar
Steriade, M., Contreras, D. and Amzica, F. (1994b) Synchronized sleep oscillations and their paroxysmal developments. Trends in Neuroscience 17: 199–208CrossRefGoogle Scholar
Steriade, M., Amzica, F. and Contreras, D. (1996a) Synchronization of fast (30–40 Hz) spontaneous cortical rhythms during brain activation. Journal of Neuroscience 16: 392–417CrossRefGoogle Scholar
Steriade, M., Contreras, D., Amzica, F. and Timofeev, I. (1996b) Synchronization of fast (30–40 Hz) spontaneous oscillations in intrathalamic and thalamocortical networks. Journal of Neuroscience 16: 2788–2808CrossRefGoogle Scholar
Steriade, M., Jones, E. G. and McCormick, D. A. (1997) Thalamus (vol. 1, Organisation and Function). Oxford: Elsevier
Steriade, M., Amzica, F., Neckelmann, D. and Timofeev, I. (1998a) Spike-wave complexes and fast runs of cortically generated seizures. II. Extra- and intracellular patterns. Journal of Neurophysiology 80: 1456–1479CrossRefGoogle Scholar
Steriade, M., Timofeev, I., Dürmüller, N. and Grenier, F. (1998b) Dynamic properties of corticothalamic neurons and local cortical interneurons generating fast rhythmic (30–40 Hz) spike bursts. Journal of Neurophysiology 79: 483–490CrossRefGoogle Scholar
Steriade, M., Timofeev, I. and Grenier, F. (1998c) Inhibitory components of cortical spike-wave seizures in vivo. Society for Neuroscience Abstracts 24: 2143Google Scholar
Steriade, M., Timofeev, I., Grenier, F. and Dürmüller, N. (1998d) Role of thalamic and cortical neurons in augmenting responses: dual intracellular recordings in vivo. Journal of Neuroscience 18: 6425–6443CrossRefGoogle Scholar
Steriade, M., Timofeev, I. and Grenier, F. (2001a) Natural waking and sleep states: a view from inside neocortical neurons. Journal of Neurophysiology 85: 1969–1985CrossRefGoogle Scholar
Steriade, M., Timofeev, I. and Grenier, F. (2001b) Intrinsic, antidromic and synaptic excitability of cortical neurons during natural waking-sleep cycle. Society for Neuroscience Abstracts 27: 240Google Scholar
Sterman, M. B. and Clemente, C. D. (1962a) Forebrain inhibitory mechanisms: cortical synchronization induced by basal forebrain stimulation. Experimental Neurology 6: 91–102CrossRefGoogle Scholar
Sterman, M. B. and Clemente, C. D. (1962b) Forebrain inhibitory mechanisms: sleep patterns induced by basal forebrain stimulation in the behaving cat. Experimental Neurology 6: 103–117CrossRefGoogle Scholar
Stevens, D. R., Greene, R. W. and McCarley, R. W. (1992) Serotonin 1 and serotonin 2 receptors hyperpolarize and depolarize separate populations of medial pontine reticular formation neurons in vitro. Neuroscience 47: 545–553CrossRefGoogle Scholar
Stewart, M. and Fox, S. E. (1991) Hippocampal theta activity in monkeys. Brain Research 538: 59–63CrossRefGoogle ScholarPubMed
Stickgold, R., Whitbee, D., Schirmer, B., Patel, V. and Hobson, J. A. (2000) Visual discrimination improvement. A multi-step process occurring during sleep. Journal of Cognitive Neuroscience 12: 246–254CrossRefGoogle ScholarPubMed
Stuart, G. and Sakmann, B. (1995) Amplification of EPSPs by axosomatic sodium channels in neocortical pyramidal neurons. Neuron 15: 1065–1076CrossRefGoogle ScholarPubMed
Sugita, S., Tanaka, E. and North, R. A. (1993) Membrane properties and synaptic potentials of three types of neurone in rat lateral amygdala. Journal of Physiology (London) 460: 705–718CrossRefGoogle ScholarPubMed
Sundstrom, L. E., Brana, C., Gatherer, M., Mepham, J. and Rougier, A. (2001) Somatostatin- and neuropeptide Y-synthesizing neurones in the fascia dentate of humans with temporal lobe epilepsy. Brain 124: 688–697CrossRefGoogle ScholarPubMed
Sutherland, G. R. and McNaughton, B. (2000) Memory traces reactivation in hippocampal and neocortical neuronal ensembles. Current Opinion in Neurobiology 10: 180–186CrossRefGoogle ScholarPubMed
Sutherling, W. W., Crandall, P. H., Cahan, L. D. and Barth, D. S. (1988) The magnetic field of epileptic spikes agrees with intracranial localizations in complex partial epilepsy. Neurology 38: 778–786CrossRefGoogle ScholarPubMed
Sutula, T., He, X. X., Cavazos, J. and Scott, G. (1988) Synaptic reorganization in the hippocampus induced by abnormal functional activity. Science 239: 1147–1150CrossRefGoogle ScholarPubMed
Suzuki, W. A. (1996) The anatomy, physiology and functions of the perirhinal cortex. Current Opinion in Neurobiology 6: 179–186CrossRefGoogle ScholarPubMed
Svensson, T. H., Bunney, B. S. and Aghajanian, G. K. (1975) Inhibition of both noradrenergic and serotonergic neurons in brain by the alpha-adrenergic agonist clonidine. Brain Research 92: 291–306CrossRefGoogle ScholarPubMed
Swann, J. W., Smith, K. L. and Brady, R. J. (1993) Localized excitatory synaptic interactions mediate the sustained depolarization of electrographic seizure in developing hippocampus. Journal of Neuroscience 13: 4680–4689CrossRefGoogle ScholarPubMed
Swann, J. W., Al-Noori, S., Jiang, M. and Lee, C. L. (2000) Spine loss and other dendritic abnormalities in epilepsy. Hippocampus 10: 617–6253.0.CO;2-R>CrossRefGoogle ScholarPubMed
Sypert, G. W. and Ward, A. A. Jr. (1971) Unidentified neuroglia potentials during propagated seizures in neocortex. Experimental Neurology 33: 239–255CrossRefGoogle ScholarPubMed
Szentágothai, J. (1978) The neuron network of the cerebral cortex: a functional interpretation. The Ferrier Lecture. Proceedings of the Royal Society (London, Series B) 201: 219–248CrossRefGoogle ScholarPubMed
Szentágothai, J. and Arbib, M. A. (1974) Conceptual models of neural organization. Neuroscience Research Program Bulletin 12: 307–510Google ScholarPubMed
Szymusiak, R. and McGinty, D. (1986) Sleep-related neuronal discharge in the basal forebrain of cats. Brain Research 370: 82–92CrossRefGoogle ScholarPubMed
Szymusiak, R. and McGinty, D. (1989) Sleep-waking discharge of basal forebrain projection neurons in cats. Brain Research Bulletin 22: 423–430CrossRefGoogle ScholarPubMed
Szymusiak, R., Shouse, M. N. and McGinty, D. (1966) Brainstem stimulation during sleep evokes abnormal rhythmic activity in thalamic neurons in feline penicillin epilepsy. Brain Research 713: 253–260CrossRefGoogle Scholar
Szymusiak, R., Steininger, T., Alam, N. and McGinty, D. (2001) Preoptic area sleep-regulating mechanisms. Archives Italiennes de Biologie 139: 77–92Google ScholarPubMed
Tamás, G., Buhl, E. H. and Somogyi, P. (1997) Fast IPSPs elicited via multiple synaptic release sites by distinct types of GABAergic neurone in the cat visual cortex. Journal of Physiology (London) 500: 715–738CrossRefGoogle ScholarPubMed
Tancredi, V., Biagini, G., D'Antuono, M., Louvel, J., Pumain, R. and Avoli, M. (2000) Spindle-like thalamocortical synchronization in a rat brain slice preparation. Journal of Neurophysiology 84: 1093–1097CrossRefGoogle Scholar
Tasker, G. J. and Dudek, F. E. (1991) Electrophysiology of GABA-mediated synaptic transmission and possible roles in epilepsy. Neurochemical Research 16: 251–262CrossRefGoogle ScholarPubMed
Tauck, D. L. and Nadler, J. V. (1985) Evidence of functional mossy fiber sprouting in hippocampal formation of kainic acid-treated rats. Journal of Neuroscience 5: 1016–1022CrossRefGoogle ScholarPubMed
Taylor-Courval, D. and Gloor, P. (1984) Behavioral alterations associated with generalized spike and wave discharges in the EEG of the cat. Experimental Neurology 83: 167–186CrossRefGoogle ScholarPubMed
Telfeian, A. E. and Connors, B. W. (1998) Layer-specific pathways for the horizontal propagation of epileptiform discharges in neocortex. Epilepsia 39: 700–708CrossRefGoogle ScholarPubMed
Temkin, O. (1971) The Falling Sickness. Baltimore: Johns Hopkins University Press
Terman, D., Bose, A. and Kopell, N. (1996) Functional reorganization in thalamocortical networks: transition between spindling and delta sleep rhythms. Proceedings of the National Academy of Sciences of the USA 93: 15417–15422CrossRefGoogle ScholarPubMed
Terzano, M. G., Parrino, L. and Spaggiari, M. C. (1988) The cyclic alternating pattern sequences in the dynamic organization of sleep. Electroencephalography and Clinical Neurophysiology 69: 437–447CrossRefGoogle Scholar
Terzano, M. G., Parrino, L., Spaggiari, M. C., Barusi, R. and Simeoni, S. (1991) Discriminatory effect of cyclic alternating pattern in focal lesioned and benign rolandic interictal spikes during sleep. Epilepsia 32: 616–628CrossRefGoogle Scholar
Thomas, J. E. and Klass, D. W. (1968) Six-per-second spike and wave pattern in the electroencephalogram. Neurology 18: 587–593CrossRefGoogle ScholarPubMed
Thompson, S. M. and Gähwiler, B. H. (1989) Activity-dependent disinhibition. I. Repetitive stimulation reduces IPSP driving force and conductance in the hippocampus in vitro. Journal of Neurophysiology 61: 501–511CrossRefGoogle ScholarPubMed
Thomson, A. M. (1988a) Inhibitory postsynaptic potentials evoked in thalamic neurons by stimulation of the reticularis nucleus evoke slow spikes in isolated rat brain slices. Neuroscience 25: 491–502CrossRefGoogle Scholar
Thomson, A. M. (1988b) Biphasic responses of thalamic neurons to GABA in isolated rat brain slices. Neuroscience 25: 503–512CrossRefGoogle Scholar
Thomson, A. M. (1997) Activity-dependent properties of synaptic transmission at two classes of connections made by rat neocortical pyramidal axons in vitro. Journal of Physiology (London) 502: 131–147CrossRefGoogle ScholarPubMed
Thomson, A. M. and Deuchars, J. (1997) Synaptic interactions in neocortical local circuits: dual intracellular recordings in vitro. Cerebral Cortex 7: 510–522CrossRefGoogle ScholarPubMed
Thomson, A. M. and West, D. C. (1993) Fluctuations in pyramid-pyramid excitatory postsynaptic potentials modified by presynaptic firing pattern and postsynaptic membrane potential using paired intracellular recordings in rat neocortex. Neuroscience 54: 329–346CrossRefGoogle ScholarPubMed
Thomson, A. M., Girldestone, D. and West, D. C. (1988) Voltage-dependent currents prolong single-axon postsynaptic potentials in layer III pyramidal neurons in rat neocortical slices. Journal of Neurophysiology 60: 1896–1907CrossRefGoogle ScholarPubMed
Thomson, A. M., Deuchars, J. and West, D. C. (1993a) Large, deep layer pyramid-pyramid single axon EPSPs in slices of rat motor cortex display paired pulse and frequency-dependent depression, mediated presynaptically and self-facilitation, mediated postsynaptically. Journal of Neurophysiology 70: 2354–2369CrossRefGoogle Scholar
Thomson, A. M., Deuchars, J. and West, D. C. (1993b) Single axon excitatory postsynaptic potentials in neocortical interneurons exhibit pronounced paired pulse facilitation. Neuroscience 54: 347–360CrossRefGoogle Scholar
Thomson, A. M., West, D. C. and Deuchars, J. (1995) Properties of single axon excitatory postsynaptic potentials elicited in spiny interneurons by action potentials in pyramidal neurons in slices of rat neocortex. Neuroscience 69: 727–738CrossRefGoogle ScholarPubMed
Thomson, A. M., West, D. C., Hahn, J. and Deuchars, J. (1996) Single axon IPSPs elicited in pyramidal cells by three classes of interneurons in slices of rat neocortex. Journal of Physiology (London) 496: 81–102CrossRefGoogle ScholarPubMed
Timofeev, I. and Steriade, M. (1996) Low-frequency rhythms in the thalamus of intact-cortex and decorticated cats. Journal of Neurophysiology 76: 4152–4168CrossRefGoogle ScholarPubMed
Timofeev, I. and Steriade, M. (1997) Fast (mainly 30–100 Hz) oscillations in the cat cerebellothalamic pathway and their synchronization with cortical potentials. Journal of Physiology (London) 504: 153–168CrossRefGoogle ScholarPubMed
Timofeev, I. and Steriade, M. (1998) Cellular mechanisms underlying intrathalamic augmenting responses of reticular and relay neurons. Journal of Neurophysiology 79: 2716–2729CrossRefGoogle ScholarPubMed
Timofeev, I., Contreras, D. and Steriade, M. (1996) Synaptic responsiveness of cortical and thalamic neurons during various phases of slow oscillation in cat. Journal of Physiology (London) 494: 265–278CrossRefGoogle ScholarPubMed
Timofeev, I., Grenier, F. and Steriade, M. (1998) Spike-wave complexes and fast runs of cortically generated seizures. IV. Paroxysmal fast runs in cortical and thalamic neurons. Journal of Neurophysiology 80: 1495–1513CrossRefGoogle ScholarPubMed
Timofeev, I., Grenier, F., Bazhenov, M., Sejnowski, T. J. and Steriade, M. (2000a) Origin of slow oscillations in deafferented cortical slabs. Cerebral Cortex 10: 1185–1199CrossRefGoogle Scholar
Timofeev, I., Grenier, F., Bazhenov, M., Sejnowski, T. J. and Steriade, M. (2000b) Impact of intrinsic properties and synaptic factors on the activity of neocortical networks in vivo. Journal of Physiology (Paris) 94: 343–355CrossRefGoogle Scholar
Timofeev, I., Bazhenov, M., Sejnowski, T. J. and Steriade, M. (2001a) Contribution of intrinsic and synaptic factors in the desynchronization of thalamic oscillatory activity. Thalamus and Related Systems 1: 53–69Google Scholar
Timofeev, I., Grenier, F. and Steriade, M. (2001b) Disfacilitation and active inhibition in the neocortex during the natural sleep-wake cycle: an intracellular study. Proceedings of the National Academy of Sciences of the USA 98: 1924–1929CrossRefGoogle Scholar
Timofeev, I., Bazhenov, M., Sejnowski, T. J. and Steriade, M. (2002a) Cortical IH takes part in the generation of paroxysmal activities. Proceedings of the National Academy of Sciences of the USA 99: 9533–9537CrossRefGoogle Scholar
Timofeev, I., Grenier, F., Bazhenov, M., Houweling, A., Sejnowski, T. J. and Steriade, M. (2002b) Short- and medium-term plasticity associated with augmenting responses in cortical slabs and spindles in intact cortex of cats in vivo. Journal of Physiology (London) 542: 583–598CrossRefGoogle Scholar
Timofeev, I., Grenier, F. and Steriade, M. (2002c) The role of chloride-dependent inhibition and the activity of fast-spiking neurons during cortical spike-wave seizures. Neuroscience 114: 1115–1132CrossRefGoogle Scholar
Tononi, G. and Cirelli, C. (2001) Some considerations on sleep and neural plasticity. Archives Italiennes de Biologie 139: 221–241Google ScholarPubMed
Tononi, G., Cirelli, C. and Shaw, P. J. (2000) The molecular correlates of sleep, waking and sleep deprivation. In The Regulation of Human (Human Frontier Workshop VIII), ed. A. Borbély, O. Hayaishi, T. J. Sejnowski and J. S. Altman, pp. 155–167, Strasbourg: Human Frontier Science Program
Topolnik, L., Steriade, M. and Timofeev, I. (2001) Neocortical deafferentation potentiates development of paroxysmal activities. Society for Neuroscience Abstracts 27: 288Google Scholar
Topolnik, L., Steriade, M. and Timofeev, I. (2003) Partial cortical deafferentation promotes development of paroxysmal activity. Submitted
Torres, E. M., Perry, T. A., Blockland, A., Wilkinson, L. S., Wiley, R. G., Lappi, D. A. and Dunnet, S. B. (1994) Behavioural, histochemical and biochemical consequences of selective immunolesion in discrete regions of the basal forebrain cholinergic system. Neuroscience 63: 95–122CrossRefGoogle Scholar
Traub, R. D. and Llinás, R. (1979) Hippocampal pyramidal cells: significance of dendritic ionic conductances for neuronal function and epileptogenesis. Journal of Neurophysiology 42: 476–496CrossRefGoogle ScholarPubMed
Traub, R. D. and Wong, R. K. S. (1981) Penicillin-induced epileptiform activity in the hippocampal slice: a model of synchronization of CA3 pyramidal cell bursting. Neuroscience 6: 223–230CrossRefGoogle ScholarPubMed
Traub, R. D., Miles, R. and Jefferys, J. G. R. (1993) Synaptic and intrinsic conductances shape picrotoxin-induced synchronized after-discharges in the guinea-pig hippocampal slices. Journal of Physiology (London) 461: 525–547CrossRefGoogle Scholar
Traub, R. D., Whittington, M. A., Stanford, I. M. and Jefferys, J. G. R. (1996) A mechanism for generation of long-range synchronous fast oscillations in the cortex. Nature 383: 621–624CrossRefGoogle ScholarPubMed
Traub, R. D., Jefferys, J. G. R. and Whittington, M. A. (1999a) Fast Oscillations in Cortical Circuits. Cambridge, MA: The MIT Press
Traub, R. D., Schmitz, D., Jefferys, J. G. R. and Draguhn, A. (1999b) High-frequency population oscillations are predicted to occur in hippocampal pyramidal neuronal networks interconnected by axoaxonal gap junctions. Neuroscience 92: 407–426CrossRefGoogle Scholar
Traub, R. D., Whittington, M. A., Bühl, E. H., LeBeau, F. N., Bibbig, A., Boyd, S., Cross, H. and Baldeweg, T. A. (2001) A possible role for gap junctions in generation of very fast EEG oscillations preceding the onset of, and perhaps initiating, seizures. Epilepsia 42: 153–170Google ScholarPubMed
Traub, R. D., Buhl, E. H., Gloveli, T. and Whittington, M. A. (2003) A model of a layer 2/3 neocortical pyramidal neuron demonstrating multiple compartment-specific firing patterns, including fast rhythmic bursting. Journal of Neurophysiology, in pressGoogle Scholar
Traynelis, S. F. and Dingledine, R. (1988) Potassium-induced spontaneous electrographic seizures in the rat hippocampal slice. Journal of Neurophysiology 59: 259–276CrossRefGoogle ScholarPubMed
Treitman, L. J. and Treitman, D. M. (1999) Genetic epilepsy – generalized. In The Epilepsies, ed. P. Kotagal and H. O. Lüders, pp. 543–549, San Diego: Academic Press
Treves, A. and Rolls, E. T. (1994) A computational analysis of the role of the hippocampus in memory. Hippocampus 4: 374–391CrossRefGoogle ScholarPubMed
Trulson, M. E. and Jacobs, B. L. (1979) Raphe unit activity in freely moving cats: correlation with level of behavioral arousal. Brain Research 163: 135–150CrossRefGoogle ScholarPubMed
Trulson, M. E., Crisp, T. and Trulson, V. M. (1984) Activity of serotonin-containing nucleus centralis superior (raphe medianus) neurons in freely moving cats. Experimental Brain Research 54: 33–44CrossRefGoogle ScholarPubMed
Tsakiridou, E., Bertollini, L., Curtis, M., Avanzini, G. and Pape, H. C. (1995) T-type calcium conductance in the reticular thalamic nucleus: a contribution to absence epilepsy. Journal of Neuroscience 15: 3110–3117CrossRefGoogle Scholar
Tseng, G. F. and Prince, D. A. (1996) Structural and functional alterations in rat corticospinal neurons following axotomy. Journal of Neurophysiology 75: 248–267CrossRefGoogle ScholarPubMed
Tseng, K. Y., Kasanetz, F., Kargieman, L., Riquelne, L. A. and Murer, M. G. (2001) Cortical slow oscillatory activity is reflected in the membrane potential and spike trains of striatal neurons in rats with chronic nigrostriatal lesions. Journal of Neuroscience 21: 6430–6439CrossRefGoogle ScholarPubMed
Tsodyks, M., Kenet, T., Grinvald, A. and Arieli, A. (1999) Linking spontaneous activity of single cortical neurons and the underlying functional architecture. Science 286: 1943–1946CrossRefGoogle ScholarPubMed
Turner, D. A. and Wheal, H. V. (1991) Excitatory synaptic potentials in kainic acid-denervated rat CA1 pyramidal neurons. Journal of Neuroscience 11: 2786–2794CrossRefGoogle ScholarPubMed
Turrini, P., Casu, M. A., Wong, T. P., Koninck, Y., Ribeiro-da-Silva, A. and Cuello, A. C. (2001) Cholinergic nerve terminals establish classical synapses in the rat cerebral cortex: synaptic pattern and age-related atrophy. Neuroscience 105: 277–285CrossRefGoogle ScholarPubMed
Tuunanen, J., Lukasiuk, K., Halonen, T. and Pitkänen, A. (1999) Status epilepticus-induced neuronal damage in the rat amygdaloid complex: distribution, time-course and mechanisms. Neuroscience 94: 473–495CrossRefGoogle ScholarPubMed
Uchida, S., Maloney, T., March, J. D., Azari, R. and Feinberg, I. (1991) Sigma (12–15 Hz) and delta (0.3–3.0 Hz) EEG oscillate reciprocally within NREM sleep. Brain Research Bulletin 27: 93–96CrossRefGoogle Scholar
Ueno, R., Honda, K., Inoue, S. and Hayaishi, O. (1983) Prostaglandin D2, a cerebral sleep-inducing substance in rats. Proceedings of the National Academy of Sciences of the USA 80: 1735–1737CrossRefGoogle ScholarPubMed
Uhl, G. R., Tran, V., Snyder, S. H. and Martin, J. B. (1985) Somatostatin receptors: distribution in rat central nervous system and human frontal cortex. Journal of Comparative Neurology 240: 266–304Google ScholarPubMed
Uhlrich, D. and Huguenard, J. R. (1996) GABAB receptor-mediated responses in GABAergic projection neurones of rat nucleus reticularis thalami in vitro. Journal of Physiology (London) 493: 845–854CrossRefGoogle Scholar
Uhlrich, D. and Huguenard, J. R. (1997) GABAA-receptor-mediated rebound burst firing and burst shunting in thalamus. Journal of Neurophysiology 78: 1748–1751CrossRefGoogle Scholar
Uhlrich, D. J., Manning, K. A. and Xue, J. T. (2002) Effects of activation of the histaminergic tuberomammillary nucleus on visual responses of neurons in the dorsal lateral geniculate nucleus. Journal of Neuroscience 22: 1098–1107CrossRefGoogle ScholarPubMed
Umbriaco, D., Watkins, K. C., Descarries, L., Cozzari, C. and Hartman, B. K. (1994) Ultrastructural and morphometric features of the acetylcholine innervation in adult rat parietal cortex. An electron microscopic study in serial sections. Journal of Comparative Neurology 348: 351–373CrossRefGoogle ScholarPubMed
Urbano, F. J., Leznik, E. and Llinás, R. R. (2001) Cortical activation patterns evoked by afferent axons stimuli at different frequencies: an in vitro voltage sensitive dye imaging study. Thalamus and Related Systems 1: 371–378Google Scholar
Brederode, J. and Spain, W. (1995) Differences in inhibitory synaptic input between layer II–III and layer V neurons of the cat neocortex. Journal of Neurophysiology 74: 1149–1166CrossRefGoogle Scholar
Vanderwolf, C. H. (1969) Hippocampal electrical activity and voluntary movement in the rat. Electroencephalography and Clinical Neurophysiology 26: 407–418CrossRefGoogle ScholarPubMed
Vanderwolf, C. H. (1988) Cerebral activity and behavior: control by central cholinergic and serotonergic systems. International Reviews of Neurobiology 30: 225–340CrossRefGoogle ScholarPubMed
Hoesen, G. W., Hyman, B. T. and Damasio, A. R. (1991) Entorhinal cortex pathology in Alzheimer's disease. Hippocampus 1: 1–8CrossRefGoogle ScholarPubMed
Luijtelaar, E. L. and Coenen, A. M. (1986) Two types of electrocortical paroxysms in an inbred strain of rats. Neuroscience Letters 70: 393–397CrossRefGoogle Scholar
Vanni-Mercier, G., Sakai, K. and Jouvet, M. (1984) Neurones spécifiques de l'éveil dans l'hypothalamus postérieur du chat. Comptes Rendus de l'Académie des Sciences (Paris) 298: 195–200Google Scholar
Velasco, F. and Velasco, M. (1990) Mesencephalic structures and tonic-clonic generalized seizures. In Generalized Epilepsy: Cellular, Molecular and Pharmacological Approach, ed. M. Avoli, P. Gloor, G. Kostopoulos and R. Naquet, pp. 368–384, Boston: Birkhäuser
Velasco, F., Velasco, M., Cepeda, C. and Munoz, H. (1980) Wakefulness-sleep modulation of cortical and subcortical somatic evoked potentials in man. Electroencephalography and Clinical Neurophysiology 48: 64–72CrossRefGoogle ScholarPubMed
Velasco, F., Velasco, M., Velasco, A. L., Jiménez, F., Márquez, I. and Rise, M. (1995) Electrical stimulation of the centromedian thalamic nucleus in the control of intractable seizures: long-term studies. Epilepsia 36: 63–71CrossRefGoogle Scholar
Velasco, F., Velasco, M., Jiménez, F., Velasco, A. L., Rojas, B. and Perez, M. L. (2001) Centromedian nucleus stimulation for epilepsy: clinical, electroencephalographic, and behavioral observations. Thalamus and Related Systems 1: 387–398Google Scholar
Velayos, J. L., Jimenez-Castellanos, J. Jr. and Reinoso-Suárez, F. (1989) Topographical organization of the projections from the reticular thalamic nucleus to the intralaminar and medial thalamic nuclei in the cat. Journal of Comparative Neurology 279: 457–469CrossRefGoogle ScholarPubMed
Vergnes, M. and Marescaux, C. (1992) Cortical and thalamic lesions in rats with genetic absence epilepsy. Journal of Neural Transmission 35 (Suppl.): 71–83Google ScholarPubMed
Vertes, R. P. and Kocsis, B. (1997) Brainstem-diencephalo-septohippocampal systems controlling the theta rhythm of the hippocampus. Neuroscience 81: 893–926Google ScholarPubMed
Villablanca, J. (1974) Role of the thalamus in sleep control: sleep-wakefulness studies of chronic cats without the thalamus: the “athalamic cat”. In Basic Sleep Mechanisms, ed. O. Petre-Quadens and J. Schlag, pp. 51–81, New York: Academic
Villablanca, J. R., Andrés, I. and Olmstead, C. E. (2001) Sleep-waking states develop independently in the isolated forebrain and brain stem following early postnatal midbrain transection in cats. Neuroscience 106: 717–731CrossRefGoogle ScholarPubMed
Krosigk, M., Bal, T. and McCormick, D. A. (1993) Cellular mechanisms of a synchronized oscillation in the thalamus. Science 261: 361–364CrossRefGoogle Scholar
Wada, J. A. and Terao, A. (1970) Effect of parachlorophenylalanine on basal forebrain stimulation. Experimental Neurology 28: 501–506CrossRefGoogle Scholar
Wadman, W. J. and Gutnick, M. J. (1993) Non-uniform propagation of epileptiform discharge in brain slices of rat neocortex. Neuroscience 53: 899–904Google Scholar
Walshe, F. M. R. (1957) The brain-stem conceived as the “highest level” of function in the nervous system: with particular reference to the “automatic apparatus” of Carpenter (1850) and to the “centrencephalic integrating system” of Penfield. Brain 80: 510–539CrossRefGoogle ScholarPubMed
Walter, G. (1936) The location of cerebral tumors by electroencephalography. Lancet 8: 305–308CrossRefGoogle Scholar
Wang, X. J. and Rinzel, J. (1993) Spindle rhythmicity in the reticularis thalami nucleus: synchronization among mutually inhibitory neurons. Neuroscience 53: 899–904CrossRefGoogle ScholarPubMed
Wang, Z. and McCormick, D. A. (1993) Control of firing mode of corticotectal and corticopontine layer V burst-generating neurons by norepinephrine, acetylcholine and 1S, 3R-ACPD. Journal of Neuroscience 13: 2199–2216CrossRefGoogle Scholar
Ward, A. A. (1975) Topical convulsants metals. In Experimental Models of Epilepsy, ed. D. P. Purpura, J. K. Penry, D. B. Tower, D. M. Woodbury and R. D. Walter, pp. 13–35, New York: Raven Press
Ward, A. A. and Schmidt, R. P. (1961) Some properties of single epileptic neurons. Archives of Neurology 5: 308–313CrossRefGoogle ScholarPubMed
Ward, A. A., Jasper, H. H. and Pope, A. (1969) Clinical and experimental challenges of the epilepsies. In Basic Mechanisms of the Epilepsies, ed. H. H. Jasper, A. A. Ward and A. Pope, pp. 1–12, Boston: Little, Brown
Watson, C. W. and Bowker, R. (1960) On the significance of circumscribed electroencephalographic abnormalities in genetic light sensitive states including cases of genetic epilepsy with “centrencephalic” epilepsy. Electroencephalography and Clinical Neurophysiology 12: 551Google Scholar
Weber, A. J., Kalil, R. E. and Behan, M. (1989) Synaptic connections between corticogeniculate axons and interneurons in the dorsal lateral geniculate nucleus of the cat. Journal of Comparative Neurology 289: 156–164CrossRefGoogle ScholarPubMed
Werth, E., Achermann, P., Dijk, D. J. and Borbély, A. (1997) Spindle frequency activity in the sleep EEG: individual differences and topographical distribution. Electroencephalography and Clinical Neurophysiology 103: 535–542CrossRefGoogle Scholar
West, W. J. (1841) On a particular form of infantile convulsions. Lancet 1: 724–725CrossRefGoogle Scholar
Westerberg, V. and Corcoran, M. E. (1987) Antagonism of central but not peripheral cholinergic receptors retards amygdala kindling in rats. Experimental Neurology 95: 194–206CrossRefGoogle Scholar
Westerfield, M., Joyner, R. W. and Moore, J. W. (1978) Temperature-sensitive conduction failure at axon branch points. Journal of Neurophysiology 41: 1–8CrossRefGoogle ScholarPubMed
Westgaard, J. H., Bonato, P. and Holte, K. A. (2002) Low-frequency oscillations (<;0.3 Hz) in the electromyographic (EMG) activity of the human trapezius muscle during sleep. Journal of Neurophysiology 88: 1177–1184CrossRefGoogle ScholarPubMed
Wheal, H. V., Bernard, C., Chad, J. E. and Cannon, R. C. (1998) Pro-epileptic changes in synaptic function can be accompanied by pro-epileptic changes in neuronal excitability. Trends in Neurosciences 21: 167–174CrossRefGoogle ScholarPubMed
White, J. C. (1940) Autonomic discharge from stimulation of the hypothalamus. In The Hypothalamus and Central Levels of Autonomic Function, ed. J. F. Fulton, S. W. Ranson and A. M. Frantz, pp. 854–863, Baltimore: Williams and Wilkins
White, J. C., Langston, J. W. and Pedley, T. A. (1977) Benign epileptiform transients of sleep: clarification of the small sharp spike controversy. Neurology 27: 1061–1068CrossRefGoogle ScholarPubMed
Wilcox, K. S., Gutnick, M. J. and Cristoph, G. R. (1988) Electrophysiological properties of neurons in the lateral habenular nucleus: an in vitro study. Journal of Neurophysiology 59: 212–225CrossRefGoogle Scholar
Wilcox, K. S., Grant, S. J., Burkhart, B. A. and Cristoph, G. R. (1989) In vivo electrophysiology of neurons in the lateral dorsal tegmental nucleus. Brain Research Bulletin 22: 557–560CrossRefGoogle Scholar
Wilder, B. J. and Morrell, F. (1967) Cellular behavior in secondary epileptic lesions. Neurology 17: 1193–1204CrossRefGoogle ScholarPubMed
Williams, D. (1953) A study of thalamic and cortical rhythms in Petit Mal. Brain 76: 50–69CrossRefGoogle ScholarPubMed
Williams, J. A. and Reiner, P. B. (1993) Noradrenaline hyperpolarizes identified rat mesopontine cholinergic neurons in vitro. Journal of Neuroscience 13: 3878–3883CrossRefGoogle ScholarPubMed
Williams, J. A., Comisarow, J., Day, J., Fibiger, H. C. and Reiner, P. B. (1994) State-dependent release of acetylcholine in rat thalamus measured by in vivo microdialysis. Journal of Neuroscience 14: 5236–5242CrossRefGoogle ScholarPubMed
Williamson, A. M., Ohara, P. T. and Ralston, H. J. (1993) Electron microscopic evidence that cortical terminals make direct contacts onto cells of the thalamic reticular nucleus in the monkey. Brain Research 631: 175–179CrossRefGoogle ScholarPubMed
Williamson, A., Telfeian, A. E. and Spencer, D. D. (1995) Prolonged GABA responses in dentate granule cells in slices isolated from patients with temporal lobe sclerosis. Journal of Neurophysiology 74: 378–387CrossRefGoogle ScholarPubMed
Williamson, R. and Wheal, H. V. (1992) The contribution of AMPA and NMDA receptors to graded bursting activity in the hippocampal CA1 region in an acute in vitro model of epilepsy. Epilepsy Research 12: 179–188CrossRefGoogle Scholar
Willmore, L. J. (1999) How does trauma cause epilepsy? In The Epilepsies – Etiologies and Prevention, ed. P. Kotagal and H. O. Lüders, pp. 289–291, San Diego: Academic Press
Wilson, C. J. (1993) The generation of natural firing patterns in neostriatal neurons. Progress in Brain Research 99: 277–297CrossRefGoogle ScholarPubMed
Wilson, C. J. and Kawaguchi, Y. (1996) The origin of two-state spontaneous membrane potential fluctuations of neostriatal spiny neurons. Journal of Neuroscience 16: 2397–2410CrossRefGoogle Scholar
Wilson, M. A. and McNaughton, B. L. (1994) Reactivation of hippocampal ensemble memories during sleep. Science 265: 676–679CrossRefGoogle ScholarPubMed
Wilson, S., Kinnier, A. and Bruce, A. (1955) Neurology. Baltimore: Williams & Wilkins
Winson, J. and Abzug, C. (1978) Neuronal transmission through hippocampal pathways dependent on behavior. Journal of Neurophysiology 41: 716–732CrossRefGoogle ScholarPubMed
Winter, O., Kok, A., Kenemans, J. L. and Elton, M. (1995) Auditory event-related potentials (AEPs) to deviant stimuli during drowsiness and sleep. Electroencephalography and Clinical Neurophysiology 96: 398–412CrossRefGoogle Scholar
Wise, S. P., Fleshman, J. W. Jr. and Jones, E. G. (1979) Maturation of pyramidal cell form in relation to developing afferent and efferent connections of rat somatic sensory cortex. Neuroscience 4: 1275–1297CrossRefGoogle ScholarPubMed
Witte, O. W. and Freund, H. J. (1999) Neuronal dysfunction, epilepsy, and postlesional brain plasticity. Advances in Neurology 81: 25–36Google ScholarPubMed
Wittner, L., Maglóczky, Z., Borhegyi, S., Halász, P., Tóth, S., Eröss, L., Szabó, Z. and Freund, T. F. (2001) Preservation of perisomatic inhibitory input of granule cells in the epileptic human dentate gyrus. Neuroscience 108: 587–600CrossRefGoogle ScholarPubMed
Wolpert, S. (1982) A New History of India. New York: Oxford University Press
Wong, R. K. S. and Stewart, M. (1992) Different firing patterns generated in dendrites and somata of CA1 pyramidal neurones in guinea-pig hippocampus. Journal of Physiology (London) 457: 675–687CrossRefGoogle ScholarPubMed
Wong, R. K. S., Prince, D. A. and Basbaum, A. I. (1979) Intradendritic recordings from hippocampal neurons. Proceedings of the National Academy of Sciences of the USA 76: 986–990CrossRefGoogle ScholarPubMed
Woody, C. D., Gruen, E. and Wang, X. F. (2003) Electrical properties affecting discharge of units of the mid and posterolateral thalamus of conscious cats. Neuroscience, in pressCrossRefGoogle ScholarPubMed
Wuarin, J. P. and Dudek, F. E. (1996) Electrographic seizures and new recurrent excitatory circuits in the dentate gyrus of hippocampal slices from kainate-treated epileptic rats. Journal of Neuroscience 16: 4438–4448CrossRefGoogle ScholarPubMed
Xiong, Z. Q., Saggau, P. and Stringer, J. L. (2000) Activity-dependent intracellular acidification correlates with the duration of seizure activity. Journal of Neuroscience 20: 1290–1296CrossRefGoogle ScholarPubMed
Yamada, T., Kameyama, S., Fuchigami, Z., Nakazumi, Y., Dickins, Q. S. and Kimura, J. (1988) Changes of short latency somatosensory evoked potential in sleep. Electroencephalography and Clinical Neurophysiology 70: 126–136CrossRefGoogle ScholarPubMed
Yamamoto, C. and McIlwain, H. (1966) Electrical activities in thin sections from the mammalian brain maintained in chemically defined media in vitro. Journal of Neurochemistry 13: 1333–1343CrossRefGoogle ScholarPubMed
Yamashita, A., Watanabe, Y. and Hayaishi, O. (1983) Autoradiographic localization of a binding protein(s) specific for prostaglandin D2 in rat brain. Proceedings of the National Academy of Sciences of the USA 80: 6114–6118CrossRefGoogle ScholarPubMed
Yang, C. R., Seamans, J. K. and Gorelova, N. (1996) Electrophysiological and morphological properties of layers V–VI principal pyramidal cells in rat prefrontal cortex in vitro. Journal of Neuroscience 16: 1904–1921CrossRefGoogle ScholarPubMed
Yang, L. and Benardo, L. S. (1997) Epileptogenesis following neocortical trauma from two sources of disinhibition. Journal of Neurophysiology 78: 2804–2810CrossRefGoogle ScholarPubMed
Yaqub, B. A. (1993) Electroclinical seizures in Lennox-Gastaut syndrome. Epilepsia 34: 120–127CrossRefGoogle ScholarPubMed
Yen, C. T., Conley, M., Hendry, S. H. C. and Jones, E. G. (1985) The morphology of physiologically identified GABAergic neurons in the somatic sensory part of the thalamic reticular nucleus in the cat. Journal of Neuroscience 5: 2254–2268CrossRefGoogle ScholarPubMed
Yeterian, E. H. and Pandya, D. N. (1989) Thalamic connections of the superior temporal sulcus in the rhesus monkey. Journal of Comparative Neurology 282: 80–97CrossRefGoogle ScholarPubMed
Ylinen, A., Bragin, A., Nádasdy, Z., Jandó, G., Szabó, I., Sik, A. and Buzsáki, G. (1995) Sharp wave-associated high-frequency oscillation (200 Hz) in the intact hippocampus: network and intracellular mechanisms. Journal of Neuroscience 15: 30–46CrossRefGoogle ScholarPubMed
Yoshida, M., Sasa, M. and Takaori, S. (1984) Serotonin-mediated inhibition from dorsal raphe nucleus of neurons in dorsal geniculate and thalamic reticular nuclei. Brain Research 290: 95–105CrossRefGoogle ScholarPubMed
Young, M. P., Tanaka, K. and Yamane, S. (1992) On oscillating neuronal responses in the visual cortex of the monkey. Journal of Neurophysiology 67: 1464–1474CrossRefGoogle ScholarPubMed
Yue, B. W. and Huguenard, J. R. (2001) The role of H-current in regulating strength and frequency of thalamic network oscillations. Thalamus and Related Systems 1: 95–103Google ScholarPubMed
Yuste, R. and Tank, D. W. (1996) Dendritic integration in mammalian neurons, a century after Cajal. Neuron 16: 701–716CrossRefGoogle ScholarPubMed
Zhang, S. J., Huguenard, J. R. and Prince, D. A. (1997) GABAA receptor-mediated Cl- currents in rat thalamic reticular and relay neurons. Journal of Neurophysiology 78: 2280–2286CrossRefGoogle ScholarPubMed
Zhang, Y., Perez-Velazquez, J. L., Tian, G. F., Wu, C. P., Skinner, F. K., Carlen, P. L. and Zhang, L. (1998) Slow oscillations (≤1 Hz) mediated by GABAergic interneuronal networks in rat hippocampus. Journal of Neuroscience 18: 9256–9268CrossRefGoogle ScholarPubMed
Zhu, J. J. and Lo, F. S. (1999) Three GABA receptor-mediated postsynaptic potentials in interneurons in the rat lateral geniculate nucleus. Journal of Neuroscience 19: 5721–5730CrossRefGoogle ScholarPubMed
Zhu, J. J. and Uhlrich, D. J. (1998) Cellular mechanisms underlying two muscarinic receptor-mediated depolarizing responses in relay cells of the rat lateral geniculate nucleus. Neuroscience 87: 767–781CrossRefGoogle ScholarPubMed
Zhu, J. J., Lytton, W. W., Xue, J. T. and Uhlrich, D. J. (1999a) An intrinsic oscillation in interneurons of the rat lateral geniculate nucleus. Journal of Neurophysiology 81: 702–711CrossRefGoogle Scholar
Zhu, J. J., Uhlrich, D. J. and Lytton, W. W. (1999b) Burst firing in identified rat geniculate interneurons. Neuroscience 91: 1445–1460CrossRefGoogle Scholar
Zifkin, B. G. and Dravet, C. (1997) Generalized convulsive seizures. In Epilepsy: A Comprehensive Textbook, ed. J. Engel Jr. and T. A. Pedley, pp. 567–577, Philadelphia: Lippincott-Raven
Zola-Morgan, S. and Squire, L. R. (1993) Neuroanatomy of memory. Annual Reviews of Neuroscience 16: 547–563CrossRefGoogle Scholar
Zuckermann, E. C. and Glaser, G. H. (1968) Hippocampal epileptic activity induced by localized ventricular perfusion with high-potassium cerebrospinal fluid. Experimental Neurology 20: 87–110CrossRefGoogle ScholarPubMed
Zygierewicz, J., Blinowska, K. J., Durka, P. J., Szelenberger, W., Niemcewicz, S. and Androsiuk, W. (1999) High resolution study of sleep spindles. Clinical Neurophysiology 110: 2136–2147CrossRefGoogle ScholarPubMed
Abel, T., Nguyen, P. V., Barad, M., Deuel, T. A., Kandel, E. R. and Bourtchouladze, R. (1997) Genetic demonstration of a role for PKA in the late phase of LTP and in hippocampus-based long-term memory. Cell 88: 615–626CrossRefGoogle ScholarPubMed
Abramson, B. P. and Chalupa, L. M. (1985) The laminar distribution of cortical connections with the tecto- and cortico-recipient zones in the cat's lateral posterior nucleus. Neuroscience 15: 81–95CrossRefGoogle ScholarPubMed
Achermann, P. and Borbély, A. (1997) Low-frequency (< Hz) oscillations in the human sleep EEG. Neuroscience 81: 213–222CrossRefGoogle Scholar
Achermann, P. and Borbély, A. (1998a) Coherence analysis of the human sleep electroencephalogram. Neuroscience 85: 1195–1208CrossRefGoogle Scholar
Achermann, P. and Borbély, A. (1998b) Temporal evolution of coherence and power in the human sleep electroencephalogram. Journal of Sleep Research 7 (Suppl. 1): 36–41CrossRefGoogle Scholar
Adey, W. R. (1967) Hippocampal states and functional relations with corticosubcortical systems in attention and learning. Progress in Brain Research 27: 228–245CrossRefGoogle Scholar
Adolphs, R., Tranel, D., Damasio, H. and Damasio, A. (1994) Impaired recognition of emotion in facial expression following bilateral damage to the human amygdala. Nature 372: 669–672CrossRefGoogle ScholarPubMed
Adrian, E. D. and Matthews, B. H. C. (1934) The Berger rhythm: potential changes from the occipital lobes in man. Brain 57: 355–384CrossRefGoogle Scholar
Agmon, A. and Connors, B. W. (1991) Thalamocortical responses of mouse somatosensory (barrel) cortex in vitro. Neuroscience 41: 365–379CrossRefGoogle ScholarPubMed
Ajmone-Marsan, C. (1975) Focal electrical stimulation. In Experimental Models of Epilepsy, ed. D. P. Purpura, J. K. Penry, D. B. Tower, D. M. Woodbury and R. D. Walter, pp. 147–172, New York: Raven Press
Aladjalova, N. A. (1964) Slow Electrical Processes in the Brain. Progress in Brain Research (vol. 7). Amsterdam: Elsevier
Albe-Fessard, D. and Buser, P. (1955) Activités intracellulaires recueillies dans le cortex sigmoïde du chat: participation des neurones pyramidaux au “potential évoqué” somesthésique. Journal de Physiologie (Paris) 47: 67–69Google Scholar
Albowitz, B. and Kuhnt, U. (1993) The contribution of intracortical connections to horizontal spread of activity in the neocortex as revealed by voltage sensitive dyes and a fast optical recording method. European Journal of Neuroscience 5: 1349–1359CrossRefGoogle Scholar
Albowitz, B. and Kuhnt, U. (1995) Epileptiform activity in the guinea-pig neocortical slice spreads preferentially along supragranular layers – recordings with voltage-sensitive dyes. European Journal of Neuroscience 7: 1273–1284CrossRefGoogle ScholarPubMed
Albrecht, D., Royl, G. and Kaneoke, Y. (1998) Very slow oscillatory activities in lateral geniculate neurons of freely moving and anesthetized rats. Neuroscience Research 32: 209–220CrossRefGoogle ScholarPubMed
Alefeld, M., Sutor, B. and Luhmann, H. J. (1998) Pattern and pharmacology of propagating epileptiform activity in mouse cerebral cortex. Experimental Neurology 153: 113–122CrossRefGoogle ScholarPubMed
Alger, B. E. and Nicoll, R. A. (1982) Feed-forward dendritic inhibition in rat hippocampal pyramidal cells studied in vitro. Journal of Physiology (London) 328: 105–123CrossRefGoogle ScholarPubMed
