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All Genetics
Citations 271-280 of 679 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Familial basilar migraine associated with a new mutation in the ATP1A2 gene
- A. Ambrosini, M. D’Onofrio, G. S. Grieco, A. Di Mambro, G. Montagna, D. Fortini, F. Nicoletti, G. Nappi, G. Sances, J. Schoenen, M. G. Buzzi, F. M. Santorelli, and F. Pierelli
Neurology 2005; 65: 1826-1828.
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- BRIEF COMMUNICATIONS
A family with McLeod syndrome and calpainopathy with clinically overlapping diseases
- A. Starling, D. Schlesinger, F. Kok, M. Rita Passos-Bueno, M. Vainzof, and M. Zatz
Neurology 2005; 65: 1832-1833.
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- EDITORIALS
A way out of the maze: Campylobacter jejuni gene polymorphisms define Guillain-Barré syndrome
- John H.J. Wokke and Leonard H. van den Berg
Neurology 2005; 65: 1350-1351.
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- ARTICLES
Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia
- G. Zanni, Y. Saillour, M. Nagara, P. Billuart, L. Castelnau, C. Moraine, L. Faivre, E. Bertini, A. Durr, A. Guichet, D. Rodriguez, V. des Portes, C. Beldjord, and J. Chelly
Neurology 2005; 65: 1364-1369.
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- ARTICLES
Campylobacter gene polymorphism as a determinant of clinical features of Guillain–Barré syndrome
- M. Koga, M. Takahashi, M. Masuda, K. Hirata, and N. Yuki
Neurology 2005; 65: 1376-1381.
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- BRIEF COMMUNICATIONS
Mutations in the glucocerebrosidase gene and Parkinson disease: Phenotype–genotype correlation
- Judith Aharon-Peretz, Samih Badarny, Hanna Rosenbaum, and Ruth Gershoni-Baruch
Neurology 2005; 65: 1460-1461.
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- BRIEF COMMUNICATIONS
POLG mutations in Alpers syndrome
- K. V. Nguyen, E. Østergaard, S. Holst Ravn, T. Balslev, E. Rubæk Danielsen, A. Vardag, P. J. McKiernan, G. Gray, and R. K. Naviaux
Neurology 2005; 65: 1493-1495.
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- BRIEF COMMUNICATIONS
Genomic microarray analysis identifies candidate loci in patients with corpus callosum anomalies
- E. H. Sherr, R. Owen, D. G. Albertson, D. Pinkel, P. D. Cotter, A. M. Slavotinek, S. W. Hetts, R. J. Jeremy, G. Schilmoeller, K. Schilmoeller, M. Wakahiro, and A. J. Barkovich
Neurology 2005; 65: 1496-1498.
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- ARTICLES
Familial aggregation, the PDE4D gene, and ischemic stroke in a genetically isolated population
- M.J.E. van Rijn, A. J.C. Slooter, A. F.C. Schut, A. Isaacs, Y. S. Aulchenko, P. J.L.M. Snijders, L. J. Kappelle, J. C. van Swieten, B. A. Oostra, and C. M. van Duijn
Neurology 2005; 65: 1203-1209.
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- BRIEF COMMUNICATIONS
Early-onset toe walking in rippling muscle disease due to a new caveolin-3 gene mutation
- Ricardo E. Madrid, Christian Kubisch, and Arthur P. Hays
Neurology 2005; 65: 1301-1303.
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