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All Genetics
Citations 231-240 of 676 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Men transmit MS more often to their children vs women: The Carter effect
- O. H. Kantarci, L. F. Barcellos, E. J. Atkinson, P. P. Ramsay, R. Lincoln, S. J. Achenbach, M. De Andrade, S. L. Hauser, and B. G. Weinshenker
Neurology 2006; 67: 305-310.
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- BRIEF COMMUNICATIONS
RLS3: Fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity
- K. M. Liebetanz, J. Winkelmann, C. Trenkwalder, B. Pütz, M. Dichgans, T. Gasser, and B. Müller-Myhsok
Neurology 2006; 67: 320-321.
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- BRIEF COMMUNICATIONS
Varicose veins associated with CADASIL result from a novel mutation in the Notch3 gene
- S. Saiki, K. Sakai, M. Saiki, Y. Kitagawa, T. Umemori, K. Murata, M. Matsui, and G. Hirose
Neurology 2006; 67: 337-339.
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- ARTICLES
A genome-wide scan and HCRTR2 candidate gene analysis in a European cluster headache cohort
- L. Baumber, C. Sjöstrand, M. Leone, H. Harty, G. Bussone, J. Hillert, R. C. Trembath, and M. B. Russell
Neurology 2006; 66: 1888-1893.
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- BRIEF COMMUNICATIONS
Family history of dementia is a risk factor for Lewy body disease
- B. K. Woodruff, N. R. Graff-Radford, T. J. Ferman, D. W. Dickson, M. W. DeLucia, J. E. Crook, Z. Arvanitakis, S. Brassler, C. Waters, W. Barker, and R. Duara
Neurology 2006; 66: 1949-1950.
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- CLINICAL/SCIENTIFIC NOTES
The Thr354Ile substitution in PSEN1:: Disease-causing mutation or polymorphism?
- Peiyee Lee, Luis Medina, and John M. Ringman
Neurology 2006; 66: 1955-1956.
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- ARTICLES
Classification of partial seizure symptoms in genetic studies of the epilepsies
- H. Choi, M. R. Winawer, S. Kalachikov, T. A. Pedley, W. A. Hauser, and R. Ottman
Neurology 2006; 66: 1648-1653.
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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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