Allen, P. J., Fish, D. R. and Smith, S. J. (1992) Very high-frequency rhythmic activity during SEEG suppression in frontal lobe epilepsy. Electroencephalography and Clinical Neurophysiology 82: 155–159CrossRefGoogle ScholarPubMed
Al-Noori, S. and Swann, J. (2000) A role for sodium and chloride in kainic acid-induced beading of inhibitory interneuron dendrites. Neuroscience 101: 337–348CrossRefGoogle ScholarPubMed
Alonso, A. and Klink, R. (1993) Differential electroresponsiveness of stellate and pyramidal-like cells of medial entorhinal cortex layer II. Journal of Neurophysiology 70: 128–143CrossRefGoogle ScholarPubMed
Alonso, A. and Köhler, C. (1984) A study of the reciprocal connection between the septum and the entorhinal area using anterograde and retrograde axonal transport methods in the rat brain. Journal of Comparative Neurology 225: 327–343CrossRefGoogle Scholar
Alonso, A. and Llinás, R. (1989) Subthreshold Na+-dependent theta-like rhythmicity in stellate cells of entorhinal cortex layer II. Nature 342: 175–177CrossRefGoogle ScholarPubMed
Alonso, A., Curtis, M. and Llinás, R. (1990) Postsynaptic Hebbian and non-Hebbian long-term potentiation of synaptic efficacy in the entorhinal cortex in slices and in isolated adult guinea pig brain. Proceedings of the National Academy of Sciences of the USA 87: 9280–9284CrossRefGoogle ScholarPubMed
Altman, J. and Bayer, S. A. (1979) Development of the diencephalons in the rat. V. Thymidine-radiographic observations on internuclear and intranuclear gradients in the thalamus. Journal of Comparative Neurology 188: 473–500CrossRefGoogle Scholar
Alvarez-Maubecin, V., Garcia-Hernandez, F., Williams, J. T. and Bockstaele, E. J. (2000) Functional coupling between neurons and glia. Journal of Neuroscience 20: 4091–4098CrossRefGoogle ScholarPubMed
Amadeo, M. and Shagass, C. (1973) Brief latency click-evoked potentials during waking and sleep in man. Psychophysiology 10: 244–250CrossRefGoogle ScholarPubMed
Amaral, D. G. and Price, J. L. (1984) Amygdalo-cortical projections in the monkey (Macaca fascicularis). Journal of Comparative Neurology 230: 465–496CrossRefGoogle Scholar
Amaral, D. G. and Witter, M. P. (1989) The three-dimensional organization of the hippocampal formation: a review of anatomical data. Neuroscience 31: 571–591CrossRefGoogle ScholarPubMed
Amaral, D. G., Price, J. L., Pitkänen, A. and Carmichael, S. T. (1992) Anatomical organization of the primate amygdaloid complex. In The Amygdala, ed. J. P. Aggleton, pp. 1–66, New York: Wiley-Liss
Amzica, F. and Massimini, M. (2000) Modulation of glia and neuronal activities by halothane. Society for Neuroscience Abstracts 26: 734Google Scholar
Amzica, F. and Massimini, M. (2002) Glia and neuronal interactions during slow wave and paroxysmal activities in the neocortex. Cerebral Cortex 12: 1101–1113CrossRefGoogle ScholarPubMed
Amzica, F. and Neckelmann, D. (1999) Membrane capacitance of cortical neurons and glia during sleep oscillations and spike-wave seizures. Journal of Neurophysiology 82: 2731–2746CrossRefGoogle ScholarPubMed
Amzica, F. and Steriade, M. (1995a) Disconnection of intracortical synaptic linkages disrupts synchronization of a slow oscillation. Journal of Neuroscience 15: 4658–4677CrossRefGoogle Scholar
Amzica, F. and Steriade, M. (1995b) Short- and long-range neuronal synchronization of the slow (< Hz) cortical oscillation. Journal of Neurophysiology 75: 20–38CrossRefGoogle Scholar
Amzica, F. and Steriade, M. (1996) Progressive cortical synchronization of ponto-geniculo-occipital potentials during rapid eye movement sleep. Neuroscience 72: 309–314CrossRefGoogle ScholarPubMed
Amzica, F. and Steriade, M. (1997) The K-complex: its slow (< Hz) rhythmicity and relation to delta waves. Neurology 49: 952–959CrossRefGoogle ScholarPubMed
Amzica, F. and Steriade, M. (1998a) Cellular substrates and laminar profile of sleep K-complex. Neuroscience 82: 671–686CrossRefGoogle Scholar
Amzica, F. and Steriade, M. (1998b) Electrophysiological correlates of sleep delta waves. Electroencephalography and Clinical Neurophysiology 107: 69–83CrossRefGoogle Scholar
Amzica, F. and Steriade, M. (1999) Spontaneous and artificial activation of neocortical seizures. Journal of Neurophysiology 82: 3123–3138CrossRefGoogle ScholarPubMed
Amzica, F. and Steriade, M. (2000) Neuronal and glial membrane potentials during sleep and paroxysmal oscillations in the cortex. Journal of Neuroscience 20: 6646–6665CrossRefGoogle Scholar
Amzica, F. and Steriade, M. (2002) The functional significance of K-complexes. Sleep Medicine Reviews 6: 139–149CrossRefGoogle ScholarPubMed
Amzica, F., Nuñez, A. and Steriade, M. (1992) Delta-frequency (1–4 Hz) oscillations of perigeniculate thalamic neurons and their modulation by light. Neuroscience 51: 285–294CrossRefGoogle Scholar
Amzica, F., Neckelmann, D. and Steriade, M. (1997) Instrumental conditioning of fast (20- to 50-Hz) oscillations in corticothalamic networks. Proceedings of the National Academy of Sciences of the USA 94: 1985–1989CrossRefGoogle ScholarPubMed
Amzica, F., Massimini, M. and Manfridi, A. (2002) Spatial buffering during slow and paroxysmal oscillations in cortical networks of glial cells in vivo. Journal of Neuroscience 22: 1042–1053CrossRefGoogle ScholarPubMed
Anderer, P., Klösch, G., Gruber, G., Trenker, E., Pascual-Marqui, R. D., Zeitlhofer, J., Barbanoj, M. J., Rappelsberger, P. and Saletu, B. (2001) Low-resolution brain electromagnetic tomography revealed simultaneously active frontal and parietal sleep spindle sources in the human cortex. Neuroscience 103: 581–592CrossRefGoogle ScholarPubMed
Andersen, P. and Andersson, S. A. (1968) Physiological Basis of the Alpha Rhythm. New York: Appleton-Century-Crofts
Andersen, P. and Sears, T. A. (1964) The role of inhibition in the phasing of spontaneous thalamocortical discharge. Journal of Physiology (London) 173: 459–480CrossRefGoogle Scholar
Andersen, P., Eccles, J. C. and Løyning, Y. (1964) Location of postsynaptic inhibitory synapses on hippocampal pyramids. Journal of Neurophysiology 27: 592–607CrossRefGoogle ScholarPubMed
Andersen, P., Blackstad, T. W. and Lømo, T. (1966) Location and identification of excitatory synapses on hippocampal pyramidal cells. Experimental Brain Research 1: 236–248CrossRefGoogle ScholarPubMed
Andersen, P., Gross, G. N., Lømo, T. and Sveen, O. (1969) Participation of inhibitory and excitatory interneurons in the control of hippocampal cortical output. In The Interneuron, ed. M. Brazier, pp. 415–465, Los Angeles: University of California Press
Andersen, P., Dingledine, R., Gjerstad, L., Langmoen, I. A. and Laursen, A. M. (1980a) Two different responses of hippocampal pyramidal cells to application of gamma-aminobutyric acid. Journal of Physiology (London) 305: 279–296CrossRefGoogle Scholar
Andersen, P., Silfvenius, H., Sundberg, S. H. and Sveen, O. (1980b) A comparison of distal and proximal dendritic synapses on CA1 pyramids in hippocampal slices in vitro. Journal of Physiology (London) 307: 273–299CrossRefGoogle Scholar
Andre, P. and Arrighi, P. (2001) Modulation of Purkinje cell response to glutamate during the sleep-waking cycle. Neuroscience 105: 731–746CrossRefGoogle ScholarPubMed
Andreasen, M. and Hablitz, J. J. (1993) Local anesthetics block transient outward potassium currents in rat neocortical neurons. Journal of Neurophysiology 69: 1966–1975CrossRefGoogle ScholarPubMed
Andrew, R. D. and Mac Vicar, B. A. (1994) Imaging cell volume changes and neuronal excitation in the hippocampal slice. Neuroscience 62: 371–383CrossRefGoogle ScholarPubMed
Annegers, J. W. (1994) The natural course of epilepsy: an epidemiologic perspective. In The Surgical Management of Epilepsy, ed. A. R. Wyler and B. P. Hermann, pp. 3–7, Boston: Butterworth-Heinemann
Araque, A., Sanzgiri, R. P., Parpura, V. and Haydon, P. G. (1998) Calcium elevation in astrocytes causes an NMDA receptor-dependent increase in the frequency of miniature synaptic currents in cultured hippocampal neurons. Journal of Neuroscience 18: 6822–6829CrossRefGoogle ScholarPubMed
Araque, A., Parpura, V., Sanzgiri, R. P. and Haydon, P. G. (1999) Tripartite synapses: glia, the unacknowledged partner. Trends in Neurosciences 22: 208–215CrossRefGoogle ScholarPubMed
Arduini, A. and Arduini, M. (1954) Effect of drugs and metabolic alterations on brainstem arousal mechanism. Journal of Pharmacology and Experimental Therapy 110: 76–85Google ScholarPubMed
Asanuma, C. (1989) Axonal arborizations of a magnocellular basal nucleus input, and their relation to the neurons in the thalamic reticular nucleus of rats. Proceedings of the National Academy of Sciences of the USA 86: 4746–4750CrossRefGoogle ScholarPubMed
Asanuma, C. (1997) Distribution of neuromodulatory inputs in the reticular and dorsal thalamic nuclei. In Thalamus, vol. 2 (Experimental and Clinical Aspects), ed. M. Steriade, E. G. Jones and D. A. McCormick, pp. 93–153, Oxford: Elsevier
Asanuma, C. and Porter, L. L. (1990) Light and electron microscopic evidence for a GABAergic projection from the caudal basal forebrain to the thalamic reticular nucleus in rats. Journal of Comparative Neurology 302: 159–172CrossRefGoogle ScholarPubMed
Aserinsky, E. and Kleitman, N. (1953) Regularly occurring periods of eye motility and concomitant phenomena during sleep. Science 118: 273–274CrossRefGoogle ScholarPubMed
Aserinsky, E. and Kleitman, N. (1955) Two types of ocular motility occurring in sleep. Journal of Applied Physiology 8: 11–18CrossRefGoogle ScholarPubMed
Aston-Jones, G. and Bloom, F. E. (1981) Activity of norepinephrine-containing locus coeruleus neurons in behaving rats anticipates fluctuations in the sleep-waking cycle. Journal of Neuroscience 1: 876–886CrossRefGoogle ScholarPubMed
Avanzini, G., Curtis, M., Panzica, F. and Spreafico, R. (1989) Intrinsic properties of nucleus reticularis thalami neurones of the rat studied in vitro. Journal of Physiology (London) 416: 111–122CrossRefGoogle ScholarPubMed
Avanzini, G., Curtis, M., Marescaux, C., Panzica, F., Spreafico, R. and Vergnes, M. (1992) Role of thalamic reticular nucleus in the generation of rhythmic thalamo-cortical activities subserving spike and waves. Journal of Neural Transmission 35 (Suppl.): 85–95Google ScholarPubMed
Avanzini, G., De Curtis, M., Pape, H. C. and Spreafico, R. (1999) Intrinsic properties of reticular thalamic neurons relevant to genetically determined spike-wave generation. In Jasper's Basic Mechanisms of the Epilepsies (3rd edn.), ed. A. V. Delgado-Escucta, W. A. Wilson, R. W. Olsen and R. J. Porter, pp. 297–309, Philadelphia: Lippincott – Williams & Wilkins
Avendaño, C., Rausell, E. and Reinoso-Suárez, F. (1985) Thalamic projections to areas 5a and 5b of the parietal cortex in the cat: a retrograde horseradish peroxidase study. Journal of Neuroscience 5: 1446–1470CrossRefGoogle ScholarPubMed
Avendaño, C., Rausell, E., Perez-Aguilar, D. and Isorna, S. (1988) Organization of the association cortical afferent connections of area 5: a retrograde tracer study in the cat. Journal of Comparative Neurology 278: 1–33CrossRefGoogle ScholarPubMed
Avoli, M. and Gloor, P. (1981) The effects of transient functional depression of the thalamus on spindles and on bilateral synchronous epileptic discharges of feline generalized penicillin epilepsy. Epilepsia 22: 443–452CrossRefGoogle ScholarPubMed
Avoli, M., Gloor, P., Kostopoulos, G. and Gotman, J. (1983) An analysis of penicillin-induced generalized spike and wave discharges using simultaneous recordings of cortical and thalamic single neurons. Journal of Neurophysiology 50: 819–837CrossRefGoogle ScholarPubMed
Avoli, M., Barbarosie, M., Lücke, A., Nagao, T., Lopantsev, V. and Köhling, R. (1996) Synchronous GABA-mediated potentials and epileptiform discharges in the rat limbic system in vitro. Journal of Neuroscience 16: 3912–3924CrossRefGoogle ScholarPubMed
Ayala, G. F., Dichter, M., Gumnit, R. J., Matsumoto, H. and Spencer, W. A. (1973) Genesis of epileptic spikes: new knowledge of cortical feedback systems suggests a neurophysiological explanation of brief paroxysms. Brain Research 52: 1–17CrossRefGoogle ScholarPubMed
Babb, T. L. (1999) Hippocampal neurophysiology in humans. In The Epilepsies – Etiologies and Prevention, ed. P. Kotagal and H. O. Lüders, pp. 167–170, San Diego: Academic Press
Babb, T. L., Pretorius, J. K., Kupfer, W. R. and Crandall, P. H. (1989) Glutamate decarboxylase-immunoreactive neurons are preserved in human epileptic hippocampus. Journal of Neuroscience 9: 2562–2574CrossRefGoogle ScholarPubMed
Bal, T. and McCormick, D. A. (1993) Mechanisms of oscillatory activity in guinea-pig nucleus reticularis thalami in vitro: a mammalian pacemaker. Journal of Physiology (London) 466: 669–691CrossRefGoogle Scholar
Bal, T. and McCormick, D. A. (1996) What stops synchronized thalamocortical oscillations?Neuron 17: 297–308CrossRefGoogle ScholarPubMed
Bal, T., Krosigk, M. and McCormick, D. A. (1995a) Synaptic and membrane mechanisms underlying synchronized oscillations in the ferret lateral geniculate nucleus in vitro. Journal of Physiology (London) 483: 641–663CrossRefGoogle Scholar
Bal, T., Krosigk, M. and McCormick, D. A. (1995b) Role of the ferret perigeniculate nucleus in the generation of synchronized oscillations in vitro. Journal of Physiology (London) 483: 665–685CrossRefGoogle Scholar
Bal, T., Debay, D. and Destexhe, A. (2000) Cortical feedback controls the frequency and synchrony of oscillations in the visual thalamus. Journal of Neuroscience 20: 7478–7488CrossRefGoogle ScholarPubMed
Baranyi, A., Szente, M. B. and Woody, C. D. (1991) Properties of associative long-lasting potentiation induced by cellular conditioning in the motor cortex of conscious cats. Neuroscience 42: 321–334CrossRefGoogle ScholarPubMed
Barnes, D. M. and Dichter, M. A. (1984) Effects of ethosuximide and tetramethylsuccinimide on cultured cortical neurons. Neurology 34: 620–625CrossRefGoogle ScholarPubMed
Barth, D. S., Sutherling, W., Engle, J. Jr. and Beatty, J. (1984) Neuromagnetic evidence of spatially distributed sources underlying epileptiform spikes in the human brain. Science 223: 293–296CrossRefGoogle ScholarPubMed
Bassetti, C., Mathis, J., Gugger, M., Lövblad, K. O. and Hess, C. W. (1996) Hypersomnia following paramedian thalamic stroke: a report of 12 patients. Annals of Neurology 39: 471–480CrossRefGoogle ScholarPubMed
Bazhenov, M., Timofeev, I., Steriade, M. and Sejnowski, T. J. (1998a) Cellular and network models for intrathalamic augmenting responses during 10-Hz stimulation. Journal of Neurophysiology 79: 2730–2748CrossRefGoogle Scholar
Bazhenov, M., Timofeev, I., Steriade, M. and Sejnowski, T. J. (1998b) Computational models of thalamocortical augmenting responses. Journal of Neuroscience 18: 6444–6465CrossRefGoogle Scholar
Bazhenov, M., Timofeev, I., Steriade, M. and Sejnowski, T. J. (1999) Self-sustained rhythmic activity in the thalamic reticular nucleus mediated by depolarizing GABAA receptor potentials. Nature Neuroscience 2: 168–174CrossRefGoogle ScholarPubMed
Bazhenov, M., Timofeev, I., Steriade, M. and Sejnowski, T. (2000) Spiking-bursting activity in the thalamic reticular nucleus initiates sequences of spindle oscillations in thalamic networks. Journal of Neurophysiology 84: 1076–1087CrossRefGoogle ScholarPubMed
Bazhenov, M., Timofeev, I., Steriade, M. and Sejnowski, T. J. (2002) Model of thalamocortical slow-wave sleep oscillations and transitions to activated states. Journal of Neuroscience 22: 8691–8704CrossRefGoogle ScholarPubMed
Beevor, C. E. and Horsley, V. (1890) A record of the results obtained by electrical excitation of the so-called motor cortex and internal capsule in an orang-outan (Simia satyrus). Philosophical Transactions of the Royal Society of London (B) 181: 129–158CrossRefGoogle Scholar
Bekisz, M. and Wróbel, A. (1993) 20 Hz rhythm of activity in visual system of perceiving cat. Acta Neurobiologiae Experimentalis (Warszaw) 53: 175–182Google ScholarPubMed
Ben-Ari, Y. (1985) Limbic seizures and brain damage produced by kainic acid: mechanisms and relevance to human temporal lobe epilepsy. Neuroscience 14: 375–403CrossRefGoogle ScholarPubMed
Ben-Ari, Y. and Represa, A. (1990) Brief seizure episodes induce long-term potentiation and mossy fibre sprouting in the hippocampus. Trends in Neurosciences 8: 312–318CrossRefGoogle Scholar
Ben-Ari, Y., Gal La Salle, G. and Champagnat, J. (1974) Lateral amygdala unit activity. I. Relationship between spontaneous and evoked activity. Electroencephalography and Clinical Neurophysiology 37: 449–461CrossRefGoogle ScholarPubMed
Ben-Ari, Y., Krnjeviæ, K., Reiffenstein, R. J. and Reinhardt, W. (1981) Inhibitory conductance changes and action of γ-aminobutyrate in rat hippocampus. Neuroscience 6: 2445–2463CrossRefGoogle ScholarPubMed
Benazzouz, A. and Hallett, M. (2000) Mechanism of action of deep brain stimulation. Neurology 55 (Suppl. 6): S13–S16Google ScholarPubMed
Benington, J. H. and Heller, H. C. (1995) Restoration of brain energy metabolism as the function of sleep. Progress of Neurobiology 45: 347–360CrossRefGoogle ScholarPubMed
Benson, D. L., Isackson, P. J., Hendry, S. H. C. and Jones, E. G. (1991) Differential gene expression for glutamic acid decarboxylase and type II calcium-calmodulin-dependent protein kinase in basal ganglia, thalamus and hypothalamus of the monkey. Journal of Neuroscience 11: 1540–1564CrossRefGoogle ScholarPubMed
Beranek, L., Obál, F. Jr., Taishi, P., Bodosi, B., Laczi, F. and Krueger, J. M. (1997) Changes in rat sleep after single and repeated injections of the long-acting somatostatin analog octreotide. American Journal of Physiology 273: R1484–1491Google ScholarPubMed
Berger, H. (1929) Uber das Elektroencephalogramm des Menschen. Archive für Psychiatrie und Nervenkrankheiten 87: 527–570CrossRefGoogle Scholar
Berger, H. (1937) Uber das Elektroencephalogramm des Menschen. Dreizehnte Mitteilung. Archive für Psychiatrie und Nervenkrankheiten 106: 577–584CrossRefGoogle Scholar
Bergmann, F., Costin, A. and Gutman, J. (1963) A low-threshold convulsive area in the rabbit's mesencephalon. Electroencephalography and Clinical Neurophysiology 15: 683–690CrossRefGoogle ScholarPubMed
Bernard, C., Hirsch, J. C. and Ben-Ari, Y. (1999) Excitation and inhibition in temporal lobe epilepsy: a close encounter. In Jasper's Basic Mechanisms of the Epilepsies (3rd edn.), ed. A. V. Delgado-Escueta, W. A. Wilson, R. W. Olsen and R. J. Porter, pp. 821–828, Philadelphia: Lippincott – Williams & Wilkins
Bernard, C., Cossart, R., Hirsch, J. C., Esclapez, M. and Ben-Ari, Y. (2000) What is GABAergic inhibition? How is it modified in epilepsy?Epilepsia 41 (Suppl. 6): S90–S95CrossRefGoogle Scholar
Bernusconi, R., Lauber, J., Marescaux, C., Vergnes, M., Martin, P., Rubio, V., Leonhardt, T., Reymann, N. and Bitiiger, H. (1992) Experimental absence seizures: potential role of gamma-hydroxybutyric acid and GABAB receptors. Journal of Neural Transmission 35 (Suppl.): 155–177Google Scholar
Bernusconi, R., Mathivet, P., Bischoff, S. and Marescaux, C. (1999) γ-Hydroxybutyric acid: an endogenous neuromodulator with abuse potential?Trends in Pharmacological Sciences 20: 135–141CrossRefGoogle Scholar
Berridge, M. J. (1998) Neuronal calcium signaling. Neuron 21: 13–26CrossRefGoogle ScholarPubMed
Berridge, M. J. (2000) Calcium signaling systems in neurons: synaptic plasticity and sleep. In The Regulation of Sleep, ed. A. A. Borbély, O. Hayaishi, T. J. Sejnowski and J. S. Altman, pp. 65–75, Strasbourg: Human Frontier Science Program
Bertram, E. H. and Scott, C. (2000) The pathological substrate of limbic epilepsy: neuronal loss in the medial dorsal thalamus nucleus as the consistent change. Epilepsia 41 (Suppl. 6): S3–S8CrossRefGoogle ScholarPubMed
Beurrier, C., Bioulac, B., Audin, J. and Hammond, C. (2001) High-frequency stimulation produces a transient blockade of voltage-gated currents in subthalamic neurons. Journal of Neurophysiology 85: 1351–1356CrossRefGoogle ScholarPubMed
Bezzi, P. and Volterra, A. (2001) A neuron-glia signaling network in the active brain. Current Opinion in Neurobiology 11: 387–394CrossRefGoogle ScholarPubMed
Bignall, K. E., Imbert, M. and Buser, P. (1966) Optic projections to non visual cortex in the cat. Journal of Neurophysiology 29: 396–409CrossRefGoogle Scholar
Bishop, P. O., Burke, W. and Hayhow, W. R. (1959) Repetitive stimulation of optic nerve and lateral geniculate synapses. Experimental Neurology 1: 534–555CrossRefGoogle ScholarPubMed
Bland, B. H. and Colom, L. V. (1993) Extrinsic and intrinsic properties underlying oscillation and synchrony in limbic cortex. Progress in Neurobiology 41: 157–208CrossRefGoogle ScholarPubMed
Blumenfeld, H. and McCormick, D. A. (2000) Corticothalamic inputs control the pattern of activity generated in thalamocortical networks. Journal of Neuroscience 20: 5153–5162CrossRefGoogle ScholarPubMed
Borbély, A. A. (1982) A two process model of sleep regulation. Human Neurobiology 1: 195–204Google ScholarPubMed
Borbély, A. A. (1984) Das Geheimnis der Schlafs. Stuttgart: Deutsche Verlags-Anstalt
Borbély, A. A. and Tobler, I. (1989) Endogenous sleep-promoting substances and sleep regulation. Physiological Reviews 69: 605–670CrossRefGoogle ScholarPubMed
Bormann, J. and Kettenmann, H. (1988) Patch clamp study of GABA receptor Cl- channels in cultured astrocytes. Proceedings of the National Academy of Sciences of the USA 85: 8336–8340CrossRefGoogle ScholarPubMed
Borst, J. G. and Sakmann, B. (1999) Depletion of calcium in the synaptic cleft of a calyx-type synapse in the rat brainstem. Journal of Physiology (London) 521: 123–133CrossRefGoogle ScholarPubMed
Bougousslavsky, J., Miklossy, J., Deruz, J. P., Regli, F. and Assai, G. (1986) Unilateral left paramedian infarction of the thalamus and midbrain: a clinico-pathological study. Journal of Neurology, Neurosurgery and Psychiatry 49: 686–694CrossRefGoogle Scholar
Bourassa, J., Pinault, D. and Deschênes, M. (1995) Corticothalamic projections from the cortical barrel field to the somatosensory thalamus in rats: a single-fiber study using biocytin as an anterograde tracer. European Journal of Neuroscience 7: 19–30CrossRefGoogle Scholar
Bouyer, J. J., Montaron, M. F., Vahnée, J. M., Albert, M. P. and Rougeul, A. (1987) Anatomical localization of cortical beta rhythm in cat. Neuroscience 22: 863–869CrossRefGoogle ScholarPubMed
Bragin, A., Engel, J. Jr., Wilson, C. L., Fried, I. and Mathern, G. W. (1999a) Hippocampal and entorhinal cortex high-frequency oscillations (100–500 Hz) in human epileptic brain and in kainic acid-treated rats with chronic seizures. Epilepsia 40: 127–137CrossRefGoogle Scholar
Bragin, A., Engel, J. Jr., Wilson, C. L., Vizentin, E. and Mathern, G. W. (1999b) Electrophysiologic analysis of a chronic seizure model after unilateral hippocampal KA injection. Epilepsia 40: 1210–1221CrossRefGoogle Scholar
Bragin, A., Wilson, C. L. and Engel, J. Jr. (2000) Chronic epileptogenesis requires development of a network of pathologically interconnected neuron clusters: a hypothesis. Epilepsia 41 (Suppl. 6): S144–S152CrossRefGoogle ScholarPubMed
Branch, C. L. and Martin, A. R. (1958) Inhibition of Betz cell activity by thalamic and cortical stimulation. Journal of Neurophysiology 21: 380–390CrossRefGoogle ScholarPubMed
Bratz, E. (1899) Ammonshornbefunde bei Epileptischen. Archives für Psychiatrie und Nervenkrankheiten 31: 820–835CrossRefGoogle Scholar
Braun, A. R., Balkin, T. J., Wesensten, N. J., Carson, R. E., Varga, M., Baldwin, P., Selbie, S., Belenky, G. and Herscovitch, P. (1997) Regional cerebral blood flow throughout the sleep-wake cycle. Brain 120: 1173–1197CrossRefGoogle ScholarPubMed
Brazier, M. A. B. (1961) A History of the Electrical Activity of the Brain. London: Pitman
Bremer, F. (1935) Cerveau “isolé” et physiologie du sommeil. Comptes Rendus de la Société de Biologie (Paris) 118: 1235–1241Google Scholar
Bremer, F. (1937) L'activité cérébrale au cours du sommeil et de la narcose. Contribution à l'étude du mécanisme du sommeil. Bulletin de l'Académie Royale de Médecine de Belgique 4: 68–86Google Scholar
Bremer, F. (1949) Considérations sur l'origine et la nature des “ondes” cérébrales. Electroencephalography and Clinical Neurophysiology 1: 177–193Google Scholar
Bremer, F. (1958a) Cerebral and cerebellar potentials. Physiological Reviews 38: 357–388CrossRefGoogle Scholar
Bremer, F. (1958b) Le processus d'excitation et d'inhibition dans les phénomènes épileptiques. In Bases Physiologiques et Aspects Cliniques de l'Épilepsie, ed. T. Alajouanine, pp. 1–35, Paris: Masson
Bremer, F. (1973) Preoptic hypnogenic area and reticular activating system. Archives Italiennes de Biologie 111: 85–111Google ScholarPubMed
Bremer, F. (1975) The isolated brain and its aftermath. In The Neurosciences: Paths of Discovery, ed. F. G. Worden, J. P. Swazey and G. A. Adelman, pp. 267–274. Cambridge, MA: The MIT Press
Bremer, F., Stoupel, N. and Reeth, P. C. (1960) Nouvelles recherches sur la facilitation et l'inhibition des potentiels évoqués corticaux dans l'éveil réticulaire. Archives Italiennes de Biologie 98: 229–247Google Scholar
Bringuier, V., Frégnac, Y., Baranyi, A., Debanne, D. and Shulz, D. E. (1997) Synaptic origin and stimulus dependency of neuronal oscillatory activity in the primary visual cortex of the cat. Journal of Physiology (London) 500: 751–774CrossRefGoogle ScholarPubMed
Brown, A. M., Schwindt, P. C. and Crill, W. E. (1993) Voltage dependence and activation kinetics of pharmacologically defined components of high-threshold calcium current in rat neocortical neurons. Journal of Neurophysiology 70: 1530–1543CrossRefGoogle ScholarPubMed
Brown, R. E., Sergeeva, O. A., Eriksson, K. S. and Haas, H. L. (2002) Convergent excitation of dorsal raphe serotonin neurons by multiple arousal systems (orexin/hypocretin, histamine and noradrenaline). Journal of Neuroscience 22: 8850–8859CrossRefGoogle Scholar
Browne, S. H., Kang, J., Akk, G., Chiang, L. W., Schulman, H., Huguenard, J. R. and Prince, D. A. (2001) Kinetic and pharmacological properties of GABAA receptors in single thalamic neurons and GABAA subunit expression. Journal of Neurophysiology 86: 2312–2322CrossRefGoogle Scholar
Browning, R. A. and Nelson, D. K. (1986) Modification of electroshock and pentylenetetrazol seizure patterns in rats after precollicular transections. Experimental Neurology 93: 546–556CrossRefGoogle ScholarPubMed
Browning, R., Maggio, R., Sahibzada, N. and Gale, K. (1993) Role of brainstem structures in seizures initiated from the deep prepiriform cortex of rats. Epilepsia 34: 393–407CrossRefGoogle ScholarPubMed
Brumberg, J. C., Nowak, L. G. and McCormick, D. A. (2000) Ionic mechanisms underlying repetitive high-frequency burst firing in supragranular cortical neurons. Journal of Neuroscience 20: 4829–4943CrossRefGoogle ScholarPubMed
Buchhalter, J. R. (1993) Animal models of inherited epilepsy. Epilepsia 34 (Suppl. 3): S31–S41CrossRefGoogle ScholarPubMed
Buckmaster, P. S., Jongen-Rêlo, A. L., Davari, S. B. and Wong, E. H. (2000) Testing the disinhibition hypothesis of epileptogenesis in vivo and during spontaneous seizures. Journal of Neuroscience 20: 6232–6240CrossRefGoogle ScholarPubMed
Budde, T., Mager, R. and Pape, H. C. (1992) Different types of potassium outward current in relay neurons acutely isolated from the lateral geniculate nucleus. European Journal of Neuroscience 4: 708–722CrossRefGoogle ScholarPubMed
Buhl, E. H., Otis, T. S. and Mody, I. (1996) Zinc-induced collapse of augmented inhibition by GABA in a temporal lobe epilepsy model. Science 271: 369–373CrossRefGoogle Scholar
Bullock, T. H. (1997) Signals and signs in the nervous system: the dynamic anatomy of electrical activity is probably information-rich. Proceedings of the National Academy of Sciences of the USA 94: 1–6CrossRefGoogle ScholarPubMed
Burns, B. D. (1951) Some properties of isolated cerebral cortex in the unanaesthetised cat. Journal of Physiology (London) 112: 156–175CrossRefGoogle Scholar
Burns, B. D. (1958) The Mammalian Cortex. London: Monographs of the Physiological Society
Burnstine, T. H., Vining, E. P., Uematsu, S. and Lesser, R. P. (1991) Multifocal independent epileptiform discharges in children: ictal correlates and surgical therapy. Neurology 41: 1223–1228CrossRefGoogle ScholarPubMed
Bush, P. C., Prince, D. A. and Miller, K. D. (1999) Increased pyramidal excitability and NMDA conductance can explain posttraumatic epileptogenesis without disinhibition: a model. Journal of Neurophysiology 82: 1748–1758CrossRefGoogle ScholarPubMed
Buzsáki, G. (1989) Two-stage model of memory trace formation: a role for “noisy” brain states. Neuroscience 31: 551–570CrossRefGoogle ScholarPubMed
Buzsáki, G. (1990) Petit-mal epilepsy and parkinsonian tremor: hypothesis of a common pacemaker. Neuroscience 36: 1–14CrossRefGoogle ScholarPubMed
Buzsáki, G. (1998) Memory consolidation during sleep: a neurophysiological perspective. Journal of Sleep Research 7 (Suppl. 1): 17–23CrossRefGoogle ScholarPubMed
Buzsáki, G. (2002) Theta oscillations in the hippocampus. Neuron, 33: 325–340CrossRefGoogle ScholarPubMed
Buzsáki, G. and Chrobak, J. J. (1995) Temporal structure in spatially organized neuronal ensembles: a role for interneuron networks. Current Opinion in Neurobiology 5: 504–510CrossRefGoogle Scholar
Buzsáki, G., Grastyan, E., Tveritskaya, I. and Czopf, J. (1979) Hippocampal evoked potentials and EEG changes during classical conditioning in the rat. Electroencephalography and Clinical Neurophysiology 47: 64–74CrossRefGoogle ScholarPubMed
Buzsáki, G., Leung, L. and Vanderwolf, C. H. (1983) Cellular bases of hippocampal EEG in the behaving rat. Brain Research Reviews 6: 139–171CrossRefGoogle Scholar
Buzsáki, G., Bickford, R. G., Armstrong, D. M., Ponomareff, G., Chen, K. S., Ruiz, R., Thal, L. G. and Gage, F. H. (1988a) Electrical activity in the neocortex of freely moving young and aged rats. Neuroscience 26: 735–744CrossRefGoogle Scholar
Buzsáki, G., Bickford, R. G., Ponomareff, G., Thal, L. J., Mandel, R. and Gage, F. H. (1988b) Nucleus basalis and thalamic control of neocortical activity in the freely moving rat. Journal of Neuroscience 8: 4007–4026CrossRefGoogle Scholar
Buzsáki, G., Kennedy, B., Solt, V. B. and Ziegler, M. (1991) Noradrenergic control of thalamic oscillations: the role of α-2 receptors. European Journal of Neuroscience 3: 222–229CrossRefGoogle Scholar
Buzsáki, G., Penttonen, M., Nádasdy, Z. and Bragin, A. (1996) Pattern and inhibition-dependent invasion of pyramidal cell dendrites by fast spikes in the hippocampus in vivo. Proceedings of the National Academy of Sciences of the USA 93: 9921–9925CrossRefGoogle ScholarPubMed
Cadilhac, J., Vlahovitch, B. and Delange, M. (1965) Considerations on the changes in epileptic discharges during the phase of eye movements. Electroencephalography and Clinical Neurophysiology 18: 96Google Scholar
Calvet, J., Calvet, M. C. and Scherrer, J. (1964) Etude stratigraphique corticale de l'activité EEG spontanée. Electroencephalography and Clinical Neurophysiology 17: 109–125CrossRefGoogle Scholar
Cannon, W. B. and Rosenblueth, A. (1949) The Supersensitivity of Denervated Structures: A Law of Denervation. New York: Macmillan
Canu, M. H. and Rougeul, A. (1992) Nucleus reticularis thalami participates in sleep spindles, not in beta rhythms concomitant with attention in cat. Comptes Rendus de l'Académie des Sciences (Paris) 315: 513–520Google Scholar
Cape, E. G. and Jones, B. E. (1998) Differential modulation of high-frequency γ-electroencephalogram activity and sleep-wake state by noradrenaline and serotonin microinjections into the region of cholinergic basalis neurons. Journal of Neuroscience 18: 2653–2666CrossRefGoogle ScholarPubMed
Cape, E. G. and Jones, B. E. (2000) Effects of glutamate versus procaine microinjections into the basal forebrain cholinergic cell area upon gamma and theta EEG activity and sleep-wake state. European Journal of Neuroscience 12: 2166–2184CrossRefGoogle ScholarPubMed
Carlen, P., Perez-Velazquez, J. L., Valiante, T. A., Jahromi, S. S. and Bardakjian, B. L. (1996) Electric coupling in epileptogenesis. In Gap Junctions in the Nervous System, ed. D. C. Spray and R. Dermietzel, pp. 289–299, Austin, TX: Landes Company
Carli, G., Diete-Spiff, K. and Pompeiano, O. (1967) Presynaptic and postsynaptic inhibition of transmission of somatic afferent volleys through the cuneate nucleus during sleep. Archives Italiennes de Biologie 105: 52–82Google ScholarPubMed
Carskadon, M. A. and Dement, W. C. (2000) Normal human sleep: an overview. In Principles and Practice of Sleep Medicine, ed. M. H. Kryger, T. Roth and W. C. Dement, pp. 15–25, Philadelphia: W. B. Saunders
Cassidi, R. M. and Gale, K. (1998) Mediodorsal thalamus plays a critical role in the development of limbic motor seizures. Journal of Neuroscience 18: 9002–9009CrossRefGoogle Scholar
Castaigne, P., Buge, A., Escourolle, R. and Mason, M. (1962) Ramollissement pédonculaire médian, tegmentothalamique avec ophtalmoplégie et hypersomnie. Revue Neurologique (Paris) 106: 357–367Google Scholar
Castro-Alamancos, M. (1999) Neocortical synchronized oscillations induced by thalamic disinhibition in vivo. Journal of Neuroscience (online) 19: RC27CrossRefGoogle ScholarPubMed
Castro-Alamancos, M. (2002a) Different temporal processing of sensory inputs in the rat thalamus during quiescent and information processing states in vivo. Journal of Physiology (London) 539: 567–578CrossRefGoogle Scholar
Castro-Alamancos, M. (2002b) Properties of primary sensory (lemniscal) synapses in the ventrobasal thalamus and the relay of high-frequency sensory inputs. Journal of Neurophysiology 87: 946–953CrossRefGoogle Scholar
Castro-Alamancos, M. and Calcagnotto, M. E. (2001) High-pass filtering of corticothalamic activity by neuromodulators released in the thalamus during arousal: in vitro and in vivo. Journal of Neurophysiology 85: 1489–1497CrossRefGoogle ScholarPubMed
Castro-Alamancos, M. A. and Connors, B. W. (1996a) Short-term plasticity of a thalamocortical pathway dynamically modulated by behavioral state. Science 272: 274–277CrossRefGoogle Scholar
Castro-Alamancos, M. A. and Connors, B. W. (1996b) Spatiotemporal properties of short-term plasticity in sensorimotor thalamocortical pathways of the rat. Journal of Neuroscience 16: 2767–2779CrossRefGoogle Scholar
Castro-Alamancos, M. A. and Connors, B. W. (1996c) Cellular mechanisms of the augmenting response: short-term plasticity in a thalamocortical pathway. Journal of Neuroscience 16: 7742–7756CrossRefGoogle Scholar
Caton, R. (1875) The electric currents of the brain. British Medical Journal 2: 278Google Scholar
Caton, R. (1887) Interim report on investigations of the electric currents of the brain. British Medical Journal (Suppl. 1): 62Google Scholar
Cauli, B., Audinat, E., Lambolez, B., Angulo, M. C., Ropert, N., Tauzuki, K., Hestrin, S. and Rossier, J. (1997) Molecular and physiological diversity of cortical nonpyramidal cells. Journal of Neuroscience 17: 3894–3906CrossRefGoogle ScholarPubMed
Cauller, L. J. and Connors, B. W. (1994) Synaptic physiology of horizontal afferents in layer I in slices of rat SI neocortex. Journal of Neuroscience 14: 751–762CrossRefGoogle ScholarPubMed
Cavazzuti, G. B., Ferrari, F., Galli, V. and Benatti, A. (1989) Epilepsy with typical absence seizures with onset during the first year of life. Epilepsia 30: 802–806CrossRefGoogle ScholarPubMed
Celio, M. R. (1986) Parvalbumin in most gamma-aminobutyric acid-containing neurons of rat cerebral cortex. Science 231: 995–997CrossRefGoogle ScholarPubMed
Cespuglio, R., Gomez, M. E., Walker, E. and Jouvet, M. (1979) Effets du refroidissement et de la stimulation des noyaux du système du raphé sur les états de vigilance chez le chat. Electroencephalography and Clinical Neurophysiology 47: 289–308CrossRefGoogle Scholar
Cespuglio, R., Faradji, H., Hahn, Z. and Jouvet, M. (1984) Voltammetric detection of brain 5-hydroxyindolamines by means of electrochemically treated carbon fibre electrodes: chronic recordings for up to one month with movable cerebral electrodes in the sleeping or waking rat. In Measurement of Neurotransmitter Release in Vivo (IBRO Handbook Series, vol. 6), ed. C. A. Marsden, pp. 173–191, New York: Wiley
Chagnac-Amitai, Y. and Connors, B. W. (1989) Synchronized excitation and inhibition driven by bursting neurons in neocortex. Journal of Neurophysiology 62: 1149–1162CrossRefGoogle ScholarPubMed
Chagnac-Amitai, Y., Luhmann, H. J. and Prince, D. A. (1990) Burst generating and regular spiking layer 5 pyramidal neurons of rat neocortex have different morphological features. Journal of Comparative Neurology 296: 598–613CrossRefGoogle ScholarPubMed
Chamberlin, N. L., Traub, R. D. and Dingledine, R. (1990) Role of EPSPs in initiation of spontaneous synchronized burst firing in rat hippocampal neurons bathed in high potassium. Journal of Neurophysiology 64: 1000–1008CrossRefGoogle ScholarPubMed
Chandler, S. H., Chase, M. H. and Nakamura, Y. (1980) Intracellular analysis of synaptic mechanisms controlling trigeminal motoneurons activity during sleep and wakefulness. Journal of Neurophysiology 44: 359–371CrossRefGoogle ScholarPubMed
Chang, H. T. (1950) The repetitive discharges of corticothalamic reverberating circuit. Journal of Neurophysiology 13: 235–257CrossRefGoogle Scholar
Charnay, Y., Bouras, C., Vallet, P. G., Golaz, J., Guntern, R. and Constantinidis, J. (1989) Immunohistochemical colocalization of delta-sleep-inducing peptide and luteinizing hormone-releasing hormone in rabbit brain neurons. Neuroscience 31: 495–505CrossRefGoogle ScholarPubMed
Charpier, S., Leresche, N., Deniau, J. M., Mahon, S., Hughes, S. W. and Crunelli, V. (1999) On the putative contribution of GABAB receptors to the electrical events occurring during spontaneous spike and wave discharges. Neuropharmacology 38: 1699–1706CrossRefGoogle Scholar
Chase, M. H. and Morales, F. R. (1983) Subthreshold excitatory activity and motoneuron discharge during REM periods of active sleep. Science 221: 1195–1198CrossRefGoogle ScholarPubMed
Chase, M. H., Chandler, S. H. and Nakamura, Y. (1980) Intracellular determination of membrane potential of trigeminal motoneurons during sleep and wakefulness. Journal of Neurophysiology 44: 349–358CrossRefGoogle ScholarPubMed
Chen, K., Baram, T. Z. and Soltesz, I. (1999) Febrile seizures in the developing brain result in persistent modifications of neuronal excitability in limbic circuits. Nature Medicine 5: 888–894CrossRefGoogle Scholar
Chen, W., Zhang, J. J., Hu, G. Y. and Wu, C. P. (1996) Electrophysiological and morphological properties of pyramidal and non-pyramidal neurons in the cat motor cortex in vitro. Neuroscience 73: 39–55CrossRefGoogle Scholar
Cherubini, E., Gaiarsa, J. L. and Ben-Ari, Y. (1991) GABA: an excitatory transmitter in early postnatal life. Trends in Neurosciences 14: 515–519CrossRefGoogle ScholarPubMed
Chervin, R. D., Pierce, P. A. and Connors, B. W. (1988) Periodicity and directionality in the propagation of epileptiform discharges across neocortex. Journal of Neurophysiology 60: 1695–1713CrossRefGoogle ScholarPubMed
Chou, T. C., Bjorkum, A. A., Gaus, S. E., Lu, J., Scammel, T. E. and Saper, C. B. (2002) Afferents to the ventrolateral preoptic nucleus. Journal of Neuroscience 22: 977–990CrossRefGoogle ScholarPubMed
Chow, A., Erisir, A., Farb, C., Nadal, M. S., Ozaita, A., Lau, D., Welker, E. and Rudy, B. (1999) K+ channel expression distinguishes subpopulations of parvalbumin- and somatostatin-containing neocortical interneurons. Journal of Neuroscience 19: 9332–9345CrossRefGoogle ScholarPubMed
Chrobak, J. J. and Buzsáki, G. (1996) High-frequency oscillations in the output networks of the hippocampal-entorhinal axis of the freely behaving rat. Journal of Neuroscience 16: 3056–3066CrossRefGoogle ScholarPubMed
Chronin, E. P. and Dudek, F. E. (1988) Chronic seizures and collateral sprouting of dentate mossy fibers after kainic acid treatment in rats. Brain Research 474: 181–184CrossRefGoogle Scholar
Chung, J. M., Huguenard, J. R. and Prince, D. A. (1993) Transient enhancement of low-threshold calcium current in thalamic relay neurons after corticectomy. Journal of Neurophysiology 70: 1–7CrossRefGoogle ScholarPubMed
Cirelli, C. and Tononi, G. (2000) Differential expression of plasticityr-elated genes in waking and sleep and their regulation by the noradrenergic system. Journal of Neuroscience 20: 9187–9194CrossRefGoogle ScholarPubMed
Cirelli, C., Pompeiano, M. and Tononi, G. (1996) Neuronal gene expression in the waking state: a role for locus coeruleus. Science 274: 1211–1215CrossRefGoogle ScholarPubMed
Cissé, Y., Timofeev, I., Grenier, F. and Steriade, M. (2001) Intracellular pairing with synaptic activation leads to neocortical plasticity. Society for Neuroscience Abstracts 27: 366Google Scholar
Cissé, Y., Grenier, F., Timofeev, I. and Steriade, M. (2003) Electrophysiological properties and input-output organization of callosal neurons in cat association cortex. Journal of Neurophysiology, in pressCrossRefGoogle ScholarPubMed
Claes, E. (1939) Contribution à l'étude physiologique de la fonction visuelle. I. Analyse oscillographique de l'activité spontanée et sensorielle de l'aire visuelle corticale chez le chat non anesthésié. Archives Internationales de Physiologie 48: 1181–1237Google Scholar
Claparède, E. (1905) Esquisse d'une théorie biologique du sommeil. Archives de Psychologie 4: 246–349Google Scholar
Clemens, B. and Majoros, E. (1987) Sleep studies in benign epilepsy of childhood with rolandic spikes. II. Analysis of discharge frequency and its relation to sleep dynamics. Epilepsia 28: 24–27CrossRefGoogle ScholarPubMed
