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All Genetics
Citations 191-200 of 676 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Genotype-phenotype associations for ARX gene duplication in X-linked mental retardation
- K. Szczaluba, M. Nawara, K. Poirier, J. Pilch, M. Gajdulewicz, K. Spodar, J. Chelly, J. Bal, and T. Mazurczak
Neurology 2006; 67: 2073-2075.
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- BRIEF COMMUNICATIONS
Comprehensive association analysis of the NOS2A gene with Parkinson disease
- C. Schulte, M. Sharma, J. C. Mueller, P. Lichtner, J. Prestel, D. Berg, and T. Gasser
Neurology 2006; 67: 2080-2082.
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- CLINICAL/SCIENTIFIC NOTES
Novel mutations in the senataxin DNA/RNA helicase domain in ataxia with oculomotor apraxia 2
- Brent L. Fogel and Susan Perlman
Neurology 2006; 67: 2083-2084.
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- CLINICAL/SCIENTIFIC NOTES
Spinocerebellar ataxia type 20 is genetically distinct from spinocerebellar ataxia type 5
- D. N. Lorenzo, S. M. Forrest, Y. Ikeda, K. A. Dick, L.P.W. Ranum, and M. A. Knight
Neurology 2006; 67: 2084-2085.
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- ARTICLES
Frequency of LRRK2 mutations in early- and late-onset Parkinson disease
- L. N. Clark, Y. Wang, E. Karlins, L. Saito, H. Mejia-Santana, J. Harris, E. D. Louis, L. J. Cote, H. Andrews, S. Fahn, C. Waters, B. Ford, S. Frucht, R. Ottman, and K. Marder
Neurology 2006; 67: 1786-1791.
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- ARTICLES
Vascular risk factors and cognitive decline among elderly male twins
- Glen L. Xiong, Brenda L. Plassman, Michael J. Helms, and David C. Steffens
Neurology 2006; 67: 1586-1591.
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- BRIEF COMMUNICATIONS
POLG1 in idiopathic Parkinson disease
- W. Tiangyou, G. Hudson, D. Ghezzi, G. Ferrari, M. Zeviani, D. J. Burn, and P. F. Chinnery
Neurology 2006; 67: 1698-1700.
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- BRIEF COMMUNICATIONS
Phenotypic homogeneity of the Huntington disease–like presentation in a SCA17 family
- S. A. Schneider, B.P.C. van de Warrenburg, T. D. Hughes, M. Davis, M. Sweeney, N. Wood, N. P. Quinn, and K. P. Bhatia
Neurology 2006; 67: 1701-1703.
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- BRIEF COMMUNICATIONS
Genetic heterogeneity of autosomal dominant nonprogressive congenital ataxia
- J. C. Jen, H. Lee, Y. H. Cha, S. F. Nelson, and R. W. Baloh
Neurology 2006; 67: 1704-1706.
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- BRIEF COMMUNICATIONS
Variation of the serotonin transporter gene SLC6A4 in the susceptibility to migraine with aura
- U. Todt, J. Freudenberg, I. Goebel, A. Heinze, K. Heinze-Kuhn, M. Rietschel, H. Göbel, and C. Kubisch
Neurology 2006; 67: 1707-1709.
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