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All Genetics
Citations 241-250 of 676 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Ataxia with oculomotor apraxia type 2: A clinical, pathologic, and genetic study
- C. Criscuolo, L. Chessa, S. Di Giandomenico, P. Mancini, F. Saccà, G. S. Grieco, M. Piane, F. Barbieri, G. De Michele, S. Banfi, F. Pierelli, N. Rizzuto, F. M. Santorelli, L. Gallosti, A. Filla, and C. Casali
Neurology 2006; 66: 1207-1210.
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- BRIEF COMMUNICATIONS
Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansions
- M. -E. Arsenault, C. Prévost, A. Lescault, C. Laberge, J. Puymirat, and J. Mathieu
Neurology 2006; 66: 1248-1250.
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- BRIEF COMMUNICATIONS
New HSN2 mutation in Japanese patient with hereditary sensory and autonomic neuropathy type 2
- M. Takagi, T. Ozawa, K. Hara, S. Naruse, T. Ishihara, J. Shimbo, S. Igarashi, K. Tanaka, O. Onodera, and M. Nishizawa
Neurology 2006; 66: 1251-1252.
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- ARTICLES
Postoperative seizures after extratemporal resections and hemispherectomy in pediatric epilepsy
- J. Mani, A. Gupta, E. Mascha, D. Lachhwani, K. Prakash, W. Bingaman, and E. Wyllie
Neurology 2006; 66: 1038-1043.
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- BRIEF COMMUNICATIONS
Sacsin-related ataxia (ARSACS): Expanding the genotype upstream from the gigantic exon
- Y. Ouyang, Y. Takiyama, K. Sakoe, H. Shimazaki, T. Ogawa, S. Nagano, Y. Yamamoto, and I. Nakano
Neurology 2006; 66: 1103-1104.
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- ARTICLES
A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia
- M. Morita, A. Al-Chalabi, P. M. Andersen, B. Hosler, P. Sapp, E. Englund, J. E. Mitchell, J. J. Habgood, J. de Belleroche, J. Xi, W. Jongjaroenprasert, H. R. Horvitz, L. -G. Gunnarsson, and R. H. Brown, Jr
Neurology 2006; 66: 839-844.
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- ARTICLES
Basilar-type migraine: Clinical, epidemiologic, and genetic features
- Malene Kirchmann, Lise Lykke Thomsen, and Jes Olesen
Neurology 2006; 66: 880-886.
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Intronic mutation in the PGK1 gene may cause recurrent myoglobinuria by aberrant splicing
- Kentaro Shirakawa, Yoshitomo Takahashi, and Hiroaki Miyajima
Neurology 2006; 66: 925-927.
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Electrophysiologic characterization in spinocerebellar ataxia 17
- F. Manganelli, A. Perretti, M. Nolano, B. Lanzillo, A. C. Bruni, G. De Michele, A. Filla, and L. Santoro
Neurology 2006; 66: 932-934.
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- ARTICLES
Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia
- N. Elleuch, C. Depienne, A. Benomar, A. M. Ouvrard Hernandez, X. Ferrer, B. Fontaine, D. Grid, C.M.E. Tallaksen, R. Zemmouri, G. Stevanin, A. Durr, and A. Brice
Neurology 2006; 66: 654-659.
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