Clements, J. R. and Grant, S. (1990) Glutamate-like immunoreactivity in neurons of the laterodorsal tegmental and pedunculopontine nuclei in the rat. Neuroscience Letters 120: 70–73CrossRefGoogle ScholarPubMed
Cobb, S. (1947) Photic driving as a cause of clinical seizures in epileptic patients. Archives of Neurology and Psychiatry (Chicago) 58: 70–71CrossRefGoogle ScholarPubMed
Cobb, S. R., Buhl, E. H., Halasy, K., Paulsen, O. and Somogyi, P. (1995) Synchronization of neuronal activity in hippocampus by individual GABAergic interneurons. Nature 378: 811–817CrossRefGoogle ScholarPubMed
Coenen, A. M. L. and Vendrik, A. J. H. (1972) Determination of the transfer ratio of cat's geniculate neurons through quasi-intracellular recordings and the relation with the level of alertness. Experimental Brain Research 14: 227–242CrossRefGoogle ScholarPubMed
Colder, B. W., Wilson, C. L., Frysinger, R. C., Chao, L. C., Harper, R. M. and Engel, J. Jr. (1996) Neuronal synchrony in relation to burst discharge in epileptic human temporal lobes. Journal of Neurophysiology 75: 2496–2508CrossRefGoogle ScholarPubMed
Collins, D. R., Lang, E. J. and Paré, D. (1999) Spontaneous activity of the perirhinal cortex in behaving cats. Neuroscience 89: 1025–1039CrossRefGoogle ScholarPubMed
Collins, D. R., Pelletier, J. G. and Paré, D. (2001) Slow and fast (gamma) neuronal oscillations in the perirhinal cortex and lateral amygdala. Journal of Neurophysiology 85: 1661–1672CrossRefGoogle ScholarPubMed
Collins, R. L. (1975) Audiogenic seizures. In Experimental Models of Epilepsy, ed. D. P. Purpura, J. K. Penry, D. B. Tower, D. M. Woodbury and R. D. Walter, pp. 347–372, New York: Raven Press
Colonnier, M. (1966) The structural design of the neocortex. In Brain and Conscious Experience, ed. J. C. Eccles, pp. 1–23, New York: Springer
Colonnier, M. (1968) Synaptic patterns on different cell types in the different laminae of the visual cortex. An electron microscope study. Brain Research 9: 268–287CrossRefGoogle ScholarPubMed
Coombs, S. J., Eccles, J. C. and Fatt, P. (1955) The electrical properties of the motoneurone membrane. Journal of Physiology (London) 130: 291–325CrossRefGoogle ScholarPubMed
Connors, B. W. (1984) Initiation of synchronized neuronal bursting in neocortex. Nature 310: 685–687CrossRefGoogle ScholarPubMed
Connors, B. W. and Amitai, Y. (1995) Functions of local circuits in neocortex: synchrony and laminae. In The Cortical Neuron, ed. M. J. Gutnick and I. Mody, pp. 123–140, New York: Oxford University Press
Connors, B. W. and Gutnick, M. J. (1990) Intrinsic firing patterns of diverse neocortical neurons. Trends in Neurosciences 13: 99–104CrossRefGoogle ScholarPubMed
Connors, B. W. and Prince, D. A. (1982) Effects of local anesthetic QX-314 on the membrane properties of hippocampal pyramidal neurons. Journal of Pharmacology and Experimental Therapy 220: 476–481Google ScholarPubMed
Connors, B. W., Gutnick, M. J. and Prince, D. A. (1982) Electrophysiological properties of neocortical neurons in vitro. Journal of Neurophysiology 48: 1302–1320CrossRefGoogle ScholarPubMed
Connors, B. W., Malenka, R. and Silva, L. R. (1988) Two inhibitory postsynaptic potentials, and GABAA and GABAB receptor-mediated responses in neocortex of rat and cat. Journal of Physiology (London) 406: 443–468CrossRefGoogle Scholar
Consolazione, A., Priestley, J. V. and Cuello, A. C. (1984) Serotonin-containing projections to the thalamus in the rat revealed by a horseradish peroxidase and peroxidase antiperoxidase double-staining technique. Brain Research 322: 233–243CrossRefGoogle ScholarPubMed
Contreras, D. and Llinás, R. (2001) Voltage-sensitive dye imaging of neocortical spatio-temporal dynamics to afferent activation frequency. Journal of Neuroscience 21: 9403–9413CrossRefGoogle Scholar
Contreras, D. and Steriade, M. (1995) Cellular basis of EEG slow rhythms: a study of dynamic corticothalamic relationships. Journal of Neuroscience 15: 604–622CrossRefGoogle ScholarPubMed
Contreras, D. and Steriade, M. (1996) Spindle oscillation: the role of corticothalamic feedback in a thalamically generated rhythm. Journal of Physiology (London) 490: 159–179CrossRefGoogle Scholar
Contreras, D., Curró Dossi, R. and Steriade, M. (1992) Bursting and tonic discharges in two classes of reticular thalamic neurons in vivo. Journal of Neurophysiology 68: 973–977CrossRefGoogle Scholar
Contreras, D., Curró Dossi, R. and Steriade, M. (1993) Electrophysiological properties of cat reticular neurones in vivo. Journal of Physiology (London) 470: 273–294CrossRefGoogle ScholarPubMed
Contreras, D., Destexhe, A., Sejnowski, T. J. and Steriade, M. (1996a) Control of spatiotemporal coherence of a thalamic oscillation by corticothalamic feedback. Science 274: 771–774CrossRefGoogle Scholar
Contreras, D., Timofeev, I. and Steriade, M. (1996b) Mechanisms of long-lasting hyperpolarizations underlying slow sleep oscillations in cat corticothalamic networks. Journal of Physiology (London) 494: 251–264CrossRefGoogle Scholar
Contreras, D., Destexhe, A., Sejnowski, T. J. and Steriade, M. (1997a) Spatiotemporal patterns of spindle oscillations in cortex and thalamus. Journal of Neuroscience 17: 1179–1196CrossRefGoogle Scholar
Contreras, D., Destexhe, A. and Steriade, M. (1997b) Spindle oscillations during cortical spreading depression in naturally sleeping cats. Neuroscience 77: 933–996Google Scholar
Contreras, D., Destexhe, A. and Steriade, M. (1997c) Intracellular and computational characterization of the intracortical inhibitory control of synchronized thalamic inputs in vivo. Journal of Neurophysiology 78: 335–350CrossRefGoogle Scholar
Contreras, D., Dürmüller, N. and Steriade, M. (1997d) Absence of a prevalent laminar distribution of IPSPs in association cortical neurons of cat. Journal of Neurophysiology 78: 2742–2753CrossRefGoogle Scholar
Corner, M. A., Pelt, J., Wolters, P. S., Baker, R. E. and Nuytinck, R. H. (2002) Physiological effects of sustained blockade of excitatory synaptic transmission on spontaneously active developing neuronal networks – an inquiry into the reciprocal linkage between intrinsic biorhythms and neuroplasticity in early ontogeny. Neuroscience and Behavioral Reviews 26: 127–185CrossRefGoogle ScholarPubMed
Cossart, R., Dinocourt, C., Hirsch, J., Merchan-Perez, A., Felipe, J., Ben-Ari, Y., Esclapez, M. and Bernard, C. (2001) Dendritic but not somatic GABAergic inhibition is decreased in experimental epilepsy. Nature Neuroscience 4: 52–62CrossRefGoogle Scholar
Coulter, D. A. (1999) Chronic epileptogenic cellular alterations in the limbic system after status epilepticus. Epilepsia 40 (Suppl. 1): S23–S33CrossRefGoogle ScholarPubMed
Coulter, D. A., Huguenard, J. R. and Prince, D. A. (1989) Characterization of ethosuximide reduction of low-threshold calcium current in thalamic neurons. Annals of Neurology 25: 582–593CrossRefGoogle ScholarPubMed
Cowan, R. L. and Wilson, C. J. (1994) Spontaneous firing patterns and axonal projections of single corticostriatal neurons in the rat medial agranular cortex. Journal of Neurophysiology 71: 17–32CrossRefGoogle ScholarPubMed
Cragg, B. G. (1975) The development of synapses in the visual system of the cat. Journal of Comparative Neurology 160: 147–166CrossRefGoogle ScholarPubMed
Creutzfeldt, O. D., Watanabe, S. and Lux, H. D. (1966) Relations between EEG phenomena and potentials of single cortical cells. I. Evoked responses after thalamic and epicortical stimulation. Electroencephalography and Clinical Neurophysiology 20: 1–18CrossRefGoogle Scholar
Crill, W. E. (1996) Persistent sodium current in mammalian central neurons. Annual Reviews of Physiology 58: 349–362CrossRefGoogle ScholarPubMed
Crochet, S. and Sakai, K. (1999) Effects of microdialysis application of monoamines on the EEG and behavioural states in the cat mesopontine tegmentum. European Journal of Neuroscience 11: 3738–3752CrossRefGoogle ScholarPubMed
Crowne, D. P. and Radcliffe, D. D. (1975) Some characteristics and functional relations of the electrical activity of the primate hippocampus and hypotheses of hippocampal function. In The Hippocampus, ed. R. L. Isaacson and J. H. Pribram, pp. 185–203, New York: Plenum
Crunelli, V. and Leresche, N. (1991) A role for GABAB receptors in excitation and inhibition of thalamocortical neurons. Trends in Neuroscience 14: 16–21CrossRefGoogle Scholar
Crunelli, V. and Leresche, N. (2002) Childhood absence epilepsy: genes, channels, neurons and networks. Nature Reviews Neuroscience 3: 371–382CrossRefGoogle ScholarPubMed
Crunelli, V., Kelly, J. S., Leresche, N. and Pirchio, M. (1987) The ventral and dorsal lateral geniculate nucleus of the rat: intracellular recordings in vitro. Journal of Physiology (London) 384: 587–601CrossRefGoogle ScholarPubMed
Crunelli, V., Haby, M., Jassik-Gerschenfeld, D., Leresche, N. and Pirchio, M. (1988) Cl- and K+-dependent inhibitory postsynaptic potentials evoked by interneurons of the rat lateral geniculate nucleus. Journal of Physiology (London) 399: 153–176CrossRefGoogle ScholarPubMed
Csicsvari, J., Hirase, H., Czurkó, A. and Buzsáki, G. (1998) Reliability and state dependence of pyramidal cell – interneuron synapses in the hippocampus: an ensemble approach in the behaving rat. Neuron 21: 179–189CrossRefGoogle ScholarPubMed
Csicsvari, J., Hirase, H., Czurkó, A., Mamiya, A. and Buzsáki, G. (1999) Fast network oscillations in the hippocampal CA1 region of the behaving rat. Journal of Neuroscience 19: RC20 (1–4), 1999CrossRefGoogle ScholarPubMed
Cunningham, E. T. and LeVay, S. (1986) Laminar and synaptic organization of the projection from the thalamic nucleus centralis to primary visual cortex in the cat. Journal of Comparative Neurology 254: 65–77CrossRefGoogle ScholarPubMed
Curró Dossi, R., Paré, D. and Steriade, M. (1991) Short-lasting nicotinic and long-lasting muscarinic depolarizing responses of thalamocortical neurons to stimulation of mesopontine cholinergic nuclei. Journal of Neurophysiology 65: 393–406CrossRefGoogle ScholarPubMed
Curró Dossi, R., Nuñez, A. and Steriade, M. (1992a) Electrophysiology of a slow (0.5–4 Hz) intrinsic oscillation of cat thalamocortical neurones in vivo. Journal of Physiology (London) 447: 215–234CrossRefGoogle Scholar
Curró Dossi, R., Paré, D. and Steriade, M. (1992b) Various types of inhibitory postsynaptic potentials in anterior thalamic cells are differentially altered by stimulation of laterodorsal tegmental cholinergic nucleus. Neuroscience 47: 279–289CrossRefGoogle Scholar
Curtis, D. R. and Eccles, J. C. (1960) Synaptic action during and after repetitive stimulation. Journal of Physiology (London) 150: 374–398CrossRefGoogle ScholarPubMed
Daikoku, S., Kawano, H., Noguchi, M., Nakanishi, J., Tokuzen, M., Chihara, K. and Nagatsu, I. (1986) GRF neurons in the rat hypothalamus. Brain Research 399: 250–261CrossRefGoogle ScholarPubMed
Dalla Bernardina, B. and Berghini, G. (1976) Rolandic spikes in children with or without epilepsy (20 subjects polygraphically studied during sleep). Epilepsia 17: 161–167CrossRefGoogle Scholar
Danober, L. and Pape, H. C. (1998) Strychnine-sensitive glycine responses in neurons of the lateral amygdala: an electrophysiological and immunocytochemical characterization. Neuroscience 85: 427–441CrossRefGoogle ScholarPubMed
Danober, L., Depaulis, A., Marescaux, C. and Vergnes, M. (1993) Effects of cholinergic drugs on genetic absence seizures in rats. European Journal of Pharmacology 234: 263–268CrossRefGoogle ScholarPubMed
Danober, L., Vergnes, M., Depaulis, A. and Marescaux, C. (1994) Nucleus basalis lesions suppress spike and wave discharges in rats with spontaneous absence epilepsy. Neuroscience 59: 531–539CrossRefGoogle ScholarPubMed
Danober, L., Depaulis, A., Vergnes, M. and Marescaux, C. (1995) Mesopontine cholinergic control over generalized non-convulsive seizures in a genetic model of absence epilepsy in the rat. Neuroscience 69: 1183–1193CrossRefGoogle Scholar
Danober, L., Deransart, C., Depaulis, A., Vergnes, M. and Marescaux, C. (1998) Pathophysiological mechanisms of genetic absence epilepsy in the rat. Progress in Neurobiology 55: 27–57CrossRefGoogle ScholarPubMed
Datta, S., Curró Dossi, R., Paré, D., Oakson, G. and Steriade, M. (1991) Substantia nigra reticulata neurons during sleep-waking states: relation with ponto-geniculo-occipital waves. Brain Research 566: 344–347CrossRefGoogle ScholarPubMed
Davenport, C. J., Brown, W. J. and Babb, T. L. (1990) Sprouting of GABAergic and mossy fibers axons in the dentate gyrus following intrahippocampal kainate in the rats. Experimental Neurology 109: 180–190CrossRefGoogle Scholar
Dawson, T. M., Bredt, D. S., Fotuhi, M., Hwang, P. M. and Snyder, S. H. (1991) Nitric oxide synthase and neuronal NADPH diaphorase are identical in brain and peripheral tissues. Proceedings of the National Academy of Sciences of the USA 88: 7797–7801CrossRefGoogle ScholarPubMed
Deans, M. R., Gibson, J. R., Sellitto, C., Connors, B. W. and Paul, D. L. (2001) Synchronous activity of inhibitory networks in neocortex requires electrical synapses containing connexin36. Neuron 31: 477–485CrossRefGoogle ScholarPubMed
Debarbieux, F., Brunton, J. and Charpak, S. (1998) Effect of bicuculline in thalamic activity: a direct blockade of IAHP in reticularis neurons. Journal of Neurophysiology 79: 2911–2918CrossRefGoogle ScholarPubMed
Curtis, M. and Avanzini, G. (2001) Interictal spikes in focal epileptogenesis. Progress in Neurobiology 63: 541–567CrossRefGoogle ScholarPubMed
DeFelipe, J. (1993) Neocortical neuronal diversity: chemical heterogeneity revealed by co-localization studies of classic transmitters, neuropeptides, calcium-binding proteins and cell surface molecules. Cerebral Cortex 3: 273–289CrossRefGoogle Scholar
DeFelipe, J. (1999) Chandelier cells and epilepsy. Brain 122: 1807–1822CrossRefGoogle ScholarPubMed
DeFelipe, J. and Farinas, I. (1992) The pyramidal neuron of the cerebral cortex: morphological and chemical characteristics of the synaptic inputs. Progress in Neurobiology 39: 563–607CrossRefGoogle ScholarPubMed
Dégenètais, E., Thierry, A. M., Glowinski, J. and Gioanni, Y. (2002) Electrophysiological properties of pyramidal neurons in the rat prefrontal cortex: an in vivo intracellular recording study. Cerebral Cortex 12: 1–16CrossRefGoogle Scholar
Gennaro, L., Ferrara, M. and Bertini, M. (2001) The boundary between wakefulness and sleep: quantitative electroencephalographic changes during the sleep onset period. Neuroscience 107: 1–11CrossRefGoogle ScholarPubMed
Deiber, M. P., Ibanez, V., Bastuji, H., Fischer, C. and Mauguière, F. (1988) Changes of middle latency auditory evoked potentials during natural sleep in humans. Neurology 39: 806–813CrossRefGoogle Scholar
Deisz, R. A., Billard, J. M. and Zieglgänsberger, W. (1997) Presynaptic and postsynaptic GABAB receptors of neocortical neurons of the rat in vitro: differences in pharmacology and ionic mechanisms. Synapse 25: 62–723.0.CO;2-D>CrossRefGoogle ScholarPubMed
DeLanerolle, N., Kim, J., Robbins, R. and Spencer, D. (1989) Hippocampal interneuron loss and plasticity in human temporal lobe epilepsy. Brain Research 495: 387–395CrossRefGoogle Scholar
Dell, P. and Padel, Y. (1965) Rapid falling asleep provoked by selective stimulation of vagal afferents in the cat. Electroencephalography and Clinical Neurophysiology 18: 725Google Scholar
Delphs, J. R. and Dichter, M. A. (1983) Effects of somatostatin on mammalian cortical neurons in culture: physiological actions and unusual dose response characteristics. Journal of Neuroscience 3: 1176–1188CrossRefGoogle Scholar
Dement, W. C. (2001) Remembering Nathaniel Kleitman. Archives Italiennes de Biologie 139: 11–17Google ScholarPubMed
Dement, W. C. and Kleitman, N. (1957) Cyclic variations in EEG during sleep and their relation to eye movements, body motility, and dreaming. Electroencephalography and Clinical Neurophysiology 9: 673–690CrossRefGoogle ScholarPubMed
Dement, W. C., Hendricksen, S., Jacobs, B. L. and Mitler, M. M. (1973) Biogenic amines, phasic events, and behavior. In Pharmacology and the Future of Man, ed. F. E. Bloom and G. H. Acheson, pp. 74–89, New York: Karger
Dempsey, E. W. and Morison, R. S. (1942) The production of rhythmically recurrent cortical potentials after localized thalamic stimulation. American Journal of Physiology 135: 293–300Google Scholar
Denti, A., McGaugh, J. L., Landfield, P. W. and Shinkman, P. G. (1970) Effects of posttrial electrical stimulation of the mesencephalic reticular formation on avoidance learning in rats. Physiology and Behavior 5: 659–662CrossRefGoogle ScholarPubMed
Deransart, C., Lé-Pham, B. T., Hirsch, E., Marescaux, C. and Depaulis, A. (2001) Inhibition of the substantia nigra suppresses absences and clonic seizures in audiogenic rats, but not tonic seizures: evidence for seizure specificity of the nigral control. Neuroscience 105: 203–211CrossRefGoogle Scholar
Dermietzel, R. and Spray, D. C. (1993) Gap junctions in the brain: where, what type, how many and why?Trends in Neurosciences 16: 186–192CrossRefGoogle Scholar
Descarries, L., Gisiger, V. and Steriade, M. (1997) Diffuse transmission by acetylcholine in the CNS. Progress in Neurobiology 53: 603–625CrossRefGoogle ScholarPubMed
Deschênes, M. and Hu, B. (1990) Electrophysiology and pharmacology of the corticothalamic input to lateral thalamic nuclei: an intracellular study in the cat. European Journal of Neuroscience 2: 140–152CrossRefGoogle Scholar
Deschênes, M., Paradis, M., Roy, J. P. and Steriade, M. (1984) Electrophysiology of neurons of lateral thalamic nuclei in cat: resting properties and burst discharges. Journal of Neurophysiology 51: 1196–1219CrossRefGoogle ScholarPubMed
Deschênes, M., Madariaga-Domich, A. and Steriade, M. (1985) Dendrodendritic synapses in cat reticularis thalami nucleus, a structural basis for thalamic spindle synchronization. Brain Research 334: 169–171Google ScholarPubMed
Desmedt, J. E. (1981) Scalp-recorded cerebral event-related potentials in man as point of entry into the analysis of cognitive processing. In The Organization of the Cerebral Cortex, ed. F. O. Schmitt, F. G. Worden, G. Adelman and S. G. Dennis, pp. 441–473, Cambridge, MA: The MIT Press
Desmedt, J. E. and Tomberg, C. (1994) Transient phase-locking of 40 Hz electrical oscillations in prefrontal and parietal human cortex reflects the process of conscious somatic perception. Neuroscience Letters 168: 126–129CrossRefGoogle ScholarPubMed
Destexhe, A. (1998) Spike-and-wave oscillations based on the properties of GABAB receptors. Journal of Neuroscience 18: 9099–9111CrossRefGoogle ScholarPubMed
Destexhe, A. and Paré, D. (1999) Impact of network activity on the integrative properties of neocortical pyramidal neurons in vivo. Journal of Neurophysiology 81: 1531–1547CrossRefGoogle ScholarPubMed
Destexhe, A. and Sejnowski, T. J. (2001) Thalamocortical Assembly. Oxford: Oxford University Press
Destexhe, A., Contreras, D., Sejnowski, T. J. and Steriade, M. (1994a) A model of spindle rhythmicity in the isolated thalamic reticular nucleus. Journal of Neurophysiology 72: 803–818CrossRefGoogle Scholar
Destexhe, A., Contreras, D., Sejnowski, T. J. and Steriade, M. (1994b) Modeling the control of reticular thalamic oscillations by neuromodulators. NeuroReport 5: 2217–2220CrossRefGoogle Scholar
Destexhe, A., Contreras, D.Steriade, M., Sejnowski, T. J. and Huguenard, J. R. (1996) In vivo, in vitro and computational analysis of dendritic calcium currents in thalamic reticular neurons. Journal of Neuroscience 16: 169–185CrossRefGoogle ScholarPubMed
Destexhe, A., Contreras, D., and Steriade, M. (1998) Mechanisms underlying the synchronizing action of corticothalamic feedback through inhibition of thalamic relay cells. Journal of Neurophysiology 79: 999–1016CrossRefGoogle ScholarPubMed
Destexhe, A., Contreras, D. and Steriade, M. (1999a) Neocortical excitability controls the coherence of thalamic-generated oscillations through corticothalamic feedback. Neuroscience 92: 427–443CrossRefGoogle Scholar
Destexhe, A., Contreras, D. and Steriade, M. (1999b) Spatiotemporal analysis of local field potentials and unit discharges in cat cerebral cortex during natural wake and sleep states. Journal of Neuroscience 19: 4595–4608CrossRefGoogle Scholar
Destexhe, A., McCormick, D. A. and Sejnowski, T. J. (1999c) Thalamic and thalamocortical mechanisms underlying 3 Hz spike-and-wave discharges. Progress in Brain Research 121: 289–307CrossRefGoogle Scholar
Destexhe, A., Contreras, D. and Steriade, M. (2001) LTS cells in cerebral cortex and their role in generating spike-and-wave oscillations. Neurocomputing 38–40: 555–563CrossRefGoogle Scholar
Détári, L. and Vanderwolf, C. H. (1987) Activity of identified cortically projecting neurones during large slow waves and cortical activation in anaesthetized rats. Brain Research 437: 1–8CrossRefGoogle ScholarPubMed
Détári, L., Juhasz, G. and Kukorelli, T. (1984) Firing properties of cat basal forebrain neurones during sleep-wakefulness cycle. Electroencephalography and Clinical Neurophysiology 58: 362–368CrossRefGoogle ScholarPubMed
Détári, L., Rasmusson, D. D. and Semba, K. (1997) Phasic relationship between the activity of basal forebrain neurons and cortical EEG in urethane-anesthetized rat. Brain Research 759: 112–121CrossRefGoogle ScholarPubMed
Devinsky, O., Ehremberg, B., Barthlen, G. M., Abramson, H. S. and Luciano, D. (1994) Epilepsy and sleep apnea syndrome. Neurology 44: 2060–2064CrossRefGoogle ScholarPubMed
Dichter, M. A. and Spencer, W. A. (1969a) Penicillin-induced interictal discharges from the cat hippocampus. I. Characteristics and topographical features. Journal of Neurophysiology 32: 649–662CrossRefGoogle Scholar
Dichter, M. A. and Spencer, W. A. (1969b) Penicllin-induced interictal discharges from the cat hippocampus. II. Mechanisms underlying origin and restriction. Journal of Neurophysiology 32: 663–687CrossRefGoogle Scholar
Dichter, M. A., Herman, C. J. and Selzer, M. (1972) Silent cells during interictal discharges and seizures in hippocampal penicillin foci. Evidence for the role of extracellular K+ in the transition from the interictal state to seizures. Brain Research 48: 173–183CrossRefGoogle Scholar
Dickson, C. T. and Alonso, A. (1997) Muscarinic induction of synchronous population activity in the entorhinal cortex. Journal of Neuroscience 17: 6729–6744CrossRefGoogle ScholarPubMed
Dickson, C. T., Kirk, I. J., Oddie, S. D. and Bland, B. H. (1995) Classification of theta-related cells in the entorhinal cortex: cell discharges are controlled by the ascending brainstem synchronizing pathway in parallel with hippocampal theta-related cells. Hippocampus 5: 306–319CrossRefGoogle ScholarPubMed
Dickson, C. T., Mena, A. R. and Alonso, A. (1997) Electroresponsiveness of medial entorhinal cortex layer III neurons in vitro. Neuroscience 81: 937–950CrossRefGoogle ScholarPubMed
Dijk, D. J. and Czeisler, C. A. (1995) Contribution of the circadian pacemaker and sleep homeostat to sleep propensity, sleep structure, electroencephalographic slow waves, and sleep spindle activity. Journal of Neuroscience 15: 3526–3538CrossRefGoogle ScholarPubMed
Dijk, D. J., Hayes, B. and Czeisler, C. A. (1993) Dynamics of electroencephalographic sleep spindles and slow wave activity in men: effect of sleep deprivation. Brain Research 626: 190–199CrossRefGoogle ScholarPubMed
Dinner, D. S. (1993) Posttraumatic epilepsy. In The Treatment of Epilepsy: Principles, ed. E. Wyllie, pp. 654–658, Philadelphia: Lea & Fibinger
Do, K. Q., Binns, K. E. and Salt, T. E. (1994) Release of the nitric oxide precursor, arginine, from the thalamus upon sensory afferent stimulation, and its effect on thalamic neurons in vivo. Neuroscience 60: 581–586CrossRefGoogle ScholarPubMed
Dolmetsch, R. E., Pajvani, U., Fife, K., Spotts, J. M. and Greenberg, M. E. (2001) Signaling to the nucleus by an L-type calcium channel-calmodulin complex through the MPA kinase pathway. Science 294: 333–339CrossRefGoogle Scholar
Domich, L., Oakson, G. and Steriade, M. (1986) Thalamic burst patterns in the naturally sleeping cat: a comparison between cortically projecting and reticularis neurones. Journal of Physiology (London) 379: 429–449CrossRefGoogle ScholarPubMed
Domich, L., Oakson, G. and Steriade, M. (1987) Thalamic and cortical spindles during early ontogenesis in kittens. Developmental Brain Research 31: 140–142CrossRefGoogle Scholar
Douglas, R. and Martin, K. (1991) A functional microcircuit for cat visual cortex. Journal of Physiology (London) 440: 735–769CrossRefGoogle ScholarPubMed
Draguhn, A., Traub, R. D., Schmitz, D. and Jefferys, J. G. (1998) Electrical coupling underlies high-frequency oscillations in the hippocampus in vitro. Nature 394: 189–192CrossRefGoogle ScholarPubMed
Drake, M. E., Weate, S. J., Newell, S. A., Padamadan, H. and Pakalnis, A. (1994) Multiple sleep latency tests in epilepsy. Clinical Electroencephalography 25: 59–62CrossRefGoogle ScholarPubMed
Dreifuss, F. E. (1997) Classification of epileptic seizures. In Epilepsy: A Comprehensive Textbook, ed. J. Engel Jr. and T. A. Pedley, pp. 517–524, Philadelphia: Lippincott-Raven
Dudek, F. E., Snow, R. S. and Taylor, C. P. (1986) Role of electrical interactions in synchronization of epileptiform bursts. Advances in Neurology 44: 593–617Google ScholarPubMed
Dulac, O. and N'Guyen, T. (1993) The Lennox-Gastaut syndrome. Epilepsia 34 (Suppl. 7): S7–S17CrossRefGoogle ScholarPubMed
Dunwiddie, T. V. (1985) The physiological role of adenosine in the central nervous system. International Review of Neurobiology 27: 63–139CrossRefGoogle ScholarPubMed
Dusser de Barenne, J. G. and McCulloch, W. S. (1938) The direct functional interrelation of sensory cortex and optic thalamus. Journal of Neurophysiology 1: 176–186CrossRefGoogle Scholar
Dzubay, J. A. and Jahr, C. E. (1999) The concentration of synaptically released glutamate outside of the climbing fiber – Purkinje cell synaptic cleft. Journal of Neuroscience 19: 5265–5274CrossRefGoogle ScholarPubMed
Eccles, J. C. (1961) Chairman's opening remarks. In The Nature of Sleep, ed. G. E. W. Wolstenholme and M. O'Connor, pp. 1–3, London: Churchill
Eccles, J. C., Libet, B. and Young, R. R. (1958) The behavior of chromatolysed motoneurones studied by intracellular recording. Journal of Physiology (London) 143: 11–40CrossRefGoogle ScholarPubMed
Eccles, J. C., Ito, M. and Szentágothai, J. (1967) The Cerebellum as a Neuronal Machine. New York: Springer
Echlin, F. A., Arnett, V. and Zoll, J. (1952) Paroxysmal high voltage discharges from isolated and partially isolated cerebral cortex as a mechanism in focal cortical epilepsy. Electroencephalography and Clinical Neurophysiology 4: 147–164CrossRefGoogle Scholar
Eckhorn, R., Bauer, R., Jordan, W., Brosch, M., Kruse, W., Munk, M. and Reitboeck, H. J. (1988) Coherent oscillations: a mechanism of feature linking in the visual cortex?Biological Cybernetics 60: 121–130CrossRefGoogle ScholarPubMed
Economo, C. von (1918) Die Encephalitis Lethargica. Vienna: Deuticke
Economo, C. (1929) Schlaftheorie. Ergebnisse der Physiologie 28: 312–339CrossRefGoogle Scholar
Egan, T. M. and North, R. A. (1985) Acetylcholine acts on m2-muscarinic receptors to excite rat locus coeruleus neurones. British Journal of Pharmacology 85: 733–735CrossRefGoogle ScholarPubMed
Eisenman, J. S. (1982) Electrophysiology of the anterior hypothalamus: thermoregulation and fever. In Pyretics and Antipyretics, ed. G. Milton, pp. 187–217, Berlin: Springer
Elton, M., Winter, O., Heslenfeld, D., Loewy, D., Campbell, K. and Kok, A. (1997) Event-related potentials to tones in the absence and presence of sleep spindles. Journal of Sleep Research 6: 78–83CrossRefGoogle ScholarPubMed
Engel, A., König, P., Kreiter, A. and Singer, W. (1991) Interhemispheric synchronization of oscillatory neuronal responses in cat visual cortex. Science 252: 1177–1179CrossRefGoogle ScholarPubMed
Engel, J. (1995) Inhibitory mechanisms of epileptic seizure generation. Advances in Neurology 67: 157–171Google ScholarPubMed
Engel, J. Jr., Henry, T. R., Risinger, M. W., Mazziotta, J. C., Sutherling, W. W., Levesque, M. F. and Phelps, M. E. (1990) Presurgical evaluation for partial epilepsy: relative contributions of chronic depth electrode recordings versus FDG-PET and scalp-sphenoidal ictal EEG. Electroencephalography and Clinical Neurophysiology 40: 1670–1677Google ScholarPubMed
Esclapez, M., Hirsch, J., Khazipov, R., Ben-Ari, Y. and Bernard, C. (1997) Operative GABAergic inhibition in hippocampal CA1 pyramidal neurons in experimental epilepsy. Proceedings of the National Academy of Sciences of the USA 94: 12151–12156CrossRefGoogle ScholarPubMed
Evarts, E. V. (1964) Temporal patterns of discharge of pyramidal tract neurons during sleep and waking. Journal of Neurophysiology 27: 152–171CrossRefGoogle ScholarPubMed
Everson, C. A., Smith, C. B. and Sokoloff, L. (1994) Effects of prolonged sleep deprivation on local rates of cerebral energy metabolism in freely moving rats. Journal of Neuroscience 14: 6769–6778CrossRefGoogle ScholarPubMed
Façon, E., Steriade, M. and Wertheimer, N. (1958) Hypersomnie prolongée engendrée par des lésions bilatérales du système activateur médial: le syndrome thrombotique de la bifurcation du tronc basilaire. Revue Neurologique (Paris) 98: 117–133Google Scholar
Faingold, C. L. and Meldrum, B. S. (1990) Excitant amino acids in epilepsy. In Generalized Epilepsy, ed. M. Avoli, P. Gloor, G. Kostopoulos and R. Naquet, pp. 102–117, Boston: Birkhäuser
Farid, H. and Adelson, E. H. (2001) Synchrony does not promote grouping in temporally structured displays. Nature Neuroscience 4: 875–876CrossRefGoogle Scholar
Farmer, S. F. (1998) Rhythmicity, synchronization and binding in human and primate motor cortex. Journal of Physiology (London) 509: 3–14CrossRefGoogle Scholar
Federico, P. and MacVicar, B. A. (1996) Imaging the induction and spread of seizure activity in the isolated brain of guinea pig: the roles of GABA and glutamate receptors. Journal of Neurophysiology 76: 3471–3492CrossRefGoogle ScholarPubMed
Feinberg, I. and Campbell, I. G. (1993) Ketamine administration during waking increases delta EEG intensity in rat sleep. Neuropharmacology 9: 41–48Google ScholarPubMed
Feindel, W. and Penfield, W. (1954) Localization of discharge in temporal lobe automatism. Archives of Neurology and Psychiatry (Chicago) 72: 605–630CrossRefGoogle ScholarPubMed
Feindel, W. and Rasmussen, T. (1991) Temporal lobectomy with amygdalectomy and minimal hippocampal resection: review of 100 cases. Canadian Journal of Neurological Sciences 18: 603–605CrossRefGoogle ScholarPubMed
Feldberg, L. A. and Sherwood, P. D. (1954) Injections of drugs into the lateral ventricle of the cat. Journal of Physiology (London) 123: 148–167CrossRefGoogle ScholarPubMed
Fencl, V., Koski, G. and Pappenheimer, J. R. (1971) Factors in cerebrospinal fluid from goats that affect sleep and activity in rats. Journal of Physiology (London) 216: 565–589CrossRefGoogle ScholarPubMed
Ferencz, I., Kokaia, M., Keep, M., Elmér, E., Metsis, M., Kokaia, Z. and Lindvall, O. (1997) Effects of cholinergic denervation on seizure development and neurotrophin messenger RNA regulation in rapid hippocampal kindling. Neuroscience 80: 389–399CrossRefGoogle ScholarPubMed
Ferencz, I., Leanza, G., Nanobashvili, A., Kokaia, M. and Lindvall, O. (2000) Basal forebrain neurons suppress amygdala kindling via cortical but not hippocampal cholinergic projections in rats. European Journal of Neuroscience 12: 2107–2116CrossRefGoogle Scholar
Ferrara, M., Gennaro, L., Curcio, G., Cristiani, R., Corvasce, C. and Bertino, M. (2002) Regional differences of the human sleep electroencephalogram in response to selective slow-wave sleep deprivation. Cerebral Cortex 12: 737–748CrossRefGoogle ScholarPubMed
Ferrier, D. (1876) The Functions of the Brain. London: Smith, Elder & Co
Ferster, D. and Lindström, S. (1985) Augmenting responses evoked in area 17 of the cat by intracortical axonal collaterals of cortico-geniculate cells. Journal of Physiology (London) 367: 217–232CrossRefGoogle Scholar
Fetz, E. E., Chen, D., Murphy, V. N. and Matsumara, M. (2000) Synaptic interactions mediating synchrony and oscillations in primate sensorimotor cortex. Journal de Physiologie (Paris) 94: 323–331CrossRefGoogle ScholarPubMed
Feucht, M., Möller, U., Witte, H., Schmidt, K., Arnold, M., Benninger, F., Steinberger, K. and Friedrich, M. H. (1998) Nonlinear dynamics of 3 Hz spike-and-wave discharges recorded during typical absence seizures in children. Cerebral Cortex 8: 524–533CrossRefGoogle ScholarPubMed
Finnerty, G. T. and Jefferys, J. G. R. (2000) 9–16 Hz oscillation precedes secondary generalization of seizures in the rat tetanus toxin model of epilepsy. Journal of Neurophysiology 83: 2217–2226CrossRefGoogle ScholarPubMed
Fischer-Perroudon, C., Mouret, J. and Jouvet, M. (1974) Sur un cas d'agrypnie (4 mois sans sommeil) au cours d'une maladie de Morvan: effet favorable du 5–hydroxytryptophane. Electroencephalography and Clinical Neurophysiology 36: 1–18CrossRefGoogle Scholar
Fiset, P., Paus, T., Daloze, T., Plourde, G., Meuret, P., Bonhomme, V., Hajj-Ali, N., Backman, S. B. and Evans, A. C. (1999) Brain mechanisms of propofol-induced loss of consciousness in humans: a positron emission tomography study. Journal of Neuroscience 19: 5506–5513CrossRefGoogle Scholar
Fish, D. R., Gloor, P., Quesney, L. F. and Olivier, A. O. (1993) Clinical responses to electrical brain stimulation of the temporal and frontal lobes in patients with epilepsy. Brain 116: 397–414CrossRefGoogle ScholarPubMed
Fisher, R. S. and Prince, D. A. (1977) Spike-wave rhythms in cat cortex induced by parenteral penicillin. I. Electroencephalographic patterns. Electroencephalography and Clinical Neurophysiology 42: 608–624CrossRefGoogle Scholar
Fisher, R. S., Buchwald, N. A., Hull, C. D. and Levine, M. S. (1988) GABAergic basal forebrain neurons project to the neocortex: the localization of glutamic acid decarboxylase and choline acetyltransferase in feline corticopetal neurons. Journal of Comparative Neurology 272: 489–502CrossRefGoogle ScholarPubMed
Fisher, R. S., Webber, W. R., Lesser, R. P., Arroyo, S. and Uematsu, S. (1992) High-frequency EEG activity at the start of seizures. Journal of Clinical Neurophysiology 9: 441–448Google ScholarPubMed
Fleidervish, I. A. and Gutnick, M. J. (1996) Kinetics of slow inactivation of persistent sodium current in layer V neurons of mouse neocortical slices. Journal of Neurophysiology 76: 2125–2130CrossRefGoogle Scholar
Foehring, R. C., Schwindt, P. C. and Crill, W. E. (1989) Norepinephrine selectively reduces slow Ca2+- and Na+-mediated currents in cat neocortical neurons. Journal of Neurophysiology 61: 245–256CrossRefGoogle ScholarPubMed
Foldvary, N. (2001) Sleep disorders in epilepsy. In Epilepsy and Sleep, ed. D. S. Dinner and H. O. Lüders, pp. 191–201, San Diego: Academic Press
Ford, B., Holmes, C. J., Mainville, L. and Jones, B. E. (1995) GABAergic neurons in the rat pontomesencephalic tegmentum: codistribution with cholinergic and other tegmental neurons projecting to the posterior lateral hypothalamus. Journal of Comparative Neurology 363: 177–196CrossRefGoogle ScholarPubMed
Foulkes, D. (1967) Nonrapid eye movement mentation. Experimental Neurology 19: 28–38CrossRefGoogle Scholar
Franck, J. E. and Schwartzkroin, P. A. (1985) Do kainite-lesioned hippocampi become epileptogenic?Brain Research 329: 309–313CrossRefGoogle ScholarPubMed
Frank, G. (1969) A study of the inter-relations of spike discharge density and sleep stages in epileptic patients. Electroencephalography and Clinical Neurophysiology 26: 238Google ScholarPubMed
Frank, M. G., Issa, N. P. and Stryker, M. P. (2001) Sleep enhances plasticity in the developing visual cortex. Neuron 30: 275–287CrossRefGoogle ScholarPubMed
Frantseva, M. V., Kokarovtseva, L., Naus, C. G., Carlen, P. L., MacFabe, D. and Perez Velazquez, J. L. (2002) Specific gap junctions enhance the neuronal vulnerability to brain traumatic injury. Journal of Neuroscience 22: 644–653CrossRefGoogle ScholarPubMed
Freeman, W. J. (1975) Mass Action in the Nervous System. New York: Academic Press
Freeman, W. J. and Dijk, B. W. (1988) Spatial patterns of visual cortical fast EEG during conditioned reflex in a rhesus monkey. Brain Research 422: 267–276CrossRefGoogle Scholar
French, C. R., Sah, P., Buckett, K. J. and Gage, P. W. (1990) A voltage-dependent persistent sodium current in mammalian hippocampal neurons. Journal of General Physiology 95: 1139–1157CrossRefGoogle ScholarPubMed
Freund, T. F. (1993) Anterograde PHAL-tracing combined with pre- and postembedding immunocytochemistry. In Immunohistochemistry, ed. A. C. Cuello, pp. 329–348, New York: Wiley
Freund, T. F. and Buzsáki, G. (1988) Alterations in excitatory and GABA-ergic inhibitory connections in hippocampal transplants. Neuroscience 27: 373–385CrossRefGoogle Scholar
Freund, T. F. and Buzsáki, G. (1996) Interneurons of the hippocampus. Hippocampus 6: 347–4703.0.CO;2-I>CrossRefGoogle ScholarPubMed
Fries, P., Neuenschwander, S., Engel, A. K., Goebel, R. and Singer, W. (2001a) Rapid feature selective neuronal synchronization through correlated latency shifting. Nature Neuroscience 4: 194–200CrossRefGoogle Scholar
Fries, P., Reynolds, J. H., Rorie, A. E. and Desimone, R. (2001b) Modulation of oscillatory neuronal synchronization by selective visual attention. Science 291: 1560–1563CrossRefGoogle Scholar
Fritsch, G. and Hitzig, E. (1870) Uber die elektrische Erregbarkeit des Grosshirns. Archive für Anatomie, Physiologie und wissenschaftliche Medizin 37: 300–332Google Scholar
Fromm, G. H. (1986) Role of inhibitory mechanisms in staring spells. Journal of Clinical Neurophysiology 3: 297–311CrossRefGoogle ScholarPubMed
Futamachi, K. J., Mutani, R. and Prince, D. A. (1974) Potassium activity in rabbit cortex. Brain Research 75: 5–25CrossRefGoogle ScholarPubMed
Gabor, A. J. and Ajmone-Marsan, C. (1968) Coexistence of focal bilateral diffuse paroxysmal discharges in epileptics. Epilepsia 10: 453–472CrossRefGoogle Scholar
Gais, S., Plihal, W., Wagner, U. and Born, J. (2000) Early sleep triggers memory for early visual discrimination skills. Nature Neuroscience 3: 1335–1339CrossRefGoogle ScholarPubMed
Gais, S., Mölle, M., Helms, K. and Born, J. (2002) Learning-dependent increases in sleep density. Journal of Neuroscience 22: 6830–6834CrossRefGoogle Scholar
Galarreta, M. and Hestrin, S. (1998) Frequency-dependent synaptic depression and the balance of excitation and inhibition in the neocortex. Nature Neuroscience 1: 587–594CrossRefGoogle ScholarPubMed
Galarreta, M. and Hestrin, S. (1999) A network of fast-spiking cells in the neocortex connected by electrical synapses. Nature 402: 72–75CrossRefGoogle ScholarPubMed
Gallopin, T., Fort, P., Eggerman, E., Cauli, B., Luppi, P. H., Rossier, J., Audinat, E., Mühlethaler, , and Serafin, M. (2000) Identification of sleep-promoting neurons in vitro. Nature 404: 992–995CrossRefGoogle ScholarPubMed
Garcia-Cairasco, N., Terra, V. C. and Doretto, M. C. (1993) Midbrain substrates of audiogenic seizures in rats. Behavioral and Brain Research 58: 57–67CrossRefGoogle ScholarPubMed
Garcia-Rill, E., Skinner, R. D., Miyazato, H. and Homma, Y. (2001) Pedunculopontine stimulation induces prolonged activation of pontine reticular neurons. Neuroscience 104: 455–465CrossRefGoogle ScholarPubMed
Gastaut, H. (1950) Combined photic and metrazol activation of the brain. Electroencephalography and Clinical Neurophysiology 2: 263–275CrossRefGoogle Scholar
Gastaut, H. (1968) Clinical and electroencephalographic correlates of generalized spike and wave bursts occurring spontaneously in man. Epilepsia 9: 179–184CrossRefGoogle ScholarPubMed
Gastaut, H. and Broughton, R. (1972) Epileptic Seizures. Clinical and Electrographic Features, Diagnosis and Treatment. Springfield, ILL: Charles C. Thomas
Gastaut, H., Roger, J. and Gastaut, Y. (1948) Les formes expérimentales de l'épilepsie humaine. I. L'épilepsie induite par la stimulation lumineuse intermittente rythmée, ou épilepsie photogénique. Revue Neurologique (Paris) 80: 161–183Google Scholar
Gastaut, H., Roger, J., Soulayrol, R., Tassinari, C. T., Régis, H., Dravet, C., Bernard, R., Pinsard, N. and Saint-Jean, M. (1966) Childhood epileptic encephalopathy with diffuse slow spike-waves (otherwise known as “petit mal variant”) or Lennox syndrome. Epilepsia 7: 139–179CrossRefGoogle Scholar
Gaudin-Chazal, G., Portalier, P., Barrit, M. C. and Puizillout, J. J. (1982) Serotonin-like immunoreactivity in paraffin-sections of the nodose ganglia of the cat. Neuroscience Letters 33: 169–172CrossRefGoogle ScholarPubMed
Gean, P. W., Shinnick-Gallagher, P. and Anderson, C. (1989) Spontaneous epileptiform activity and alterations of GABA- and NMDA-mediated neurotransmission in amygdala neurons kindled in vivo. Brain Research 494: 177–181CrossRefGoogle Scholar
Gevins, A., Smith, E. M., McEvoy, L. and Yu, D. (1997) High-resolution EEG mapping of cortical activation related to working memory: effects of task difficulty, type of processing, and practice. Cerebral Cortex 7: 374–385CrossRefGoogle ScholarPubMed
Giaretta, D., Avoli, M. and Gloor, P. (1987) Intracellular recordings in precruciate neurons during spike and wave discharges of feline generalized penicillin epilepsy. Brain Research 405: 68–79CrossRefGoogle Scholar
Gibbs, E. L. and Gibbs, F. A. (1947) Diagnostic and localizing value of electroencephalographic studies in sleep. Research Publications of the Association for the Research of Nervous and Mental Diseases 26: 366–376Google Scholar
Gibbs, F. A. and Gibbs, E. L. (1952) Atlas of Electroencephalography, 2nd edn. Cambridge, MA: Addison-Wesley
Gibbs, F. A., Gibbs, E. L. and Lennox, W. G. (1937) Epilepsy: a paroxysmal cerebral dysrhythmia. Brain 60: 377–388CrossRefGoogle Scholar
Gibbs, F. A., Gibbs, E. L. and Lennox, W. G. (1938) Cerebral dysrhythmias of epilepsy: measures for their control. Archives of Neurology and Psychiatry (Chicago) 39: 298CrossRefGoogle Scholar
Gibbs, F. A., Gibbs, E. L. and Lennox, W. G. (1939) The influence of the blood sugar level on the wave and spike formation in petit mal epilepsy. Archives of Neurology and Psychiatry (Chicago) 47: 1111–1116CrossRefGoogle Scholar
Gibbs, J. W., Berkow-Schroeder, G. and Coulter, D. A. (1996) GABAA receptor function in developing rat thalamic reticular neurons: whole cell recordings of GABA-mediated currents and modulation by clonazepam. Journal of Neurophysiology 76: 2568–2579CrossRefGoogle ScholarPubMed
Gibbs, J. W., Shumate, M. D. and Coulter, D. A. (1997) Differential epilepsy-associated alterations in postsynaptic GABAA receptor function in dentate granule cells and CA1 neurons. Journal of Neurophysiology 77: 1924–1938CrossRefGoogle Scholar
Gibson, J. R., Beierlein, M. and Connors, B. W. (1999) Two networks of electrically coupled inhibitory neurons in neocortex. Nature 402: 75–79CrossRefGoogle ScholarPubMed
Gilbert, C. D. (1992) Horizontal integration and cortical dynamics. Neuron 9: 1–13CrossRefGoogle ScholarPubMed
Gilbert, C. D. and Wiesel, T. N. (1983) Clustered intrinsic connections in cat visual cortex. Journal of Neuroscience 3: 1116–1133CrossRefGoogle ScholarPubMed
Gilliland, M. A., Bergmann, B. M. and Rechtschaffen, A. (1989) Sleep deprivation in the rat. VIII. High EEG amplitude sleep deprivation. Sleep 12: 53–59CrossRefGoogle ScholarPubMed
Girgis, M. (1980) Participation of muscarinic cholinergic receptors may be an important requirement of the kindling process. Experimental Neurology 70: 458–461CrossRefGoogle ScholarPubMed
Glenn, L. L. and Dement, W. C. (1981) Membrane potential, synaptic activity and excitability of hindlimb motoneurons during wakefulness and sleep. Journal of Neurophysiology 46: 839–854CrossRefGoogle ScholarPubMed
Glenn, L. L. and Steriade, M. (1982) Discharge rate and excitability of cortically projecting intralaminar thalamic neurons during waking and sleep states. Journal of Neuroscience 2: 1287–1404CrossRefGoogle ScholarPubMed
Glenn, L. L., Hada, J., Roy, J. P., Deschênes, M. and Steriade, M. (1982) Anterograde tracer and field potential analysis of the neocortical layer I projection from the nucleus ventralis medialis of the thalamus in cat. Neuroscience 7: 1861–1877CrossRefGoogle ScholarPubMed
Gloor, P. (1969) Hans Berger on the Electroencephalogram of Man. Amsterdam: Elsevier (Suppl. no. 28 of Electroencephalography and Clinical Neurophysiology)
Gloor, P. (1976) Generalized and widespread bilateral paroxysmal abnormalities. In Handbook of Electroencephalography and Clinical Neurophysiology, vol. 11/B, ed. A. Rémond, pp. 11B52–11B87, Amsterdam: Elsevier
Gloor, P. (1987) Volume conductor principles: their application to the surface and depth electroencephalogram. In Presurgical Evaluation of Epileptics, ed. H. G. Wieser and C. E. Elger, pp. 59–68, Berlin: Springer
Gloor, P. (1991) Mesial temporal sclerosis: historical background and an overview from a modern perspective. In Epilepsy Surgery, ed. H. Lüders, pp. 689–703, New York: Raven Press
Gloor, P. (1992) Role of the amygdala in temporal lobe epilepsy. In The Amygdala: Neurobiological Aspects of Emotion, Memory, and Mental Dysfunction, ed. J. P. Aggleton, pp. 505–538, New York: Wiley-Liss
Gloor, P. (1997) The Temporal Lobe and Limbic System. New York: Oxford University Press
Gloor, P. and Fariello, R. G. (1988) Generalized epilepsy: some of its cellular mechanisms differ from those of focal epilepsy. Trends in Neuroscience 11: 63–68CrossRefGoogle ScholarPubMed
Gloor, P., Ball, G. and Schaul, N. (1977) Brain lesions that produce delta waves. Neurology 27: 326–333CrossRefGoogle ScholarPubMed
Gloor, P., Olivier, A., Quesney, L. F., Anderman, F. and Horowitz, S. (1982) The role of the limbic system in experiential phenomena of temporal lobe epilepsy. Annals of Neurology 12: 129–144CrossRefGoogle ScholarPubMed
Gloor, P., Avoli, M. and Kostopoulos, G. (1990) Thalamocortical relationships in generalized epilepsy with bilaterally synchronous spike-and-wave discharges. In Generalized Epilepsies, ed. M. Avoli, P. Gloor, G. Kostopoulos and R. Naquet, pp. 190–212, Boston: Birkhäuser
Goff, W. R., Allison, T., Shapiro, A. and Rosner, B. S. (1966) Cerebral somatosensory responses evoked during sleep in man. Electroencephalography and Clinical Neurophysiology 21: 1–9CrossRefGoogle ScholarPubMed
Gökyigit, A. and Caliskan, A. (1995) Diffuse spike-wave seizures of 9–year duration without behavioral change or intellectual decline. Epilepsia 36: 210–213CrossRefGoogle ScholarPubMed
Goldensohn, E. S. and Purpura, D. P. (1963) Intracellular potentials of cortical neurons during focal epileptogenic discharges. Science 139: 840–842CrossRefGoogle ScholarPubMed
Goldman-Rakic, P. S. (1987) Circuitry of the prefrontal cortex and the regulation of behavior by representational memory. In Handbook of Physiology (vol. V, The Nervous System), ed. F. Plum and V. B. Mountcastle, pp. 373–417, Bethesda: American Physiological Society
Goldman-Rakic, P. S. (1988) Changing concepts of cortical connectivity: parallel distributed cortical networks. In Neurobiology of Neocortex, ed. P. Kakic and W. Singer, pp. 177–202, New York: Wiley
Goldring, N. L., Jung, H. Y., Mickus, T. and Spruston, N. (1999) Dendritic calcium spikes initiation and repolarization are controlled by distinct potassium channel subtypes in CA1 pyramidal neurons. Journal of Neuroscience 19: 8789–8798CrossRefGoogle Scholar
Goldring, S., Edwards, I., Harding, G. W. and Bernardo, K. L. (1992) Results of anterior temporal lobectomy that spares the amygdala in patients with complex partial seizures. Journal of Neurosurgery 77: 185–193CrossRefGoogle ScholarPubMed
Golomb, D., Wang, X. J. and Rinzel, J. (1994) Synchronization properties of spindle oscillations in a thalamic reticular nucleus model. Journal of Neurophysiology 72: 1109–1126CrossRefGoogle Scholar
Golshani, P. and Jones, E. G. (1999) Synchronized paroxysmal activity in the developing thalamocortical network mediated by corticothalamic projections and “silent” synapses. Journal of Neuroscience 19: 2865–2875CrossRefGoogle ScholarPubMed
Golshani, P., Liu, X. B. and Jones, E. G. (2001) Differences in quantal amplitude reflect GluR4–subunit number at corticothalamic synapses on two populations of thalamic neurons. Proceedings of the National Academy of Sciences of the USA 98: 4172–4177CrossRefGoogle ScholarPubMed
Gomez, M. R. and Westmoreland, B. F. (1987) Absence seizures. In Clinical Medicine and the Nervous System: Epilepsy – Electroclinical Syndromes, ed. H. Lüders and R. P. Lesser, pp. 105–129, New York: Springer
Gonchar, Y. and Burkhalter, A. (1997) Three distinct families of GABAergic neurons in rat visual cortex. Cerebral Cortex 7: 347–358CrossRefGoogle ScholarPubMed
Gotman, J. and Marciani, M. G. (1985) Electroencephalographic spiking activity, drug levels and seizure occurrence in epileptic patients. Annals of Neurology 17: 597–603CrossRefGoogle ScholarPubMed
Gottselig, J. M., Bassetti, C. L. and Achermann, P. (2002) Power and coherence of sleep spindle frequency activity following hemispheric strokes. Brain 125: 373–383CrossRefGoogle Scholar
Gowers, W. R. (1885) Epilepsy and Other Chronic Convulsive Disorders. New York: William Wood
Grace, A. A. and Bunney, B. S. (1979) Paradoxical GABA excitation of nigral dopaminergic cells: indirect mediation through reticulata inhibitory neurons. European Journal of Pharmacology 59: 211–218CrossRefGoogle ScholarPubMed
Grace, A. A. and Bunney, B. S. (1985) Opposing effects of striatonigral feed-back pathways on midbrain dopamine cell activity. Brain Research 333: 271–284CrossRefGoogle Scholar
Gray, C. M. and McCormick, D. A. (1996) Chattering cells: superficial pyramidal neurons contributing to the generation of synchronous oscillations in the visual cortex. Science 274: 109–113CrossRefGoogle ScholarPubMed
Gray, C. M., König, P., Engel, A. K. and Singer, W. (1989) Stimulus-specific neuronal oscillations in cat visual cortex exhibit inter-columnar synchronization which reflects global stimulus properties. Nature 338: 334–337CrossRefGoogle Scholar
Gray, C. M., Engel, A. K., König, P. and Singer, W. (1990) Stimulus-dependent neuronal oscillations in cat visual cortex: receptive field properties and feature dependence. European Journal of Neuroscience 2: 607–619CrossRefGoogle ScholarPubMed
Gray, E. G. (1959) Axo-somatic and axo-dendritic synapses of the cerebral cortex: an electron microscope study. Journal of Anatomy 93: 420–433Google Scholar
Graybiel, A. M. and Elde, R. P. (1983) Somatostatin-like immunoreactivity characterizes neurons of the nucleus reticularis thalami in the cat and monkey. Journal of Neuroscience 3: 1303–1321CrossRefGoogle ScholarPubMed
Graybiel, A. M. and Ragsdale, C. W. (1979) Fiber connections of the basal ganglia. In Development and Chemical Specificity of Neurons, ed. M. Cuénod, G. W. Kreutzberg and F. E. Bloom, pp. 239–283, Amsterdam: Elsevier
Green, J. D. (1969) The hippocampus. Physiological Reviews 44: 561–608CrossRefGoogle Scholar
Greene, R. W., Haas, H. L. and McCarley, R. W. (1986) A low-threshold calcium spike mediates firing pattern alterations in pontine reticular neurons. Science 234: 738–740CrossRefGoogle ScholarPubMed
Grenier, F., Timofeev, I. and Steriade, M. (1998) Leading role of thalamic over cortical neurons during postinhibitory rebound excitation. Proceedings of National Academy of Sciences of the USA 95: 13929–13934CrossRefGoogle ScholarPubMed
Grenier, F., Timofeev, I. and Steriade, M. (2001) Focal synchronization of ripples (80–200 Hz) in neocortex and their neuronal correlates. Journal of Neurophysiology 86: 1884–1898CrossRefGoogle ScholarPubMed
Grenier, F., Timofeev, I. and Steriade, M. (2002) Thalamic short-term plasticity and its impact on the neocortex. Thalamus and Related Systems 1: 331–340Google Scholar
Grenier, F., Timofeev, I. and Steriade, M. (2003) Neocortical ripples (80–200 Hz) and their role in initiation of electrical seizures. Journal of Neurophysiology, in pressGoogle Scholar
Grill, W. M. and McIntyre, C. C. (2001) Extracellular excitation of central neurons: implications for the mechanisms of deep brain stimulation. Thalamus and Related Systems 1: 269–277Google Scholar
Gritti, I., Mainville, L. and Jones, B. E. (1994) Projections of GABAergic and cholinergic basal forebrain and GABAergic preoptic-anterior hypothalamic neurons to the posterior lateral hypothalamus of the rat. Journal of Comparative Neurology 339: 251–268CrossRefGoogle ScholarPubMed
Grossman, R. G. and Hampton, T. (1968) Depolarization of cortical glial cells during electrical activity. Brain Research 11: 316–324CrossRefGoogle Scholar
Grüner, J. E., Hirsch, J. C. and Sotelo, C. (1974) Ultrastructural features of the isolated suprasylvian gyrus in the cat. Journal of Comparative Neurology 154: 1–28CrossRefGoogle ScholarPubMed
Guberman, A., Gloor, P. and Sherwin, A. L. (1975) Response of generalized epilepsy in the cat to ethosuximide and diphenylhydantoin. Neurology 25: 758–764CrossRefGoogle ScholarPubMed
Gulyas, A. I., Miles, R., Sok, A., Toth, K., Tamamaki, N. and Freund, T. F. (1993) Hippocampal pyramidal cells excite inhibitory neurons through a single release site. Nature 366: 683–687CrossRefGoogle ScholarPubMed
Gupta, A., Wang, Y. and Markram, H. (2000) Organizing principles for a diversity of GABAergic interneurons and synapses in the neocortex. Science 287: 273–278CrossRefGoogle ScholarPubMed
Gutfreund, Y., Yarom, Y. and Segev, I. (1995) Subthreshold oscillations and resonant frequency in guinea-pig cortical neurons: physiology and modelling. Journal of Physiology (London) 483: 621–640CrossRefGoogle ScholarPubMed
Gutnick, M. J. and Mody, I. (eds.) (1995) The Cortical Neuron. Oxford: Oxford University Press
Gutnick, M. J., Heinemann, U. and Prince, D. A. (1979) Stimulus induced and seizure related changes in extracellular potassium concentration in cat thalamus (VPL). Electroencephalography and Clinical Neurophysiology 47: 329–344CrossRefGoogle Scholar
Gutnick, M. J., Connors, B. W. and Prince, D. A. (1982) Mechanisms of neocortical epileptogenesis in vitro. Journal of Neurophysiology 48: 1321–1335CrossRefGoogle ScholarPubMed
Gutnick, M. J., Amitai, Y. and Barkai, E. (1992) Chronic models of cortical epilepsy: experimental manipulations leading to long-term reorganization of local neocortical circuitry. In Molecular Neurobiology of Epilepsy, ed. J. Engel Jr., C. Wasterlain, E. A. Cavalheiro, U. Heinemann and G. Avanzini, pp. 221–229, Amsterdam: Elsevier
Haas, H. L. and Greene, R. W. (1986) Effects of histamine on hippocampal pyramidal cells of the rat in vitro. Experimental Brain Research 62: 123–130CrossRefGoogle ScholarPubMed
Halasz, P. (1991) Runs of rapid spikes in sleep: a characteristic EEG expression of generalized malignant epileptic encephalopathies. A conceptual review with new pharmacological data. Epilepsy Research (Suppl.) 2: 49–71Google ScholarPubMed
Halgren, E., Smith, M. E. and Stapleton, J. M. (1985) Hippocampal field potentials evoked by repeated vs nonrepeated words. In Electrical Activity of the Archicortex, ed. G. Buzsáki and C. H. Vanderwolf, pp. 67–81, Budapest: Akademiai Kiadó
Hallanger, A. E. and Wainer, B. H. (1988) Ultrastructure of ChAT-immunoreactive synaptic terminals in the thalamic reticular nucleus of the rat. Journal of Comparative Neurology 278: 486–497CrossRefGoogle ScholarPubMed
Hallanger, A. E., Levey, A. I., Lee, H. J., Rye, D. B. and Wainer, B. H. (1987) The origins of cholinergic and other subcortical afferents to the thalamus in the rat. Journal of Comparative Neurology 262: 105–124CrossRefGoogle ScholarPubMed
Halliwell, J. V. (1986) M-current in human neocortical neurones. Neuroscience Letters 67: 1–6CrossRefGoogle ScholarPubMed
Halpern, L. M. (1972) Chronically isolated aggregates of mammalian cerebral cortical neurons studied in situ. In Experimental Models of Epilepsy, ed. D. P. Purpura, J. F. Penry, D. B. Tower, D. M. Woodbury and R. D. Walter, pp. 197–221, New York: Raven
Han, Z. S., Buhl, E. H., Lorinczi, Z. and Somogyi, P. (1993) A high degree of spatial selectivity in the axonal and dendritic domains of physiologically identified local-circuit neurons in the dentate gyrus of the rat hippocampus. European Journal of Neuroscience 5: 395–410CrossRefGoogle ScholarPubMed
Hansen, J. C. and Hillyard, S. (1980) Endogenous brain potentials associated with auditory selective attention. Electroencephalography and Clinical Neurophysiology 49: 277–290CrossRefGoogle Scholar
Harding, B. N. and Powell, T. P. S. (1972) An electron microscopic study of afferent fibre connexions to the monkey thalamus from motor cortex and basal ganglia. Journal of Anatomy 111: 503–504Google ScholarPubMed
Haulica, I., Ababei, L., Branisteanu, D. and Topoliceanu, F. (1973) Preliminary data on the possible hypnogenic role of adenosine. Journal of Neurochemistry 21: 1019–1020CrossRefGoogle ScholarPubMed
Hayaishi, O. (1988) Sleep-wake regulation by prostaglandin D2 and E2. Journal of Biological Chemistry 263: 14593–14596Google ScholarPubMed
Heath, R. (1954) Studies in Schizophrenia: A Multidisciplinary Approach to Mind-Brain Relationships. Cambridge, MA: Harvard University Press
Heilman, K. M., Bowers, D., Coslett, H. B., Whelan, H. and Watson, R. T. (1985) Direction hypokinesia: prolonged reaction times for leftward movements in patients with right hemisphere lesions and neglect. Neurology 35: 855–860CrossRefGoogle Scholar
Heinemann, U. and Pumain, R. (1981) Effects of tetrodotoxin on changes in extracellular free calcium induced by repetitive electrical stimulation and iontophoretic application of excitatory amino acids in the sensorimotor cortex of cats. Neuroscience Letters 21: 87–91CrossRefGoogle Scholar
Heinemann, U., Gabriel, S., Jauch, R., Schulze, K., Kivi, A., Eilers, A., Kovacs, R. and Lehmann, T. N. (2000) Alterations of glial cell function in temporal lobe epilepsy. Epilepsia 41: S185–S189CrossRefGoogle ScholarPubMed
Heller, H. C., Glotzbach, S., Grahn, D. and Radeke, C. (1988) Sleep-dependent changes in the thermoregulatory system. In Clinical Physiology of Sleep, ed. R. Lydic and J. F. Biebuyck, pp. 145–169, Bethesda: American Physiological Society
Hennevin, E., Hars, B., Maho, C. and Bloch, V. (1995) Processing of learned information in paradoxical sleep: relevance for memory. Behavioral and Brain Research 69: 125–135CrossRefGoogle ScholarPubMed
Herculano-Houzel, S., Munk, M. H. J., Neuenschwander, S. and Singer, W. (1999) Precisely synchronized oscillatory firing patterns require electroencephalographic activation. Journal of Neuroscience 19: 3992–4010CrossRefGoogle ScholarPubMed
Herkenham, M. (1987) Mismatches between neurotransmitter and receptor localization in brain: observations and implications. Neuroscience 23: 1–38CrossRefGoogle Scholar
Hernández-Cruz, A. and Pape, H. C. (1989) Identification of two calcium currents in acutely dissociated neurons from the rat lateral geniculate nucleus. Journal of Neurophysiology 61: 1270–1283CrossRefGoogle ScholarPubMed
Hess, G. and Gustafsson, B. (1990) Changes in field excitatory postsynaptic potential shape induced by tetanization in the CA1 region of the guinea-pig hippocampal slice. Neuroscience 37: 61–69CrossRefGoogle ScholarPubMed
Hess, W. R. (1944) Das Schlafsyndrom als Folge dienzephaler Reizung. Helvetica Physiologica et Pharmacologica Acta 2: 305–344Google Scholar
Hestrin, S. and Armstrong, W. E. (1996) Morphology and physiology of cortical neurons in layer I. Journal of Neuroscience 16: 5290–5300CrossRefGoogle ScholarPubMed
Hikosaka, O. and Wurtz, R. H. (1983) Visual and oculomotor function of monkey substantia nigra pars reticulata. IV: relation of substantia nigra to superior colliculus. Journal of Neurophysiology 49: 1285–1301CrossRefGoogle ScholarPubMed
Hille, B. (1992) Ionic Channels of Excitable Membranes. Sunderland, MA: Sinauer
Hirsch, J. C. and Burnod, Y. (1987) A synaptically evoked late hyperpolarization in the rat dorsolateral geniculate neurons in vitro. Neuroscience 23: 457–468CrossRefGoogle ScholarPubMed
Hirsch, J. C., Fourment, A. and Marc, M. E. (1983) Sleep-related variations of membrane potential in the lateral geniculate body relay neurons of the cat. Brain Research 259: 308–312CrossRefGoogle ScholarPubMed
Hirsch, J. C., Quesada, O., Esclapez, M., Gozlan, H., Ben-Ari, Y. and Bernard, C. L. (1996) Enhanced NMDAR-dependent epileptiform activity is controlled by oxidizing agents in a chronic model of temporal lobe epilepsy. Journal of Neurophysiology 76: 4185–4189CrossRefGoogle Scholar
Hobson, J. A. and Pace-Schott, E. F. (2002) The cognitive neuroscience of sleep: neuronal systems, consciousness and learning. Nature Reviews Neuroscience 3: 679–693CrossRefGoogle Scholar
Hobson, J. A., McCarley, R. W. and Wyzinski, P. W. (1975) Sleep cycle oscillation: reciprocal discharge by two brain stem neuronal groups. Science 189: 55–58CrossRefGoogle ScholarPubMed
Hobson, J. A., Pace-Schott, E. and Stickgold, R. (2000) Dreaming and the brain: toward a cognitive neuroscience of conscious states. Brain and Behavioral Sciences 23: 793–842CrossRefGoogle Scholar
Hoffman, D. A., Magee, J. C., Colbert, C. M. and Johnston, D. (1997) K+ channel regulation of signal propagation in dendrites of hippocampal pyramidal neurons. Nature 387: 869–875CrossRefGoogle ScholarPubMed
Hoffman, S. N., Salin, P. A. and Prince, D. A. (1994) Chronic neocortical epileptogenesis in vitro. Journal of Neurophysiology 71: 1762–1772CrossRefGoogle ScholarPubMed
Hoffman, W. H. and Haberly, L. B. (1991) Bursting induced epileptiform EPSPs in slices of piriform cortex are generated by deep cells. Journal of Neuroscience 11: 2021–2031CrossRefGoogle ScholarPubMed
Hofle, N., Paus, T., Reutens, D., Fiset, P., Gotman, J., Evans, A. C. and Jones, B. E. (1997) Regional cerebral blood flow changes as a function of delta and spindle activity during slow wave sleep in humans. Journal of Neuroscience 17: 4800–4808CrossRefGoogle ScholarPubMed
Homma, Y., Skinner, R. D. and Garcia-Rill, E. (2002) Effects of pedunculopontine nucleus (PPN) stimulation on caudal pontine reticular formation (PnC) neurons in vitro. Journal of Neurophysiology 87: 3033–3047CrossRefGoogle ScholarPubMed
Honda, T. and Semba, K. (1995) An ultrastructural study of cholinergic and non-cholinergic neurons in the laterodorsal and pedunculopontine tegmental nuclei in the rat. Neuroscience 68: 837–853CrossRefGoogle ScholarPubMed
Hoogland, P. V., Wouterlood, F. G., Welker, E. and Loos, H. (1991) Ultrastructure of giant and small thalamic terminals of cortical origin: a study of the projections from the barrel cortex in mice using Phaseolus vulgaris-leucoagglutinin (PHA-L). Experimental Brain Research 87: 159–172CrossRefGoogle Scholar
Horne, J. (1988) Why We Sleep. Oxford: Oxford University Press
Hosford, D. A., Clark, S., Cao, Z., Wilson, W. A. Jr., Lin, F. H., Morrisett, R. A. and Huin, A. (1992) The role of GABAB receptor activation in absence seizures of lethargic (Ih/Ih) mice. Science 257: 398–401CrossRefGoogle Scholar
Hosford, D. A., Caddick, S. J. and Lin, F. H. (1997) Generalized epilepsies: emerging insights into cellular and genetic mechanisms. Current Opinion in Neurology 10: 115–120CrossRefGoogle ScholarPubMed
Houser, C. R. and Esclapez, M. (1996) Vulnerability and plasticity of the GABA system in the pilocarpine model of spontaneous recurrent seizures. Epilepsy Research 26: 207–218CrossRefGoogle ScholarPubMed
Houser, C. R., Vaughan, J. E., Barber, R. P. and Roberts, E. (1980) GABA neurons are the major cell type of the nucleus reticularis thalami. Brain Research 200: 341–354CrossRefGoogle ScholarPubMed
Houser, C. R., Miyashiro, J. E., Swartz, B. E., Walsh, G. O., Rich, J. R. and Delgado-Escueta, A. V. (1990) Altered patterns of dynorphin immunoreactivity suggest mossy fiber reorganization in human hippocampal epilepsy. Journal of Neuroscience 10: 267–282CrossRefGoogle ScholarPubMed
Houweling, A., Bazhenov, M., Timofeev, I., Steriade, M. and Sejnowski, T. J. (1999) Cortical and thalamic components of augmenting responses: a modelling study. Neurocomputing 26–27: 735–742CrossRefGoogle Scholar
Houweling, A. R., Bazhenov, M., Timofeev, I., Grenier, F., Steriade, M. and Sejnowski, T. J. (2002) Frequency-selective augmenting responses by short-term synaptic depression in cat neocortex. Journal of Physiology (London) 542: 599–617CrossRefGoogle ScholarPubMed
Hu, B., Bouhassira, D., Steriade, M. and Deschênes, M. (1988) The blockage of ponto-geniculo-occipital waves in the cat lateral geniculate nucleus by nicotinic antagonists. Brain Research 473: 394–397CrossRefGoogle ScholarPubMed
Hu, B., Steriade, M. and Deschênes, M. (1989a) The effects of peribrachial stimulation on reticular thalamic neurons: the blockage of spindle waves. Neuroscience 31: 1–12CrossRefGoogle Scholar
Hu, B., Steriade, M. and Deschênes, M. (1989b) The effects of brainstem peribrachial stimulation on neurons of the lateral geniculate nucleus. Neuroscience 31: 13–24CrossRefGoogle Scholar
Hu, B., Steriade, M. and Deschênes, M. (1989c) The cellular mechanism of thalamic ponto-geniculo-occipital waves. Neuroscience 31: 25–35CrossRefGoogle Scholar
Hubel, D. H. (1960) Single unit activity in lateral geniculate body and optic tract of unrestrained cats. Journal of Physiology (London) 150: 91–104CrossRefGoogle ScholarPubMed
Hudson, L. P., Munoz, D. G., Miller, L., McLahlan, R. S., Girvin, J. P. and Blume, W. T. (1993) Amygdaloid sclerosis in temporal lobe epilepsy. Annals of Neurology 33: 622–631CrossRefGoogle ScholarPubMed
Hughes, J. R. (1980) Two forms of the 6/sec spike and wave complex. Electroencephalography and Clinical Neurophysiology 48: 535–550CrossRefGoogle ScholarPubMed
Huguenard, J. R. (1996) Low-threshold calcium currents in central nervous system neurons. Annual Review of Physiology 58: 329–348CrossRefGoogle ScholarPubMed
Huguenard, J. R. (1999) Neuronal circuitry of thalamocortical epilepsy and mechanisms of antiabsence drug action. Advances in Neurology 79: 991–999Google ScholarPubMed
Huguenard, J. R. and Prince, D. A. (1992) A novel T-type current underlies prolonged Ca2+-dependent burst firing in GABAergic neurons of rat thalamic reticular nucleus. Journal of Neuroscience 12: 3804–3817CrossRefGoogle Scholar
Huguenard, J. R. and Prince, D. A. (1994a) Clonazepam suppresses GABAB-mediated inhibition in thalamic relay neurons through effects in nucleus reticularis. Journal of Neurophysiology 71: 2576–2581CrossRefGoogle Scholar
Huguenard, J. R. and Prince, D. A. (1994b) Intrathalamic rhythmicity studied in vitro: nominal T current modulation causes robust anti-oscillatory effects. Journal of Neuroscience 14: 5485–5502CrossRefGoogle Scholar
Huguenard, J. R., Chung, J. M. and Prince, D. A. (1996) Excitability changes in thalamic and neocortical neurons after injury. In Progressive Nature of Epileptogenesis (Epilepsy Research, Suppl. 12), ed. U. Heinemann, pp. 129–135, Amsterdam: Elsevier
Huntsman, M. M. and Huguenard, J. R. (2000) Nucleus-specific differences in GABAA receptor mediated inhibition are enhanced during thalamic development. Journal of Neurophysiology 83: 350–358CrossRefGoogle Scholar
Huntsman, M. M., Porcello, D. M., Homanics, G. E., DeLorey, T. M. and Huguenard, J. R. (1999) Reciprocal inhibitory connections and network synchrony in the mammalian thalamus. Science 283: 541–543CrossRefGoogle ScholarPubMed
IFSECN (1974) A glossary of terms most commonly used by clinical electroencephalographers. Electroencephalography and Clinical Neurophysiology 37: 538–548CrossRef
Imig, T. J. and Reale, R. A. (1981) Ipsilateral corticocortical projections related to binaural columns in cat primary auditory cortex. Journal of Comparative Neurology 203: 1–14CrossRefGoogle ScholarPubMed
Immon, H., Ito, K., Dauphin, L. and McCarley, R. W. (1996) Electrical stimulation of the cholinergic laterodorsal tegmental nucleus elicits scopolamine-sensitive excitatory postsynaptic potentials in medial pontine reticular formation neurons. Neuroscience 74: 393–401CrossRefGoogle Scholar
Inglis, W. L. and Semba, K. (1996) Colocalization of ionotropic glutamate receptor subunits with NADPH-diaphorase-containing neurons in the rat mesopontine tegmentum. Journal of Comparative Neurology 368: 17–323.0.CO;2-N>CrossRefGoogle ScholarPubMed
Ingvar, D. H., Sjölund, B. and Ardo, A. (1976) Correlation between ECG frequency, cerebral oxygen uptake and blood flow. Electroencephalography and Clinical Neurophysiology 41: 268–276CrossRefGoogle Scholar
Innocenti, B., Parpura, V. and Haydon, P. G. (2000) Imaging extracellular waves of glutamate during calcium signaling in cultured astrocytes. Journal of Neuroscience 20: 1800–1808CrossRefGoogle ScholarPubMed
Isokawa, M. and Levesque, M. F. (1991) Increased NMDA responses and dendritic degeneration in human epileptic hippocampal neurons in slices. Neuroscience Letters 132: 212–216CrossRefGoogle ScholarPubMed
Ito, H., Halldin, C. and Farde, L. (1999) Localization of 5–HT1A receptors in the living human brain using [carbonyl-11C]WAY-100635: PET with anatomic standardization technique. Journal of Nuclear Medicine 40: 102–109Google Scholar
Ito, K. and McCarley, R. W. (1984) Alterations in membrane potential and excitability of cat medial pontine reticular formation neurons during changes in naturally occurring sleep-wake states. Brain Research 292: 169–175CrossRefGoogle ScholarPubMed
Ito, K., Yanagihara, M., Imon, L., Dauphin, L. and McCarley, R. W. (2002) Intracellular recordings of pontine medial gigantocellular tegmental field neurons in the naturally sleeping cat: behavioral state-related activity and soma size difference in order of recruitment. Neuroscience, 114: 23–37CrossRefGoogle ScholarPubMed
Iyer, K. S. and McCann, S. M. (1987) Delta sleep inducing peptide (DSIP) stimulates growth hormone (GH) release in the rat by hypothalamic and pituitary actions. Peptides 8: 45–48CrossRefGoogle ScholarPubMed
Jackson, J. H. (1864) Illustrations of diseases of the nervous system: clinical lectures and reports by the medical staff of the London hospital. London Hospital Reports 1: 337–387Google Scholar
Jackson, J. H. (1931) Selected Writings of John Hughlings Jackson (vol. 1, On Epilepsy and Epileptiform Convulsions), ed. J. Taylor, London: Hodder and Stroughton
Jacobs, K. M., Graber, K. D., Kharazia, V. N., Parada, I. and Prince, D. A. (2000) Postlesional epilepsy: the ultimate brain plasticity. Epilepsia 41 (Suppl. 6): S153–S161CrossRefGoogle ScholarPubMed
Jacobsen, R. B., Uhlrich, D. and Huguenard, J. R. (2001) GABAB and NMDA receptors contribute to spindle-like oscillations in rat thalamus in vitro. Journal of Neurophysiology 86: 1365–1375CrossRefGoogle Scholar
Jahnsen, H. and Llinás, R. (1984a) Electrophysiological properties of guinea-pig thalamic neurones: an in vitro study. Journal of Physiology (London) 349: 205–226CrossRefGoogle Scholar
Jahnsen, H. and Llinás, R. (1984b) Ionic basis for electroresponsiveness and oscillatory properties of guinea-pig thalamic neurones in vitro. Journal of Physiology (London) 349: 227–247CrossRefGoogle Scholar
Jandó, G., Carpi, D., Kandel, A., Urioste, R., Horvath, Z., Pierre, E., Vati, D., Vadasz, C. and Buzsáki, G. (1995) Spike-and-wave epilepsy in rats: sex differences and inheritance of physiological traits. Neuroscience 64: 301–317CrossRefGoogle ScholarPubMed
Jasper, H. H. (1949) Diffuse projection systems: the integrative action of the thalamic reticular system. Electroencephalography and Clinical Neurophysiology 1: 405–420CrossRefGoogle ScholarPubMed
Jasper, H. H. (1969) Mechanism of propagation. In Brain Mechanisms of the Epilepsies, ed. H. H. Jasper, A. A. Ward and A. Pope, pp. 421–438, Boston: Little, Brown
Jasper, H. H. (1975) Application of experimental models to human epilepsy. In Experimental Models of Epilepsy, ed. D. P. Purpura, J. K. Penry, D. B. Tower, D. M. Woodbury and R. D. Walter, pp. 585–601, New York: Raven Press
Jasper, H. H. (1981) Problems relating cellular or modular specificity to cognitive functions: importance of state-dependent reactions. In The Organization of the Cerebral Cortex, ed. F. O. Schmitt, F. G. Worden, G. Adelman and S. G. Dennis, pp. 375–393, Cambridge, MA: The MIT Press
Jasper, H. H. (1990) Historical introduction. In Generalized Epilepsies, ed. M. Avoli, P. Gloor, G. Kostopoulos and R. Naquet, pp. 1–15, Boston: Birkhäuser
Jasper, H. H. and Droogleever-Fortuyn, J. (1949) Experimental studies on the functional anatomy of petit-mal epilepsy. Research Publications of the Association of Nervous and Mental Diseases 26: 272–298Google Scholar
Jasper, H. H. and Hawkes, W. A. (1938) Electroencephalography. IV. Localization of seizure waves in epilepsy. Archives of Neurology (Chicago) 39: 885–901CrossRefGoogle Scholar
Jasper, H. H. and Kershman, J. (1941) Electroencephalographic classification of the epilepsies. Archives of Neurology and Psychiatry 45: 903–943CrossRefGoogle Scholar
Jasper, H. H. and Shagass, C. (1941) Conscious time judgments related to conditioned time intervals and voluntary control of the alpha rhythm. Journal of Experimental Psychology 28: 503–508CrossRefGoogle Scholar
Jasper, H. H. and Tessier, J. (1971) Acetylcholine liberation from cerebral cortex during paradoxical (REM) sleep. Science 172: 601–602CrossRefGoogle ScholarPubMed
Jasper, H. H., Pertuiset, B. and Flaniginn, H. (1951) EEG and cortical electrogram in patients with temporal lobe epilepsy. Archives of Neurology and Psychiatry (Chicago) 65: 272–290CrossRefGoogle Scholar
Jasper, H. H., Ward, A. A. Jr. and Pope, A. (eds) (1969) Basic Mechanisms of the Epilepsies. Boston: Little, Brown
Jeanmonod, D., Magnin, M., Morel, A., Siegemund, M., Cancro, A., Lanz, M., Llinás, R., Ribary, U., Kronberg, E., Schulman, J. and Zonenshayn, M. (2001) Thalamocortical dysrhythmia. II. Clinical and surgical aspects. Thalamus and Related Systems 1: 245–254Google Scholar
Jefferson, G. (1958) Reticular formation and clinical neurology. In Reticular Formation of the Brain, ed. H. H. Jasper, L. D. Proctor, R. S. Knighton, W. C. Noshay and R. T. Costello, pp. 729–738, Boston: Little, Brown
Jefferys, J. G. R. (1995) Nonsynaptic modulation of neuronal activity in the brain: electric currents and extracellular ions. Physiological Reviews 75: 689–723CrossRefGoogle ScholarPubMed
Jefferys, J. G. R. and Haas, H. L. (1982) Synchronized bursting of CA1 pyramidal cells in absence of synaptic transmission. Nature 300: 448–450CrossRefGoogle ScholarPubMed
Jensen, F. E., Holmes, G. L., Lombroso, C. T., Blume, H. K. and Firkusny, I. R. (1992) Age-dependent changes in long-term seizures susceptibility and behavior after hypoxia in rats. Epilepsia 33: 971–980CrossRefGoogle ScholarPubMed
Jensen, M. S. and Yaari, Y. (1997) Role of intrinsic burst firing, potassium accumulation, and electrical coupling in the elevated postassium model of hippocampal epilepsy. Journal of Neurophysiology 77: 1224–1233CrossRefGoogle Scholar
Jensen, M. S., Cherubini, E. and Yaari, Y. (1993) Opponent effects of potassium on GABAA-mediated postsynaptic inhibition in the rat hippocampus. Journal of Neurophysiology 69: 764–771CrossRefGoogle ScholarPubMed
Jensen, M. S., Azouz, R. and Yaari, Y. (1994) Variant firing patterns in rat hippocampal pyramidal cells modulated by extracellular potassium. Journal of Neurophysiology 71: 831–839CrossRefGoogle ScholarPubMed
Jensen, M. S., Azouz, R. and Yaari, Y. (1996) Spike afterdepolarization and burst generation in adult rat hippocampal CA1 pyramidal cells. Journal of Physiology (London) 492: 199–210CrossRefGoogle Scholar
Jobert, M., Poiseau, E., Jähnig, P., Schulz, H. and Kubicki, S. (1992) Topographical analysis of sleep spindle activity. Neuropsychobiology 26: 210–217CrossRefGoogle ScholarPubMed
Johnston, D. and Brown, T. H. (1981) Giant spike potential hypothesis for epileptiform activity. Science 211: 294–297CrossRefGoogle ScholarPubMed
Johnston, D. and Brown, T. H. (1984) The synaptic nature of the paroxysmal depolarizing shift in hippocampal neurons. Annals of Neurology 16 (Suppl.): S65–S75CrossRefGoogle ScholarPubMed
Johnston, D., Magee, J. C., Colbert, C. M. and Cristie, B. R. (1996) Active properties of neuronal dendrites. Annual Reviews of Neuroscience 19: 165–186CrossRefGoogle ScholarPubMed
Johnston, D., Hoffman, D. A., Magee, J. C., Poolos, N. P., Watanabe, S., Colbert, C. M. and Migliore, M. (2000) Dendritic potassium channels in hippocampal pyramidal neurons. Journal of Physiology (London) 525: 75–81CrossRefGoogle ScholarPubMed
Jones, B. E. (1995) Reticular formation: cytoarchitecture, transmitters, and projections. In The Rat Nervous System, 2nd edn., ed. G. Paxinos, pp. 155–171, New York: Academic
Jones, B. E. (2000) Basic mechanisms of sleep-wake states. In Principles and Practice of Sleep Medicine, ed. M. H. Kryger, T. Toth and W. C. Dement, pp. 134–154, Philadelphia: Saunders
Jones, E. G. (1975) Varieties and distribution of non-pyramidal cells in the somatic sensory cortex of the squirrel monkey. Journal of Comparative Neurology 160: 205–268CrossRefGoogle ScholarPubMed
Jones, E. G. (1985) The Thalamus. New York: Plenum
Jones, E. G. (1995) Overview: basic elements of the cortical network. In The Cortical Neuron, ed. M. J. Gutnick and I. Mody, pp. 111–122, New York: Oxford University Press
Jones, E. G. (1998) What are local circuits? In Neurobiology of Neocortex, ed. P. Rakic and W. Singer, pp. 137–152, New York: Wiley
Jones, E. G. (2000) Cortical and subcortical contributions to activity-dependent plasticity in primate somatosensory cortex. Annual Reviews of Neuroscience 23: 1–37CrossRefGoogle ScholarPubMed
Jones, E. G. (2001) The thalamic matrix and thalamocortical synchrony. Trends in Neurosciences 24: 595–601CrossRefGoogle ScholarPubMed
Jones, E. G. and Powell, T. P. S. (1969) An electron microscopic study of the mode of transmission of cortico-thalamic fibres within the sensory relay nuclei of the thalamus. Proceedings of the Royal Society of London (Series B) 172: 173–185CrossRefGoogle Scholar
Jones, E. G., Coulter, J. D. and Hendry, S. H. C. (1978) Intracortical connectivity of architectonic fields in somatic sensory, motor and parietal cortex of monkeys. Journal of Comparative Neurology 181: 291–348CrossRefGoogle ScholarPubMed
Jones, M. S. and Barth, D. S. (1999) Spatiotemporal organization of fast (>200 Hz) electrical oscillations in rat vibrissa/barrel cortex. Journal of Neurophysiology 82: 1599–1609CrossRefGoogle ScholarPubMed
Jones, M. S., MacDonald, K. D., Choi, B., Dudek, F. E. and Barth, D. S. (2000) Intracellular correlates of fast (>200 Hz) electrical oscillations in rat somatosensory cortex. Journal of Neurophysiology 84: 1505–1518CrossRefGoogle ScholarPubMed
Jones, R. S. and Heinemann, V. (1988) Synaptic and intrinsic responses of medial entorhinal cortical cells in normal and magnesium-free medium in vitro. Journal of Neurophysiology 59: 1476–1496CrossRefGoogle ScholarPubMed
Jouvet, M. (1962) Recherches sur les structures nerveuses et les mécanismes responsables des différentes phases du sommeil physiologique. Archives Italiennes de Biologie 100: 125–206Google Scholar
Jouvet, M. (1965) Paradoxical sleep – a study of its nature and mechanisms. Progress in Brain Research 18: 20–57CrossRefGoogle ScholarPubMed
Jouvet, M. (1972) The role of monoamines and acetylcholine-containing neurons in the regulation of the sleep-waking cycle. Ergebnisse der Physiologie 64: 166–307Google ScholarPubMed
Jouvet, M. (1986) Programmation génétique itérative et sommeil paradoxal. Confrontations Psychiatriques 27: 153–181Google Scholar
Jouvet, M. (1988) The regulation of paradoxical sleep by the hypothalamo-hypophysis. Archives Italiennes de Biologie 126: 259–274Google ScholarPubMed
Jouvet, M. (1992) Le Château des Songes. Paris: Odile Jacob
Jouvet, M. (1999) The Paradox of Sleep. Cambridge, MA: The MIT Press
Jouvet, M. and Michel, F. (1959) Corrélations électromyographiques du sommeil chez le chat décortiqué et mésencéphalique chronique. Comptes Rendus de la Société de Biologie (Paris) 153: 422–425Google Scholar
Jouvet, M., Michel, F. and Courjon, J. (1959) Sur un stade d'activité électrique cérébrale rapide au cours du sommeil physiologique. Comptes Rendus de la Société de Biologie (Paris) 153: 1024–1028Google Scholar
Jouvet-Mounier, D., Astic, L. and Lacote, D. (1970) Ontogenesis of the states of sleep in rat, cat, and guinea-pig during the first postnatal month. Developmental Psychobiology 2: 216–239CrossRefGoogle ScholarPubMed
Jung, R. (1962) Blocking of petit-mal attacks by sensory arousal and inhibition of attacks by an active change in attention during the epileptic aura. Epilepsia 3: 435–437CrossRefGoogle Scholar
Kammermeier, P. J. and Jones, S. W. (1997) High-voltage-activated calcium currents in neurons acutely isolated from the ventrobasal nucleus of the rat thalamus. Journal of Neurophysiology 77: 465–475CrossRefGoogle ScholarPubMed
Kamondi, A., Williams, J. A., Hutcheon, B. and Reiner, P. B. (1992) Membrane properties of mesopontine cholinergic neurons studied with the whole-cell patch-clamp technique: implications for behavioral state control. Journal of Neurophysiology 68: 1359–1372CrossRefGoogle ScholarPubMed
Kamondi, A., Acsády, L. and Buzsáki, G. (1998) Dendritic spikes are enhanced by cooperative network activity in the intact hippocampus. Journal of Neuroscience 18: 3919–3928CrossRefGoogle ScholarPubMed
Kamphuis, W., Huisman, E., Dreijer, A. M., Ghijsen, W. E., Verhage, M. and Lopes da Silva, F. H. (1990) Kindling increases the K+-evoked Ca2+-dependent release of endogenous GABA in area CA1 of rat hippocampus. Brain Research 511: 63–70CrossRefGoogle ScholarPubMed
Kandel, A. and Buzsáki, G. (1997) Cellular-synaptic generation of sleep spindles, spike-and-wave discharges, and evoked thalamocortical responses in the neocortex of rat. Journal of Neuroscience 17: 6783–6797CrossRefGoogle ScholarPubMed
Kandel, E. R. and Spencer, W. A. (1961) Electrophysiology of hippocampal neurons. I. After-potentials and repetitive firing. Journal of Neurophysiology 24: 243–259CrossRefGoogle ScholarPubMed
Kandel, E. R., Spencer, W. A. and Brinley, F. J. Jr. (1961) Electrophysiology of hippocampal neurons. I. Sequential invasion and synaptic organization. Journal of Neurophysiology 24: 225–242CrossRefGoogle ScholarPubMed
Kang, J., Jiang, L., Goldman, S. A. and Nedergaard, M. (1998) Astrocyte-mediated potentiation of inhibitory synaptic transmission. Nature Neuroscience 1: 683–692CrossRefGoogle ScholarPubMed
Kang, Y. and Kayano, F. (1994) Electrophysiological and morphological characteristics of layer VI pyramidal cells in the cat motor cortex. Journal of Neurophysiology 72: 578–591CrossRefGoogle ScholarPubMed
Kang, Y. and Kitai, S. T. (1990) Electrophysiological properties of pedunculopontine neurons and their postsynaptic responses following stimulation of substantia nigra reticulata. Brain Research 535: 79–95CrossRefGoogle ScholarPubMed
Kao, C. Q. and Coulter, D. A. (1997) Physiology and pharmacology of corticothalamic stimulation-evoked responses in rat somatosensory thalamic neurons in vitro. Journal of Neurophysiology 77: 2661–2676CrossRefGoogle ScholarPubMed
