Myoclonus and extrapyramidal diseases

Neurophysiologie Clinique

Volumn 36, Issue 5-6, 2006, Pages 319-325

  Defebvre, L ^a  

^a IFR114 ^*  (France)

Author keywords

EEG; Huntington's disease; Lewy body dementia; Multiple system atrophy; Myoclonus; Parkinson's disease; Somatosensory evoked potentials

Indexed keywords

ARTICLE; CLINICAL FEATURE; CORTICOBASAL DEGENERATION; DENTATORUBROPALLIDOLUYSIAN ATROPHY; DIFFUSE LEWY BODY DISEASE; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; DYSTONIA; ELECTROENCEPHALOGRAM; ELECTROPHYSIOLOGY; EVOKED SOMATOSENSORY RESPONSE; EXTRAPYRAMIDAL SYNDROME; HUMAN; HUNTINGTON CHOREA; MYOCLONUS; PARKINSON DISEASE; PARKINSONISM; PROGRESSIVE SUPRANUCLEAR PALSY; SHY DRAGER SYNDROME; SYMPTOM; BRAIN CORTEX; ELECTROENCEPHALOGRAPHY; PATHOPHYSIOLOGY; REVIEW; TAUOPATHY;

BASAL GANGLIA DISEASES; CEREBRAL CORTEX; DYSTONIC DISORDERS; ELECTROENCEPHALOGRAPHY; EVOKED POTENTIALS, SOMATOSENSORY; HUMANS; MULTIPLE SYSTEM ATROPHY; MYOCLONUS; PARKINSON DISEASE; TAUOPATHIES;

EID: 33847408907     PISSN: 09877053     EISSN: 17697131     Source Type: Journal    
DOI: 10.1016/j.neucli.2006.11.003     Document Type: Article

References (42)

1. Asmus F., and Gasser T. Inherited myoclonus dystonia. Adv. Neurol. 94 (2004) 113-119
2. Burkhardt C.R., Filley C.M., Kleinscmidt-DeMasters B.K., De la Monte S., Norenberg M.D., and Schneck S.A. Diffuse Lewy body disease and progressive dementia. Neurology 38 (1988) 1520-1528
3. Carella F., Scaioli V., Ciano C., Birelli S., Oliva D., and Girotti F. Adult onset myoclonic Huntington's disease. Mov. Disord. 8 (1993) 201-205
4. Cassim F., Derambure P., Defebvre L., Bourriez J.L., Destée A., and Guieu J.D. Exploration neurophysiologiste des tremblements. Neurophysiol. Clin. 30 (2000) 81-96
5. Cassim F. Les dystonies myocloniques. Rev. Neurol. 159 (2003) 892-899
6. Caviness J.N., Adler C.H., Beach T.G., Wetjen K.L., and Caselli R.J. Myoclonus in Lewy body disorders. Adv. Neurol. 89 (2002) 23-30
7. Caviness J.N., Adler C.H., Beach T.G., Wetjen K.L., and Caselli R.J. Small amplitude cortical myoclonus in Parkinson's disease: physiology and clinical observations. Mov. Disord. 17 (2002) 657-662
8. Caviness J.N., Adler C.H., Caselli R.J., et al. Electrophysiology of the myoclonus in dementia with Lewy bodies. Neurology 60 (2003) 523-524
9. Caviness J.N., Adler C.H., Newman S., Caselli R.J., and Muenter M.D. Cortical myoclonus in Levodopa-responsive parkinsonism. Mov. Disord. 13 (1998) 540-544
10. Caviness J.N., and Kurth M. Cortical myoclonus in Huntington's disease associated with an enlarged somatosensory. Mov. Disord. 12 (1997) 1046-1051
11. Caviness J.N. Myoclonus and neurodegenerative disease-what's in a name?. Parkinsonism Relat. Disord. 9 (2003) 185-192
12. Chen R., Ashy P., and Lang A.E. Stimulus-sensitive myoclonus in akinetic-rigid syndromes. Brain 115 (1992) 1875-1888
13. Clouston P.D., Lim C.L., Fung V., Yannikas C., and Morris J.G.L. Brainstem myoclonus in a patient with non-dopa-responsive parkinsonism. Mov. Disord. 11 (1996) 404-410
14. Gasser T. Inherited myoclonus-dystonia syndrome. Adv. Neurol. 78 (1998) 325-334
15. Grimes D.A., Han F., Lang A.E., St George-Hyssop P., Racacho L., and Bulman D.E. A novel locus for inherited myoclonus-dystonia on 18p11. Neurology 59 (2002) 1183-1186
16. Grosse P., Kühn A., Cordivari C., and Brown P. Coherence analysis in the myoclonus of corticobasale degeneration. Mov. Disord. 18 (2003) 1345-1350
17. Kofler M., Muller J., Reggiani L., and Wenning G.K. Somatosensory evoked potentials in progressive supranuclear palsy. J. Neurol. Sci. 179 (2000) 85-91
18. Kofler M., Muller J., Wenning G.K., Reggiani L., Hollosi P., Bosch S., et al. The auditory startle reaction in parkinsonian disorders. Mov. Disord. 16 (2001) 62-71
19. Kurihara T., Landau W.M., and Torack R.M. Progressive supranuclear palsy with action myoclonus seizures. Neurology 24 (1974) 219-223
20. Lou J.S., Valls-Solé J., and Toro C. Hallett. Facial action myoclonus in patients with olivopontocerebellar atrophy. Mov. Disord. 9 (1994) 223-226
21. Lu C.S., Ikeda A., Terada K., Mima T., Nagamine T., Fukuyama H., et al. Electrophysiological studies of early stage corticobasal degeneration. Mov. Disord. 13 (1998) 140-146
22. Matsunaga K., Uozumi T., Qingrui L., Hashimoto T., and Tsuji S. Amantadine-induced cortical myoclonus. Neurology 56 (2001) 279-280
23. Nygaard T.G., Raymond D., and Chen C. Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31. Ann. Neurol. 46 (1999) 794-798
24. Okuma Y., Fujishima K., Miwa H., Mori H., and Mizuno Y. Myoclonic tremulous movements in multiple system atrophy are a form of cortical myoclonus. Mov. Disord. 20 (2005) 451-456
25. Patel S., and Slater P. Analysis of the brain lesions involved in myoclonus produced by intracerebral picrotoxin. Neurosciences 20 (1987) 687-693
26. Quinn N., Rothwell J.C., Thompson P.D., and Marsden C.D. Hereditary myoclonic dystonia, hereditary torsion dystonia, and hereditary essential myoclonus: an area of confusion. Adv. Neurol. 50 (1988) 391-401
27. Rodriguez M.E., Artieda J., Zubieta J.L., and Obeso J.A. Reflex myoclonus in olivopontocerebellar atrophy. J. Neurol. Neurosurg. Psychiatry 57 (1994) 316-319
28. Salazar G., Valls-Sole J., Marti M.J., Chang H., and Tolosa E. Postural and action myoclonus in patients with parkinsonian type multiple system atrophy. Mov. Disord. 15 (2000) 77-83
29. Sawle G.V., Brooks D.J., Marsden C.D., and Frakowiak R.S. Corticobasal degeneration. A unique pattern of regional cortical oxygen hypometabolism and striatal fluorodopa uptake demonstrated by positron emission tomography. Brain 114 (1991) 541-556
30. Shafiq M., and Lang A.E. Myoclonus in parkinsonian disorders. Adv. Neurol. 89 (2002) 77-83
31. Strafella A., Ashby P., and Lang E. Reflex myoclonus in cortical-basal ganglionic degeneration involves a transcortical pathway. Mov. Disord. 12 (1997) 360-369
32. Suyama N., Kobayashi S., Isino H., Iijima M., and Imaoka K. Progressive supranuclear palsy with palatal myoclonus. Acta Neuropathol. (Berl.) 94 (1997) 290-293
33. Thompson P.D., Bhatia K.P., Brown P., et al. Cortical myoclonus in Huntington's disease. Mov. Disord. 9 (1994) 633-641
34. Thompson P.D., Day B.L., Rothwell J.C., Brown P., Britton T.C., and Marsden C.D. The myoclonus in corticobasal degeneration evidence for two forms of cortical reflex myoclonus. Brain 117 (1994) 1197-1207
35. Thompson P.D., and Shibasaki H. Myoclonus in corticobasal degeneration and other neurodegenerations. Adv Neurol 82 (2000) 69-81
36. Vardi J., Glaubman H., Rabey J.M., and Streiffler M. Myoclonic attacks induced by l-Dopa and bromocriptin in Parkinson patients: a sleep EEG study. J. Neurol. 218 (1978) 35-42
37. Vidailhet M., Tassin J., Durif F., Nivelon-Chevallier A., Agid Y., Brice A., et al. A major locus for several phenotypes of myoclonus-dystonia on chromosome 7q. Neurology 56 (2001) 1213-1216
38. Wakabayashi K., Ikeuchi T., Ishikawa A., and Takahashi H. Multiple system atrophy with severe involvement of the motor cortical areas and cerebral white matter. J. Neurol. Sci. 156 (1998) 114-117
39. Warner T.T., Williams L.D., Walker W.H., Flinter F., Robb S.A., Bundey S.E., et al. A clinical and molecular genetic study of dentatorubro pallidoluysian atrophy in four European families. Ann. Neurol. 37 (1995) 452-459
40. Wenning G.K., Tison F., Ben Shlomo Y., Daniel S.E., and Quinn N.P. Multiple system atrophy: a review of 203 pathologically proven cases. Mov. Disord. (1997) 133-147
41. Wenning G.K., Ben Shlomo Y., Magalhaes M., Daniel S.E., and Quinn N.P. Clinical features and natural history of multiple system atrophy. Brain 117 (1994) 835-845
42. Zimprich A., Grabowski M., Asmus F., Naumann M., Berg D., Bertram M., et al. Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome. Nat. Genet. 29 (2001) 66-69