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All Genetics
Citations 241-250 of 679 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Clinical use of genotype to predict chemosensitivity in oligodendroglial tumors
- C. Walker, B. Haylock, D. Husband, K. A. Joyce, D. Fildes, M. D. Jenkinson, T. Smith, J. Broome, D. G. du Plessis, and P. C. Warnke
Neurology 2006; 66: 1661-1667.
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- ARTICLES
The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V
- O. Dubourg, H. Azzedine, R. Ben Yaou, J. Pouget, A. Barois, V. Meininger, D. Bouteiller, M. Ruberg, A. Brice, and E. LeGuern
Neurology 2006; 66: 1721-1726.
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- BRIEF COMMUNICATIONS
Autosomal recessive ataxia with peripheral neuropathy and elevated AFP: Novel mutations in SETX
- T. Asaka, H. Yokoji, J. Ito, K. Yamaguchi, and A. Matsushima
Neurology 2006; 66: 1580-1581.
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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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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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