Kapas, L., Obal, F. Jr. and Krueger, J. M. (1993) Humoral regulation of sleep. International Reviews of Neurobiology 35: 131–160CrossRefGoogle Scholar
Karni, A., Tanne, D., Rubenstein, B. S., Askenasy, J. J. M. and Sagi, D. (1994) Dependence on REM sleep of overnight improvement of a perceptual skill. Science 265: 679–682CrossRefGoogle ScholarPubMed
Kato, N. (1990) Cortico-thalamo-cortical projection between visual cortices. Brain Research 509: 150–152CrossRefGoogle ScholarPubMed
Kawaguchi, Y. (1993) Groupings of nonpyramidal and pyramidal cells with specific physiological and morphological characteristics in rat frontal cortex. Journal of Neurophysiology 69: 416–431CrossRefGoogle ScholarPubMed
Kawaguchi, Y. (1995) Physiological subgroups of nonpyramidal cells with specific morphological characteristics in layers II/III of rat frontal cortex. Journal of Neuroscience 15: 2638–2655CrossRefGoogle Scholar
Kawaguchi, Y. and Kubota, Y. (1993) Correlation of physiological subgroups of nonpyramidal cells with parvalbumin- and calbindinD28k-immunoreactive neurons in layer V of rat frontal cortex. Journal of Neurophysiology 70: 387–396CrossRefGoogle Scholar
Kawaguchi, Y. and Kubota, Y. (1996) Physiological and morphological identification of somatostatin- or vasoactive intestinal polypeptide-containing cells among GABAergic cell subtypes in rat frontal cortex. Journal of Neuroscience 16: 2701–2715CrossRefGoogle ScholarPubMed
Kawaguchi, Y. and Kubota, Y. (1997) GABAergic cell subtypes and their synaptic connections in rat frontal cortex. Cerebral Cortex 7: 476–486CrossRefGoogle ScholarPubMed
Kayama, Y., Sugitani, M. and Iwama, K. (1982) Effects of locus coeruleus stimulation on neuronal activities of dorsal lateral geniculate nucleus and perigeniculate reticular nucleus of the rat. Neuroscience 7: 655–666CrossRefGoogle ScholarPubMed
Keifer, J. C., Baghdoyan, H. A., Becker, L. and Lydic, R. (1994) Halothane decreases pontine acetylcholine release and increases spindles. NeuroReport 5: 577–580CrossRefGoogle ScholarPubMed
Kellaway, P. (1985) Sleep and epilepsy. Epilepsia 26 (Suppl. 1): 15–30CrossRefGoogle ScholarPubMed
Kellaway, P. and Frost, J. D. Jr. (1983) Biorhythmic modulation of epileptic events. In Recent Advances in Epilepsy (vol. 1), ed. T. A. Pedley and B. S. Meldrum, pp. 139–154, London: Churchill-Livingstone
Kellaway, P., Crawley, J. W. and Kagawa, N. (1960) Paroxysmal pain and autonomic disturbances of cerebral origin: a specific electroclinical syndrome. Epilepsia 1: 466–483CrossRefGoogle Scholar
Kellaway, P., Hrachovy, R. A., Frost, J. D. Jr. and Zion, T. (1979) Precise characterization and quantification of infantile spasms. Annals of Neurology 6: 214–218CrossRefGoogle ScholarPubMed
Kellaway, P., Frost, J. D. Jr. and Crawley, J. W. (1980) Time modulation of spike-and-wave activity in generalized epilepsy. Annals of Neurology 8: 491–500CrossRefGoogle ScholarPubMed
Kellaway, P., Frost, J. D. Jr. and Crawley, J. W. (1990) The relations between sleep spindles and spike-and-wave bursts in human epilepsy. In Generalized Epilepsy, ed. M. Avoli, P. Gloor, G. Kostopoulos and R. Naquet, pp. 36–48, Boston: Birkhäuser
Keller, A. (1993) Intrinsic synaptic organization of the motor cortex. Cerebral Cortex 3: 43–51CrossRefGoogle ScholarPubMed
Kennedy, C., Gillin, J. C., Mendelson, W., Suda, S., Miyaoka, M., Ito, M., Nakamura, R. K., Storch, F. I., Pettigrew, K., Mishkin, M. and Sokoloff, L. (1982) Local cerebral glucose utilization in non-rapid eye movement sleep. Nature 297: 325–327CrossRefGoogle ScholarPubMed
Kettenmann, H. and Schachner, M. (1985) Pharmacological properties of γ-aminobutyric acid-, glutamate-, and aspartate-induced depolarizations in cultured astrocytes. Journal of Neuroscience 5: 3295–3301CrossRefGoogle ScholarPubMed
Khateb, A., Serafin, M. and Mühlethaler, M. (1989) Midbrain reticular neurones in vitro are sensitive to amines and opiates. Society of Neuroscience Abstracts 15: 451Google Scholar
Khateb, A., Serafin, M., Jones, B. E., Alonso, A. and Mühlethaler, M. (1991) Pharmacological study of basal forebrain neurons in guinea pig brain slices. Society for Neuroscience Abstracts 17: 881Google Scholar
Khateb, A., Fort, P., Alonso, A., Jones, B. E. and Mühlethaler, M. (1993) Pharmacological and immunohistochemical evidence for serotonergic modulation of cholinergic nucleus basalis neurons. European Journal of Neuroscience 5: 541–547CrossRefGoogle ScholarPubMed
Khazipov, R., Esclapez, M., Caillard, O., Bernard, C., Khalikov, I., Tyzio, R., Hirsch, J., Dzhala, V., Berger, B. and Ben-Ari, Y. (2001) Early development of neuronal activity in the primate hippocampus in utero. Journal of Neuroscience 21: 9770–9781CrossRefGoogle ScholarPubMed
Kia, H. K., Miquel, M. C., Brisorgeuil, M. J., Daval, G., Riad, M., Mestikawy, S., Hamon, M. and Verge, D. (1996) Immunocytochemical localization of serotonin 1A receptors in the rat central nervous system. Journal of Comparative Neurology 365: 289–3053.0.CO;2-1>CrossRefGoogle Scholar
Killam, K. F., Killam, E. K. and Naquet, R. (1967) An animal model of light sensitive epilepsy. Electroencephalography and Clinical Neurophysiology 22: 497–513CrossRefGoogle ScholarPubMed
Kim, D., Song, I., Keum, S., Lee, T., Jeong, M. J., Kim, S. S., McEnery, M. W. and Shin, H. S. (2001) Lack of the burst firing of thalamocortical relay neurons and resistance to absence seizures in mice lacking α1G T-type Ca2+ channels. Neuron 31: 35–45CrossRefGoogle Scholar
Kim, U. and McCormick, D. A. (1998) Functional and ionic properties of a slow afterhyperpolarization in ferret perigeniculate neurons in vitro. Journal of Neurophysiology 80: 1222–1235CrossRefGoogle ScholarPubMed
Kim, U., Bal, T. and McCormick, D. A. (1995) Spindle waves are propagating synchronized oscillations in the ferret LGNd in vitro. Journal of Neurophysiology 74: 1301–1323CrossRefGoogle ScholarPubMed
Kim, U., Sanchez-Vives, M. V. and McCormick, D. A. (1997) Functional dynamics of GABAergic inhibition in the thalamus. Science 278: 130–134CrossRefGoogle ScholarPubMed
Kinomura, S., Larsson, J., Gulyás, B. and Roland, P. (1996) Activation by attention of the human reticular formation and thalamic intralaminar nuclei. Science 271: 512–515CrossRefGoogle ScholarPubMed
Kita, Y. and Kitai, S. T. (1990) Electrophysiological properties of pedunculopontine neurons and their postsynaptic responses following stimulation of substantia nigra pars reticulata. Brain Research 535: 79–95Google Scholar
Kitsikis, A. and Steriade, M. (1981) Immediate behavioral effects of kainic acid injections into the midbrain reticular core. Behavioral Brain Research 3: 361–380CrossRefGoogle ScholarPubMed
Kleitman, N. (1963) Sleep and Wakefulness. Chicago: University of Chicago Press
Kleitman, N. (1993) Basic rest-activity cycle. In Encyclopedia of Sleep and Dreaming, ed. M. A. Carskadon, pp. 65–66, New York: Macmillan
Klink, R. and Alonso, A. (1997a) Muscarinic modulation of the oscillatory and repetitive firing properties of entorhinal cortex layer II neurons. Journal of Neurophysiology 77: 1813–1828CrossRefGoogle Scholar
Klink, R. and Alonso, A. (1997b) Ionic mechanisms of muscarinic depolarization in entorhinal cortex layer II neurons. Journal of Neurophysiology 77: 1829–1843CrossRefGoogle Scholar
Klüver, H. and Bucy, P. C. (1937) An analysis of certain effects of bilateral lobectomy in the rhesus monkey, with special reference to “psychic blindness”. Journal of Psychology 5: 33–54CrossRefGoogle Scholar
Knight, A. R. and Bowery, N. G. (1992) GABA receptors in rats with spontaneous generalized nonconvulsive epilepsy. Journal of Neural Transmission 35 (Suppl.): 189–196Google ScholarPubMed
Knowles, W. D. and Schwartzkroin, P. A. (1981) Local circuit synaptic interactions in hippocampal brain slices. Journal of Neuroscience 1: 318–322CrossRefGoogle ScholarPubMed
Kobayashi, K., Nishibayashi, N., Ohtsuka, Y., Oka, E. and Ohtahara, S. (1994) Epilepsy with electrical status epilepticus during slow sleep and secondary bilateral synchrony. Epilepsia 35: 1097–1103CrossRefGoogle ScholarPubMed
Konorski, J. (1967) Integrative Activity of the Brain. Chicago: University of Chicago Press
Kosaka, T., Kosaka, K., Hataguchi, Y., Nagatsu, I., Wu, J. Y., Ottersen, O. P., Storm-Mathisen, J. and Hama, K. (1987) Catecholaminergic neurons containing GABA-like and/or glutamic acid decarboxylase-like immunoreactivities in various brain regions of the rat. Experimental Brain Research 66: 191–201CrossRefGoogle ScholarPubMed
Kostopoulos, G. (1992) The tottering mouse: a critical review of its usefulness in the study of neuronal mechanisms underlying epilepsy. Journal of Neural Transmission 35 (Suppl.): 21–36Google Scholar
Kostopoulos, G. (2000) Spike-and-wave discharges of absence seizures as a transformation of sleep spindles: the continuing development of a hypothesis. Clinical Neurophysiology 111 (Suppl. 2): S27–S38CrossRefGoogle ScholarPubMed
Kotagal, P. (1995) Multifocal independent spike syndrome: relationship to hypsarrhthymia and the slow spike-wave (Lennox-Gastaut) syndrome. Clinical Electroencephalography 26: 23–29CrossRefGoogle ScholarPubMed
Kotila, M. and Waltimo, O. (1992) Epilepsy after stroke. Epilepsia 33: 495–498CrossRefGoogle ScholarPubMed
Koukkou, M. and Lehmann, D. (1968) EEG and memory storage in sleep experiments with humans. Electroencephalography and Clinical Neurophysiology 25: 455–462CrossRefGoogle ScholarPubMed
Kreindler, A. (1965) Experimental Epilepsy. Progress in Brain Research (vol. 19), Amsterdam: Elsevier
Kreindler, A. and Steriade, M. (1963) Functional differentiation within the amygdaloid complex inferred from peculiarities of afterdischarges. Electroencephalography and Clinical Neurophysiology 15: 811–826CrossRefGoogle Scholar
Kreindler, A. and Steriade, M. (1964) EEG patterns of arousal and sleep induced by stimulating various amygdaloid levels in the cat. Archives Italiennes de Biologie 102: 576–586Google ScholarPubMed
Kreindler, A., Zuckermann, E., Steriade, M. and Chimion, D. (1958) Electroclinical features of the convulsive fit induced experimentally through stimulation of the brain stem. Journal of Neurophysiology 21: 430–436CrossRefGoogle Scholar
Krnjević, K., Pumain, R. and Renaud, L. (1971) The mechanisms of excitation by acetylcholine in the cerebral cortex. Journal of Physiology (London) 215: 247–268CrossRefGoogle Scholar
Krueger, J. M. and Toth, L. A. (1994) Cytokines as regulators of sleep. Annals of New York Academy of Sciences 739: 299–310CrossRefGoogle Scholar
Krueger, J. M., Pappenheimer, J. R. and Karnovsky, M. L. (1982) Sleep-promoting effects of muramyl peptides. Proceedings of the National Academy of Sciences of the USA 79: 6102–6106CrossRefGoogle ScholarPubMed
Krueger, J. M., Walter, J., Karnovsky, M. L., Chedid, L., Choay, J. P., Lefrancier, P. and Lederer, E. (1984) Muramyl peptides. Variation of somnogenic activity with structure. Journal of Experimental Medicine 159: 68–76CrossRefGoogle ScholarPubMed
Krueger, J. M., Obal, F. Jr. and Fang, J. (1999) Humoral regulation of physiological sleep: cytokines and GHRH. Journal of Sleep Research 8 (Suppl. 1): 53–59CrossRefGoogle ScholarPubMed
Krushinsky, L. V. (1962) Study of pathophysiological mechanism of cerebral haemorrhages provoked by reflex epileptic seizures in rats. Epilepsia 3: 363–380CrossRefGoogle Scholar
Kudrimoti, H. S., Barnes, C. A. and McNaughton, B. L. (1999) Reactivation of hippocampal cell assemblies: effects of behavioral state, experience, and EEG dynamics. Journal of Neuroscience 19: 4090–4101CrossRefGoogle ScholarPubMed
Lacaille, J. C. and Schwartzkroin, P. A. (1988a) Stratum lacunosum-moleculare interneurons of hippocampal CA1 region. I. Intracellular response characteristics, synaptic responses and morphology. Neuroscience 8: 1400–1410CrossRefGoogle Scholar
Lacaille, J. C. and Schwartzkroin, P. A. (1988b) Stratum lacunosum-moleculare interneurons of hippocampal CA1 region. II. Intrasomatic and intradendritic recordings of local circuit synaptic interactions. Neuroscience 8: 1411–1424CrossRefGoogle Scholar
Lai, Y. Y., Clements, J. R. and Siegel, J. M. (1993) Glutamatergic and cholinergic projections to the pontine inhibitory area identified with horseradish peroxidase retrograde transport and immunohistochemistry. Journal of Comparative Neurology 336: 321–330CrossRefGoogle ScholarPubMed
Lampl, I., Reichova, I. and Ferster, D. (1999) Synchronous membrane potential fluctuations in neurons of the cat visual cortex. Neuron 22: 361–374CrossRefGoogle ScholarPubMed
Lancel, M., Riezen, H. and Glatt, A. (1992) The time course of σ activity and slow-wave activity during NREMS in cortical and thalamic EEG of the cat during baseline and after 12 hours of wakefulness. Brain Research 596: 285–295CrossRefGoogle ScholarPubMed
Landisman, C. E., Long, M. A., Beierlein, M., Deans, M. R., Paul, D. L. and Connors, B. W. (2002) Electrical synapses in the thalamic reticular nucleus. Journal of Neuroscienc 22: 1002–1009Google ScholarPubMed
Lang, E. J. and Paré, D. (1997) Synaptic and synaptically activated intrinsic conductances underlie inhibitory potentials in cat lateral amygdaloid projection neurons in vivo. Journal of Neurophysiology 77: 353–363CrossRefGoogle ScholarPubMed
Lang, E. J. and Paré, D. (1998) Synaptic responses of interneurons of the cat lateral amygdaloid nucleus. Neuroscience 83: 877–889CrossRefGoogle ScholarPubMed
Laureys, S., Peigneux, P., Phillips, C., Fuchs, S., Degueldre, C., Aerts, J., Del Fiore, G., Petiau, C., Luxen, A., Linden, M., Cleeremans, A., Smith, C. and Maquet, P. (2001) Experience-dependent changes in cerebral functional connectivity during human rapid eye movement sleep. Neuroscience 105: 521–525CrossRefGoogle ScholarPubMed
Lavoie, B. and Parent, A. (1994) Pedunculopontine nucleus in the squirrel monkey: distribution of cholinergic and monoaminergic neurons in the mesopontine tegmentum with evidence for the presence of glutamate in cholinergic neurons. Journal of Comparative Neurology 344: 190–209CrossRefGoogle ScholarPubMed
LeDoux, J. E. (1996) The Emotional Brain. New York: Simon and Schuster
LeDoux, J. E., Cicchetti, P., Xagoraris, A. and Romanski, L. M. (1990) The lateral amygdaloid nucleus: sensory interface of the amygdala in fear conditioning. Journal of Neuroscience 10: 1062–1069CrossRefGoogle ScholarPubMed
Lee, K. and McCormick, D. A. (1996) Abolition of spindle oscillations by serotonin and norepinephrine in the ferret lateral geniculate and perigeniculate nuclei in vitro. Neuron 17: 309–321CrossRefGoogle ScholarPubMed
Lehmann, T. N., Gabriel, S., Kovacs, R., Eilers, A., Kivi, A., Schulze, K., Lanksch, W. R., Meencke, H. J. and Heinemann, U. (2000) Alterations in neuronal connectivity in area CA1 of hippocampal slices from temporal lobe epilepsy patients and pilocarpine-treated epileptic rats. Epilepsia 41 (Suppl. 6): S190–S194CrossRefGoogle ScholarPubMed
Lemieux, J. F. and Blume, W. T. (1986) Topographical evolution of spike-wave complexes. Brain Research 373: 275–287CrossRefGoogle ScholarPubMed
Lennox, W. G. (1951) Phenomena and correlates of the psychomotor triad. Archives of Neurology 1: 357–371CrossRefGoogle ScholarPubMed
Lennox, W. G. and Lennox, M. A. (1960) Epilepsy and Related Disorders. London: Churchill
Leonard, C. S. and Llinás, R. R. (1990) Electrophysiology of mammalian pedunculopontine and laterodorsal tegmental neurons in vitro: implications for the control of REM sleep. In Brain Cholinergic Systems, ed. M. Steriade and D. Biesold, pp. 205–223, Oxford: Oxford University Press
Leonard, C. S. and Llinás, R. R. (1994) Serotonergic and cholinergic inhibition of mesopontine cholinergic neurons controlling REM sleep: an in vitro electrophysiological study. Neuroscience 59: 309–330CrossRefGoogle Scholar
Leonard, C. S., Rao, S. and Sanchez, R. M. (1995) Patterns of neuromodulation and the nitric oxide signaling pathway in mesopontine cholinergic neurons. Seminars in the Neurosciences, ed. M. Steriade, 7: 319–328CrossRefGoogle Scholar
Leonard, C. S., Michaelis, E. K. and Mitchell, K. M. (2001) Activity-dependent nitric oxide concentration dynamics in the laterodorsal tegmental nucleus in vitro. Journal of Neurophysiology 86: 2159–2172CrossRefGoogle ScholarPubMed
Leresche, N., Jassik-Gerschenfeld, D., Haby, M., Soltesz, I. and Crunelli, V. (1990) Pacemaker-like and other types of spontaneous membrane potential oscillations of thalamocortical cells. Neuroscience Letters 113: 72–77CrossRefGoogle ScholarPubMed
Leresche, N., Lightowler, S., Soltesz, I., Jassik-Gerschenfeld, D. and Crunelli, V. (1991) Low-frequency oscillatory activities intrinsic to rat and cat thalamocortical cells. Journal of Physiology (London) 441: 155–174CrossRefGoogle ScholarPubMed
Leresche, N., Parri, H. R., Erdemli, G., Guyon, A., Turner, J. P., Williams, S. R., Asprodini, E. and Crunelli, V. (1998) On the action of the anti-absence drug ethosuximide in the rat and cat thalamus. Journal of Neuroscience 18: 4842–4853CrossRefGoogle ScholarPubMed
Leresche, N., Asprodini, E., Emri, Z., Cope, D. W. and Crunelli, V. (2000) Somatostatin inhibits GABAergic transmission in the sensory thalamus via presynaptic receptors. Neuroscience 98: 513–522CrossRefGoogle ScholarPubMed
Leschinger, A., Stabel, J., Igelmund, P. and Heinemann, U. (1993) Pharmacological and electrographic properties of epileptiform activity induced by elevated K+ and lowered Ca2+ and Mg2+ concentration in rat hippocampal slices. Experimental Brain Research 96: 230–240CrossRefGoogle ScholarPubMed
Letinic, K. and Rakic, P. (2001) Telencephalic origin of human thalamic GABAergic neurons. Nature Neuroscience 4: 931–936CrossRefGoogle ScholarPubMed
Lévesque, M., Charara, A., Gagnon, S., Parent, A. and Deschênes, M. (1996) Corticostriatal projections from layer V cells in rat are collaterals of long-range corticofugal axons. Brain Research 709: 311–315CrossRefGoogle Scholar
Levi, G. and Gallo, V. (1995) Release of neuroactive amino acids from glia. In Neuroglia, ed. H. Kettenmann and B. R. Ransom, pp. 815–826, New York: Oxford University Press
Li, C. L. and McIlwain, H. (1957) Maintenance of resting membrane potentials in slices of mammalian cerebral cortex and other tissues in vitro. Journal of Physiology (London) 139: 178–190CrossRefGoogle ScholarPubMed
Li, X. G., Somogyi, P., Ylinen, A. and Buzsáki, G. (1994) The hippocampal CA3 network: an in vivo intracellular labeling study. Journal of Comparative Neurology 339: 181–208CrossRefGoogle Scholar
Lin, J. S., Sakai, K. and Jouvet, M. (1988) Evidence for histaminergic arousal mechanisms in the hypothalamus of cats. Neuropharmacology 27: 111–122CrossRefGoogle Scholar
Lin, J. S., Sakai, K., Vanni-Mercier, G. and Jouvet, M. (1989) A critical role of the posterior hypothalamus in the mechanisms of wakefulness determined by microinjections of muscimol in freely moving cats. Brain Research 479: 225–240CrossRefGoogle ScholarPubMed
Lingenhoehl, K., Brom, R., Heid, J., Beck, P., Froestl, W., Kaupmann, K., Bettler, B. and Mosbacher, J. (1999) γ-hydroxybutyrate is a weak agonist at recombinant GABAB receptors. Neuropharmacology 38: 1667–1674CrossRefGoogle Scholar
Lipman, I. J. and Hughes, J. R. (1968) Rhythmic mid-temporal discharges. Electroencephalography and Clinical Neurophysiology 27: 43–47CrossRefGoogle Scholar
Lisman, J. E. (1997) Bursts as a unit of neural information: making unreliable synapses reliable. Trends in Neurosciences 20: 38–43CrossRefGoogle ScholarPubMed
Litt, B., Esteller, R., Echauz, J., D'Alessandro, M., Shor, R., Henry, T., Pennell, P., Epstein, C., Bakay, R., Dichter, M. and Vachtsevanos, G. (2001) Epileptic seizures may begin hours in advance of clinical onset: a report of five patients. Neuron 30: 51–64CrossRefGoogle ScholarPubMed
Liu, X. B. and Jones, E. G. (1999) Predominance of corticothalamic synaptic inputs to thalamic reticular nucleus neurons in the rat. Journal of Comparative Neurology 414: 67–793.0.CO;2-Z>CrossRefGoogle ScholarPubMed
Liu, X. B., Warren, R. A. and Jones, E. G. (1995) Synaptic distribution of afferents from reticular nucleus in ventroposterior nucleus of cat thalamus. Journal of Comparative Neurology 352: 187–202CrossRefGoogle ScholarPubMed
Liu, X. B., Bolea, S., Golshani, P. and Jones, E. G. (2001) Differentiation of corticothalamic and collateral thalamocortical synapses on mouse reticular nucleus by EPSC amplitude and AMPA receptor subunit composition. Thalamus and Related Systems 1: 15–29Google Scholar
Liu, Z., Vergnes, M., Depaulis, A. and Marescaux, C. (1992) Involvement of intrathalamic GABAB neurotransmission in the control of absence seizures in the rat. Neuroscience 48: 87–93CrossRefGoogle ScholarPubMed
Livingstone, M. S. and Hubel, D. H. (1981) Effects of sleep and arousal on the processing of visual information in the cat. Nature 291: 554–561CrossRefGoogle ScholarPubMed
Llinás, R. R. (1964) Mechanisms of supraspinal action upon spinal cord activities. Differences between reticular and cerebellar inhibitory action upon alpha extensor motorneurones. Journal of Neurophysiology 27: 1117–1126CrossRefGoogle Scholar
Llinás, R. R. (1985) Electrotonic transmission in the mammalian central nervous system. In Gap Junctions, ed. M. V. L. Bennett, pp. 337–353, New York: Cold Harbor Spring
Llinás, R. R. (1988) The intrinsic electrophysiological properties of mammalian neurons: insights into central nervous system function. Science 242: 1654–1664CrossRefGoogle ScholarPubMed
Llinás, R. R. and Paré, D. (1991) Of dreaming and wakefulness. Neuroscience 44: 521–535CrossRefGoogle ScholarPubMed
Llinás, R. R. and Ribary, U. (1993) Coherent 40-Hz oscillation characterizes dream state in humans. Proceedings of the National Academy of Sciences of the USA 90: 2078–2081CrossRefGoogle ScholarPubMed
Llinás, R. R. and Terzuolo, C. A. (1964) Mechanisms of supraspinal actions upon spinal cord activities. Reticular inhibitory mechanisms on alpha-extensor motoneurons. Journal of Neurophysiology 27: 579–591CrossRefGoogle ScholarPubMed
Llinás, R., Grace, A. A. and Yarom, Y. (1991) In vitro neurons in mammalian cortical layer 4 exhibit intrinsic oscillatory activity in the 10- to 50-Hz frequency range. Proceedings of the National Academy of Sciences of the USA 88: 897–901CrossRefGoogle ScholarPubMed
Llinás, R., Ribary, U., Jeanmonod, D., Kronberg, E. and Mitra, P. P. (1999) Thalamocortical dysrhythmia: a neurological and neuropsychiatric syndrome characterized by magneto-encephalography. Proceedings of the National Academy of Sciences of the USA 96: 15222–15227CrossRefGoogle Scholar
Llinás, R., Ribary, U., Jenamonod, D., Cancro, R., Kronberg, E., Schulman, J., Zonenshayn, M., Magnin, M., Morel, A. and Siegemund, M. (2001) Thalamocortical dysrhythmia. I. Functional and imaging aspects. Thalamus and Related Systems 1: 237–244Google Scholar
Loiseau, P. (1992) Human absence epilepsies. Journal of Neural Transmission 35 (Suppl.): 1–6Google ScholarPubMed
Loomis, A. L., Harvey, N. and Hobart, G. A. (1938) Distribution of disturbance patterns in the human electroencephalogram, with special reference to sleep. Journal of Neurophysiology 1: 413–430CrossRefGoogle Scholar
Lopantsev, V. and Avoli, M. (1998) Participation of GABAA-mediated inhibition in ictal-like discharges in the rat entorhinal cortex. Journal of Neurophysiology 79: 352–360CrossRefGoogle Scholar
Lopes da Silva, F. H., Rotterdam, A., Storm van Leeuwen, W. and Tielen, A. M. (1970) Dynamic characteristics of visual evoked potentials in the dog. II. Beta frequency selectivity in evoked potentials and background activity. Electroencephalography and Clinical Neurophysiology 29: 260–268CrossRefGoogle ScholarPubMed
Lopes da Silva, F. H., Witter, M. P., Boeijinga, P. H. and Lohman, A. H. M. (1990) Anatomic organization and physiology of the limbic system. Physiological Reviews 70: 453–511CrossRefGoogle Scholar
Lopes da Silva, F. H., Kamphuis, W., Titulaer, M., Vreugdenhil, M. and Wadman, W. J. (1995) An experimental model of progressive epilepsy: the development of kindling of the hippocampus of the rat. Italian Journal of Neurological Sciences 16: 45–57CrossRefGoogle ScholarPubMed
LoPiccolo, M. A. (1977) Behavioral and Neuronal Effects of EEG Synchronizing Stimuli in the Cat. Ph.D. Thesis, McMaster University, Hamilton (Ontario)
Lorente de Nó, R. (1933) Studies on the structure of the cerebral cortex. I. The area entorhinalis. Journal of Psychology and Neurology 45: 381–438Google Scholar
Loszádi, D. A. (1995) Organization of connections between the thalamic reticular and the anterior thalamic nuclei in the rat. Journal of Comparative Neurology 358: 233–246CrossRefGoogle Scholar
Lothman, E. W., Bertram, E. H. and Stringer, J. L. (1991) Functional anatomy of hippocampal seizures. Progress in Neurobiology 37: 1–82CrossRefGoogle ScholarPubMed
Loup, F., Wieser, H. G., Yonekawa, Y., Aguzzi, A. and Fritschy, J. M. (2000) Selective alterations in GABAA receptor subtypes in human temporal lobe epilepsy. Journal of Neuroscience 20: 5401–5419CrossRefGoogle ScholarPubMed
Lübke, J. I., Greene, R. W., Semba, K., Kamondi, A., McCarley, R. W. and Reiner, P. B. (1992) Serotonin hyperpolarizes cholinergic low-threshold burst neurons in the rat laterodorsal tegmental nucleus in vitro. Proceedings of the National Academy of Sciences of the USA 89: 743–747CrossRefGoogle Scholar
Luciani, L. (1911) Fisiologia dell'uomo. Milano: Societa Editrice Libraria
Lucretius, T. C. (1988) On the Nature of the Universe (translated by R. E. Latham). London: Penguin Books
Lüders, H. O., Engel, J. Jr. and Munari, C. (1993) General principles. In Surgical Treatment of the Epilepsies, ed. J. Engel Jr., pp. 137–153, New York: Raven
Luhmann, H. J., Mittmann, T., Schmidt-Kastner, R., Eysel, U. T., Mudrick-Donnon, L. A. and Heinemann, U. (1999) Hyperexcitability after focal lesions and transient ischemia in rat neocortex. In Progressive Nature of Epileptogenesis (Epilepsy Research, Suppl. 12), ed. U. Heinemann, pp. 119–128, Amsterdam: Elsevier
Lüthi, A. and McCormick, D. A. (1998) Periodicity of thalamic synchronized oscillations: the role of Ca2+-mediated upregulation of IH. Neuron 20: 553–63CrossRefGoogle ScholarPubMed
Lux, H. D. and Neher, E. (1973) The equilibrium time course of [K+]o in cat cortex. Experimental Brain Research 17: 190–205CrossRefGoogle Scholar
Lydic, R., McCarley, R. W. and Hobson, J. A. (1987) Serotonin neurons and sleep. II. Time course of dorsal raphe discharge frequency, PGO waves, and behavioral states. Archives Italiennes de Biologie 126: 1–28Google Scholar
Lytton, W. W. and Sejnowski, T. J. (1991) Simulation of cortical pyramidal neurons synchronized by inhibitory interneurons. Journal of Neurophysiology 66: 1059–1079CrossRefGoogle ScholarPubMed
Lytton, W. W., Contreras, D., Destexhe, A. and Steriade, M. (1997) Dynamic interactions determine partial thalamic quiescence in a computer network model of spike-and-wave seizures. Journal of Neurophysiology 77: 1679–1696CrossRefGoogle Scholar
MacDonald, K. D., Fifkova, E., Jones, M. S. and Barth, D. S. (1998) Focal stimulation of the thalamic reticular nucleus induces focal gamma waves in cortex. Journal of Neurophysiology 79: 474–477CrossRefGoogle ScholarPubMed
Macnish, R. (1830) The Philosophy of Sleep. Glasgow: M'Phun
MacVicar, B. A. (1985) Depolarizing prepotentials are Na+-dependent in CA1 pyramidal neurons. Brain Research 333: 378–381CrossRefGoogle ScholarPubMed
MacVicar, B. A. and Dudek, F. E. (1981) Electrotonic coupling between pyramidal cells: a direct demonstration in rat hippocampal slices. Science 213: 782–785CrossRefGoogle ScholarPubMed
MacVicar, B. A. and Dudek, F. E. (1982) Electrotonic coupling between granule cells of rat dentate gyrus. Physiological and anatomical evidence. Journal of Neurophysiology 47: 579–592CrossRefGoogle ScholarPubMed
MacVicar, B. A., Tse, F. W., Crichton, S. A. and Kettenmann, H. (1989) GABA-activated Cl- channels in astrocytes of hippocampal slices. Journal of Neuroscience 9: 3577–3583CrossRefGoogle ScholarPubMed
Maffei, L., Moruzzi, G. and Rizzolatti, G. (1965) Influence of sleep and wakefulness on the response of lateral geniculate units to sinewave photic stimulation. Archives Italiennes de Biologie 103: 596–608Google ScholarPubMed
Magee, J., Hoffman, D., Colbert, C. and Johnston, D. (1998) Electrical and calcium signaling in dendrites of hippocampal pyramidal neurons. Annual Reviews of Physiology 60: 327–346CrossRefGoogle ScholarPubMed
Magill, P. J., Bolam, P. and Bevan, M. D. (2000) Relationship of activity in the subthalamic nucleus – globus pallidus network to cortical EEG. Journal of Neuroscience 20: 820–833CrossRefGoogle Scholar
Magill, P. J., Bolam, J. P. and Bevan, M. D. (2001) Dopamine regulates the impact of the cerebral cortex on the subthalamic nucleus-globus pallidus network. Neuroscience 106: 313–330CrossRefGoogle ScholarPubMed
Magistris, M. R., Mouradian, M. S. and Gloor, P. (1988) Generalized convulsions induced by pentylenetetrazol in the cat: participation of forebrain, brainstem, and spinal cord. Epilepsia 29: 379–388CrossRefGoogle ScholarPubMed
Mahon, S., Deniau, J. M. and Charpier, S. (2001) Relationship between EEG potentials and intracellular activity of striatal and cortico-striatal neurons: an in vivo study under different anesthetics. Cerebral Cortex 11: 360–373CrossRefGoogle Scholar
Mahowald, M. K. and Schenck, C. H. (1997) Sleep disorders. In Epilepsy: A Comprehensive Textbook, ed. J. Engel Jr. and T. A. Pedley, pp. 2705–2715, Philadelphia: Lippincot-Raven
Malow, B. A., Fromes, G. A. and Aldrich, M. S. (1997) Usefulness of polysomnography in epilepsy patients. Neurology 48: 1389–1394CrossRefGoogle ScholarPubMed
Manaye, K. F., Zweig, R., Wu, D., Hersh, L. B., Lacalle, S., Saper, C. B. and German, D. C. (1999) Quantification of cholinergic and select non-cholinergic mesopontine neuronal populations in the human brain. Neuroscience 89: 759–770CrossRefGoogle ScholarPubMed
Mangan, P. S., Scott, C. A., Williamson, J. M. and Bertram, E. H. III (2000) Aberrant neuronal physiology in the basal nucleus of the amygdala in a model of chronic limbic epilepsy. Neuroscience 101: 377–391CrossRefGoogle Scholar
Manganotti, P., Zanette, G., Beltramello, A., Puppini, G., Miniussi, C., Maravita, A., Santorum, E., Marzi, C. A., Fiaschi, A. and Dalla Bernardina, B. (1999) Spike topography and fMRI in benign rolandic epilepsy with spikes evoked by tapping stimulation. Electroencephalography and Clinical Neurophysiology 107: 88–92CrossRefGoogle Scholar
Manor, Y., Koch, C. and Segev, I. (1991) Effect of geometrical irregularities on propagation delay in axonal trees. Biophysical Journal 60: 1424–1437CrossRefGoogle ScholarPubMed
Mao, B. Q., Hamzei-Sichani, F., Aronov, D., Froemke, R. C. and Yuste, R. (2001) Dynamics of spontaneous activity in neocortical slices. Neuron 32: 883–898CrossRefGoogle ScholarPubMed
Maquet, P. (2000) Functional neuroimaging of normal human sleep by positron emission tomography. Journal of Sleep Research 9: 207–231CrossRefGoogle ScholarPubMed
Maquet, P. and Phillips, C. (1998) Functional imaging of human sleep. Journal of Sleep Research 7 (Suppl. 1): 42–47CrossRefGoogle ScholarPubMed
Maquet, P., Dive, D., Salmon, E., Sadzot, B., Franco, G., Poirrier, R. and Franck, G. (1992) Cerebral glucose utilization during stage 2 sleep in man. Brain Research 571: 149–153CrossRefGoogle ScholarPubMed
Maquet, P., Péters, J. M., Aerts, J., Delfiore, G., Degueldre, C., Luxen, A. and Franck, G. (1996) Functional neuro-anatomy of human rapid-eye-movement sleep and dreaming. Nature 383: 163–166CrossRefGoogle Scholar
Maquet, P., Degueldre, C., Delfiore, G., Aerts, J., Péters, J. P., Luxen, A. and Franck, G. (1997) Functional neuroanatomy of human slow wave sleep. Journal of Neuroscience 17: 2807–2812CrossRefGoogle ScholarPubMed
Maquet, P., Laureys, S., Peigneux, P., Fuchs, S., Petiau, C., Phillips, C., Aerts, J., Del Fiore, G., Degueldre, C., Meulemans, T., Luxen, A., Franck, G., Van der Linden, M., Smith, C. and Cleeremans, A. (2000) Experience-dependent changes in cerebral activation during human REM sleep
Marco, P. and DeFelipe, J. (1997) Altered synaptic circuitry in the human temporal neocortex removed from epileptic patients. Experimental Brain Research 114: 1–10CrossRefGoogle ScholarPubMed
Marcus, E. M. and Watson, C. W. (1966) Bilateral synchronous spike-wave electrographic patterns in the cat. Archives of Neurology (Chicago) 14: 601–610CrossRefGoogle ScholarPubMed
Marcus, E. M., Watson, C. W. and Simon, S. A. (1968a) An experimental model of some varieties of petit mal epilepsy. Electrical-behavioral correlations of acute bilateral epileptogenic foci in cerebral cortex. Epilepsia 9: 233–248CrossRefGoogle Scholar
Marcus, E. M., Watson, C. W. and Simon, S. A. (1968b) Behavioral correlates of acute bilateral symmetrical epileptogenic foci in monkey cerebral cortex. Brain Research 9: 370–373CrossRefGoogle Scholar
Marescaux, C., Vergnes, M. and Bernusconi, R. (1992a) GABAB receptor antagonists: potential new anti-absence drugs. Journal of Neural Transmission 35 (Suppl.): 179–188Google Scholar
Marescaux, C., Vergnes, M. and Depaulis, A. (1992b) Genetic absence epilepsy in rats from Strasbourg – a review. Journal of Neural Transmission 35 (Suppl.): 37–69Google Scholar
Margerison, J. H. and Corsellis, J. A. N. (1966) Epilepsy and the temporal lobe: a clinical, electroencephalographic and neuropathological study of the brain in epilepsy, with particular reference to the temporal lobes. Brain 89: 499–530CrossRefGoogle ScholarPubMed
Marini, G., Macchi, G. and Mancia, M. (1992) Potentiation of electroencephalographic spindles by ibotenate microinjections into nucleus reticularis thalami of cats. Neuroscience 51: 759–762CrossRefGoogle ScholarPubMed
Mariño, J., Canedo, A. and Aguilar, J. (2000) Sensorimotor cortical influences on cuneate nucleus rhythmic activity in the anesthetized cat. Neuroscience 95: 657–673CrossRefGoogle ScholarPubMed
Markram, H. (1997) A network of tufted layer 5 pyramidal neurons. Cerebral Cortex 7: 523–533CrossRefGoogle ScholarPubMed
Markram, H. and Sakmann, B. (1994) Calcium transients in dendrites of neocortical neurons evoked by single subthreshold excitatory postsynaptic potentials via low-voltage-activated calcium channels. Proceedings of the National Academy of Sciences of the USA 91: 5207–5211CrossRefGoogle ScholarPubMed
Markram, H., Lübke, J., Frötscher, M., Roth, A. and Sakmann, B. (1997a) Physiology and anatomy of synaptic connections between thick tufted pyramidal neurones in the developing rat neocortex. Journal of Physiology (London) 500: 409–440CrossRefGoogle Scholar
Markram, H., Lübke, J., Frötscher, M. and Sakmann, B. (1997b) Regulation of synaptic efficacy by coincidence of postsynaptic APs and EPSPs. Science 275: 213–215CrossRefGoogle Scholar
Markram, H., Wang, M. and Tsodycs, M. (1998) Differential signaling via the same axon of neocortical pyramidal neurons. Proceedings of the National Academy of Sciences of the USA 95: 5323–5328CrossRefGoogle ScholarPubMed
Marshall, L. H. (1987) An annotated interview with Giuseppe Moruzzi, 1910–1986. Experimental Neurology 97: 225–242CrossRefGoogle Scholar
Marshall, L. H. and Magoun, H. W. (1998) Discoveries in the Human Brain – Neuroscience Prehistory, Brain Structure, and Function. Totowa, NJ: Humana Press
Marshall, L., Mölle, M., Fehm, H. L. and Born, J. (1998) Scalp recorded direct current brain potentials during human sleep. European Journal of Neuroscience 10: 1167–1178CrossRefGoogle ScholarPubMed
Martin, J. H. (1991) Autoradiographic estimation of the extent of reversible inactivation produced by microinjections of lidocaine and muscimol in the rat. Neuroscience Letters 127: 160–164CrossRefGoogle ScholarPubMed
Martin, J. H. and Ghez, C. (1988) Red nucleus and motor cortex: parallel motor systems for the initiation and control of skilled movement. Behavioral Brain Research 28: 217–223CrossRefGoogle ScholarPubMed
Martin, S. J., Grimwood, P. D. and Morris, R. G. M. (2000) Synaptic plasticity and memory: an evaluation of the hypothesis. Annual Reviews of Neuroscience 23: 649–711CrossRefGoogle ScholarPubMed
Martina, M., Royer, S. and Paré, D. (1999) Physiological properties of central medial and central lateral amygdala neurons. Journal of Neurophysiology 82: 1843–1854CrossRefGoogle ScholarPubMed
Martina, M., Vida, I. and Jonas, P. (2000) Distal initiation and active propagation of action potentials in interneuron dendrites. Science 287: 295–300CrossRefGoogle ScholarPubMed
Mason, A. and Larkman, A. (1990) Correlations between morphology and electrophysiology of pyramidal neurons in slices of rat visual cortex. II. Electrophysiology. Journal of Neuroscience 10: 1415–1428CrossRefGoogle ScholarPubMed
Masselmo, M. E. (1999) Neuromodulation: acetylcholine and memory consolidation. Trends in Cognitive Sciences 3: 351–359CrossRefGoogle Scholar
Massimini, M. and Amzica, F. (2001) Extracellular calcium fluctuations and intracellular potentials in the cortex during the slow sleep oscillation. Journal of Neurophysiology 85: 1346–1350CrossRefGoogle ScholarPubMed
Mathern, G. W., Babb, T. L., Pretorius, J. K. and Leite, J. P. (1995) Reactive synaptogenesis and neuron densities for neuropeptide Y, somatostatin, and glutamate decarboxylase immunoreactivity in the epileptogenic human fascia dentate. Journal of Neuroscience 15: 3990–4004CrossRefGoogle Scholar
Matsumoto, H. and Ajmone-Marsan, C. (1964) Cortical cellular phenomena in experimental epilepsy. Experimental Neurology 9: 286–304CrossRefGoogle ScholarPubMed
Matsumoto, H., Ayala, G. F. and Gumnit, R. J. (1969) Neuronal behavior and triggering mechanism in cortical epileptic focus. Journal of Neurophysiology 32: 688–703CrossRefGoogle ScholarPubMed
Mauguière, P. (1992) A consensus statement on relative merits of EEG and MEG. Electroencephalography and Clinical Neurophysiology 82: 317–319Google ScholarPubMed
McAllister, A. K., Katz, L. C. and Lo, D. C. (1999) Neurotrophins and synaptic plasticity. Annual Reviews of Neuroscience 22: 295–318CrossRefGoogle ScholarPubMed
McCarley, R. W. and Hobson, J. A. (1975) Neuronal excitability modulation over the sleep cycle: a structural and mathematical model. Science 189: 58–60CrossRefGoogle ScholarPubMed
McCarley, R. W. and Massequoi, S. G. (1986) A limit cycle mathematical model of the REM sleep oscillator system. American Journal of Physiology 251: R1033–R1036Google ScholarPubMed
McCarley, R. W., Benoit, O. and Barrionuevo, G. (1983) Lateral geniculate nucleus unitary discharge in sleep and waking: state- and rate-specific aspects. Journal of Neurophysiology 50: 798–818CrossRefGoogle ScholarPubMed
McCormick, D. A. (1989) GABA as an inhibitory neurotransmitter in the human cerebral cortex. Journal of Neurophysiology 62: 1018–1027CrossRefGoogle ScholarPubMed
McCormick, D. A. (1991) Functional properties of a slowly inactivating potassium current IAs in guinea pig dorsal lateral geniculate relay neurons. Journal of Neurophysiology 66: 1176–1189CrossRefGoogle ScholarPubMed
McCormick, D. A. (1992) Neurotransmitter actions in the thalamus and cerebral cortex and their role in neuromodulation of thalamocortical activity. Progress in Neurobiology 39: 337–388CrossRefGoogle ScholarPubMed
McCormick, D. A. and Contreras, D. (2001) On the cellular and network bases of epileptic seizures. Annual Reviews of Physiology 63: 815–846CrossRefGoogle ScholarPubMed
McCormick, D. A. and Krosigk, M. (1992) Corticothalamic activation modulates thalamic firing through glutamate metabotropic receptors. Proceedings of the National Academy of Sciences of the USA 89: 2774–2778CrossRefGoogle ScholarPubMed
McCormick, D. A. and Pape, H. C. (1988) Acetylcholine inhibits identified interneurons in the cat lateral geniculate nucleus. Nature 334: 246–248CrossRefGoogle ScholarPubMed
McCormick, D. A. and Pape, H. C. (1990a) Properties of a hyperpolarization-activated cation current and its role in rhythmic oscillation in thalamic relay neurones. Journal of Physiology (London) 431: 291–318CrossRefGoogle Scholar
McCormick, D. A. and Pape, H. C. (1990b) Noradrenergic and serotonergic modulation of a hyperpolarization-activated cation current in thalamic relay cells. Journal of Physiology (London) 431: 319–342CrossRefGoogle Scholar
McCormick, D. A. and Prince, D. A. (1986) Acetylcholine induces burst firing in thalamic reticular neurones by activating a K+ conductance. Nature 319: 147–165CrossRefGoogle Scholar
McCormick, D. A. and Prince, D. A. (1987) Actions of acetylcholine in the guinea pig and cat medial and lateral geniculate nuclei, in vitro. Journal of Physiology (London) 392: 147–165CrossRefGoogle ScholarPubMed
McCormick, D. A. and Prince, D. A. (1988) Noradrenergic modulation of firing pattern in guinea pig and cat thalamic neurones, in vitro. Journal of Neurophysiology 59: 978–996CrossRefGoogle Scholar
McCormick, D. A. and Wang, Z. (1991) Serotonin and noradrenaline excite GABAergic neurones of the guinea-pig and cat nucleus reticularis thalami. Journal of Physiology (London) 442: 235–255CrossRefGoogle ScholarPubMed
McCormick, D. A. and Williamson, A. (1991) Modulation of neuronal firing mode in cat and guinea-pig LGNd by histamine: possible cellular mechanisms of histaminergic control of arousal. Journal of Neuroscience 11: 3188–3199CrossRefGoogle ScholarPubMed
McCormick, D. A., Connors, B. W., Lighthall, J. W. and Prince, D. A. (1985) Comparative electrophysiology of pyramidal and sparsely spiny stellate neurons of the neocortex. Journal of Neurophysiology 54: 782–806CrossRefGoogle ScholarPubMed
McDonald, A. J. (1994) Calretinin immunoreactive neurons in the basolateral amygdala of the rat and monkey. Brain Research 667: 238–242CrossRefGoogle ScholarPubMed
