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Myoclonus; see Movement Disorders/myoclonus
Citations 11-14 of 14 total displayed.
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Past content
(since Apr 2003):
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- ARTICLES
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy
- R. Nabbout, E. Gennaro, B. Dalla Bernardina, O. Dulac, F. Madia, E. Bertini, G. Capovilla, C. Chiron, G. Cristofori, M. Elia, E. Fontana, R. Gaggero, T. Granata, R. Guerrini, M. Loi, L. La Selva, M. L. Lispi, A. Matricardi, A. Romeo, V. Tzolas, D. Valseriati, P. Veggiotti, F. Vigevano, L. Vallée, F. Dagna Bricarelli, A. Bianchi, and F. Zara
Neurology 2003; 60: 1961-1967.
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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
Benign adult familial myoclonic epilepsy: Genetic heterogeneity and allelism with ADCME
- F.A. de Falco, P. Striano, A. de Falco, S. Striano, R. Santangelo, A. Perretti, P. Balbi, M. Cecconi, and F. Zara
Neurology 2003; 60: 1381-1385.
[Abstract]
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- CLINICAL/SCIENTIFIC NOTES
Efficacy of levetiracetam in a patient with Unverricht-Lundborg progressive myoclonic epilepsy
- P. Kinrions, N. Ibrahim, K. Murphy, A.-E. Lehesjoki, I. Järvela, and N. Delanty
Neurology 2003; 60: 1394-1395.
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