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All Genetics
Citations 571-580 of 679 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
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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- BRIEF COMMUNICATIONS
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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- BRIEF COMMUNICATIONS
Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13
- S.E. Noble-Topham, D.A. Dyment, M.Z. Cader, R. Ganapathy, J.D. Brown, G.P.A. Rice, and G.C. Ebers
Neurology 2002; 59: 1099-1101.
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- BRIEF COMMUNICATIONS
Heterogeneity of presenile dementia with bone cysts (Nasu–Hakola disease): Three genetic forms
- T. Kondo, K. Takahashi, N. Kohara, Y. Takahashi, S. Hayashi, H. Takahashi, H. Matsuo, M. Yamazaki, K. Inoue, K. Miyamoto, and T. Yamamura
Neurology 2002; 59: 1105-1107.
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- BRIEF COMMUNICATIONS
Presenilin-1 mutation (E280G), spastic paraparesis, and cranial MRI white-matter abnormalities
- S. O’Riordan, P. McMonagle, J. C. Janssen, N. C. Fox, M. Farrell, J. Collinge, M. N. Rossor, and M. Hutchinson
Neurology 2002; 59: 1108-1110.
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- CLINICAL/SCIENTIFIC NOTES
The absence of survival motor neuron 2 gene may play a role in multifocal motor neuropathy
- R. Rojas-García, E. Tizzano, I. Cuscó, E. Gallardo, M. J. Barceló, I. de Andrés, P. Larrodé, J. F. Martí-Massó, J. A. Martínez-Matos, M. Povedano, B. Rallo, S. Serrano, M. Baiget, and I. Illa
Neurology 2002; 59: 1112-1113.
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- BRIEF COMMUNICATIONS
Ullrich disease: Collagen VI deficiency: EM suggests a new basis for muscular weakness
- H. Ishikawa, K. Sugie, K. Murayama, M. Ito, N. Minami, I. Nishino, and I. Nonaka
Neurology 2002; 59: 920-923.
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Novel mutation in X-linked Charcot-Marie-Tooth disease associated with CNS impairment
- Hideshi Kawakami, Ken Inoue, Ichiro Sakakihara, and Shigenobu Nakamura
Neurology 2002; 59: 923-926.
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- ARTICLES
Association of µ-opioid receptor subunit gene and idiopathic generalized epilepsy
- H. Wilkie, A. Osei–Lah, B. Chioza, L. Nashef, D. McCormick, P. Asherson, and A. J. Makoff
Neurology 2002; 59: 724-728.
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