McDonald, A. J. and Augustine, J. R. (1993) Localization of GABA-like immunoreactivity in the monkey amygdala. Neuroscience 52: 281–294CrossRefGoogle ScholarPubMed
McGinty, D. J. and Harper, R. M. (1976) Dorsal raphe neurons: depression of firing during sleep in cats. Brain Research 101: 569–575CrossRefGoogle ScholarPubMed
McGinty, D. J. and Sterman, M. B. (1968) Sleep suppression after basal forebrain lesions in the cat. Science 160: 1253–1255CrossRefGoogle ScholarPubMed
McKeown, M. J. and McNamara, J. O. (2001) When do epileptic seizures really begin?Neuron 30: 1–3CrossRefGoogle ScholarPubMed
McKeown, M. J., Humphries, C., Iragui, V. and Sejnowski, T. J. (1999) Spatially fixed patterns account for the spike and wave features in absence seizures. Brain Tomography 12: 107–116CrossRefGoogle ScholarPubMed
McNaughton, B. L., Barnes, C. A. and Andersen, P. (1981) Synaptic efficacy and EPSP summation in granule cells of rat fascia dentata studied in vitro. Journal of Neurophysiology 46: 952–966CrossRefGoogle ScholarPubMed
Meeren, H. K. M., Pijn, J. P. M., Luijtelaar, E. J. L. M., Coenen, A. M. L. and Lopes da Silva, F. H. (2002) Cortical focus drives widespread corticothalamic networks during spontaneous absence seizures in rats. Journal of Neuroscience 22: 1480–1495CrossRefGoogle ScholarPubMed
Meis, S., Munsch, T. and Pape, H. C. (2002) Antioscillatory effects of nociceptin/orphanin FQ in synaptic networks of the rat thalamus. Journal of Neuroscience 22: 718–727CrossRefGoogle ScholarPubMed
Merica, H., Blois, R., Fortune, R. D. and Gaillard, J. M. (1997) Evolution of delta activity within the nonREM sleep episode: a biphasic hypothesis. Physiology and Behavior 62: 213–219CrossRefGoogle ScholarPubMed
Merlet, I., Garcia-Larrea, L., Grégoire, M. C., Lavenne, F. and Mauguière, F. (1996) Source propagation of interictal spikes in temporal lobe epilepsy. Brain 119: 377–392CrossRefGoogle ScholarPubMed
Metherate, R., Cox, C. L. and Ashe, J. H. (1992) Cellular bases of neocortical activation: modulation of neural oscillations by the nucleus basalis and endogenous acetylcholine. Journal of Neuroscience 12: 4701–4711CrossRefGoogle ScholarPubMed
Miles, R. and Wong, R. K. S. (1983) Single neurones can initiate synchronized population discharges in the hippocampus. Nature 306: 371–373CrossRefGoogle ScholarPubMed
Miles, R. and Wong, R. K. S. (1987) Latent synaptic pathways revealed after titanic stimulation in the hippocampus. Nature 329: 724–726CrossRefGoogle Scholar
Miles, R., Toth, K., Gulyas, A. I., Hajos, N. and Freund, T. F. (1996) Differences between somatic and dendritic inhibition in the hippocampus. Neuron 16: 815–823CrossRefGoogle ScholarPubMed
Miller, L. A., McLachlan, R. S., Bouwer, M. S., Hudson, L. P. and Munoz, M. G. (1994) Amygdalar sclerosis: preoperative indicators and outcome after temporal lobe lobectomy. Journal of Neurology, Neurosurgery and Psychiatry 57: 1099–1105CrossRefGoogle Scholar
Minamimoto, T. and Kimura, M. (2002) Participation of the thalamic CM-Pf complex in attentional orienting. Journal of Neurophysiology 87: 3090–3101CrossRefGoogle ScholarPubMed
Mineff, E. M. and Weinberg, R. J. (2000) Differential synaptic distribution of AMPA receptor subunits in the ventral posterior and reticular thalamic nuclei of the rat. Neuroscience 101: 969–982CrossRefGoogle ScholarPubMed
Mitchell, S. J. and Ranck, J. B. J. (1980) Generation of theta rhythm in medial entorhinal cortex of freely moving rats. Brain Research 189: 49–66CrossRefGoogle ScholarPubMed
Miyauchi, T., Nomura, Y., Ohno, S., Kishimoto, H. and Matsushita, M. (1988) Positron emission tomography in three cases of Lennox-Gastaut syndrome. Japanese Journal of Psychiatry Neurology 42: 795–804Google ScholarPubMed
Mody, I. (1998) Ion channels in epilepsy. International Review of Neurobiology 42: 199–226CrossRefGoogle ScholarPubMed
Mogilner, A. I., Benabid, A. L. and Rezai, A. (2001) Brain stimulation: current applications and future prospects. Thalamus and Related Systems 1: 255–267Google Scholar
Mölle, M., Marshall, L., Gais, S. and Born, J. (2003) Grouping of spindle activity during slow oscillations in human non-REM sleep. Journal of Neuroscience 22: 10941–10947CrossRefGoogle Scholar
Monckton, J. E. and McCormick, D. A. (2002) The neuromodulatory role of serotonin in the ferret thalamus. Journal of Neurophysiology, in pressCrossRefGoogle ScholarPubMed
Montero, V. M. (1987) Ultrastructural identification of synaptic terminals from the axon of type 3 interneurons in the cat lateral geniculate nucleus. Journal of Comparative Neurology 264: 268–283CrossRefGoogle ScholarPubMed
Montero, V. M. (1991) A quantitative study of synaptic contacts on interneurons and relay cells of the cat lateral geniculate nucleus. Experimental Brain Research 86: 257–270CrossRefGoogle ScholarPubMed
Montero, V. M. and Singer, W. (1985) Ultrastructural identification of somata and neural processes immunoreactive to antibodies against glutamic acid decarboxylase (GAD) in the dorsal lateral geniculate nucleus of the cat. Experimental Brain Research 59: 151–165CrossRefGoogle ScholarPubMed
Moody, W. J. Jr., Futamachi, K. J. and Prince, D. A. (1974) Extracellular potassium activity during epileptogenesis. Experimental Neurology 42: 248–263CrossRefGoogle ScholarPubMed
Morales, F. R. and Chase, M. H. (1978) Intracellular recording of lumbar motoneuron membrane potential during sleep and wakefulness. Experimental Neurology 62: 821–827CrossRefGoogle ScholarPubMed
Morimoto, K., Dragunow, M. and Goddard, G. V. (1986) Deep prepyriform cortex kindling and its relation to amygdala kindling in the rat. Experimental Neurology 94: 637–648CrossRefGoogle ScholarPubMed
Morin, D. and Steriade, M. (1981) Development from primary to augmenting responses in the somatosensory system. Brain Research 205: 49–66CrossRefGoogle ScholarPubMed
Morin, F., Beaulieu, C. and Lacaille, J. C. (1998) Selective loss of GABA neurons in area CA1 of the rat hippocampus after intraventricular kainate. Epilepsy Research 32: 363–369CrossRefGoogle ScholarPubMed
Morison, R. S. and Bassett, D. L. (1945) Electrical activity of the thalamus and basal ganglia in decorticated cats. Journal of Neurophysiology 8: 309–314CrossRefGoogle Scholar
Morison, R. S. and Dempsey, E. W. (1942) Mechanism of thalamocortical augmentation and repetition. American Journal of Physiology 138: 297–308Google Scholar
Morrell, F. (1960) Secondary epileptogenic lesions. Epilepsia 1: 538–560CrossRefGoogle ScholarPubMed
Morrison, J. H. and Foote, S L. (1986) Noradrenergic and serotoninergic innervation of cortical, thalamic and tectal visual structures in old and new world monkeys. Journal of Comparative Neurology 243: 117–138CrossRefGoogle ScholarPubMed
Moruzzi, G. (1964) The historical development of the deafferentation hypothesis of sleep. Proceedings of the American Philosophical Society 108: 19–28Google Scholar
Moruzzi, G. (1966) The functional significance of sleep with particular regard to the brain mechanisms underlying consciousness. In Brain and Conscious Experience, ed. J. C. Eccles, pp. 345–379, New York: Springer
Moruzzi, G. (1969) Sleep and instinctive behavior. Archives Italiennes de Biologie 107: 175–216Google ScholarPubMed
Moruzzi, G. (1972) The sleep-waking cycle. Ergebnisse der Physiologie 64: 1–165Google ScholarPubMed
Moruzzi, G. and Magoun, H. W. (1949) Brain stem reticular formation and activation of the EEG. Electroencephalography and Clinical Neurophysiology 1: 455–473CrossRefGoogle ScholarPubMed
Mountcastle, V. B. (1997) The columnar organization of the neocortex. Brain 120: 701–722CrossRefGoogle ScholarPubMed
Mountcastle, V. B. (1998) Perceptual Neuroscience – The Cerebral Cortex. Cambridge, MA: Harvard University Press
Mouret, J. and Coindet, J. (1980) Polygraphic evidence against a critical role of the raphe nuclei in sleep in the rat. Brain Research 186: 273–287CrossRefGoogle ScholarPubMed
Mulle, C., Steriade, M. and Deschênes, M. (1985) Absence of spindle oscillations in the cat anterior thalamic nuclei. Brain Research 334: 169–171CrossRefGoogle ScholarPubMed
Mulle, C., Madariaga, A. and Deschênes, M. (1986) Morphology and electrophysiological properties of reticularis thalami neurons in cat: in vivo study of a thalamic pacemaker. Journal of Neuroscience 6: 2134–2145CrossRefGoogle ScholarPubMed
Munk, M. H. J., Roelfsema, P. R., König, P., Engel, A. K. and Singer, W. (1996) Role of reticular activation in the modulation of intracortical synchronization. Science 272: 271–274CrossRefGoogle ScholarPubMed
Murthy, V. N. and Fetz, E. E. (1992) Coherent 25- to 35-Hz oscillations in the sensorimotor cortex of awake behaving monkeys. Proceedings of National Academy of Sciences of the USA 89: 5670–5674CrossRefGoogle ScholarPubMed
Murthy, V. N. and Fetz, E. E. (1997a) Oscillatory activity in sensorimotor cortex of awake monkeys: synchronization of local field potentials and relation to behavior. Journal of Neurophysiology 76: 3949–3967CrossRefGoogle Scholar
Murthy, V. N. and Fetz, E. E. (1997b) Synchronization of neurons during local field potential oscillations in sensorimotor cortex of awake monkeys. Journal of Neurophysiology 76: 3968–3982CrossRefGoogle Scholar
Nadler, J. V., Perry, B. W. and Cotman, C. W. (1978) Preferential vulnerability of hippocampus to intraventricular kainic acid. In Kainic Acid as a Tool in Neurobiology, ed. E. G. McGeer, J. W. Olney and P. L. McGeer, pp. 219–237, New York: Raven Press
Nagao, T., Alonso, A. and Avoli, M. (1996) Epileptiform activity induced by pilocarpine in the rat hippocampal-entorhinal slice preparation. Neuroscience 72: 399–408CrossRefGoogle ScholarPubMed
Nagy, J. I., Yamamoto, T., Shiosaka, S., Dewar, K. M., Whittaker, M. E. and Hertzberg, E. L. (1988) Immunohistochemical localization of gap junction protein in rat CNS: a preliminary account. In Gap Junctions, ed. E. L. Hertzberg and R. G. Johnson, pp. 375–389, New York: A. R. Liss
Nakabayashi, T., Uchida, S., Maehara, T., Hirai, N., Nakamura, M., Arakaki, H., Shimisu, H. and Okubo, Y. (2001) Absence of sleep spindles in human medial and basal temporal lobes. Psychiatry and Clinical Neuroscience 55: 57–65CrossRefGoogle ScholarPubMed
Nakamura, A., Nakashima, M., Sugao, T., Kanemoto, H., Fukumura, Y. and Shiomi, H. (1988) Potent antinociceptive effect of centrally administered delta-sleep-inducing peptide (DSIP). European Journal of Pharmacology 155: 247–253CrossRefGoogle Scholar
Nakamura, A., Nakashima, M., Sakai, K., Niwa, M., Nozaki, M. and Shiomi, H. (1989) Delta-sleep-inducing peptide (DSIP) stimulates the release of immunoreactive Met-enkephalin from rat lower brainstem slices in vitro. Brain Research 481: 165–168CrossRefGoogle ScholarPubMed
Naquet, R. and Meldrum, B. S. (1975) In Experimental Models of Epilepsy, ed. D. P. Purpura, J. K. Penry, D. B. Tower, D. M. Woodbury and R. D. Walter, pp. 373–406, New York: Raven Press
Naquet, R. and Valin, A. (1990) Focal discharges in photosensitive generalized epilepsy. In Generalized Epilepsy, ed. M. Avoli, P. Gloor, G. Kostopoulos and R. Naquet, pp. 273–285, Boston: Birkhäuser
Nathan, T., Jensen, M. S. and Lambert, J. D. (1990) The slow inhibitory postsynaptic potential in rat hippocampal CA1 neurones is blocked by intracellular injection of QX-314. Neuroscience Letters 110: 309–313CrossRefGoogle ScholarPubMed
Nauta, W. J. H. (1946) Hypothalamic regulation of sleep in rats. Experimental study. Journal of Neurophysiology 9: 285–316CrossRefGoogle ScholarPubMed
Neckelmann, D., Amzica, F. and Steriade, M. (1998) Spike-wave complexes and fast components of cortically generated seizures. III. Synchronizing mechanisms. Journal of Neurophysiology 80: 1480–1494CrossRefGoogle ScholarPubMed
Neckelmann, D., Amzica, F. and Steriade, M. (2000) Changes in neuronal conductance during different components of cortically generated spike-wave seizures. Neuroscience 96: 475–485CrossRefGoogle ScholarPubMed
Nelson, J. P., McCarley, R. W. and Hobson, J. A. (1983) REM sleep burst neurons, PGO waves, and eye movement information. Journal of Neurophysiology 50: 784–797CrossRefGoogle ScholarPubMed
Neugebauer, V., Keele, N. B. and Shinnick-Gallagher, P. (1997) Epileptogenesis in vivo enhances the sensitivity of inhibitory presynaptic metabotropic glutamate receptors in basolateral amygdala neurons in vitro. Journal of Neuroscience 17: 983–995CrossRefGoogle ScholarPubMed
Nicholson, C. (1980) Modulation of extracellular calcium and its functional implications. Federation Proceedings 39: 1519–1523Google ScholarPubMed
Nicoll, R. A., Malenka, R. C. and Kauer, J. A. (1990) Functional comparison of neurotransmitter receptor subtypes in mammalian central nervous system. Physiological Reviews 70: 513–565CrossRefGoogle ScholarPubMed
Niedermeyer, E. (1965) Sleep electroencephalograms in petit mal. Archives of Neurology 12: 625–630CrossRefGoogle ScholarPubMed
Niedermeyer, E. (1969) The Lennox-Gastaut syndrome: a severe type of childhood epilepsy. Deutsche Zeitschrift für Nervenheilkrankheiten 195: 263–282Google ScholarPubMed
Niedermeyer, E. (1993) Historical aspects. In Electroencephalography: Basic Principles, Clinical Applications and Related Field, 3rd edn., ed. E. Niedermeyer and F. Lopes da Silva, pp. 1–14, Baltimore: Williams & Wilkins
Niedermeyer, E. (1999a) Abnormal EEG patterns (epileptic and paroxysmal). In Electroencephalography: Basic Principles, Clinical Applications and Related Fields, 4th edn., ed. E. Niedermeyer and F. Lopes da Silva, pp. 235–260, Baltimore: Williams & Wilkins
Niedermeyer, E. (1999b) Epileptic seizure disorders. In Electroencephalography: Basic Principles, Clinical Applications and Related Fields, 4th edn., ed. E. Niedermeyer and F. Lopes da Silva, pp. 476–585, Baltimore: Williams & Wilkins
Nielsen, T. (2000) Cognition in REM and NREM sleep. Brain and Behavioral Sciences 23: 851–866CrossRefGoogle ScholarPubMed
Nishimura, Y., Kitagawa, H., Saitoh, K., Asahi, M., Itoh, K., Yoshioka, K., Asahara, T., Tanaka, T. and Yamamoto, T. (1996) The burst firing in the layer III and V pyramidal neurons of the cat sensorimotor cortex in vitro. Brain Research 727: 212–216CrossRefGoogle ScholarPubMed
Nishimura, Y., Asahi, M., Saitoh, K., Kitagawa, H., Kumazawa, Y., Itoh, K., Lin, M., Akamine, T., Shibuyam, H., Asahara, T. and Yamamoto, T. (2001) Ionic mechanisms underlying burst firing of layer III sensorimotor cortical neurons of the cat: and in vitro slice study. Journal of Neurophysiology 86: 771–781CrossRefGoogle ScholarPubMed
Nitecka, L., Tremblay, E., Charton, G., Bouillot, J. P., Berger, M. L. and Ben-Ari, Y. (1984) Maturation of kainic acid seizure-brain damage syndrome in the rat. II. Histopathological sequelae. Neuroscience 13: 1073–1094CrossRefGoogle ScholarPubMed
Nitz, D. and Siegel, J. M. (1997a) GABA release in the dorsal raphe nucleus: role in the control of REM sleep. American Journal of Physiology 273: R451–455Google Scholar
Nitz, D. and Siegel, J. M. (1997b) GABA release in the locus coeruleus as a function of sleep/wake state. Neuroscience 78: 795–801CrossRefGoogle Scholar
Noachtar, S. (2001) Generalized epilepsy and sleep. In Epilepsy and Sleep, ed. D. S. Dinner and H. O. Lüders, pp. 75–83, San Diego: Academic Press
Noebels, J. L. (1984) A single error of noradrenergic axon growth synchronizes central neurons. Nature 310: 409–411CrossRefGoogle Scholar
Noebels, J. L. (1999) Single-gene models of epilepsy. Advances in Neurology 79: 227–238Google ScholarPubMed
Nosjean, A., Arluison, M. and Laguzzi, R. F. (1987) Increase in paradoxical sleep after destruction of serotoninergic innervation in the nucleus tractus solitarius of the rat. Neuroscience 23: 469–481CrossRefGoogle ScholarPubMed
Nuñez, A. (1996) Unit activity of rat basal forebrain neurons: relationship to cortical activity. Neuroscience 72: 757–766CrossRefGoogle ScholarPubMed
Nuñez, A., Amzica, F. and Steriade, M. (1992a) Intrinsic and synaptically generated delta (1–4 Hz) rhythms in dorsal lateral geniculate neurons and their modulation by light-induced fast (30–70 Hz) events. Neuroscience 51: 269–284CrossRefGoogle Scholar
Nuñez, A., Amzica, F. and Steriade, M. (1992b) Intracellular evidence for incompatibility between spindle and delta oscillations in thalamocortical neurons of cat. Neuroscience 48: 75–85CrossRefGoogle Scholar
Nuñez, A., Amzica, F. and Steriade, M. (1992c) Voltage-dependent fast (20–40 Hz) oscillations in long-axoned neocortical neurons. Neuroscience 51: 7–10CrossRefGoogle Scholar
Nuñez, A., Amzica, F. and Steriade, M. (1993) Electrophysiology of cat association cortical neurons in vivo: intrinsic properties and synaptic responses. Journal of Neurophysiology 70: 418–430CrossRefGoogle ScholarPubMed
Obál, F. Jr., Alfoldi, P., Cady, A. B., Johannsen, L., Sary, G. and Krueger, J. M. (1988) Growth hormone-releasing factor enhances sleep in rats and rabbits. American Journal of Physiology 255: R310–316Google ScholarPubMed
Obál, F. Jr., Payne, L., Kapas, L., Opp, M. and Krueger, J. M. (1991) Inhibition of growth hormone-releasing factor suppresses both sleep and growth hormone secretion in the rat. Brain Research 557: 149–153CrossRefGoogle ScholarPubMed
O'Brien, J. L., Goldensohn, E. S. and Hoefer, R. T. (1959) Electroencephalographic abnormalities in addition to bilaterally synchronous 3 cycle per second spike and wave activity in petit mal. Electroencephalography and Clinical Neurophysiology 13: 747–761CrossRefGoogle Scholar
Oertel, W. H., Graybiel, A. M., Mugnaini, E., Elde, R. P., Schmechel, D. E. and Kopin, I. J. (1983) Coexistence of glutamic acid decarboxylase and somatostatin-like immunoreactivity in neurons of the feline nucleus reticularis thalami. Journal of Neuroscience 3: 1322–1332CrossRefGoogle ScholarPubMed
Ogawa, J. (1963) Midbrain reticular influences upon single neurons in lateral geniculate nucleus. Science 139: 343–344CrossRefGoogle ScholarPubMed
Ohara, P. T. and Lieberman, A. R. (1985) The thalamic reticular nucleus of the adult rat: experimental anatomical studies. Journal of Neurocytology 14: 365–411CrossRefGoogle ScholarPubMed
Ojima, H. (1994) Terminal morphology and distribution of corticothalamic fibers originating from layers 5 and 6 of cat primary auditory cortex. Cerebral Cortex 4: 646–663CrossRefGoogle ScholarPubMed
Okasaki, M. M., Evenson, D. A. and Nadler, J. V. (1995) Hippocampal mossy fiber sprouting and synapse formation after status epilepticus in rats: visualization after retrograde transport of biocytin. Journal of Comparative Neurology 352: 515–534CrossRefGoogle Scholar
O'Leary, J. L. and Goldring, S. (1976) Science and Epilepsy. New York: Raven Press
Orkand, R. K. (1969) Neuroglial-neuronal interactions. In Basic Mechanisms of the Epilepsies, ed. H. H. Jasper, A. A. Ward Jr. and A. Pope, pp. 737–746, Boston: Little, Brown
Otis, T. S., Koninck, Y. and Mody, I. (1994) Lasting potentiation of inhibition is associated with an increased number of γ-aminobutyric acid type A receptors activated during miniature inhibitory postsynaptic currents. Proceedings of the National Academy of Sciences of the USA 91: 7698–7702CrossRefGoogle ScholarPubMed
Pabst, M. J., Beranova-Giorgianni, S. and Krueger, J. M. (1999) Effects of muramyl peptides on macrophages, monokines and sleep. Neuroimmunomodulation 6: 261–283CrossRefGoogle ScholarPubMed
Pape, H. C. (1995) Nitric oxide: an adequate modulatory link between biological oscillators and control systems in the mammalian brain. Seminars in the Neurosciences 7: 329–340CrossRefGoogle Scholar
Pape, H. C. (1996) Queer current and pacemaker: the hyperpolarization-activated cation current in neurons. Annual Reviews of Physiology 58: 299–327CrossRefGoogle ScholarPubMed
Pape, H. C. and Eysel, U. T. (1987) Modulatory actions of the reticular transmitters norepinephrine and 5–hydroxytryptamine (serotonin) in the cat's visual thalamus. Society for Neuroscience Abstracts 13: 86Google Scholar
Pape, H. C. and Mager, R. (1992) Nitric oxide controls oscillatory activity in thalamocortical neurons. Neuron 9: 441–448CrossRefGoogle ScholarPubMed
Pape, H. C. and McCormick, D. A. (1989) Noradrenaline and serotonin selectively modulate thalamic burst firing by enhancing a hyperpolarization-activated cation current. Nature 340: 715–718CrossRefGoogle ScholarPubMed
Pape, H. C. and McCormick, D. A. (1995) Electrophysiological and pharmacological properties of interneurons in the cat dorsal lateral geniculate nucleus. Neuroscience 68: 1105–1125CrossRefGoogle ScholarPubMed
Pape, H. C., Budde, T., Mager, R. and Kisvrday, Z. F. (1994) Prevention of Ca2+-mediated action potentials in GABAergic local circuit neurones of rat thalamus by a transient K+ current. Journal of Physiology (London). 478: 403–422CrossRefGoogle Scholar
Pappenheimer, J. R., Miller, T. B. and Goodrich, C. A. (1967) Sleep-promoting effects of cerebrospinal fluid from sleep-deprived goats. Proceedings of the National Academy of Sciences of the USA 58: 513–517CrossRefGoogle ScholarPubMed
Paré, D. and Gaudreau, H. (1996) Projection cells and interneurons of the lateral and basolateral amygdala: distinct firing patterns and differential relation to theta and delta rhythms in conscious cats. Journal of Neuroscience 16: 3334–3350CrossRefGoogle ScholarPubMed
Paré, D. and Lang, E. J. (1998) Calcium electrogenesis in neocortical pyramidal neurons in vivo. European Journal of Neuroscience 10: 3164–3170CrossRefGoogle ScholarPubMed
Paré, D. and Llinás, R. (1995) Conscious and pre-conscious processes as seen from the standpoint of sleep-waking cycle neurophysiology. Neuropsychologia 33: 1155–1168CrossRefGoogle ScholarPubMed
Paré, D. and Smith, Y. (1993) Distribution of GABA immunoreactivity in the amygdaloid complex of the cat. Neuroscience 57: 1061–1076CrossRefGoogle ScholarPubMed
Paré, D. and Smith, Y. (1994) GABAergic projection from the intercalated cell masses of the amygdala to the basal forebrain in cats. Journal of Comparative Neurology 344: 33–49CrossRefGoogle ScholarPubMed
Paré, D. and Smith, Y. (1996) Thalamic collaterals of corticostriatal axons: their termination field and synaptic targets in cats. Journal of Comparative Neurology 372: 551–5673.0.CO;2-3>CrossRefGoogle ScholarPubMed
Paré, D. and Steriade, M. (1990) Control of mamillothalamic axis by brainstem cholinergic laterodorsal tegmental afferents: possible involvement in mnemonic processes. In Brain Cholinergic Systems, ed. M. Steriade and D. Biesold, pp. 337–354, Oxford: Oxford University Press
Paré, D., Steriade, M., Deschênes, M. and Oakson, G. (1987) Physiological properties of anterior thalamic nuclei, a group devoid of inputs from the reticular thalamic nucleus. Journal of Neurophysiology 57: 1669–1685CrossRefGoogle ScholarPubMed
Paré, D., Smith, Y., Parent, A. and Steriade, M. (1988) Projections of upper brainstem cholinergic and non-cholinergic neurons of cat to intralaminar and reticular thalamic nuclei. Neuroscience 25: 69–88CrossRefGoogle ScholarPubMed
Paré, D., Steriade, M., Deschênes, M. and Bouhassira, D. (1990) Prolonged enhancement of anterior thalamic synaptic responsiveness by stimulation of a brainstem cholinergic group. Journal of Neuroscience 10: 20–33CrossRefGoogle ScholarPubMed
Paré, D., Curró Dossi, R. and Steriade, M. (1991) Three types of inhibitory postsynaptic potentials generated by interneurons in the anterior thalamic complex of cat. Journal of Neurophysiology 66: 1190–1204CrossRefGoogle ScholarPubMed
Paré, D., Smith, Y. and Paré, J. F. (1995) Intra-amygdaloid projections of the basolateral and basomedial nuclei in the cat: Phaseolus vulgaris-leucoagglutinin anterograde tracing at the light electron microscopic level. Neuroscience 69: 567–583CrossRefGoogle ScholarPubMed
Paré, D., Shink, E., Gaudreau, H., Destexhe, A. and Lang, E. J. (1998) Impact of spontaneous synaptic activity on the resting properties of cat neocortical pyramidal neurons in vivo. Journal of Neurophysiology 79: 1450–1460CrossRefGoogle ScholarPubMed
Paré, D., Collins, D. R. and Pelletier, J. G. (2002) Amygdala oscillations and the consolidation of emotional memories. Trends in Cognitive Sciences 6: 306–314CrossRefGoogle ScholarPubMed
Parent, A. and Steriade, M. (1984) Midbrain tegmental projections of nucleus reticularis thalami of cat and monkey: a retrograde transport and antidromic identification study. Journal of Comparative Neurology 229: 548–558CrossRefGoogle Scholar
Parent, A., Paré, D., Smith, Y. and Steriade, M. (1988) Basal forebrain cholinergic and non-cholinergic projections to the thalamus and brainstem in cats and monkeys. Journal of Comparative Neurology 277: 281–301CrossRefGoogle Scholar
Parmeggiani, P. L. (1988) Thermoregulation during sleep from the view point of homeostasis. In Clinical Physiology of Sleep, ed. R. Lydic and J. F. Biebuyck, pp. 159–179, Bethesda: American Physiological Society
Parmeggiani, P. L., Azzaroni, A., Cevolani, D. and Ferrari, G. (1986) Polygraphic study of anterior hypothalamic-preoptic neuron thermosensitivity during sleep. Electroencephalography and Clinical Neurophysiology 63: 289–295CrossRefGoogle ScholarPubMed
Parmentier, R., Ohtsu, H., Djebarra-Hannas, Z., Valatx, J. L., Watanabe, T. and Lin, J. S. (2002) Anatomical, physiological, and pharmacological characteristics of histidine decarboxylase knock-out mice: evidence for the role of brain histamine in behavioral and sleep-wake control. Journal of Neuroscience 22: 7695–7711CrossRefGoogle ScholarPubMed
Parpura, V., Basarsky, T. A., Liu, F., Jeftinija, K. and Haydon, P. G. (1994) Glutamate-mediated astrocyte-neuron signaling. Nature 369: 744–747CrossRefGoogle Scholar
Parri, H. R. and Crunelli, V. (1998) Sodium current in rat and cat thalamocortical neurons: role of a non-inactivating component in tonic and burst firing. Journal of Neuroscience 18: 854–867CrossRefGoogle ScholarPubMed
Parri, H. R., Gould, T. M. and Crunelli, V. (2001) Spontaneous astrocytic Ca2+ oscillations in situ drive NMDAR-mediated neuronal excitation. Nature Neuroscience 4: 803–812CrossRefGoogle ScholarPubMed
Passouant, P. (1984) Historical aspects of sleep and epilepsy. In Epilepsy and Sleep Deprivation, ed. R. Degen and E. Niedermeyer, pp. 67–73, Amsterdam: Elsevier
Patry, F. L. (1931) The relation of time of day, sleep and other factors to the incidence of epileptic seizures. American Journal of Psychiatry 10: 789–813CrossRefGoogle Scholar
Pavlides, C. and Winson, J. (1989) Influences of hippocampal place cell firing in awake state on the activity of these cells during subsequent sleep episodes. Journal of Neuroscience 9: 2907–2918CrossRefGoogle ScholarPubMed
Pavlov, I. P. (1923) “Innere Hemmung” der bedingten Reflexe und der Schlaf – ein und derselbe Prozess. Skandinavische Archive für Physiologie 44: 42–58Google Scholar
Pedley, R. A. (1987) Epilepsy. In A Textbook of Clinical Neurology, ed. A. M. Halliday, S. R. Butler and R. Paul, pp. 231–268, New York: Wiley
Pedroarena, C. and Llinás, R. (1997) Dendritic calcium conductances generate high-frequency oscillation in thalamocortical neurons. Proceedings of the National Academy of Sciences of the USA 94: 24–28CrossRefGoogle ScholarPubMed
Pedroarena, C. and Llinás, R. (2001) Interactions of synaptic and intrinsic electroresponsiveness determine corticothalamic activation dynamics. Thalamus and Related Systems 1: 3–14Google Scholar
Pellegrini, A., Musgrave, J. and Gloor, P. (1979) Role of afferent input of subcortical origin in the genesis of bilaterally synchronous epileptic discharges of feline generalized penicillin epilepsy. Experimental Neurology 64: 155–173CrossRefGoogle ScholarPubMed
Pellegrini, A., Curró Dossi, R., Dal Pos, F., Ermani, M., Zanotto, I. and Testa, F. (1989) Ethosuximide alters intrathalamic and thalamocortical synchronizing mechanisms: a possible explanation of its antiabsence effect. Brain Research 497: 344–360CrossRefGoogle ScholarPubMed
Peña, E. and Geijo-Barrientos, E. (1996) Laminar localization, morphology, and physiological properties of pyramidal neurons that have low-threshold calcium current in the guinea-pig medial frontal cortex. Journal of Neuroscience 16: 5301–5311CrossRefGoogle ScholarPubMed
Penfield, W. and Jasper, H. H. (1954) Epilepsy and the Functional Anatomy of the Human Brain. Boston: Little, Brown
Penfield, W. and Rasmussen, T. (1950) The Cerebral Cortex of Man. A Clinical Study of Localization of Function. New York: Macmillan Co
Penry, J. K., Porter, R. J. and Dreifuss, F. E. (1971) Patterns of paroxysmal abnormal discharges in twelve-hour telemetered EEGs of untreated children with absence (petit mal) seizures. Neurology 21: 392Google Scholar
Perez-Velazquez, J. L. and Carlen, P. L. (1999) Synchronization of GABAergic interneuronal networks during seizure-like activity in the rat horizontal hippocampal slice. European Journal of Neuroscience 1111: 4110–4118CrossRefGoogle Scholar
Perez-Velazquez, J. L. and Carlen, P. L. (2000) Gap junctions, synchrony and seizures. Trends in Neurosciences 23: 68–74CrossRefGoogle ScholarPubMed
Perez-Velazquez, J. L., Valiante, T. A. and Carlen, P. L. (1994) Modulation of gap junctional mechanisms during calcium-free induced field burst activity: a possible role for electrotonic coupling in epileptogenesis. Journal of Neuroscience 14: 4308–4317CrossRefGoogle ScholarPubMed
Perkins, K. L. and Wong, R. K. S. (1995) Intracellular QX-314 blocks the hyperpolarization-activated inward current IQ in hippocampal CA1 pyramidal cells. Journal of Neurophysiology 73: 911–915CrossRefGoogle ScholarPubMed
Perreault, M. C., Qin, Y., Heggelund, P. and Zhu, J. J. (2003) Postsynaptic development of GABAergic signaling in the rat lateral geniculate nucleus: presynaptic dendritic mechanisms. Journal of Physiology (London) 546: 137–148CrossRefGoogle Scholar
Perreault, P. and Avoli, M. (1992) 4-Aminopyridine-induced epileptiform activity and a GABA-mediated long-lasting depolarization in the rat hippocampus. Journal of Neuroscience 12: 104–115CrossRefGoogle Scholar
Perrin, F., Garcia-Larrea, L., Mauguière, F. and Bastuji, H. (1999) A differential brain response to the subject's own name persists during sleep. Clinical Neurophysiology 110: 2153–2164CrossRefGoogle ScholarPubMed
Petsche, H. (1962) Pathophysiologie und Klinik des Petit-Mal. Wiener Zeitschrift für Nervenheilkrankheiten 19: 345–442Google Scholar
Petsche, H., Pockberger, H. and Rappelsberger, P. (1984) On the search for the sources of the electroencephalogram. Neuroscience 11: 1–27CrossRefGoogle ScholarPubMed
Piéron, H. (1913) Le Problème Physiologique du Sommeil. Paris: Masson
Pinault, D. (1996) A novel single-cell staining procedure performed in vivo under electrophysiological control: morpho-functional features of juxtacellularly labelled thalamic cells and other central neurons with biocytin or Neurobiotin. Journal of Neuroscience Methods 65: 113–136CrossRefGoogle ScholarPubMed
Pinault, D. and Deschênes, M. (1992a) Voltage-dependent 40-Hz oscillations in rat reticular thalamic neurons in vivo. Neuroscience 51: 245–258CrossRefGoogle Scholar
Pinault, D. and Deschênes, M. (1992b) Control of 40-Hz firing of reticular thalamic cells by neurotransmitters. Neuroscience 51: 259–268CrossRefGoogle Scholar
Pinault, D., Smith, Y. and Deschênes, M. (1997) Dendrodendritic and axoaxonic synapses in the thalamic reticular nucleus of the adult rat. Journal of Neuroscience 17: 3215–3233CrossRefGoogle ScholarPubMed
Pinault, D., Leresche, N., Charpier, S., Deniau, J. M., Marescaux, C., Vergnes, M. and Crunelli, V. (1998) Intracellular recordings in thalamic neurones during spontaneous spike and wave discharges in rats with absence epilepsy. Journal of Physiology (London) 509: 449–456CrossRefGoogle ScholarPubMed
Pinault, D., Vergnes, M. and Marescaux, C. (2001) Medium-voltage 5–9 Hz oscillations give rise to spike-and-wave discharges in a genetic model of absence epilepsy: in vivo dual extracellular recordings of thalamic relay and reticular neurons. Neuroscience 105: 181–201CrossRefGoogle Scholar
Pirchio, M., Turner, J. P., Williams, S. R., Asprodini, E. and Crunelli, V. (1997) Postnatal development of membrane properties and δ oscillations in thalamocortical neurons of the cat dorsal lateral geniculate nucleus. Journal of Neuroscience 17: 5428–5444CrossRefGoogle ScholarPubMed
Plihal, W. and Born, J. (1997) Effects of early and late nocturnal sleep on declarative and procedural memory. Journal of Cognitive Neuroscience 9: 534–547CrossRefGoogle ScholarPubMed
Plum, F. (1991) Coma and related global disturbances of the human conscious state. In Cerebral Cortex (vol. 9, Normal and Altered States of Function), ed. A. Peters and E. G. Jones, pp. 359–425, New York: Plenum
Pohlmann-Eden, B., Hoch, D. B., Cochius, J. I. and Chiappa, K. H. (1996) Periodic lateralized epileptiform discharges – a critical review. Journal of Clinical Neurophysiology 13: 519–530CrossRefGoogle ScholarPubMed
Pollen, D. A. (1964) Intracellular studies of cortical neurons during thalamic induced wave and spike. Electroencephalography and Clinical Neurophysiology 17: 398–404CrossRefGoogle ScholarPubMed
Pollen, D. and Lux, H. (1966) Conductance changes during inhibitory postsynaptic potentials in normal and strychninized cortical neurons. Journal of Neurophysiology 29: 367–381CrossRefGoogle ScholarPubMed
Pompeiano, O. (1967a) The neurophysiological mechanisms of the postural and motor events during desynchronized sleep. Proceedings of the Association for the Research of Nervous and Mental Diseases 45: 351–423Google Scholar
Pompeiano, O. (1967b) Sensory inhibition during motor activity in sleep. In Neurophysiological Basis of Normal and Abnormal Motor Activities, ed. M. D. Yahr and D. P. Purpura, pp. 323–375, New York: Raven Press
Pool, J. L. (1954) Psychosurgery in older people. Journal of American Geriatric Society 2: 456–465CrossRefGoogle ScholarPubMed
Porkka-Heiskanen, T., Strecker, R. E., Thakkar, M., Bjorkum, A. A., Greene, R. W. and McCarley, R. W. (1997) Adenosine: a mediator of the sleep-inducing effects of prolonged wakefulness. Science 276: 1265–1268CrossRefGoogle ScholarPubMed
Portas, C. M., Thakkar, M., Rainnie, D. G., Greene, R. W. and McCarley, R. W. (1997) Role of adenosine in behavioral state modulation: a microdialysis study in the freely moving cat. Neuroscience 79: 225–235CrossRefGoogle ScholarPubMed
Portas, C. M., Krakow, K., Allen, P., Josephs, O., Armony, J. L. and Frith, C. D. (2000) Auditory processing across the sleep-wake cycle: simultaneous EEG and fMRI monitoring in humans. Neuron 28: 991–999CrossRefGoogle ScholarPubMed
Porter, R. J. (1993) The absence epilepsies. Epilepsia 34 (Suppl. 3): S42–S48CrossRefGoogle ScholarPubMed
Preuss, T. M. and Goldman-Rakic, P. S. (1987) Crossed corticothalamic and thalamocortical connections of macaque prefrontal cortex. Journal of Comparative Neurology 257: 269–281CrossRefGoogle ScholarPubMed
Prevett, M. C., Duncan, J. S., Jones, T., Fish, D. R. and Brooks, D. J. (1995) Demonstration of thalamic activation during typical absence seizures during H215O and PET. Neurology 45: 1396–1402CrossRefGoogle Scholar
Price, J. L. and Amaral, D. (1981) An autoradiographic study of the projections of the central nucleus of the monkey amygdala. Journal of Neuroscience 1: 1242–1259CrossRefGoogle ScholarPubMed
Prince, D. A. (1968) Inhibition in “epileptic” neurons. Experimental Neurology 21: 467–485CrossRefGoogle ScholarPubMed
Prince, D. A. (1975) Topical convulsants drugs and metabolic antagonists. In Experimental Models of Epilepsy, ed. D. P. Purpura, J. K. Penry, D. B. Tower, D. M. Woodbury and R. D. Walter, pp. 51–83, New York: Raven Press
Prince, D. A. (1983) Ionic mechanisms in cortical and hippocampal epileptogenesis. In Basic Mechanisms of Neuronal Hyperexcitability, ed. H. H. Jasper and N. M. van Gelder, pp. 217–238, New York: Alan R. Liss
Prince, D. A. and Farrell, D. (1963) “Centrencephalic” spike-wave discharges following parenteral injection of penicillin in the cat. Neurology 19: 309–310Google Scholar
Prince, D. A. and Jacobs, K. (1998) Inhibitory function in two models of chronic epileptogenesis. Epilepsy Research 32: 83–92CrossRefGoogle ScholarPubMed
Prince, D. A. and Shanzer, S. (1966) Effects of anesthetics upon the EEG response to reticular stimulation of slow synchrony. Electroencephalography and Clinical Neurophysiology 21: 578–588CrossRefGoogle ScholarPubMed
Prince, D. A. and Tseng, G. F. (1993) Epileptogenesis in chronically injured cortex: in vitro studies. Journal of Neurophysiology 69: 1276–1291CrossRefGoogle ScholarPubMed
Puizillout, J. J. and Ternaux, J. (1974) Endormement vago-aortique après section sagittale médiane du tronc cérébral et après administration de p-chlophenylalanine or destruction des noyaux du raphé. Brain Research 70: 9–42CrossRefGoogle Scholar
Puizillout, J. J., Gaudin-Chazal, G., Daszuta, A., Seyfritz, N. and Ternaux, J. P. (1979) Release of endogenous serotonin from encéphale isolé cats. II. Correlations with raphe neuronal activity and sleep and wakefulness. Journal de Physiologie (Paris) 75: 531–537Google ScholarPubMed
Puizillout, J. J., Gaudin-Chazal, G. and Bras, H. (1984) Vagal mechanisms in sleep regulation. In Sleep Mechanisms, ed. A. Borbély and J. L. Valatx, pp. 19–38 (Suppl. 8 of Experimental Brain Research), Berlin: Springer
Pumain, R., Menini, C., Heinemann, U., Louvel, J. and Silva-Barrat, C. (1985) Chemical synaptic transmission is not necessary for epileptic seizures to persist in the baboon Papio papio. Experimental Neurology 89: 250–258CrossRefGoogle Scholar
Purpura, D. P. (1970) Operations and processes in thalamic and synaptically related neural subsystems. In The Neuroscience: Second Study Program, ed. F. O. Schmitt, pp. 458–470, New York: Rockefeller University Press
Purpura, D. P. and Cohen, B. (1962) Intracellular recording from thalamic neurons during recruiting responses. Journal of Neurophysiology 25: 621–635CrossRefGoogle ScholarPubMed
Purpura, D. P. and Shofer, R. J. (1963) Intracellular recording from thalamic neurons during reticulocortical activation. Journal of Neurophysiology 26: 494–505CrossRefGoogle ScholarPubMed
Purpura, D. P., McMurtry, J. G. and Maekawa, K. (1966) Synaptic events in ventrolateral thalamic neurons during suppression of recruiting responses by brain stem reticular stimulation. Brain Research 1: 63–76CrossRefGoogle ScholarPubMed
Purpura, D. P., Bodick, N., Suzuki, K., Rapin, I. and Wurtzelmann, S. (1982) Microtubule disarray in cortical dendrites and neurobehavioral failure. I. Golgi and electron microscope studies. Brain Research 281: 287–297CrossRefGoogle Scholar
Qin, Y. L., McNaughton, B. L., Skaggs, W. E. and Barnes, C. A. (1997) Memory reprocessing in corticocortical and hippocampocortical neurons ensembles. Philosophical Transactions of the Royal Society (London, Series B) 352: 1525–1533CrossRefGoogle ScholarPubMed
Quirk, G. J., Muller, R. U., Kubie, J. L. and Ranck, J. B. Jr. (1992) The positional firing properties of medial entorhinal neurons: description and comparison with hippocampal place cells. Journal of Neuroscience 12: 1945–1963CrossRefGoogle ScholarPubMed
Racine, R. J., Burnham, W. M., Gilbert, M. and Kairiss, E. W. (1986) Kindling mechanisms. I. Electrophysiological studies. In Kindling 3, ed. J. A. Wada, pp. 263–282, New York: Raven
Raczkowski, D. and Fitzpatrick, D. (1989) Organization of cholinergic synapses in the cat's dorsal lateral geniculate and perigeniculate nuclei. Journal of Comparative Neurology 288: 231–254Google ScholarPubMed
Radulovacki, M. (1985) Role of adenosine in sleep in rats. Review of Clinical and Basic Pharmacology 5: 327–339Google ScholarPubMed
Raichle, M. E. (1998) Behind the scenes of functional brain imaging: a historical and physiological perspective. Proceedings of the National Academy of Sciences of the USA 95: 765–772CrossRefGoogle ScholarPubMed
Rainey, W. T. and Jones, E. G. (1983) Spatial distribution of individual medial lemniscal axons in the thalamic ventrobasal complex of the cat. Experimental Brain Research 49: 229–246CrossRefGoogle ScholarPubMed
Rainnie, D. G., Holmes, K. H. and Shinnick-Gallagher, P. (1992) Kindling-induced long-lasting changes in synaptic transmission in the basolateral amygdala. Journal of Neurophysiology 67: 443–454CrossRefGoogle ScholarPubMed
Rainnie, D. G., Grünze, H. C. R., McCarley, R. W. and Greene, R. W. (1994) Adenosine inhibition of mesopontine cholinergic neurons: implications for EEG arousal. Science 263: 689–692CrossRefGoogle ScholarPubMed
Ralston, B. and Ajmone-Marsan, C. (1956) Thalamic control of certain normal and abnormal cortical rhythms. Electroencephalography and Clinical Neurophysiology 8: 559–582CrossRefGoogle Scholar
Ramm, P. and Frost, B. J. (1983) Regional metabolic activity in the rat brain during sleep-like activity. Sleep 6: 196–216CrossRefGoogle Scholar
Rámon y Cajal, S. (1911) Histologie du Système Nerveux de l'Homme et des Vertéés (2 vol.), translated by L. Azoulay. Paris: Maloine. Also the 1952 edition, Madrid: Consejo Superior de Investigaciones Scientificas, Instituto Rámon y Cajal
Rasmusson, D. D., Clow, K. and Szerb, J. C. (1994) Modification of neocortical acetylcholine release and electroencephalogram desynchronization due to brainstem stimulation by drugs applied to the basal forebrain. Neuroscience 60: 665–677CrossRefGoogle ScholarPubMed
Rasmusson, D. D., Szerb, J. C. and Jordan, J. L. (1996) Differential effects of α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid and N-methyl-d-aspartate receptor antagonists applied to the basal forebrain on cortical acetylcholine release and EEG desynchronization. Neuroscience 72: 419–427CrossRefGoogle Scholar
