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Genetic Disorders
Citations 161-170 of 396 total displayed.
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Past content
(since Jan 1998):
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- Neurological Reviews
Finding the Causes of Inherited Neuropathies
- Steven S. Scherer
Arch Neurol 2006; 63: 812-816.
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- Original Contributions
Stroke and Memory Performance in Elderly Persons Without Dementia
- Christiane Reitz; Jose A. Luchsinger; Ming-Xin Tang; Jennifer Manly; Richard Mayeux
Arch Neurol 2006; 63: 571-576.
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- Neurological Reviews
Implications of Genetics on the Diagnosis and Care of Patients With Parkinson Disease
- Christine Klein
Arch Neurol 2006; 63: 328-334.
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- Original Contributions
Lewy Body Pathology in Familial Alzheimer Disease: Evidence for Disease- and Mutation-Specific Pathologic Phenotype
- James B. Leverenz; Mark A. Fishel; Elaine R. Peskind; Thomas J. Montine; David Nochlin; Ellen Steinbart; Murray A. Raskind; Gerard D. Schellenberg; Thomas D. Bird; Debby Tsuang
Arch Neurol 2006; 63: 370-376.
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- Original Contributions
Association of Apolipoprotein E Genotype and Alzheimer Disease in African Americans
- Jill R. Murrell; Brandon Price; Kathleen A. Lane; Olusegun Baiyewu; Oye Gureje; Adesola Ogunniyi; Frederick W. Unverzagt; Valerie Smith-Gamble; Sujuan Gao; Hugh C. Hendrie; Kathleen S. Hall
Arch Neurol 2006; 63: 431-434.
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- Original Contributions
Depression, Apolipoprotein E Genotype, and the Incidence of Mild Cognitive Impairment: A Prospective Cohort Study
- