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Neurology
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Myoclonus

Citations 41-49 of 49 total displayed.

Past content (since Sep 2001):

BRIEF COMMUNICATIONS
Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy
T. Sugawara, E. Mazaki–Miyazaki, K. Fukushima, J. Shimomura, T. Fujiwara, S. Hamano, Y. Inoue, and K. Yamakawa
Neurology 2002; 58: 1122-1124. [Abstract] [Full text] [PDF]  

ARTICLES
Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME)
P. Labauge, L. O. Amer, M. Simonetta-Moreau, F. Attané, C. Tannier, M. Clanet, G. Castelnovo, I. An-Gourfinkel, Y. Agid, A. Brice, A. Ducros, and E. LeGuern
Neurology 2002; 58: 941-944. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Multifocal myoclonus due to verapamil overdose
Lata Vadlamudi and Eelco F.M. Wijdicks
Neurology 2002; 58: 984. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Familial nocturnal facio-mandibular myoclonus mimicking sleep bruxism
R. Vetrugno, F. Provini, G. Plazzi, C. Lombardi, R. Liguori, E. Lugaresi, and P. Montagna
Neurology 2002; 58: 644-647. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Palatal tremor and myorhythmia in Hashimoto’s encephalopathy
J. C. Erickson, H. Carrasco, J. B. Grimes, B. Jabbari, and K. R. Cannard
Neurology 2002; 58: 504-505. [Full text] [PDF]  

ARTICLES
Myoclonus dystonia: Possible association with obsessive–compulsive disorder and alcohol dependence
R. Saunders–Pullman, J. Shriberg, G. Heiman, D. Raymond, K. Wendt, P. Kramer, K. Schilling, R. Kurlan, C. Klein, L. J. Ozelius, N. J. Risch, and S. B. Bressman
Neurology 2002; 58: 242-245. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Spasm of the sternocleidomastoid muscle induced by vagal nerve stimulation
J. Iriarte, J. Artieda, M. Alegre, E. Schlumberger, E. Urrestarazu, M. A. Pastor, and C. Viteri
Neurology 2001; 57: 2319-2320. [Full text] [PDF]  

ARTICLES
Hyperexcitable cortical responses in progressive myoclonic epilepsy: A TMS study
P. Manganotti, S. Tamburin, G. Zanette, and A. Fiaschi
Neurology 2001; 57: 1793-1799. [Abstract] [Full text] [PDF]  

ARTICLES
Unverricht–Lundborg disease in a five-generation Arab family: Instability of dodecamer repeats
A. Mazarib, L. Xiong, M.Y. Neufeld, M. Birnbaum, A.D. Korczyn, M. Pandolfo, and S.F. Berkovic
Neurology 2001; 57: 1050-1054. [Abstract] [Full text] [PDF]  

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 Movement Disorders
 All Movement Disorders
 Dystonia
 Blepharospasm
 Gait disorders/ataxia
 Cerebellum
 Huntington's disease
 Basal ganglia
 Parkinson's disease/Parkinsonism
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 Progressive supranuclear palsy
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 Multiple system atrophy
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 Myoclonus
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