Rechtschaffen, A. (1998) Current perspectives on the function of sleep. Perspectives in Biology and Medicine 41: 359–390CrossRefGoogle ScholarPubMed
Rechtschaffen, A., Lovell, R. A., Freedman, D., Whitehead, W. E. and Aldrich, M. (1973) The effect of parachlorophenylalanine on sleep in the rat: some implications for the serotonin sleep hypothesis. In Serotonin and Behavior, ed. J. Barchas and E. Usdin, pp. 401–418, New York: Academic
Rechtschaffen, A., Bergmann, B. M., Everson, C. A., Kushida, C. A. and Gilliland, M. A. (1989a) Sleep deprivation in the rat. I. Conceptual issues. Sleep 12: 1–4CrossRefGoogle Scholar
Rechtschaffen, A., Bergmann, B. M., Everson, C. A., Kushida, C. A. and Gilliland, M. A. (1989b) Sleep deprivation in the rat. X. Integration and discussion of the findings. Sleep 12: 68–87Google Scholar
Reiher, J., Lebel, M. and Klass, D. W. (1977) Small sharp spikes (SSS): reassessment of electroencephalographic characteristics and clinical significance. Electroencephalography and Clinical Neurophysiology 43: 775Google Scholar
Rempe, D. A., Bertram, E. H., Williamson, J. M. and Lothman, E. W. (1997) Interneurons in area CA1, stratum radiatum and stratum oriens remain functionally connected to excitatory synaptic input in chronically epileptic animals. Journal of Neurophysiology 78: 1504–1515CrossRefGoogle ScholarPubMed
Renaud, L., Kelly, J. and Provini, L. (1974) Synaptic inhibition in pyramidal tract neurons: membrane potential and conductance changes evoked by pyramidal tract and cortical surface stimulation. Journal of Neurophysiology 37: 1144–1155CrossRefGoogle ScholarPubMed
Reutens, D. C., Bye, A. M., Hopkins, I. J., Danks, A., Somerville, E., Walsh, J., Bleasel, A., Ouvrier, R., McKenzie, R. A. and Manson, J. I. (1993) Corpus callosotomy for intractable epilepsy: seizure outcome and prognostic factors. Epilepsia 34: 904–909CrossRefGoogle ScholarPubMed
Ribak, C. E. and Peterson, G. M. (1991) Intragranular mossy fibers in rats and gerbils form synapses with the somata and proximal dendrites of basket cells in the dentate gyrus. Hippocampus 1: 355–364CrossRefGoogle ScholarPubMed
Riou, F., Cespuglio, R. and Jouvet, M. (1982) Endogenous peptides and sleep in the rat. III. The hypnogenic properties of vasoactive intestinal peptide. Neuropeptides 2: 265–277CrossRefGoogle Scholar
Rodin, E. (1999) Decomposition and mapping of generalized spike-wave complexes. Clinical Neurophysiology 110: 1868–1875CrossRefGoogle ScholarPubMed
Roffwarg, H. P., Muzio, J. N. and Dement, W. C. (1966) Ontogenetic development of the human sleep-dream cycle. Science 152: 604–619CrossRefGoogle ScholarPubMed
Roger, A., Rossi, G. F. and Zirondoli, A. (1956) Le rôle des afférences des nerfs craniens dans le maintien de l'etat vigile de la preparation “encéphale isolé”. Electroencephalography and Clinical Neurophysiology 8: 1–13CrossRefGoogle Scholar
Romanski, L. M. and LeDoux, J. E. (1992) Equipotentiality of thalamo-amygdala and thalamo-cortico-amygdala circuits in auditory fear conditioning. Journal of Neuroscience 12: 4501–4509CrossRefGoogle ScholarPubMed
Rosen, A. S. and Andrew, R. D. (1990) Osmotic effects upon excitability in rat neocortical slices. Neuroscience 38: 579–590CrossRefGoogle ScholarPubMed
Ross, J. J., Johnson, L. C. and Walter, R. D. (1966) Spike and wave discharges during stages of sleep. Annals of Neurology 14: 399–407Google Scholar
Roth, M., Shaw, J. and Green, J. (1956) The form, voltage distribution and physiological significance of the K-complex. Electroencephalography and Clinical Neurophysiology 8: 385–402CrossRefGoogle ScholarPubMed
Rougeul-Buser, A., Bouyer, J. J., Montaron, M. F. and Buser, P. (1983) Patterns of activities in the ventrobasal thalamus and somatic cortex SI during behavioural immobility in the awake cat: focal waking rhythms. Experimental Brain Research 7 (Suppl.): 69–87CrossRefGoogle Scholar
Roy, J. P., Clercq, M., Steriade, M. and Deschênes, M. (1984) Electrophysiology of neurons of the lateral thalamic nuclei in cat: mechanisms of long-lasting hyperpolarizations. Journal of Neurophysiology 51: 1220–1235CrossRefGoogle ScholarPubMed
Roy, S. A., Dear, S. P. and Alloway, K. D. (2001) Long-range cortical synchronization without concomitant oscillations in the somatosensory system of anesthetized cats. Journal of Neuroscience 21: 1795–1808CrossRefGoogle ScholarPubMed
Royer, S., Martina, M. and Paré, D. (1999) An inhibitory interface gates impulse traffic between the input and output stations of the amygdala. Journal of Neuroscience 19: 10575–10583CrossRefGoogle ScholarPubMed
Royer, S., Martina, M. and Paré, D. (2000a) Polarized synaptic interactions between intercalated neurons of the amygdala. Journal of Neurophysiology 83: 3509–3518CrossRefGoogle Scholar
Royer, S., Martina, M. and Paré, D. (2000b) Bistable behavior of inhibitory neurons controlling impulse traffic through amygdala: role of a slowly deinactivating K+ current. Journal of Neuroscience 20: 9034–9039CrossRefGoogle Scholar
Rubboli, G., Meletti, S., Gardella, E., Zaniboni, A., D'Orsi, G., Dravet, C. and Tassinari, C. A. (1999) Photic reflex myoclonus: a neuropphysiological study in progressive myoclonus epilepsies. Epilepsia 40 (Suppl. 4): 50–58CrossRefGoogle ScholarPubMed
Ruch-Monachon, M. A., Jaffre, M. and Haefely, W. (1976) Drugs and PGO waves in the lateral geniculate body of the curarized cat. IV. The effects of acetylcholine, GABA and benzodiazepines on PGO wave activity. Archives Internationales de Pharmacodynamie et Thérapie 219: 308–325Google ScholarPubMed
Rudy, B. and McBain, C. J. (2001) Kv3 channels: voltage-gated K+ channels designed for high-frequency repetitive firing. Trends in Neurosciences 24: 517–526CrossRefGoogle ScholarPubMed
Russchen, F. T., Amaral, D. G. and Price, J. L. (1985) The afferent connections of the substantia innominata in the monkey, Macaca fascicularis. Journal of Comparative Neurology 242: 1–27CrossRefGoogle ScholarPubMed
Sadler, R. M. and Blume, W. T. (1989) Significance of bisynchronous spike-wave in patients with temporal lobe spikes. Epilepsia 30: 143–146CrossRefGoogle ScholarPubMed
Sakai, K. and Crochet, S. (2000) Serotonergic dorsal raphe neurons cease firing by disfacilitation during paradoxical sleep. NeuroReport 11: 3237–3241CrossRefGoogle ScholarPubMed
Sakai, K. and Crochet, S. (2001a) Differentiation of presumed serotonergic dorsal raphe neurons in relation to behavior and wake-sleep states. Neuroscience 104: 1141–1155CrossRefGoogle Scholar
Sakai, K. and Crochet, S. (2001b) Role of dorsal raphe neurons in paradoxical sleep generation in the cat: no evidence for a serotonergic mechanisms. European Journal of Neuroscience 13: 103–112Google Scholar
Sakai, K. and Jouvet, M. (1980) Brain stem PGO-on cells projecting directly to the cat dorsal lateral geniculate nucleus. Brain Research 194: 500–505CrossRefGoogle ScholarPubMed
Sakai, K., El Mansari, M. and Jouvet, M. (1990) Inhibition by carbachol microinjections of presumptive cholinergic PGO-on neurons in freely moving cats. Brain Research 527: 213–223CrossRefGoogle ScholarPubMed
Sakai, K., Crochet, S. and Onoe, H. (2001) Pontine structures and mechanisms involved in the generation of paradoxical (REM) sleep. Archives Italiennes de Biologie 139: 93–107Google ScholarPubMed
Sakakura, H. (1968) Spontaneous and evoked unitary activities of cat lateral geniculate neurons in sleep and wakefulness. Japanese Journal of Physiology 18: 23–42CrossRefGoogle ScholarPubMed
Sallanon, M., Sakai, K., Buda, C., Puymartin, M. and Jouvet, M. (1986) Augmentation du sommeil paradoxal, induite par l'injection d'acide iboténique dans l'hypothalamus ventrolatéral postérieur, chez le chat. Comptes Rendus de l'Académie de Sciences (Paris) 303: 175–179Google Scholar
Sallanon, M., Denoyer, M., Kitahama, K., Aubert, C., Gay, N. and Jouvet, M. (1989) Long-lasting insomnia induced by preoptic lesions and its transient reversal by muscimol injection into the posterior hypothalamus in the cat. Neuroscience 32: 669–683CrossRefGoogle ScholarPubMed
Sammaritano, M., Gigli, G. L. and Gotman, J. (1991) Interictal spiking during wakefulness and sleep and the localization of foci in temporal lobe epilepsy. Neurology 41: 290–297CrossRefGoogle ScholarPubMed
Samoriski, G. M. and Applegate, C. D. (1997) Repeated generalized seizures induce time-dependent changes in the behavioral seizure response independent of continued seizure induction. Journal of Neuroscience 17: 5581–5590CrossRefGoogle ScholarPubMed
Sanchez, R. and Leonard, C. S. (1996) NMDA-receptor-mediated synaptic currents in guinea pig laterodorsal tegmental neurons in vitro. Journal of Neurophysiology 76: 1101–1111CrossRefGoogle ScholarPubMed
Sanchez-Vives, M. V. and McCormick, D. A. (1997a) Functional properties of perigeniculate inhibition of dorsal lateral geniculate nucleus thalamocortical neurons in vitro. Journal of Neuroscience 17: 8880–8893CrossRefGoogle Scholar
Sanchez-Vives, M. V. and McCormick, D. A. (1997b) Inhibitory interactions between perigeniculate GABAergic neurons. Journal of Neuroscience 17: 8894–8908CrossRefGoogle Scholar
Sanchez-Vives, M. V. and McCormick, D. A. (2000) Cellular and network mechanisms of rhythmic recurrent activity in neocortex. Nature Neuroscience 3: 1027–1034CrossRefGoogle ScholarPubMed
Sanchez-Vives, M. V., Bal, T. and McCormick, D. A. (1997) Inhibitory interactions between perigeniculate GABAergic neurons. Journal of Neuroscience 17: 8894–8908CrossRefGoogle ScholarPubMed
Saper, C. B., Chou, T. C. and Scammell, T. E. (2001) The sleep switch: hypothalamic control of sleep and wakefulness. Trends in Neurosciences 24: 726–731CrossRefGoogle ScholarPubMed
Sato, S., Dreifuss, F. E. and Penry, J. K. (1973) The effects of sleep on spike-wave discharges in absence seizures. Neurology 23: 1335–1345CrossRefGoogle Scholar
Sato, S., White, B. G., Penry, J. K., Dreifuss, F. E., Sackellares, J. C. and Kupferberg, H. J. (1982) Valproic acid versus ethosuximide in the treatment of absence seizures. Neurology 32: 157–163CrossRefGoogle ScholarPubMed
Saunders, M. G. and Westmoreland, B. F. (1979) The EEG in evaluation of disorders affecting the brain diffusely. In Current Practice of Clinical Electroencephalography, ed. D. W. Klass and D. D. Daly, pp. 343–379, New York: Raven Press
Sawyer, S. F., Tepper, J. M. and Groves, P. M. (1994) Cerebellar-responsive neurons in the thalamic ventroanterior-ventrolateral complex of rats: light and electron microscopy. Neuroscience 63: 725–745CrossRefGoogle ScholarPubMed
Scharfman, H. E., Goodman, J. H., Du, F. and Schwarcz, R. (1998) Chronic changes in synaptic responses of entorhinal and hippocampal neurons after amino-oxyacetic acid (AOAA)-induced entorhinal cortical neuron loss. Journal of Neurophysiology 80: 3031–3046CrossRefGoogle ScholarPubMed
Scheibel, M. E., Crandall, P. H. and Scheibel, A. B. (1974) The hippocampal-dentate complex in temporal lobe epilepsy. Epilepsia 15: 55–80CrossRefGoogle ScholarPubMed
Scherg, M., Bast, T. and Berg, P. (1999) Multiple source analysis of interictal spikes: goals, requirements and clinical value. Journal of Clinical Neurophysiology 16: 214–224CrossRefGoogle ScholarPubMed
Schiff, N. D., Labar, D. R. and Victor, J. D. (1999) Common dynamics in temporal lobe seizures and absence seizures. Neuroscience 91: 417–428CrossRefGoogle ScholarPubMed
Schwartzkroin, P. A. (1975) Characteristics of CA1 neurons recorded intracellularly in the hippocampal in vitro slice preparation. Brain Research 85: 423–432CrossRefGoogle ScholarPubMed
Schwartzkroin, P. A. (1977) Further characteristics of hippocampal CA1 cells in vitro. Brain Research 128: 53–68CrossRefGoogle ScholarPubMed
Schwartzkroin, P. A. (1983) Local circuit considerations and intrinsic neuronal properties involved in hyperexcitability and cell synchronization. In Basic Mechanisms of Neuronal Hyperexcitability, ed. H. H. Jasper and N. M. van Gelder, pp. 75–105, New York: Alan R. Liss
Schwartzkroin, P. A. and Mueller, A. L. (1987) Electrophysiology of hippocampal neurons. In Cerebral Cortex (vol. 6, Further Aspects of Cortical Function, Including Hippocampus), ed. E. G. Jones and A. Peters, pp. 295–343, New York: Plenum
Schwartzkroin, P. A. and Prince, D. A. (1978) Cellular and field potential properties of epileptogenic hippocampal slices. Brain Research 147: 117–130CrossRefGoogle ScholarPubMed
Schwartzkroin, P. A. and Prince, D. A. (1980) Changes in excitatory and inhibitory synaptic potentials leading to epileptogenic activity. Brain Research 183: 61–73CrossRefGoogle ScholarPubMed
Schwindt, P. C. and Crill, W. E. (1995) Amplification of synaptic currents by persistent sodium conductance in apical dendrite of neocortical neurons. Journal of Neurophysiology 74: 2220–2224CrossRefGoogle Scholar
Schwindt, P. C., Spain, W. J., Foehring, R. C., Stafstrom, C. E., Chubb, M. C. and Crill, W. E. (1988a) Multiple potassium conductances and their functions in neurons from cat sensorimotor cortex in vitro. Journal of Neurophysiology 59: 424–449CrossRefGoogle Scholar
Schwindt, P. C., Spain, W. J., Foehring, R. C., Chubb, M. C. and Crill, W. E. (1988b) Slow conductances in neurons from cat sensorimotor cortex in vitro and their role in slow excitability changes. Journal of Neurophysiology 59: 450–467CrossRefGoogle Scholar
Schwindt, P. C., Spain, W. J. and Crill, W. E. (1989) Long-lasting reduction of excitability by a sodium-dependent potassium current in cat neocortical neurons. Journal of Neurophysiology 61: 233–244CrossRefGoogle ScholarPubMed
Scott, D. E. (1993) The History of Epileptic Therapy: Account of How Medication was Discovered. Pearl River, NY: The Parthenon Publishing Group
Seidenbecher, T. and Pape, H. C. (2001) Contribution of intralaminar thalamic nuclei to spike-and-wave-discharges during spontaneous seizures in a genetic model of absence epilepsy. European Journal of Neuroscience 13: 1537–1546CrossRefGoogle Scholar
Seidenbecher, T., Staak, R. and Pape, H. T. (1998) Relations between cortical and thalamic cellular activities during absence seizures in rats. European Journal of Neuroscience 10: 1103–1112CrossRefGoogle ScholarPubMed
Sejnowski, T. J. and Destexhe, A. (2000) Why do we sleep?Brain Research 886: 208–223CrossRefGoogle ScholarPubMed
Semba, K. and Fibiger, H. (1992) Afferent connections of the laterodorsal and the pedunculopontine tegmental nuclei in the rat: a retro- and anterograde transport and immunohistochemical study. Journal of Comparative Neurology 323: 387–410CrossRefGoogle ScholarPubMed
Semba, K., Reiner, P. B., McGeer, E. G. and Fibiger, H. (1989) Brainstem projecting neurons in the rat basal forebrain: neurochemical, topographical, and physiological distinctions from cortically projecting cholinergic neurons. Brain Research Bulletin 22: 501–509CrossRefGoogle ScholarPubMed
Señaris, R. M., Humphrey, P. P. A. and Emson, P. C. (1994) Distribution of somatostatin receptors 1, 2 and 3 mRNA in rat brain and pituitary. European Journal of Neuroscience 6: 1883–1896CrossRefGoogle ScholarPubMed
Sernagor, E., Yarom, Y. and Werman, R. (1986) Sodium-dependent regenerative responses in dendrites of axotomized motoneurons in the cat. Proceedings of the National Academy of Sciences of the USA 83: 7966–7970CrossRefGoogle ScholarPubMed
Servit, Z. (1959) Audiogenic epilepsy in rats as a model of reflex mechanisms in the pathogenesis of epileptic seizures. Journal of Experimental Medical Sciences 3: 37–44Google Scholar
Seyfried, T. N. and Todorova, M. (1999) Experimental models of epilepsy. In The Epilepsies, ed. P. Kotagal and H. O. Lüders, pp. 527–542, San Diego: Academic Press
Shadlen, M. N. and Movshon, J. A. (1999) Synchrony unbound: a critical evaluation of the temporal binding hypothesis. Neuron 24: 67–77CrossRefGoogle ScholarPubMed
Shatz, C. J. (1983) The prenatal development of the cat's retinogeniculate pathway. Journal of Neuroscience 3: 482–499CrossRefGoogle ScholarPubMed
Shatz, C. J. and Rakic, P. (1981) The genesis of efferent connections from the visual cortex of fetal rhesus monkey. Journal of Comparative Neurology 196: 287–308CrossRefGoogle ScholarPubMed
Sheer, D. (1984) Focused arousal, 40 Hz, and dysfunction. In Selfregulation of the Brain and Behavior, ed. T. Ebert, pp. 64–84, Berlin: Springer
Sherin, J. E., Shiromani, P. J., McCarley, R. W. and Saper, C. B. (1996) Activation of preoptic neurons during sleep. Science 271: 216–219CrossRefGoogle ScholarPubMed
Sherrington, C. S. (1955) Man on his Nature. New York: Doubleday
Shibasaki, H. and Neshige, R. (1987) Photic cortical reflex myoclonus. Annals of Neurology 22: 252–257CrossRefGoogle ScholarPubMed
Shibata, M., Blatteis, C. M., Krueger, J. M., Obál, F. Jr. and Opp, M. (1989) Pyrogenic, inflammatory and somnogenic responses to cytokines: differential modes of action. In Thermoregulation Research and Clinical Applications, ed. P. Lomax and E. Schanbaun, pp. 69–73, Basel: Karger
Shima, K., Nakahama, H. and Yamamoto, M. (1986) Firing properties of two types of nucleus raphe dorsalis neurons during the sleep-waking cycle and their responses to sensory stimuli. Brain Research 399: 317–326CrossRefGoogle ScholarPubMed
Shoham, S. and Krueger, J. M. (1988) Muramyl dipeptide-induced sleep and fever: effects of ambient temperature and time of injections. American Journal of Physiology 255: R157–165Google ScholarPubMed
Shoham, S., Davenne, D., Cady, A. B., Dinarello, C. A. and Krueger, J. M. (1987) Recombinant tumor necrosis factor and interleukin 1 enhance slow-wave sleep. American Journal of Physiology 253: R142–149Google ScholarPubMed
Shouse, M. N. (2001) Physiology underlying relationship of epilepsy and sleep. In Epilepsy and Sleep, ed. D. S. Dinner and H. O. Lüders, pp. 43–62, San Diego: Academic Press
Shouse, M. N., Martins da Silva, A. and Sammaritano, M. (1996) Circadian rhythm, sleep, and epilepsy. Journal of Clinical Neurophysiology 13: 32–50CrossRefGoogle ScholarPubMed
Siapas, A. G. and Wilson, M. A. (1998) Coordinated interactions between hippocampal ripples and cortical spindles during slow-wave sleep. Neuron 21: 1123–1128CrossRefGoogle ScholarPubMed
Sik, A., Penttonen, M., Ylinen, A. and Buzsáki, G. (1995) Hippocampal CA1 interneurons: an in vivo intracellular study. Journal of Neuroscience 15: 6651–6665CrossRefGoogle Scholar
Silva, A. J., Kogan, J. H., Frankland, P. W. and Kida, S. (1998) CREB and memory. Annual Reviews of Neuroscience 21: 127–148CrossRefGoogle ScholarPubMed
Silva-Barrat, C., Champagnat, J., Leiva, J. and Pavlik, V. (1994) Noradrenaline mediates paradoxical effects on rat neocortical neurons after GABA withdrawal. Journal of Neurophysiology 71: 1139–1150CrossRefGoogle ScholarPubMed
Silveira, D. C., Holmes, G. L., Schachter, S. C., Geula, C. and Schomer, D. L. (2000) Increased susceptibility to generalized seizures after immunolesions of the basal forebrain cholinergic neurons in rats. Brain Research 878: 223–227CrossRefGoogle ScholarPubMed
Simon, N. R., Lopes da Silva, F. H. and Manshanden, I. (1999) Preliminary results from a whole-head MEG study of sleep. In Recent Advances in Biomagnetism, ed. T. Yoshimoto, pp. 373–376, Sendai: Tohoku University Press
Simon, N. R., Mandshanden, I. and Lopes da Silva, F. H. (2000) A MEG study of sleep. Brain Research 860: 64–76CrossRefGoogle Scholar
Singer, W. (1977) Control of thalamic transmission by corticofugal and ascending pathways in the visual system. Physiological Reviews 57: 386–420CrossRefGoogle ScholarPubMed
Singer, W. (1990a) Search for coherence: a basic principle of cortical self-organization. Concepts in Neuroscience 1: 1–26Google Scholar
Singer, W. (1990b) Role of acetylcholine in use-dependent plasticity of the visual cortex. In Brain Cholinergic Systems, ed. M. Steriade and D. Biesold, pp. 314–336, Oxford: Oxford University Press
Slaght, S., Charpier, S., Deniau, J. M., Leresche, N. and Crunelli, V. (2000) In vivo intracellular recordings in neurones of the nucleus reticularis thalami during spike and wave discharges in the GAERS genetic model of absence epilepsy. Society of Neuroscience Abstracts 26: 735Google Scholar
Slaght, S. J., Leresche, N., Deniau, J. M., Crunelli, V. and Charpier, S. (2002) Activity of thalamic reticular neurons during spontaneous genetically determined spike and wave discharges. Journal of Neuroscience 22: 2323–2334CrossRefGoogle ScholarPubMed
Sloviter, R. S. (1987) Decreased hippocampal inhibition and a selective loss of interneurons in experimental epilepsy. Science 235: 73–76CrossRefGoogle Scholar
Sloviter, R. S. (1992) Possible functional consequences of synaptic reorganization in the dentate gyrus of kainite-treated rats. Neuroscience Letters 137: 91–96CrossRefGoogle Scholar
Smart, T. G., Xie, X. and Krishek, B. J. (1994) Modulation of inhibitory and excitatory amino acid receptor ion channels by zinc. Progress in Neurobiology 42: 393–441CrossRefGoogle ScholarPubMed
Smith, K. A. and Fisher, R. S. (1996) The selective GABAB antagonist CGP-35348 blocks spike-wave bursts in the cholesterol synthesis rat absence epilepsy model. Brain Research 729: 147–150Google ScholarPubMed
Smith, T. G. and Purpura, D. P. (1960) Electrophysiological studies on epileptogenic lesions of cat cortex. Electroencephalography and Clinical Neurophysiology 12: 59–82CrossRefGoogle ScholarPubMed
Smith, Y., Paré, D., Deschênes, M., Parent, A. and Steriade, M. (1988) Cholinergic and non-cholinergic projections from the upper brainstem to the visual thalamus in the cat. Experimental Brain Research 70: 166–180Google ScholarPubMed
Snead, O. C. (1995) Basic mechanisms of generalized absence seizures. Annals of Neurology 37: 146–157CrossRefGoogle ScholarPubMed
Snead, O. C., Depaulis, A., Vergnes, M. and Marescaux, C. (1999) Absence epilepsy: advances in experimental animal models. In Jasper's Basic Mechanisms of the Epilepsies, ed. A. V. Delgado-Escueta, W. Wilson, R. W. Olsen and R. J. Porter, 253–278, New York: Raven
Snead, O. C., Banerjee, P. K., Burnham, M. and Hampson, D. (2000) Modulation of absence seizures by the GABAAreceptor: a critical role for metabotropic glutamate receptor (mGluR4). Journal of Neuroscience 20: 6218–6224CrossRefGoogle Scholar
Snyder, S. H. and Bredt, D. A. (1991) Nitric oxide as a neuronal messenger. Trends in Pharmacological Sciences 12: 125–128CrossRefGoogle ScholarPubMed
Soderling, T. R. and Derkach, V. A. (2000) Postsynaptic protein phosphorylation and LTP. Trends in Neurosciences 23: 75–80CrossRefGoogle ScholarPubMed
Sohal, V. S., Huntsman, M. M. and Huguenard, J. R. (2000) Reciprocal inhibitory connections regulate the spatiotemporal properties of intrathalamic oscillations. Journal of Neuroscience 20: 1735–1745CrossRefGoogle ScholarPubMed
Solomon, J. S., Doyle, J. F., Burkhalter, H. and Nerbonne, J. M. (1993) Differential expression of hyperpolarization-activated currents reveals distinct classes of visual cortical projection neurons. Journal of Neuroscience 13: 5082–5091CrossRefGoogle ScholarPubMed
Soltesz, I. and Crunelli, V. (1992) GABAA and pre- and post-synaptic GABAB receptor-mediated responses in the lateral geniculate nucleus. In Progress in Brain Research (vol. 90), ed. R. R. Mize, R. E. Marc and A. M. Sillito, pp. 151–169, Amsterdam: Elsevier
Soltesz, I., Lightowler, S., Leresche, N., Jassik-Gerschenfeld, D. and Crunelli, V. (1991) Two inward currents and the transformation of low-frequency oscillations of rat and cat thalamocortical cells. Journal of Physiology (London) 441: 175–197CrossRefGoogle ScholarPubMed
Somogyi, P. (1977) A specific “axo-axonal” interneuron in the visual cortex of the rat. Brain Research 136: 345–350CrossRefGoogle ScholarPubMed
Somogyi, P. (1989) Synaptic organisation of GABAergic neurons and GABAA receptors in the lateral geniculate nucleus and visual cortex. In Retina Research Foundation Symposium, vol. 2, Neural mechanisms of visual perception, ed. D. K. T. Lam and C. D. Gilbert, pp. 35–62, Woodlands, TX: Portfolio
Somogyi, P. and Cowey, A. (1981) Combined Golgi and electron microscopic study on the synapses formed by double bouquet cells in the visual cortex of the cat and monkey. Journal of Comparative Neurology 195: 547–566CrossRefGoogle ScholarPubMed
Somogyi, P. and Freund, T. F. (1989) Immunocytochemistry and synaptic relationships of physiologically characterized, HRP-filled neurons. In Neuroanatomical Tract-Tracing Methods (vol. 2), ed. L. Heimer and L. Zaborsky, pp. 239–264, New York: Plenum
Somogyi, P. and Soltesz, I. (1986) Immunogold demonstration of GABA synaptic terminals of intracellularly recorded, horseradish peroxidase-filled basket cells and clutch cells in the cat's visual cortex. Neuroscience 19: 1051–1065CrossRefGoogle ScholarPubMed
Somogyi, P., Hajdu, F. and Tömböl, T. (1978) Ultrastructure of the anterior ventral and anterior medial nuclei of the cat thalamus. Experimental Brain Research 31: 417–431CrossRefGoogle ScholarPubMed
Somogyi, P., Smith, A. D., Nunzi, M. G., Gorio, A., Takagi, H. and Wu, J. Y. (1983) Glutamate decarboxylase immunoreactivity in the hippocampus of the cat: distribution of immunoreactive synaptic terminals with special reference to the axon initial segment of pyramidal neurons. Journal of Neuroscience 3: 1450–1468CrossRefGoogle ScholarPubMed
Somogyi, P., Freund, T. F., Hodgson, A. J., Somogyi, J., Beroukas, D. and Chubb, I. W. (1985) Identified axo-axonic cells are immunoreactive for GABA in the hippocampus and visual cortex of cats. Brain Research 332: 143–149CrossRefGoogle Scholar
Somogyi, P., Tamás, G., Lujan, R. and Buhl, E. H. (1998) Salient features of synaptic organisation in the cerebral cortex. Brain Research Reviews 26: 113–135CrossRefGoogle ScholarPubMed
Sontheimer, H., Kettenmann, H., Backus, K. H. and Schachner, M. (1988) Glutamate opens Na+/K+ channels in cultured astrocytes. Glia 1: 328–336CrossRefGoogle ScholarPubMed
Spencer, S. S. and Spencer, D. D. (1994) Entorhinal-hippocampal interactions in medial temporal lobe epilepsy. Epilepsia 35: 721–727CrossRefGoogle ScholarPubMed
Spencer, S. S., Williamson, P. D., Spencer, D. D. and Mattson, R. H. (1987) Human hippocampal seizure spread studied by depth and subdural recording: the hippocampal commissure. Epilepsia 28: 479–489CrossRefGoogle ScholarPubMed
Spencer, S. S., Kim, J., DeLanerolle, N. and Spencer, D. D. (1999) Differential neuronal and glia relations with parameters of ictal discharge in mesial temporal lobe epilepsy. Epilepsia 40: 708–712CrossRefGoogle ScholarPubMed
Spencer, W. A. and Brookhart, J. M. (1961) Electrical patterns of augmenting and recruiting waves in the depths of the sensorimotor cortex of cat. Journal of Neurophysiology 24: 26–49CrossRefGoogle Scholar
Spencer, W. A. and Kandel, E. R. (1961) Electrophysiology of hippocampal neurons. IV. Fast pre-potentials. Journal of Neurophysiology 24: 272–285CrossRefGoogle Scholar
Spreafico, R., Curtis, M., Frassoni, C. and Avanzini, G. (1988) Electrophysiological characteristics of morphologically identified reticular thalamic neurons from rat slices. Neuroscience 27: 629–638CrossRefGoogle ScholarPubMed
Spreafico, R., Frassoni, C., Regondi, M. C., Arcelli, P. and De Biasi, S. (1993) Interneurons in the mammalian thalamus, a marker of species? In Thalamic Networks for Relay and Modulation, ed. D. Minciacchi, M. Molinari, G. Macchi and E. G. Jones, pp. 17–28, New York: Pergamon Press
Squire, L. R. (1987) Memory and Brain. New York: Oxford University Press
Squire, L. R., Cohen, N. J. and Nadel, L. (1984) The medial temporal region and memory consolidation: a new hypthesis. In Memory Consolidation, ed. H. Weingartner and E. Parker, pp. 185–201, Hillsdale: Erlbaum
Staak, R. and Pape, H. C. (2001) Contribution of GABAA and GABAB receptors to thalamic neuronal activity during spontaneous absence seizures in rats. Journal of Neuroscience 21: 1378–1384CrossRefGoogle Scholar
Staba, R. J., Wilson, C. L., Bragin, A., Fried, I. and Engel, J. Jr. (2002) Sleep states differentiate single neuron activity recorded from human epileptic hippocampus, entorhinal cortex, and subiculum. Journal of Neuroscience 22: 5694–5704CrossRefGoogle ScholarPubMed
Stafstrom, C. E., Schwindt, P. C., Chubb, M. C. and Crill, W. E. (1985) Properties of persistent sodium conductance and calcium conductance of layer V neurons from cat sensorimotor cortex in vitro. Journal of Neurophysiology 53: 153–170CrossRefGoogle Scholar
Staley, K. J., Soldo, B. L. and Proctor, W. R. (1995) Ionic mechanisms of neuronal excitation by inhibitory GABAA receptors. Science 269: 977–981CrossRefGoogle ScholarPubMed
Stefan, H. and Snead, O. C. Jr. (1997) Absence seizures. In Epilepsy: A Comprehensive Textbook, ed. J. Engel Jr. and T. A. Pedley, pp. 579–590, Philadelphia: Lippincot-Raven
Steinhäuser, C. and Gallo, V. (1996) News on glutamate receptors on glial cells. Trends in Neurosciences 19: 339–345CrossRefGoogle ScholarPubMed
Steininger, T. L., Rye, D. B. and Wainer, B. H. (1992) Afferent projections to the cholinergic pedunculopontine tegmental nucleus and adjacent midbrain extrapyramidal area in the albino rat. Journal of Comparative Neurology 321: 515–543CrossRefGoogle ScholarPubMed
Steininger, T. L., Gong, H., McGinty, D. and Szymusiak, R. (2001) Subregional organization of preoptic/anterior hypothalamic projections to arousal-related monoaminergic cell groups. Journal of Comparative Neurology 429: 638–6533.0.CO;2-Y>CrossRefGoogle ScholarPubMed
Steriade, M. (1960) Mechanisms of facilitation and inhibition in focal cortical epilepsy induced by penicillin. Studies and Research in Neurology 5: 463–471 (in Romanian)Google Scholar
Steriade, M. (1964) Development of evoked responses into self-sustained activity within amygdalo-hippocampal circuits. Electroencephalography and Clinical Neurophysiology 16: 221–236CrossRefGoogle Scholar
Steriade, M. (1970) Ascending control of thalamic and cortical responsiveness. International Review of Neurobiology 12: 87–144CrossRefGoogle ScholarPubMed
Steriade, M. (1974) Interneuronal epileptic discharges related to spike-and-wave cortical seizures in behaving monkeys. Electroencephalography and Clinical Neurophysiology 37: 247–263CrossRefGoogle ScholarPubMed
Steriade, M. (1976) Cortical inhibition during sleep and waking. In Mechanisms in Transmission of Signal for Conscious Behavior, ed. T. Desiraju, pp. 209–248, Amsterdam: Elsevier
Steriade, M. (1978) Cortical long-axoned cells and putative interneurons during the sleep-waking cycle. Behavioral and Brain Sciences 3: 465–514CrossRefGoogle Scholar
Steriade, M. (1981) Mechanisms underlying cortical activation: neuronal organization and properties of the midbrain reticular core and intralaminar thalamic nuclei. In Brain Mechanisms of Perceptual Awareness and Purposeful Behavior, ed. O. Pompeiano and C. Ajmone-Marsan, pp. 327–377, New York: Raven Press
Steriade, M. (1984) The excitatory-inhibitory sequence in thalamic and neocortical cells: state-related changes and regulatory systems. In Dynamic Aspects of Neocortical Function, ed. G. M. Edelman, W. E. Gall and W. M. Cowan, pp. 107–157, New York: Wiley
Steriade, M. (1990) Spindling, incremental thalamocortical responses, and spike-wave epilepsy. In Generalized Epilepsy, ed. M. Avoli, P. Gloor, G. Kostopoulos and R. Naquet, pp. 161–180, Boston: Birkäuser
Steriade, M. (1991) Alertness, quiet sleep, dreaming. In Cerebral Cortex (vol. 9, Normal and Altered States of Function), ed. A. Peters and E. G. Jones, pp. 279–357, New York: Plenum
Steriade, M. (1995) Two channels in the cerebellothalamocortical system. Journal of Comparative Neurology 354: 57–70CrossRefGoogle ScholarPubMed
Steriade, M. (1997a) Synchronized activities of coupled oscillators in the cerebral cortex and thalamus at different levels of vigilance. Cerebral Cortex 7: 583–604CrossRefGoogle Scholar
Steriade, M. (1997b) Thalamic substrates of disturbances in states of vigilance and consciousness in humans. In Thalamus (vol. 2, Experimental and Clinical aspects), ed. M. Steriade, E. G. Jones and D. A. McCormick, pp. 721–742, Oxford: Elsevier
Steriade, M. (1998) Corticothalamic networks, oscillations, and plasticity. In Consciousness: At the Frontiers of Neuroscience (vol. 77, Advances in Neurology), ed. H. H. Jasper, L. Descarries, V. F. Castellucci and S. Rossignol, pp. 105–134, Philadelphia: Lippincott-Raven
Steriade, M. (1999a) Cellular substrates of brain rhythms. In Electroencephalography: Basic Principles, Clinical Applications, and Related Fields, 4th edn., ed. E. Niedermeyer and F. Lopes Da Silva, pp. 28–75, Baltimore: Williams & Wilkins
Steriade, M. (1999b) Coherent oscillations and short-term plasticity in corticothalamic networks. Trends in Neurosciences 22: 337–345CrossRefGoogle Scholar
Steriade, M. (2000) Corticothalamic resonance, states of vigilance, and mentation. Neuroscience 101: 243–276CrossRefGoogle ScholarPubMed
Steriade, M. (2001a) Impact of network activities on neuronal properties in corticothalamic systems. Journal of Neurophysiology 86: 1–39CrossRefGoogle Scholar
Steriade, M. (2001b) The Intact and Sliced Brain. Cambridge, MA: The MIT Press
Steriade, M. (2001c) The GABAergic reticular nucleus: a preferential target of corticothalamic projections. Proceedings of the National Academy of Sciences of the USA 98: 3625–3627CrossRefGoogle Scholar
Steriade, M. (2003) Presynaptic dendrites of thalamic local-circuit neurons and sculpting inhibition during activated states. Journal of Physiology (London) 546: 1CrossRefGoogle ScholarPubMed
Steriade, M. and Amzica, F. (1994) Dynamic coupling among neocortical neurons during evoked and spontaneous spike-wave seizure activity. Journal of Neurophysiology 72: 2051–2069CrossRefGoogle ScholarPubMed
Steriade, M. and Amzica, F. (1996) Intracortical and corticothalamic coherency of fast spontaneous oscillations. Proceedings of National Academy of Sciences of the USA 93: 2533–2538CrossRefGoogle ScholarPubMed
Steriade, M. and Amzica, F. (1998) Coalescence of sleep rhythms and their chronology in corticothalamic networks. Sleep Research Online 1: 1–10Google ScholarPubMed
Steriade, M. and Amzica, F. (1999) Intracellular study of excitability in the seizure-prone neocortex in vivo. Journal of Neurophysiology 82: 3108–3122CrossRefGoogle ScholarPubMed
Steriade, M. and Buzsáki, G. (1990) Parallel activation of thalamic and cortical neurons by brainstem and basal forebrain cholinergic systems. In Brain Cholinergic Systems, ed. M. Steriade and D. Biesold, pp. 3–63, Oxford: Oxford University Press
Steriade, M. and Contreras, D. (1995) Relations between cortical and thalamic cellular events during transition from sleep pattern to paroxysmal activity. Journal of Neuroscience 15: 623–642CrossRefGoogle Scholar
Steriade, M. and Contreras, D. (1998) Spike-wave complexes and fast runs of cortically generated seizures. I. Role of neocortex and thalamus. Journal of Neurophysiology 80: 1439–1455CrossRefGoogle ScholarPubMed
Steriade, M. and Demetrescu, M. (1960) Unspecific systems of inhibition and facilitation of potentials evoked by intermittent light. Journal of Neurophysiology 23: 602–617CrossRefGoogle Scholar
Steriade, M. and Deschênes, M. (1974) Inhibitory processes and interneuronal apparatus in motor cortex during sleep and waking. II. Recurrent and afferent inhibition of pyramidal tract neurons. Journal of Neurophysiology 37: 1093–1113CrossRefGoogle ScholarPubMed
Steriade, M. and Deschênes, M. (1984) The thalamus as a neuronal oscillator. Brain Research Reviews 8: 1–63CrossRefGoogle Scholar
Steriade, M. and Deschênes, M. (1987) Inhibitory processes in the thalamus. Journal of Mind and Behavior 8: 559–572Google Scholar
Steriade, M. and Deschênes, M. (1988) Intrathalamic and brainstem-thalamic networks involved in resting and alert states. In Cellular Thalamic Mechanisms, ed. M. Bentivoglio and R. Spreafico, pp. 37–62, Amsterdam: Elsevier
Steriade, M. and Glenn, L. L. (1982) Neocortical and caudate projections of intralaminar thalamic neurons and their synaptic excitation from the midbrain reticular core. Journal of Neurophysiology 48: 352–371CrossRefGoogle ScholarPubMed
Steriade, M. and Llinás, R. R. (1988) The functional states of the thalamus and the associated neuronal interplay. Physiological Reviews 68: 649–742CrossRefGoogle ScholarPubMed
Steriade, M. and McCarley, R. W. (1990) Brainstem Control of Wakefulness and Sleep. New York: Plenum
Steriade, M. and Morin, D. (1981) Reticular influences on primary and augmenting responses in the somatosensory cortex. Brain Research 205: 67–80CrossRefGoogle ScholarPubMed
Steriade, M. and Timofeev, I. (1997) Short-term plasticity during intrathalamic augmenting responses in decorticated cats. Journal of Neuroscience 17: 3778–3795CrossRefGoogle ScholarPubMed
Steriade, M. and Timofeev, I. (2001) Corticothalamic operations through prevalent inhibition of thalamocortical neurons. Thalamus and Related Systems 1: 225–236Google Scholar
Steriade, M. and Timofeev, I. (2002a) Generators of ictal and interictal electroencephalograms associated with infantile spasms: intracellular studies of cortical and thalamic neurons. International Review of Neurobiology 49: 77–98CrossRefGoogle Scholar
Steriade, M. and Timofeev, I. (2002b) Neuronal plasticity during sleep oscillations in corticothalamic systems. In Sleep and Brain Plasticity, ed. P. Maquet, R. Stickgold and C. S. Smith, in press, Oxford: Oxford University Press
Steriade, M. and Wyzinski, P. (1972) Cortically elicited activities in thalamic reticularis neurons. Brain Research 42: 514–520CrossRefGoogle ScholarPubMed
Steriade, M. and Yossif, G. (1974) Spike-and-wave afterdischarges in cortical somatosensory neurons of cat. Electroencephalography and Clinical Neurophysiology 37: 633–648CrossRefGoogle ScholarPubMed
Steriade, M., Iosif, G. and Apostol, V. (1969) Responsiveness of thalamic and cortical motor relays during arousal and various stages of sleep. Journal of Neurophysiology 32: 251–265CrossRefGoogle Scholar
Steriade, M., Apostol, V. and Oakson, G. (1971) Control of unitary activities in cerebellothalamic pathway during wakefulness and synchronized sleep. Journal of Neurophysiology 34: 389–413CrossRefGoogle ScholarPubMed
Steriade, M., Wyzinski, P. and Apostol, V. (1972) Corticofugal projections governing rhythmic thalamic activity. In Corticothalamic Projections and Sensorimotor Activities, ed. T. L. Frigyesi, E. Rinvik and M. D. Yahr, pp. 221–272. New York: Raven Press
Steriade, M., Deschênes, M. and Oakson, G. (1974a) Inhibitory processes and interneuronal apparatus in motor cortex during sleep and waking. I. Background firing and synaptic responsiveness of pyramidal tract neurons and interneurons. Journal of Neurophysiology 37: 1065–1092CrossRefGoogle Scholar
Steriade, M., Deschênes, M., Wyzinski, P. and Hallé, J. P. (1974b) Input-output organization of the motor cortex during sleep and waking. In Basic Sleep Mechanisms, ed. O. Petre-Quadens and J. Schlag, pp. 144–200, New York: Academic Press
Steriade, M., Oakson, G. and Diallo, A. (1976) Cortically elicited spike-wave afterdischarges in thalamic neurons. Electroencephalography and Clinical Neurophysiology 41: 641–644CrossRefGoogle Scholar
Steriade, M., Diallo, A., Oakson, G. and White-Guay, B. (1977a) Some synaptic inputs and ascending projections of lateral posterior thalamic neurons. Brain Research 131: 39–53CrossRefGoogle Scholar
Steriade, M., Oakson, G. and Diallo, A. (1977b) Reticular influences on lateralis posterior thalamic neurons. Brain Research 131: 55–71CrossRefGoogle Scholar
Steriade, M., Kitsikis, A. and Oakson, G. (1979a) Excitatory-inhibitory processes in parietal association neurons during reticular activation and sleep-waking cycle. Sleep 1: 339–355CrossRefGoogle Scholar
Steriade, M., Kitsikis, A. and Oakson, G. (1979b) Selectively REM-related increased firing rates in association interneurons during sleep: possible implications for learning. In Brain Mechanisms in Memory and Learning, ed. M. A. Brazier, pp. 47–52, New York: Raven Press
Steriade, M., Parent, A. and Hada, J. (1984) Thalamic projections of nucleus reticularis thalami: a study using retrograde transport of horseradish peroxidase and double fluorescent tracers. Journal of Comparative Neurology 229: 531–547CrossRefGoogle ScholarPubMed
Steriade, M., Deschênes, M., Domich, L. and Mulle, C. (1985) Abolition of spindle oscillations in thalamic neurons disconnected from nucleus reticularis thalami. Journal of Neurophysiology 54: 1473–1497CrossRefGoogle ScholarPubMed
Steriade, M., Domich, L. and Oakson, G. (1986) Reticularis thalami neurons revisited: activity changes during shifts in states of vigilance. Journal of Neuroscience 6: 68–81CrossRefGoogle ScholarPubMed
Steriade, M., Domich, L., Oakson, G. and Deschênes, M. (1987a) The deafferented reticularis thalami nucleus generates spindle rhythmicity. Journal of Neurophysiology 57: 260–273CrossRefGoogle Scholar
Steriade, M., Parent, A., Paré, D. and Smith, Y. (1987b) Cholinergic and non-cholinergic neurons of cat basal forebrain project to reticular and mediodorsal thalamic nuclei. Brain Research 408: 372–376CrossRefGoogle Scholar
Steriade, M., Paré, D., Parent, A. and Smith, Y. (1988) Projections of cholinergic and non-cholinergic neurons of the brainstem core to relay and associational thalamic nuclei in the cat and macaque monkey. Neuroscience 25: 47–67CrossRefGoogle ScholarPubMed
Steriade, M., Datta, S., Paré, D., Oakson, G. and Curró Dossi, R. (1990a) Neuronal activities in brainstem cholinergic nuclei related to tonic activation processes in thalamocortical systems. Journal of Neuroscience 10: 2541–2559CrossRefGoogle Scholar
Steriade, M., Jones, E. G. and Llinás, R. R. (1990b) Thalamic Oscillations and Signaling. New York: Wiley-Interscience
Steriade, M., Paré, D., Datta, S., Oakson, G. and Curró Dossi, R. (1990c) Different cellular types in mesopontine cholinergic nuclei related to ponto-geniculo-occipital waves. Journal of Neuroscience 10: 2560–2579CrossRefGoogle Scholar
Steriade, M., Gloor, P., Llinás, R. R., Lopes da Silva, F. H. and Mesulam, M. M. (1990d) Basic mechanisms of cerebral rhythmic activities. Electroencephalography and Clinical Neurophysiology 76: 481–508CrossRefGoogle Scholar
Steriade, M., Curró Dossi, R. and Nuñez, A. (1991a) Network modulation of a slow intrinsic oscillation of cat thalamocortical neurons implicated in sleep delta waves: cortical potentiation and brainstem cholinergic suppression. Journal of Neuroscience 11: 3200–3217CrossRefGoogle Scholar
Steriade, M., Curró Dossi, R., Paré, D. and Oakson, G. (1991b) Fast oscillations (20–40 Hz) in thalamocortical systems and their potentiation by mesopontine cholinergic nuclei in the cat. Proceedings of the National Academy of Sciences of the USA 88: 4396–4400CrossRefGoogle Scholar
Steriade, M., Amzica, F. and Nuñez, A. (1993a) Cholinergic and noradrenergic modulation of the slow (∼0.3 Hz) oscillation in neocortical cells. Journal of Neurophysiology 70: 1384–1400CrossRefGoogle Scholar
Steriade, M., Contreras, D., Curró Dossi, R. and Nuñez, A. (1993b) The slow (<1 Hz) oscillation in reticular thalamic and thalamocortical neurons: scenario of sleep rhythm generation in interacting thalamic and neocortical networks. Journal of Neuroscience 13: 3284–3299CrossRefGoogle Scholar
Steriade, M., Curró Dossi, R. and Contreras, D. (1993c) Electrophysiological properties of intralaminar thalamocortical cells discharging rhythmic (∼40 Hz) spike-bursts at ∼1000 Hz during waking and rapid eye movement sleep. Neuroscience 56: 1–9CrossRefGoogle Scholar
Steriade, M., McCormick, D. A. and Sejnowski, T. J. (1993d) Thalamocortical oscillation in the sleeping and aroused brain. Science 262: 679–685CrossRefGoogle Scholar
Steriade, M., Nuñez, A. and Amzica, F. (1993e) A novel slow (<1 Hz) oscillation of neocortical neurons in vivo: depolarizing and hyperpolarizing components. Journal of Neuroscience 13: 3252–3265CrossRefGoogle Scholar
Steriade, M., Nuñez, A. and Amzica, F. (1993f) Intracellular analysis of relations between the slow (<1 Hz) neocortical oscillation and other sleep rhythms. Journal of Neuroscience 13: 3266–3283CrossRefGoogle Scholar
Steriade, M., Amzica, F. and Contreras, D. (1994a) Cortical and thalamic cellular correlates of electroencephalographic burst-suppression. Electroencephalography and Clinical Neurophysiology 90: 1–16CrossRefGoogle Scholar
Steriade, M., Contreras, D. and Amzica, F. (1994b) Synchronized sleep oscillations and their paroxysmal developments. Trends in Neuroscience 17: 199–208CrossRefGoogle Scholar
Steriade, M., Amzica, F. and Contreras, D. (1996a) Synchronization of fast (30–40 Hz) spontaneous cortical rhythms during brain activation. Journal of Neuroscience 16: 392–417CrossRefGoogle Scholar
Steriade, M., Contreras, D., Amzica, F. and Timofeev, I. (1996b) Synchronization of fast (30–40 Hz) spontaneous oscillations in intrathalamic and thalamocortical networks. Journal of Neuroscience 16: 2788–2808CrossRefGoogle Scholar
Steriade, M., Jones, E. G. and McCormick, D. A. (1997) Thalamus (vol. 1, Organisation and Function). Oxford: Elsevier
Steriade, M., Amzica, F., Neckelmann, D. and Timofeev, I. (1998a) Spike-wave complexes and fast runs of cortically generated seizures. II. Extra- and intracellular patterns. Journal of Neurophysiology 80: 1456–1479CrossRefGoogle Scholar
Steriade, M., Timofeev, I., Dürmüller, N. and Grenier, F. (1998b) Dynamic properties of corticothalamic neurons and local cortical interneurons generating fast rhythmic (30–40 Hz) spike bursts. Journal of Neurophysiology 79: 483–490CrossRefGoogle Scholar
Steriade, M., Timofeev, I. and Grenier, F. (1998c) Inhibitory components of cortical spike-wave seizures in vivo. Society for Neuroscience Abstracts 24: 2143Google Scholar
Steriade, M., Timofeev, I., Grenier, F. and Dürmüller, N. (1998d) Role of thalamic and cortical neurons in augmenting responses: dual intracellular recordings in vivo. Journal of Neuroscience 18: 6425–6443CrossRefGoogle Scholar
Steriade, M., Timofeev, I. and Grenier, F. (2001a) Natural waking and sleep states: a view from inside neocortical neurons. Journal of Neurophysiology 85: 1969–1985CrossRefGoogle Scholar
Steriade, M., Timofeev, I. and Grenier, F. (2001b) Intrinsic, antidromic and synaptic excitability of cortical neurons during natural waking-sleep cycle. Society for Neuroscience Abstracts 27: 240Google Scholar
Sterman, M. B. and Clemente, C. D. (1962a) Forebrain inhibitory mechanisms: cortical synchronization induced by basal forebrain stimulation. Experimental Neurology 6: 91–102CrossRefGoogle Scholar
Sterman, M. B. and Clemente, C. D. (1962b) Forebrain inhibitory mechanisms: sleep patterns induced by basal forebrain stimulation in the behaving cat. Experimental Neurology 6: 103–117CrossRefGoogle Scholar
Stevens, D. R., Greene, R. W. and McCarley, R. W. (1992) Serotonin 1 and serotonin 2 receptors hyperpolarize and depolarize separate populations of medial pontine reticular formation neurons in vitro. Neuroscience 47: 545–553CrossRefGoogle Scholar
Stewart, M. and Fox, S. E. (1991) Hippocampal theta activity in monkeys. Brain Research 538: 59–63CrossRefGoogle ScholarPubMed
Stickgold, R., Whitbee, D., Schirmer, B., Patel, V. and Hobson, J. A. (2000) Visual discrimination improvement. A multi-step process occurring during sleep. Journal of Cognitive Neuroscience 12: 246–254CrossRefGoogle ScholarPubMed
Stuart, G. and Sakmann, B. (1995) Amplification of EPSPs by axosomatic sodium channels in neocortical pyramidal neurons. Neuron 15: 1065–1076CrossRefGoogle ScholarPubMed
Sugita, S., Tanaka, E. and North, R. A. (1993) Membrane properties and synaptic potentials of three types of neurone in rat lateral amygdala. Journal of Physiology (London) 460: 705–718CrossRefGoogle ScholarPubMed
Sundstrom, L. E., Brana, C., Gatherer, M., Mepham, J. and Rougier, A. (2001) Somatostatin- and neuropeptide Y-synthesizing neurones in the fascia dentate of humans with temporal lobe epilepsy. Brain 124: 688–697CrossRefGoogle ScholarPubMed
Sutherland, G. R. and McNaughton, B. (2000) Memory traces reactivation in hippocampal and neocortical neuronal ensembles. Current Opinion in Neurobiology 10: 180–186CrossRefGoogle ScholarPubMed
Sutherling, W. W., Crandall, P. H., Cahan, L. D. and Barth, D. S. (1988) The magnetic field of epileptic spikes agrees with intracranial localizations in complex partial epilepsy. Neurology 38: 778–786CrossRefGoogle ScholarPubMed
Sutula, T., He, X. X., Cavazos, J. and Scott, G. (1988) Synaptic reorganization in the hippocampus induced by abnormal functional activity. Science 239: 1147–1150CrossRefGoogle ScholarPubMed
Suzuki, W. A. (1996) The anatomy, physiology and functions of the perirhinal cortex. Current Opinion in Neurobiology 6: 179–186CrossRefGoogle ScholarPubMed
Svensson, T. H., Bunney, B. S. and Aghajanian, G. K. (1975) Inhibition of both noradrenergic and serotonergic neurons in brain by the alpha-adrenergic agonist clonidine. Brain Research 92: 291–306CrossRefGoogle ScholarPubMed
Swann, J. W., Smith, K. L. and Brady, R. J. (1993) Localized excitatory synaptic interactions mediate the sustained depolarization of electrographic seizure in developing hippocampus. Journal of Neuroscience 13: 4680–4689CrossRefGoogle ScholarPubMed
Swann, J. W., Al-Noori, S., Jiang, M. and Lee, C. L. (2000) Spine loss and other dendritic abnormalities in epilepsy. Hippocampus 10: 617–6253.0.CO;2-R>CrossRefGoogle ScholarPubMed
Sypert, G. W. and Ward, A. A. Jr. (1971) Unidentified neuroglia potentials during propagated seizures in neocortex. Experimental Neurology 33: 239–255CrossRefGoogle ScholarPubMed
Szentágothai, J. (1978) The neuron network of the cerebral cortex: a functional interpretation. The Ferrier Lecture. Proceedings of the Royal Society (London, Series B) 201: 219–248CrossRefGoogle ScholarPubMed
Szentágothai, J. and Arbib, M. A. (1974) Conceptual models of neural organization. Neuroscience Research Program Bulletin 12: 307–510Google ScholarPubMed
Szymusiak, R. and McGinty, D. (1986) Sleep-related neuronal discharge in the basal forebrain of cats. Brain Research 370: 82–92CrossRefGoogle ScholarPubMed
Szymusiak, R. and McGinty, D. (1989) Sleep-waking discharge of basal forebrain projection neurons in cats. Brain Research Bulletin 22: 423–430CrossRefGoogle ScholarPubMed
Szymusiak, R., Shouse, M. N. and McGinty, D. (1966) Brainstem stimulation during sleep evokes abnormal rhythmic activity in thalamic neurons in feline penicillin epilepsy. Brain Research 713: 253–260CrossRefGoogle Scholar
Szymusiak, R., Steininger, T., Alam, N. and McGinty, D. (2001) Preoptic area sleep-regulating mechanisms. Archives Italiennes de Biologie 139: 77–92Google ScholarPubMed
Tamás, G., Buhl, E. H. and Somogyi, P. (1997) Fast IPSPs elicited via multiple synaptic release sites by distinct types of GABAergic neurone in the cat visual cortex. Journal of Physiology (London) 500: 715–738CrossRefGoogle ScholarPubMed
Tancredi, V., Biagini, G., D'Antuono, M., Louvel, J., Pumain, R. and Avoli, M. (2000) Spindle-like thalamocortical synchronization in a rat brain slice preparation. Journal of Neurophysiology 84: 1093–1097CrossRefGoogle Scholar
Tasker, G. J. and Dudek, F. E. (1991) Electrophysiology of GABA-mediated synaptic transmission and possible roles in epilepsy. Neurochemical Research 16: 251–262CrossRefGoogle ScholarPubMed
Tauck, D. L. and Nadler, J. V. (1985) Evidence of functional mossy fiber sprouting in hippocampal formation of kainic acid-treated rats. Journal of Neuroscience 5: 1016–1022CrossRefGoogle ScholarPubMed
Taylor-Courval, D. and Gloor, P. (1984) Behavioral alterations associated with generalized spike and wave discharges in the EEG of the cat. Experimental Neurology 83: 167–186CrossRefGoogle ScholarPubMed
Telfeian, A. E. and Connors, B. W. (1998) Layer-specific pathways for the horizontal propagation of epileptiform discharges in neocortex. Epilepsia 39: 700–708CrossRefGoogle ScholarPubMed
Temkin, O. (1971) The Falling Sickness. Baltimore: Johns Hopkins University Press
Terman, D., Bose, A. and Kopell, N. (1996) Functional reorganization in thalamocortical networks: transition between spindling and delta sleep rhythms. Proceedings of the National Academy of Sciences of the USA 93: 15417–15422CrossRefGoogle ScholarPubMed
Terzano, M. G., Parrino, L. and Spaggiari, M. C. (1988) The cyclic alternating pattern sequences in the dynamic organization of sleep. Electroencephalography and Clinical Neurophysiology 69: 437–447CrossRefGoogle Scholar
Terzano, M. G., Parrino, L., Spaggiari, M. C., Barusi, R. and Simeoni, S. (1991) Discriminatory effect of cyclic alternating pattern in focal lesioned and benign rolandic interictal spikes during sleep. Epilepsia 32: 616–628CrossRefGoogle Scholar
Thomas, J. E. and Klass, D. W. (1968) Six-per-second spike and wave pattern in the electroencephalogram. Neurology 18: 587–593CrossRefGoogle ScholarPubMed
Thompson, S. M. and Gähwiler, B. H. (1989) Activity-dependent disinhibition. I. Repetitive stimulation reduces IPSP driving force and conductance in the hippocampus in vitro. Journal of Neurophysiology 61: 501–511CrossRefGoogle ScholarPubMed
Thomson, A. M. (1988a) Inhibitory postsynaptic potentials evoked in thalamic neurons by stimulation of the reticularis nucleus evoke slow spikes in isolated rat brain slices. Neuroscience 25: 491–502CrossRefGoogle Scholar
Thomson, A. M. (1988b) Biphasic responses of thalamic neurons to GABA in isolated rat brain slices. Neuroscience 25: 503–512CrossRefGoogle Scholar
Thomson, A. M. (1997) Activity-dependent properties of synaptic transmission at two classes of connections made by rat neocortical pyramidal axons in vitro. Journal of Physiology (London) 502: 131–147CrossRefGoogle ScholarPubMed
Thomson, A. M. and Deuchars, J. (1997) Synaptic interactions in neocortical local circuits: dual intracellular recordings in vitro. Cerebral Cortex 7: 510–522CrossRefGoogle ScholarPubMed
Thomson, A. M. and West, D. C. (1993) Fluctuations in pyramid-pyramid excitatory postsynaptic potentials modified by presynaptic firing pattern and postsynaptic membrane potential using paired intracellular recordings in rat neocortex. Neuroscience 54: 329–346CrossRefGoogle ScholarPubMed
Thomson, A. M., Girldestone, D. and West, D. C. (1988) Voltage-dependent currents prolong single-axon postsynaptic potentials in layer III pyramidal neurons in rat neocortical slices. Journal of Neurophysiology 60: 1896–1907CrossRefGoogle ScholarPubMed
Thomson, A. M., Deuchars, J. and West, D. C. (1993a) Large, deep layer pyramid-pyramid single axon EPSPs in slices of rat motor cortex display paired pulse and frequency-dependent depression, mediated presynaptically and self-facilitation, mediated postsynaptically. Journal of Neurophysiology 70: 2354–2369CrossRefGoogle Scholar
Thomson, A. M., Deuchars, J. and West, D. C. (1993b) Single axon excitatory postsynaptic potentials in neocortical interneurons exhibit pronounced paired pulse facilitation. Neuroscience 54: 347–360CrossRefGoogle Scholar
Thomson, A. M., West, D. C. and Deuchars, J. (1995) Properties of single axon excitatory postsynaptic potentials elicited in spiny interneurons by action potentials in pyramidal neurons in slices of rat neocortex. Neuroscience 69: 727–738CrossRefGoogle ScholarPubMed
Thomson, A. M., West, D. C., Hahn, J. and Deuchars, J. (1996) Single axon IPSPs elicited in pyramidal cells by three classes of interneurons in slices of rat neocortex. Journal of Physiology (London) 496: 81–102CrossRefGoogle ScholarPubMed
Timofeev, I. and Steriade, M. (1996) Low-frequency rhythms in the thalamus of intact-cortex and decorticated cats. Journal of Neurophysiology 76: 4152–4168CrossRefGoogle ScholarPubMed
Timofeev, I. and Steriade, M. (1997) Fast (mainly 30–100 Hz) oscillations in the cat cerebellothalamic pathway and their synchronization with cortical potentials. Journal of Physiology (London) 504: 153–168CrossRefGoogle ScholarPubMed
Timofeev, I. and Steriade, M. (1998) Cellular mechanisms underlying intrathalamic augmenting responses of reticular and relay neurons. Journal of Neurophysiology 79: 2716–2729CrossRefGoogle ScholarPubMed
Timofeev, I., Contreras, D. and Steriade, M. (1996) Synaptic responsiveness of cortical and thalamic neurons during various phases of slow oscillation in cat. Journal of Physiology (London) 494: 265–278CrossRefGoogle ScholarPubMed
Timofeev, I., Grenier, F. and Steriade, M. (1998) Spike-wave complexes and fast runs of cortically generated seizures. IV. Paroxysmal fast runs in cortical and thalamic neurons. Journal of Neurophysiology 80: 1495–1513CrossRefGoogle ScholarPubMed
Timofeev, I., Grenier, F., Bazhenov, M., Sejnowski, T. J. and Steriade, M. (2000a) Origin of slow oscillations in deafferented cortical slabs. Cerebral Cortex 10: 1185–1199CrossRefGoogle Scholar
Timofeev, I., Grenier, F., Bazhenov, M., Sejnowski, T. J. and Steriade, M. (2000b) Impact of intrinsic properties and synaptic factors on the activity of neocortical networks in vivo. Journal of Physiology (Paris) 94: 343–355CrossRefGoogle Scholar
Timofeev, I., Bazhenov, M., Sejnowski, T. J. and Steriade, M. (2001a) Contribution of intrinsic and synaptic factors in the desynchronization of thalamic oscillatory activity. Thalamus and Related Systems 1: 53–69Google Scholar
Timofeev, I., Grenier, F. and Steriade, M. (2001b) Disfacilitation and active inhibition in the neocortex during the natural sleep-wake cycle: an intracellular study. Proceedings of the National Academy of Sciences of the USA 98: 1924–1929CrossRefGoogle Scholar
Timofeev, I., Bazhenov, M., Sejnowski, T. J. and Steriade, M. (2002a) Cortical IH takes part in the generation of paroxysmal activities. Proceedings of the National Academy of Sciences of the USA 99: 9533–9537CrossRefGoogle Scholar
Timofeev, I., Grenier, F., Bazhenov, M., Houweling, A., Sejnowski, T. J. and Steriade, M. (2002b) Short- and medium-term plasticity associated with augmenting responses in cortical slabs and spindles in intact cortex of cats in vivo. Journal of Physiology (London) 542: 583–598CrossRefGoogle Scholar
Timofeev, I., Grenier, F. and Steriade, M. (2002c) The role of chloride-dependent inhibition and the activity of fast-spiking neurons during cortical spike-wave seizures. Neuroscience 114: 1115–1132CrossRefGoogle Scholar
Tononi, G. and Cirelli, C. (2001) Some considerations on sleep and neural plasticity. Archives Italiennes de Biologie 139: 221–241Google ScholarPubMed
Tononi, G., Cirelli, C. and Shaw, P. J. (2000) The molecular correlates of sleep, waking and sleep deprivation. In The Regulation of Human (Human Frontier Workshop VIII), ed. A. Borbély, O. Hayaishi, T. J. Sejnowski and J. S. Altman, pp. 155–167, Strasbourg: Human Frontier Science Program
Topolnik, L., Steriade, M. and Timofeev, I. (2001) Neocortical deafferentation potentiates development of paroxysmal activities. Society for Neuroscience Abstracts 27: 288Google Scholar
Topolnik, L., Steriade, M. and Timofeev, I. (2003) Partial cortical deafferentation promotes development of paroxysmal activity. Submitted
Torres, E. M., Perry, T. A., Blockland, A., Wilkinson, L. S., Wiley, R. G., Lappi, D. A. and Dunnet, S. B. (1994) Behavioural, histochemical and biochemical consequences of selective immunolesion in discrete regions of the basal forebrain cholinergic system. Neuroscience 63: 95–122CrossRefGoogle Scholar
Traub, R. D. and Llinás, R. (1979) Hippocampal pyramidal cells: significance of dendritic ionic conductances for neuronal function and epileptogenesis. Journal of Neurophysiology 42: 476–496CrossRefGoogle ScholarPubMed
Traub, R. D. and Wong, R. K. S. (1981) Penicillin-induced epileptiform activity in the hippocampal slice: a model of synchronization of CA3 pyramidal cell bursting. Neuroscience 6: 223–230CrossRefGoogle ScholarPubMed
Traub, R. D., Miles, R. and Jefferys, J. G. R. (1993) Synaptic and intrinsic conductances shape picrotoxin-induced synchronized after-discharges in the guinea-pig hippocampal slices. Journal of Physiology (London) 461: 525–547CrossRefGoogle Scholar
Traub, R. D., Whittington, M. A., Stanford, I. M. and Jefferys, J. G. R. (1996) A mechanism for generation of long-range synchronous fast oscillations in the cortex. Nature 383: 621–624CrossRefGoogle ScholarPubMed
Traub, R. D., Jefferys, J. G. R. and Whittington, M. A. (1999a) Fast Oscillations in Cortical Circuits. Cambridge, MA: The MIT Press
Traub, R. D., Schmitz, D., Jefferys, J. G. R. and Draguhn, A. (1999b) High-frequency population oscillations are predicted to occur in hippocampal pyramidal neuronal networks interconnected by axoaxonal gap junctions. Neuroscience 92: 407–426CrossRefGoogle Scholar
Traub, R. D., Whittington, M. A., Bühl, E. H., LeBeau, F. N., Bibbig, A., Boyd, S., Cross, H. and Baldeweg, T. A. (2001) A possible role for gap junctions in generation of very fast EEG oscillations preceding the onset of, and perhaps initiating, seizures. Epilepsia 42: 153–170Google ScholarPubMed
Traub, R. D., Buhl, E. H., Gloveli, T. and Whittington, M. A. (2003) A model of a layer 2/3 neocortical pyramidal neuron demonstrating multiple compartment-specific firing patterns, including fast rhythmic bursting. Journal of Neurophysiology, in pressGoogle Scholar
Traynelis, S. F. and Dingledine, R. (1988) Potassium-induced spontaneous electrographic seizures in the rat hippocampal slice. Journal of Neurophysiology 59: 259–276CrossRefGoogle ScholarPubMed
Treitman, L. J. and Treitman, D. M. (1999) Genetic epilepsy – generalized. In The Epilepsies, ed. P. Kotagal and H. O. Lüders, pp. 543–549, San Diego: Academic Press
Treves, A. and Rolls, E. T. (1994) A computational analysis of the role of the hippocampus in memory. Hippocampus 4: 374–391CrossRefGoogle ScholarPubMed
Trulson, M. E. and Jacobs, B. L. (1979) Raphe unit activity in freely moving cats: correlation with level of behavioral arousal. Brain Research 163: 135–150CrossRefGoogle ScholarPubMed
Trulson, M. E., Crisp, T. and Trulson, V. M. (1984) Activity of serotonin-containing nucleus centralis superior (raphe medianus) neurons in freely moving cats. Experimental Brain Research 54: 33–44CrossRefGoogle ScholarPubMed
Tsakiridou, E., Bertollini, L., Curtis, M., Avanzini, G. and Pape, H. C. (1995) T-type calcium conductance in the reticular thalamic nucleus: a contribution to absence epilepsy. Journal of Neuroscience 15: 3110–3117CrossRefGoogle Scholar
Tseng, G. F. and Prince, D. A. (1996) Structural and functional alterations in rat corticospinal neurons following axotomy. Journal of Neurophysiology 75: 248–267CrossRefGoogle ScholarPubMed
Tseng, K. Y., Kasanetz, F., Kargieman, L., Riquelne, L. A. and Murer, M. G. (2001) Cortical slow oscillatory activity is reflected in the membrane potential and spike trains of striatal neurons in rats with chronic nigrostriatal lesions. Journal of Neuroscience 21: 6430–6439CrossRefGoogle ScholarPubMed
Tsodyks, M., Kenet, T., Grinvald, A. and Arieli, A. (1999) Linking spontaneous activity of single cortical neurons and the underlying functional architecture. Science 286: 1943–1946CrossRefGoogle ScholarPubMed
Turner, D. A. and Wheal, H. V. (1991) Excitatory synaptic potentials in kainic acid-denervated rat CA1 pyramidal neurons. Journal of Neuroscience 11: 2786–2794CrossRefGoogle ScholarPubMed
Turrini, P., Casu, M. A., Wong, T. P., Koninck, Y., Ribeiro-da-Silva, A. and Cuello, A. C. (2001) Cholinergic nerve terminals establish classical synapses in the rat cerebral cortex: synaptic pattern and age-related atrophy. Neuroscience 105: 277–285CrossRefGoogle ScholarPubMed
Tuunanen, J., Lukasiuk, K., Halonen, T. and Pitkänen, A. (1999) Status epilepticus-induced neuronal damage in the rat amygdaloid complex: distribution, time-course and mechanisms. Neuroscience 94: 473–495CrossRefGoogle ScholarPubMed
Uchida, S., Maloney, T., March, J. D., Azari, R. and Feinberg, I. (1991) Sigma (12–15 Hz) and delta (0.3–3.0 Hz) EEG oscillate reciprocally within NREM sleep. Brain Research Bulletin 27: 93–96CrossRefGoogle Scholar
Ueno, R., Honda, K., Inoue, S. and Hayaishi, O. (1983) Prostaglandin D2, a cerebral sleep-inducing substance in rats. Proceedings of the National Academy of Sciences of the USA 80: 1735–1737CrossRefGoogle ScholarPubMed
Uhl, G. R., Tran, V., Snyder, S. H. and Martin, J. B. (1985) Somatostatin receptors: distribution in rat central nervous system and human frontal cortex. Journal of Comparative Neurology 240: 266–304Google ScholarPubMed
Uhlrich, D. and Huguenard, J. R. (1996) GABAB receptor-mediated responses in GABAergic projection neurones of rat nucleus reticularis thalami in vitro. Journal of Physiology (London) 493: 845–854CrossRefGoogle Scholar
Uhlrich, D. and Huguenard, J. R. (1997) GABAA-receptor-mediated rebound burst firing and burst shunting in thalamus. Journal of Neurophysiology 78: 1748–1751CrossRefGoogle Scholar
Uhlrich, D. J., Manning, K. A. and Xue, J. T. (2002) Effects of activation of the histaminergic tuberomammillary nucleus on visual responses of neurons in the dorsal lateral geniculate nucleus. Journal of Neuroscience 22: 1098–1107CrossRefGoogle ScholarPubMed
Umbriaco, D., Watkins, K. C., Descarries, L., Cozzari, C. and Hartman, B. K. (1994) Ultrastructural and morphometric features of the acetylcholine innervation in adult rat parietal cortex. An electron microscopic study in serial sections. Journal of Comparative Neurology 348: 351–373CrossRefGoogle ScholarPubMed
Urbano, F. J., Leznik, E. and Llinás, R. R. (2001) Cortical activation patterns evoked by afferent axons stimuli at different frequencies: an in vitro voltage sensitive dye imaging study. Thalamus and Related Systems 1: 371–378Google Scholar
Brederode, J. and Spain, W. (1995) Differences in inhibitory synaptic input between layer II–III and layer V neurons of the cat neocortex. Journal of Neurophysiology 74: 1149–1166CrossRefGoogle Scholar
Vanderwolf, C. H. (1969) Hippocampal electrical activity and voluntary movement in the rat. Electroencephalography and Clinical Neurophysiology 26: 407–418CrossRefGoogle ScholarPubMed
Vanderwolf, C. H. (1988) Cerebral activity and behavior: control by central cholinergic and serotonergic systems. International Reviews of Neurobiology 30: 225–340CrossRefGoogle ScholarPubMed
Hoesen, G. W., Hyman, B. T. and Damasio, A. R. (1991) Entorhinal cortex pathology in Alzheimer's disease. Hippocampus 1: 1–8CrossRefGoogle ScholarPubMed
Luijtelaar, E. L. and Coenen, A. M. (1986) Two types of electrocortical paroxysms in an inbred strain of rats. Neuroscience Letters 70: 393–397CrossRefGoogle Scholar
Vanni-Mercier, G., Sakai, K. and Jouvet, M. (1984) Neurones spécifiques de l'éveil dans l'hypothalamus postérieur du chat. Comptes Rendus de l'Académie des Sciences (Paris) 298: 195–200Google Scholar
Velasco, F. and Velasco, M. (1990) Mesencephalic structures and tonic-clonic generalized seizures. In Generalized Epilepsy: Cellular, Molecular and Pharmacological Approach, ed. M. Avoli, P. Gloor, G. Kostopoulos and R. Naquet, pp. 368–384, Boston: Birkhäuser
Velasco, F., Velasco, M., Cepeda, C. and Munoz, H. (1980) Wakefulness-sleep modulation of cortical and subcortical somatic evoked potentials in man. Electroencephalography and Clinical Neurophysiology 48: 64–72CrossRefGoogle ScholarPubMed
Velasco, F., Velasco, M., Velasco, A. L., Jiménez, F., Márquez, I. and Rise, M. (1995) Electrical stimulation of the centromedian thalamic nucleus in the control of intractable seizures: long-term studies. Epilepsia 36: 63–71CrossRefGoogle Scholar
Velasco, F., Velasco, M., Jiménez, F., Velasco, A. L., Rojas, B. and Perez, M. L. (2001) Centromedian nucleus stimulation for epilepsy: clinical, electroencephalographic, and behavioral observations. Thalamus and Related Systems 1: 387–398Google Scholar
Velayos, J. L., Jimenez-Castellanos, J. Jr. and Reinoso-Suárez, F. (1989) Topographical organization of the projections from the reticular thalamic nucleus to the intralaminar and medial thalamic nuclei in the cat. Journal of Comparative Neurology 279: 457–469CrossRefGoogle ScholarPubMed
Vergnes, M. and Marescaux, C. (1992) Cortical and thalamic lesions in rats with genetic absence epilepsy. Journal of Neural Transmission 35 (Suppl.): 71–83Google ScholarPubMed
Vertes, R. P. and Kocsis, B. (1997) Brainstem-diencephalo-septohippocampal systems controlling the theta rhythm of the hippocampus. Neuroscience 81: 893–926Google ScholarPubMed
Villablanca, J. (1974) Role of the thalamus in sleep control: sleep-wakefulness studies of chronic cats without the thalamus: the “athalamic cat”. In Basic Sleep Mechanisms, ed. O. Petre-Quadens and J. Schlag, pp. 51–81, New York: Academic
Villablanca, J. R., Andrés, I. and Olmstead, C. E. (2001) Sleep-waking states develop independently in the isolated forebrain and brain stem following early postnatal midbrain transection in cats. Neuroscience 106: 717–731CrossRefGoogle ScholarPubMed
Krosigk, M., Bal, T. and McCormick, D. A. (1993) Cellular mechanisms of a synchronized oscillation in the thalamus. Science 261: 361–364CrossRefGoogle Scholar
Wada, J. A. and Terao, A. (1970) Effect of parachlorophenylalanine on basal forebrain stimulation. Experimental Neurology 28: 501–506CrossRefGoogle Scholar
Wadman, W. J. and Gutnick, M. J. (1993) Non-uniform propagation of epileptiform discharge in brain slices of rat neocortex. Neuroscience 53: 899–904Google Scholar
Walshe, F. M. R. (1957) The brain-stem conceived as the “highest level” of function in the nervous system: with particular reference to the “automatic apparatus” of Carpenter (1850) and to the “centrencephalic integrating system” of Penfield. Brain 80: 510–539CrossRefGoogle ScholarPubMed
Walter, G. (1936) The location of cerebral tumors by electroencephalography. Lancet 8: 305–308CrossRefGoogle Scholar
Wang, X. J. and Rinzel, J. (1993) Spindle rhythmicity in the reticularis thalami nucleus: synchronization among mutually inhibitory neurons. Neuroscience 53: 899–904CrossRefGoogle ScholarPubMed
Wang, Z. and McCormick, D. A. (1993) Control of firing mode of corticotectal and corticopontine layer V burst-generating neurons by norepinephrine, acetylcholine and 1S, 3R-ACPD. Journal of Neuroscience 13: 2199–2216CrossRefGoogle Scholar
Ward, A. A. (1975) Topical convulsants metals. In Experimental Models of Epilepsy, ed. D. P. Purpura, J. K. Penry, D. B. Tower, D. M. Woodbury and R. D. Walter, pp. 13–35, New York: Raven Press
Ward, A. A. and Schmidt, R. P. (1961) Some properties of single epileptic neurons. Archives of Neurology 5: 308–313CrossRefGoogle ScholarPubMed
Ward, A. A., Jasper, H. H. and Pope, A. (1969) Clinical and experimental challenges of the epilepsies. In Basic Mechanisms of the Epilepsies, ed. H. H. Jasper, A. A. Ward and A. Pope, pp. 1–12, Boston: Little, Brown
Watson, C. W. and Bowker, R. (1960) On the significance of circumscribed electroencephalographic abnormalities in genetic light sensitive states including cases of genetic epilepsy with “centrencephalic” epilepsy. Electroencephalography and Clinical Neurophysiology 12: 551Google Scholar
Weber, A. J., Kalil, R. E. and Behan, M. (1989) Synaptic connections between corticogeniculate axons and interneurons in the dorsal lateral geniculate nucleus of the cat. Journal of Comparative Neurology 289: 156–164CrossRefGoogle ScholarPubMed
Werth, E., Achermann, P., Dijk, D. J. and Borbély, A. (1997) Spindle frequency activity in the sleep EEG: individual differences and topographical distribution. Electroencephalography and Clinical Neurophysiology 103: 535–542CrossRefGoogle Scholar
West, W. J. (1841) On a particular form of infantile convulsions. Lancet 1: 724–725CrossRefGoogle Scholar
Westerberg, V. and Corcoran, M. E. (1987) Antagonism of central but not peripheral cholinergic receptors retards amygdala kindling in rats. Experimental Neurology 95: 194–206CrossRefGoogle Scholar
Westerfield, M., Joyner, R. W. and Moore, J. W. (1978) Temperature-sensitive conduction failure at axon branch points. Journal of Neurophysiology 41: 1–8CrossRefGoogle ScholarPubMed
Westgaard, J. H., Bonato, P. and Holte, K. A. (2002) Low-frequency oscillations (<;0.3 Hz) in the electromyographic (EMG) activity of the human trapezius muscle during sleep. Journal of Neurophysiology 88: 1177–1184CrossRefGoogle ScholarPubMed
Wheal, H. V., Bernard, C., Chad, J. E. and Cannon, R. C. (1998) Pro-epileptic changes in synaptic function can be accompanied by pro-epileptic changes in neuronal excitability. Trends in Neurosciences 21: 167–174CrossRefGoogle ScholarPubMed
White, J. C. (1940) Autonomic discharge from stimulation of the hypothalamus. In The Hypothalamus and Central Levels of Autonomic Function, ed. J. F. Fulton, S. W. Ranson and A. M. Frantz, pp. 854–863, Baltimore: Williams and Wilkins
White, J. C., Langston, J. W. and Pedley, T. A. (1977) Benign epileptiform transients of sleep: clarification of the small sharp spike controversy. Neurology 27: 1061–1068CrossRefGoogle ScholarPubMed
Wilcox, K. S., Gutnick, M. J. and Cristoph, G. R. (1988) Electrophysiological properties of neurons in the lateral habenular nucleus: an in vitro study. Journal of Neurophysiology 59: 212–225CrossRefGoogle Scholar
Wilcox, K. S., Grant, S. J., Burkhart, B. A. and Cristoph, G. R. (1989) In vivo electrophysiology of neurons in the lateral dorsal tegmental nucleus. Brain Research Bulletin 22: 557–560CrossRefGoogle Scholar
Wilder, B. J. and Morrell, F. (1967) Cellular behavior in secondary epileptic lesions. Neurology 17: 1193–1204CrossRefGoogle ScholarPubMed
Williams, D. (1953) A study of thalamic and cortical rhythms in Petit Mal. Brain 76: 50–69CrossRefGoogle ScholarPubMed
Williams, J. A. and Reiner, P. B. (1993) Noradrenaline hyperpolarizes identified rat mesopontine cholinergic neurons in vitro. Journal of Neuroscience 13: 3878–3883CrossRefGoogle ScholarPubMed
Williams, J. A., Comisarow, J., Day, J., Fibiger, H. C. and Reiner, P. B. (1994) State-dependent release of acetylcholine in rat thalamus measured by in vivo microdialysis. Journal of Neuroscience 14: 5236–5242CrossRefGoogle ScholarPubMed
Williamson, A. M., Ohara, P. T. and Ralston, H. J. (1993) Electron microscopic evidence that cortical terminals make direct contacts onto cells of the thalamic reticular nucleus in the monkey. Brain Research 631: 175–179CrossRefGoogle ScholarPubMed
Williamson, A., Telfeian, A. E. and Spencer, D. D. (1995) Prolonged GABA responses in dentate granule cells in slices isolated from patients with temporal lobe sclerosis. Journal of Neurophysiology 74: 378–387CrossRefGoogle ScholarPubMed
Williamson, R. and Wheal, H. V. (1992) The contribution of AMPA and NMDA receptors to graded bursting activity in the hippocampal CA1 region in an acute in vitro model of epilepsy. Epilepsy Research 12: 179–188CrossRefGoogle Scholar
Willmore, L. J. (1999) How does trauma cause epilepsy? In The Epilepsies – Etiologies and Prevention, ed. P. Kotagal and H. O. Lüders, pp. 289–291, San Diego: Academic Press
Wilson, C. J. (1993) The generation of natural firing patterns in neostriatal neurons. Progress in Brain Research 99: 277–297CrossRefGoogle ScholarPubMed
Wilson, C. J. and Kawaguchi, Y. (1996) The origin of two-state spontaneous membrane potential fluctuations of neostriatal spiny neurons. Journal of Neuroscience 16: 2397–2410CrossRefGoogle Scholar
Wilson, M. A. and McNaughton, B. L. (1994) Reactivation of hippocampal ensemble memories during sleep. Science 265: 676–679CrossRefGoogle ScholarPubMed
Wilson, S., Kinnier, A. and Bruce, A. (1955) Neurology. Baltimore: Williams & Wilkins
Winson, J. and Abzug, C. (1978) Neuronal transmission through hippocampal pathways dependent on behavior. Journal of Neurophysiology 41: 716–732CrossRefGoogle ScholarPubMed
Winter, O., Kok, A., Kenemans, J. L. and Elton, M. (1995) Auditory event-related potentials (AEPs) to deviant stimuli during drowsiness and sleep. Electroencephalography and Clinical Neurophysiology 96: 398–412CrossRefGoogle Scholar
Wise, S. P., Fleshman, J. W. Jr. and Jones, E. G. (1979) Maturation of pyramidal cell form in relation to developing afferent and efferent connections of rat somatic sensory cortex. Neuroscience 4: 1275–1297CrossRefGoogle ScholarPubMed
Witte, O. W. and Freund, H. J. (1999) Neuronal dysfunction, epilepsy, and postlesional brain plasticity. Advances in Neurology 81: 25–36Google ScholarPubMed
Wittner, L., Maglóczky, Z., Borhegyi, S., Halász, P., Tóth, S., Eröss, L., Szabó, Z. and Freund, T. F. (2001) Preservation of perisomatic inhibitory input of granule cells in the epileptic human dentate gyrus. Neuroscience 108: 587–600CrossRefGoogle ScholarPubMed
Wolpert, S. (1982) A New History of India. New York: Oxford University Press
Wong, R. K. S. and Stewart, M. (1992) Different firing patterns generated in dendrites and somata of CA1 pyramidal neurones in guinea-pig hippocampus. Journal of Physiology (London) 457: 675–687CrossRefGoogle ScholarPubMed
Wong, R. K. S., Prince, D. A. and Basbaum, A. I. (1979) Intradendritic recordings from hippocampal neurons. Proceedings of the National Academy of Sciences of the USA 76: 986–990CrossRefGoogle ScholarPubMed
Woody, C. D., Gruen, E. and Wang, X. F. (2003) Electrical properties affecting discharge of units of the mid and posterolateral thalamus of conscious cats. Neuroscience, in pressCrossRefGoogle ScholarPubMed
Wuarin, J. P. and Dudek, F. E. (1996) Electrographic seizures and new recurrent excitatory circuits in the dentate gyrus of hippocampal slices from kainate-treated epileptic rats. Journal of Neuroscience 16: 4438–4448CrossRefGoogle ScholarPubMed
Xiong, Z. Q., Saggau, P. and Stringer, J. L. (2000) Activity-dependent intracellular acidification correlates with the duration of seizure activity. Journal of Neuroscience 20: 1290–1296CrossRefGoogle ScholarPubMed
Yamada, T., Kameyama, S., Fuchigami, Z., Nakazumi, Y., Dickins, Q. S. and Kimura, J. (1988) Changes of short latency somatosensory evoked potential in sleep. Electroencephalography and Clinical Neurophysiology 70: 126–136CrossRefGoogle ScholarPubMed
Yamamoto, C. and McIlwain, H. (1966) Electrical activities in thin sections from the mammalian brain maintained in chemically defined media in vitro. Journal of Neurochemistry 13: 1333–1343CrossRefGoogle ScholarPubMed
Yamashita, A., Watanabe, Y. and Hayaishi, O. (1983) Autoradiographic localization of a binding protein(s) specific for prostaglandin D2 in rat brain. Proceedings of the National Academy of Sciences of the USA 80: 6114–6118CrossRefGoogle ScholarPubMed
Yang, C. R., Seamans, J. K. and Gorelova, N. (1996) Electrophysiological and morphological properties of layers V–VI principal pyramidal cells in rat prefrontal cortex in vitro. Journal of Neuroscience 16: 1904–1921CrossRefGoogle ScholarPubMed
Yang, L. and Benardo, L. S. (1997) Epileptogenesis following neocortical trauma from two sources of disinhibition. Journal of Neurophysiology 78: 2804–2810CrossRefGoogle ScholarPubMed
Yaqub, B. A. (1993) Electroclinical seizures in Lennox-Gastaut syndrome. Epilepsia 34: 120–127CrossRefGoogle ScholarPubMed
Yen, C. T., Conley, M., Hendry, S. H. C. and Jones, E. G. (1985) The morphology of physiologically identified GABAergic neurons in the somatic sensory part of the thalamic reticular nucleus in the cat. Journal of Neuroscience 5: 2254–2268CrossRefGoogle ScholarPubMed
Yeterian, E. H. and Pandya, D. N. (1989) Thalamic connections of the superior temporal sulcus in the rhesus monkey. Journal of Comparative Neurology 282: 80–97CrossRefGoogle ScholarPubMed
Ylinen, A., Bragin, A., Nádasdy, Z., Jandó, G., Szabó, I., Sik, A. and Buzsáki, G. (1995) Sharp wave-associated high-frequency oscillation (200 Hz) in the intact hippocampus: network and intracellular mechanisms. Journal of Neuroscience 15: 30–46CrossRefGoogle ScholarPubMed
Yoshida, M., Sasa, M. and Takaori, S. (1984) Serotonin-mediated inhibition from dorsal raphe nucleus of neurons in dorsal geniculate and thalamic reticular nuclei. Brain Research 290: 95–105CrossRefGoogle ScholarPubMed
Young, M. P., Tanaka, K. and Yamane, S. (1992) On oscillating neuronal responses in the visual cortex of the monkey. Journal of Neurophysiology 67: 1464–1474CrossRefGoogle ScholarPubMed
Yue, B. W. and Huguenard, J. R. (2001) The role of H-current in regulating strength and frequency of thalamic network oscillations. Thalamus and Related Systems 1: 95–103Google ScholarPubMed
Yuste, R. and Tank, D. W. (1996) Dendritic integration in mammalian neurons, a century after Cajal. Neuron 16: 701–716CrossRefGoogle ScholarPubMed
Zhang, S. J., Huguenard, J. R. and Prince, D. A. (1997) GABAA receptor-mediated Cl- currents in rat thalamic reticular and relay neurons. Journal of Neurophysiology 78: 2280–2286CrossRefGoogle ScholarPubMed
Zhang, Y., Perez-Velazquez, J. L., Tian, G. F., Wu, C. P., Skinner, F. K., Carlen, P. L. and Zhang, L. (1998) Slow oscillations (≤1 Hz) mediated by GABAergic interneuronal networks in rat hippocampus. Journal of Neuroscience 18: 9256–9268CrossRefGoogle ScholarPubMed
Zhu, J. J. and Lo, F. S. (1999) Three GABA receptor-mediated postsynaptic potentials in interneurons in the rat lateral geniculate nucleus. Journal of Neuroscience 19: 5721–5730CrossRefGoogle ScholarPubMed
Zhu, J. J. and Uhlrich, D. J. (1998) Cellular mechanisms underlying two muscarinic receptor-mediated depolarizing responses in relay cells of the rat lateral geniculate nucleus. Neuroscience 87: 767–781CrossRefGoogle ScholarPubMed
Zhu, J. J., Lytton, W. W., Xue, J. T. and Uhlrich, D. J. (1999a) An intrinsic oscillation in interneurons of the rat lateral geniculate nucleus. Journal of Neurophysiology 81: 702–711CrossRefGoogle Scholar
Zhu, J. J., Uhlrich, D. J. and Lytton, W. W. (1999b) Burst firing in identified rat geniculate interneurons. Neuroscience 91: 1445–1460CrossRefGoogle Scholar
Zifkin, B. G. and Dravet, C. (1997) Generalized convulsive seizures. In Epilepsy: A Comprehensive Textbook, ed. J. Engel Jr. and T. A. Pedley, pp. 567–577, Philadelphia: Lippincott-Raven
Zola-Morgan, S. and Squire, L. R. (1993) Neuroanatomy of memory. Annual Reviews of Neuroscience 16: 547–563CrossRefGoogle Scholar
Zuckermann, E. C. and Glaser, G. H. (1968) Hippocampal epileptic activity induced by localized ventricular perfusion with high-potassium cerebrospinal fluid. Experimental Neurology 20: 87–110CrossRefGoogle ScholarPubMed
Zygierewicz, J., Blinowska, K. J., Durka, P. J., Szelenberger, W., Niemcewicz, S. and Androsiuk, W. (1999) High resolution study of sleep spindles. Clinical Neurophysiology 110: 2136–2147CrossRefGoogle ScholarPubMed

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  • References
  • Mircea Steriade, Université Laval, Québec
  • Book: Neuronal Substrates of Sleep and Epilepsy
  • Online publication: 23 September 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511541711.007
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  • References
  • Mircea Steriade, Université Laval, Québec
  • Book: Neuronal Substrates of Sleep and Epilepsy
  • Online publication: 23 September 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511541711.007
Available formats
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  • References
  • Mircea Steriade, Université Laval, Québec
  • Book: Neuronal Substrates of Sleep and Epilepsy
  • Online publication: 23 September 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511541711.007
Available formats
×