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All Genetics
Citations 361-370 of 676 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy
- D. D’Agostino, M. Bertelli, S. Gallo, S. Cecchin, E. Albiero, P. G. Garofalo, A. Gambardella, J.-M. St. Hilaire, H. Kwiecinski, E. Andermann, and M. Pandolfo
Neurology 2004; 63: 1500-1502.
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- BRIEF COMMUNICATIONS
Clinical phenotype of Brazilian families with spinocerebellar ataxia 10
- H. A.G. Teive, B. B. Roa, S. Raskin, P. Fang, W. O. Arruda, Y. Correa Neto, R. Gao, L. C. Werneck, and T. Ashizawa
Neurology 2004; 63: 1509-1512.
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- BRIEF COMMUNICATIONS
Long-term course of L-dopa-responsive dystonia caused by tyrosine hydroxylase deficiency
- A. Schiller, R. A. Wevers, G. C.H. Steenbergen, N. Blau, and H. H. Jung
Neurology 2004; 63: 1524-1526.
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- BRIEF COMMUNICATIONS
Coincidence of two genetic forms of Charcot–Marie–Tooth disease in a single family
- C. Verny, N. Ravisé, A-L. Leutenegger, F. Pouplard, O. Dubourg, S. Tardieu, F. Dubas, A. Brice, E. Genin, and E. LeGuern
Neurology 2004; 63: 1527-1529.
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- EDITORIALS
Posterior cortical dementia: Lost but not forgetting
- Charles J. Duffy
Neurology 2004; 63: 1148-1149.
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- EDITORIALS
Resident and Fellow Page Update
- Karen C. Johnston
Neurology 2004; 63: 1154.
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- ARTICLES
Clinical, genetic, and neuropathologic characteristics of posterior cortical atrophy
- D. F. Tang-Wai, N. R. Graff-Radford, B. F. Boeve, D. W. Dickson, J. E. Parisi, R. Crook, R. J. Caselli, D. S. Knopman, and R. C. Petersen
Neurology 2004; 63: 1168-1174.
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- EXPEDITED BRIEF COMMUNICATION
A polymorphism of the hypocretin receptor 2 gene is associated with cluster headache
- I. Rainero, S. Gallone, W. Valfrè, M. Ferrero, G. Angilella, C. Rivoiro, E. Rubino, P. De Martino, L. Savi, M. Ferrone, and L. Pinessi
Neurology 2004; 63: 1286-1288.
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- CLINICAL/SCIENTIFIC NOTES
A new SBF2 mutation in a family with recessive demyelinating Charcot-Marie-Tooth (CMT4B2)
- F. L. Conforti, M. Muglia, R. Mazzei, A. Patitucci, P. Valentino, A. Magariello, T. Sprovieri, F. Bono, C. Bergmann, A. L. Gabriele, G. Peluso, R. Nisticò, J. Senderek, and A. Quattrone
Neurology 2004; 63: 1327-1328.
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- BRIEF COMMUNICATIONS
Bias in parental transmission of the HLA-DR3 allele in Sardinian multiple sclerosis
- M. G. Marrosu, C. Sardu, E. Cocco, G. Costa, M. R. Murru, C. Mancosu, R. Murru, M. Lai, and P. Contu
Neurology 2004; 63: 1084-1086.
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