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All Genetics
Citations 271-280 of 676 total displayed.
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Past content
(since Jan 2001):
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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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- BRIEF COMMUNICATIONS
Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene
- D. Haubenberger, R. E. Bittner, S. Rauch-Shorny, F. Zimprich, C. Mannhalter, L. Wagner, I. Mineva, K. Vass, E. Auff, and A. Zimprich
Neurology 2005; 65: 1304-1305.
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- CLINICAL/SCIENTIFIC NOTES
RAS pathway activation and an oncogenic RAS mutation in sporadic pilocytic astrocytoma
- Mukesh K. Sharma, Barbara A. Zehnbauer, Mark A. Watson, and David H. Gutmann
Neurology 2005; 65: 1335-1336.
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- ARTICLES
Neuroradiologic and clinicopathologic features of oculoleptomeningeal type amyloidosis
- M. Nakamura, T. Yamashita, M. Ueda, K. Obayashi, T. Sato, T. Ikeda, Y. Washimi, T. Hirai, Y. Kuwahara, M. T. Yamamoto, M. Uchino, and Y. Ando
Neurology 2005; 65: 1051-1056.
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