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Myoclonus
Citations 31-40 of 49 total displayed.
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Past content
(since Sep 2001):
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- BRIEF COMMUNICATIONS
Cerebellar activation in opsoclonus: An fMRI study
- C. Helmchen, H. Rambold, A. Sprenger, C. Erdmann, and F. Binkofski
Neurology 2003; 61: 412-415.
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- BRIEF COMMUNICATIONS
Mutations in the  -sarcoglycan gene found to be uncommon in seven myoclonus–dystonia families
- F. Han, A. E. Lang, L. Racacho, D. E. Bulman, and D. A. Grimes
Neurology 2003; 61: 244-246.
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- BRIEF COMMUNICATIONS
Hereditary myoclonus–dystonia associated with epilepsy
- E. M.J. Foncke, C. Klein, J. H.T.M. Koelman, P. L. Kramer, K. Schilling, B. Müller, J. Garrels, P. de Carvalho Aguiar, L. Liu, A. de Froe, J. D. Speelman, L. J. Ozelius, and M. A.J. Tijssen
Neurology 2003; 60: 1988-1990.
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- BRIEF COMMUNICATIONS
A novel mutation in the -sarcoglycan gene causing myoclonus–dystonia syndrome
- L. E. Hjermind, L. M. Werdelin, H. Eiberg, B. Krag–Olsen, E. Dupont, and S. A. Sørensen
Neurology 2003; 60: 1536-1539.
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N-acetylcysteine and Unverricht–Lundborg disease Variable response and possible side effects
- M.J.J. Edwards, I.P. Hargreaves, S.J.R. Heales, S.J. Jones, V. Ramachandran, K.P. Bhatia, and S. Sisodiya
Neurology 2002; 59: 1447-1449.
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- ARTICLES
A novel locus for inherited myoclonus-dystonia on 18p11
- D. A. Grimes, F. Han, A. E. Lang, P. St. George-Hyssop, L. Racacho, and D. E. Bulman
Neurology 2002; 59: 1183-1186.
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Phenotypic features of myoclonus-dystonia in three kindreds
- D. O. Doheny, M. F. Brin, C. E. Morrison, C. J. Smith, R. H. Walker, S. Abbasi, B. Müller, J. Garrels, L. Liu, P. de Carvalho Aguiar, K. Schilling, P. Kramer, D. de Leon, D. Raymond, R. Saunders-Pullman, C. Klein, S. B. Bressman, B. Schmand, M. A.J. Tijssen, L. J. Ozelius, and J. M. Silverman
Neurology 2002; 59: 1187-1196.
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Autosomal dominant GTP-CH deficiency presenting as a dopa-responsive myoclonus-dystonia syndrome
- V. Leuzzi, Ca. Carducci, Cl. Carducci, F. Cardona, C. Artiola, and I. Antonozzi
Neurology 2002; 59: 1241-1243.
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- BRIEF COMMUNICATIONS
Clinical findings of a myoclonus-dystonia family with two distinct mutations
- D. Doheny, F. Danisi, C. Smith, C. Morrison, M. Velickovic, D. de Leon, S. B. Bressman, J. Leung, L. Ozelius, C. Klein, X. O. Breakefield, M. F. Brin, and J. M. Silverman
Neurology 2002; 59: 1244-1246.
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X-linked myoclonic epilepsy with spasticity and intellectual disability: Mutation in the homeobox gene ARX
- I. E. Scheffer, R. H. Wallace, F. L. Phillips, P. Hewson, K. Reardon, G. Parasivam, P. Stromme, S. F. Berkovic, J. Gecz, and J. C. Mulley
Neurology 2002; 59: 348-356.
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