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All Genetics
Citations 571-580 of 676 total displayed.
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Past content
(since Jan 2001):
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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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- BRIEF COMMUNICATIONS
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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- BRIEF COMMUNICATIONS
Genetic association of  2-macroglobulin polymorphisms with AD in southern Italy
- M. Zappia, R. Cittadella, I. Manna, G. Nicoletti, V. Andreoli, S. Bonavita, A. Gambardella, and A. Quattrone
Neurology 2002; 59: 756-758.
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- BRIEF COMMUNICATIONS
Expression of X-linked bulbospinal muscular atrophy (Kennedy disease) in two homozygous women
- Brian J. Schmidt, Cheryl R. Greenberg, Diane J. Allingham–Hawkins, and Elizabeth L. Spriggs
Neurology 2002; 59: 770-772.
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- CLINICAL/SCIENTIFIC NOTES
Adverse effects of phenytoin given for late-onset seizures in adults with Down syndrome
- John A. Tsiouris, Paul J. Patti, Omer Tipu, and Simhachalam Raguthu
Neurology 2002; 59: 779-780.
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