Contents
Open Peer Commentary
Comparing Chronometrie methods
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- 19 May 2011, p. 276
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Co-transmitters, modulation, and the peripheral nervous system
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- 19 May 2011, p. 430
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Homeostatic motivational function and theory
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- 19 May 2011, p. 111
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None in a million: results of mass screening for eidetic ability using objective tests published in newspapers and magazines
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- 19 May 2011, p. 612
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On the inadequacy of a homeostatic model: where do we go from here?
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- 19 May 2011, pp. 111-112
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Tracing eidetic imagery
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- 19 May 2011, pp. 612-613
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Do mental events have durations?
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- 19 May 2011, pp. 277-278
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Thank goodness we do not need a definition of modulation
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- 19 May 2011, p. 430
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On Bloch's Law and “ideal observers.”
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- 19 May 2011, p. 278
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Eidetic imagery, occipital EEG activity, and palinopsia
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- 19 May 2011, p. 613
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Defining neuromodulation
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- 19 May 2011, pp. 430-431
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Thirst is controlled by regulatory stimuli, but drinking may partly escape them
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- 19 May 2011, p. 112
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Neuronal communication and synaptic modulation: experimental evidence vs. conceptual categories
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- 19 May 2011, pp. 431-433
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Internal and external regulatory process and the ecology of motivation
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- 19 May 2011, pp. 112-113
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Relative timing of sensory transduction
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- 19 May 2011, pp. 278-279
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The visualization continuum
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- 19 May 2011, p. 614
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Aspects of communication related to axoplasmic transport
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- 19 May 2011, p. 433
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Critical duration, supersummation, and the narrow domain of strength-duration experiments
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- 19 May 2011, pp. 279-281
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Eidetic imagery is not a ghost
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- 19 May 2011, pp. 614-615
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Homeostasis is insufficient to account for subtlety of behavior
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- 19 May 2011, p. 113
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