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  • Print publication year: 2013
  • Online publication date: October 2013

Chapter 5 - Functional MRI of motor signs in Parkinson’s disease

References

1. AlbinRL, YoungAB, PenneyJB. The functional anatomy of basal ganglia disorders. Trends Neurosci. 1989;12(10):366–75.
2. DeLongMR. Primate models of movement disorders of basal ganglia origin. Trends Neurosci. 1990;13(7):281–5.
3. PlayfordED, JenkinsIH, PassinghamRE, et al. Impaired mesial frontal and putamen activation in Parkinson’s disease: a positron emission tomography study. Ann Neurol. 1992;32(2):151–61.
4. JahanshahiM, JenkinsIH, BrownRG, et al. Self-initiated versus externally triggered movements. I. An investigation using measurement of regional cerebral blood flow with PET and movement-related potentials in normal and Parkinson’s disease subjects. Brain. 1995;118(Pt 4):913–33.
5. RascolO, SabatiniU, CholletF, et al. Supplementary and primary sensory motor area activity in Parkinson’s disease. Regional cerebral blood flow changes during finger movements and effects of apomorphine. Arch Neurol. 1992;49(2):144–8.
6. RascolO, SabatiniU, FabreN, et al. The ipsilateral cerebellar hemisphere is overactive during hand movements in akinetic parkinsonian patients. Brain. 1997;120(Pt 1):103–10.
7. SamuelM, Ceballos-BaumannAO, BlinJ, et al. Evidence for lateral premotor and parietal overactivity in Parkinson’s disease during sequential and bimanual movements. A PET study. Brain. 1997;120(Pt 6):963–76.
8. WuT, WangL, HallettM, LiK, ChanP.Neural correlates of bimanual anti-phase and in-phase movements in Parkinson’s disease. Brain. 2010;133(Pt 8):2394–409.
9. SabatiniU, BoulanouarK, FabreN, et al. Cortical motor reorganization in akinetic patients with Parkinson’s disease: a functional MRI study. Brain. 2000;123(Pt 2):394–403.
10. HaslingerB, ErhardP, KampfeN, et al. Event-related functional magnetic resonance imaging in Parkinson’s disease before and after levodopa. Brain. 2001;124(Pt 3):558–70.
11. RiddingMC, InzelbergR, RothwellJC. Changes in excitability of motor cortical circuitry in patients with Parkinson’s disease. Ann Neurol. 1995;37(2):181–8.
12. ZiemannU, BrunsD, PaulusW.Enhancement of human motor cortex inhibition by the dopamine receptor agonist pergolide: evidence from transcranial magnetic stimulation. Neurosci Lett. 1996;208(3):187–90.
13. BuhmannC, GlaucheV, SturenburgHJ, et al. Pharmacologically modulated fMRI–cortical responsiveness to levodopa in drug-naive hemiparkinsonian patients. Brain. 2003;126(Pt 2):451–61.
14. YuH, SternadD, CorcosDM, VaillancourtDE. Role of hyperactive cerebellum and motor cortex in Parkinson’s disease. Neuroimage. 2007;35(1):222–33.
15. EckertT, PeschelT, HeinzeHJ, RotteM.Increased pre-SMA activation in early PD patients during simple self-initiated hand movements. J Neurol. 2006;253(2):199–207.
16. WuT, HallettM.A functional MRI study of automatic movements in patients with Parkinson’s disease. Brain. 2005;128(Pt 10):2250–9.
17. CerasaA, HagbergGE, PeppeA, et al. Functional changes in the activity of cerebellum and frontostriatal regions during externally and internally timed movement in Parkinson’s disease. Brain Res Bull. 2006;71(1–3):259–69.
18. SenS, KawaguchiA, TruongY, LewisMM, HuangX.Dynamic changes in cerebello-thalamo-cortical motor circuitry during progression of Parkinson’s disease. Neuroscience. 2010;166(2):712–19.
19. WuT, WangL, HallettM, et al. Effective connectivity of brain networks during self-initiated movement in Parkinson’s disease. Neuroimage. 2011;55(1):204–15.
20. FristonKJ, BuechelC, FinkGR, et al. Psychophysiological and modulatory interactions in neuroimaging. Neuroimage. 1997;6(3):218–29.
21. WuT, ChanP, HallettM.Effective connectivity of neural networks in automatic movements in Parkinson’s disease. Neuroimage. 2010;49(3):2581–7.
22. WuT, HallettM.Neural correlates of dual task performance in patients with Parkinson’s disease. J Neurol Neurosurg Psychiatry. 2008;79(7):760–6.
23. D’EspositoM, DetreJA, AlsopDC, et al. The neural basis of the central executive system of working memory. Nature. 1995;378(6554):279–81.
24. CorbettaM, ShulmanGL. Control of goal-directed and stimulus-driven attention in the brain. Nat Rev Neurosci. 2002;3(3):201–15.
