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Myoclonus; see Movement Disorders/myoclonus
Citations 1-10 of 12 total displayed.
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Most recent content
(27 May 2008):
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- ARTICLES
Novel mutations in Myoclonin1/EFHC1 in sporadic and familial juvenile myoclonic epilepsy
- M. T. Medina, T. Suzuki, M. E. Alonso, R. M. Durón, I. E. Martínez-Juárez, J. N. Bailey, D. Bai, Y. Inoue, I. Yoshimura, S. Kaneko, M. C. Montoya, A. Ochoa, A. Jara Prado, M. Tanaka, J. Machado-Salas, S. Fujimoto, M. Ito, S. Hamano, K. Sugita, Y. Ueda, M. Osawa, H. Oguni, F. Rubio-Donnadieu, K. Yamakawa, and A. V. Delgado-Escueta
Neurology 2008; 70: 2137-2144.
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Past content
(since Apr 2003):
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- ARTICLES
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus
- C. La Morgia, A. Achilli, L. Iommarini, P. Barboni, M. Pala, A. Olivieri, C. Zanna, S. Vidoni, C. Tonon, R. Lodi, R. Vetrugno, B. Mostacci, R. Liguori, R. Carroccia, P. Montagna, M. Rugolo, A. Torroni, and V. Carelli
Neurology 2008; 70: 762-770.
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- ARTICLES
Clinical and neuropathologic study of a French family with a mutation in the neuroserpin gene
- I. Gourfinkel-An, C. Duyckaerts, A. Camuzat, C. Meyrignac, P. Sonderegger, M. Baulac, and A. Brice
Neurology 2007; 69: 79-83.
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- NEUROIMAGES
Opsoclonus-myoclonus syndrome associated with cytomegalovirus encephalitis
- I. Zaganas, G. Prinianakis, N. Xirouchaki, and M. Mavridis
Neurology 2007; 68: 1636.
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- NEUROIMAGES
Spinal myoclonus following herpes zoster radiculitis
- A. Estraneo, A. M. Saltalamacchia, and V. Loreto
Neurology 2007; 68: E4.
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- BRIEF COMMUNICATIONS
A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A
- J. C. Mulley, P. Nelson, S. Guerrero, L. Dibbens, X. Iona, J. M. McMahon, L. Harkin, J. Schouten, S. Yu, S. F. Berkovic, and I. E. Scheffer
Neurology 2006; 67: 1094-1095.
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- CLINICAL/SCIENTIFIC NOTES
Age-related electrical status epilepticus during sleep and epileptic negative myoclonus in DRPLA
- K. Kobayashi, H. Hata, M. Oka, M. Ito, H. Yoshinaga, K. Kashihara, and Y. Ohtsuka
Neurology 2006; 66: 772-773.
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- BRIEF COMMUNICATIONS
Progressive myoclonus epilepsy with polyglucosans (Lafora disease): Evidence for a third locus
- E. M. Chan, S. Omer, M. Ahmed, L. R. Bridges, C. Bennett, S. W. Scherer, and B. A. Minassian
Neurology 2004; 63: 565-567.
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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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