25. HalsbandU, ItoN, TanjiJ, FreundHJ. The role of premotor cortex and the supplementary motor area in the temporal control of movement in man. Brain. 1993;116(Pt 1):243–66.
26. IvryRB. The representation of temporal information in perception and motor control. Curr Opin Neurobiol. 1996;6(6):851–7.
27. PashlerH.Dual-task interference in simple tasks: data and theory. Psychol Bull. 1994;116(2):220–44.
28. ColletteF, OlivierL, Van der LindenM, et al. Involvement of both prefrontal and inferior parietal cortex in dual-task performance. Brain Res Cogn Brain Res. 2005;24(2):237–51.
29. RoweJ, StephanKE, FristonK, et al. Attention to action in Parkinson’s disease: impaired effective connectivity among frontal cortical regions. Brain. 2002;125(Pt 2):276–89.
30. BuchelC, FristonK.Assessing interactions among neuronal systems using functional neuroimaging. Neural Netw. 2000;13(8–9):871–82.
31. JueptnerM, StephanKM, FrithCD, et al. Anatomy of motor learning. I. Frontal cortex and attention to action. J Neurophysiol. 1997;77(3):1313–24.
32. LewisMM, SlagleCG, SmithAB, et al. Task specific influences of Parkinson’s disease on the striato-thalamo-cortical and cerebello-thalamo-cortical motor circuitries. Neuroscience. 2007;147(1):224–35.
33. PierantozziM, PalmieriMG, MarcianiMG, et al. Effect of apomorphine on cortical inhibition in Parkinson’s disease patients: a transcranial magnetic stimulation study. Exp Brain Res. 2001;141(1):52–62.
34. FokiT, PirkerW, KlingerN, et al. FMRI correlates of apraxia in Parkinson’s disease patients OFF medication. Exp Neurol. 2010;225(2):416–22.
35. LewisMM, DuG, SenS, et al. Differential involvement of striato- and cerebello-thalamo-cortical pathways in tremor- and akinetic/rigid-predominant Parkinson’s disease. Neuroscience. 2011;177:230–9.
36. BartelsAL, de JongBM, GiladiN, et al. Striatal dopa and glucose metabolism in PD patients with freezing of gait. Mov Disord. 2006;21(9):1326–32.
37. HanakawaT, FukuyamaH, KatsumiY, HondaM, ShibasakiH.Enhanced lateral premotor activity during paradoxical gait in Parkinson’s disease. Ann Neurol. 1999;45(3):329–36.
38. FabreN, BrefelC, SabatiniU, et al. Normal frontal perfusion in patients with frozen gait. Mov Disord. 1998;13(4):677–83.
39. MatsuiH, UdakaF, MiyoshiT, et al. Three-dimensional stereotactic surface projection study of freezing of gait and brain perfusion image in Parkinson’s disease. Mov Disord. 2005;20(10):1272–7.
40. SnijdersAH, LeunissenI, BakkerM, et al. Gait-related cerebral alterations in patients with Parkinson’s disease with freezing of gait. Brain. 2011;134(Pt 1):59–72.
41. JenkinsIH, FernandezW, PlayfordED, et al. Impaired activation of the supplementary motor area in Parkinson’s disease is reversed when akinesia is treated with apomorphine. Ann Neurol. 1992;32(6):749–57.
42. RascolO, SabatiniU, CholletF, et al. Normal activation of the supplementary motor area in patients with Parkinson’s disease undergoing long-term treatment with levodopa. J Neurol Neurosurg Psychiatry. 1994;57(5):567–71.
43. NgB, PalmerS, AbugharbiehR, McKeownMJ. Focusing effects of L-dopa in Parkinson’s disease. Hum Brain Mapp. 2010;31(1):88–97.
44. WuT, LongX, ZangY, et al. Regional homogeneity changes in patients with Parkinson’s disease. Hum Brain Mapp. 2009;30(5):1502–10.
45. PhillipsMD, BakerKB, LoweMJ, et al. Parkinson disease: pattern of functional MR imaging activation during deep brain stimulation of subthalamic nucleus – initial experience. Radiology. 2006;239(1):209–16.
46. ArantesPR, CardosoEF, BarreirosMA, et al. Performing functional magnetic resonance imaging in patients with Parkinson’s disease treated with deep brain stimulation. Mov Disord. 2006;21(8):1154–62.
47. Ceballos-BaumannAO, BoeckerH, BartensteinP, et al. A positron emission tomographic study of subthalamic nucleus stimulation in Parkinson disease: enhanced movement-related activity of motor-association cortex and decreased motor cortex resting activity. Arch Neurol. 1999;56(8):997–1003.
48. LimousinP, GreeneJ, PollakP, et al. Changes in cerebral activity pattern due to subthalamic nucleus or internal pallidum stimulation in Parkinson’s disease. Ann Neurol. 1997;42(3):283–91.
49. SubramanianL, HindleJV, JohnstonS, et al. Real-time functional magnetic resonance imaging neurofeedback for treatment of Parkinson’s disease. J Neurosci. 2011;31(45):16309–17.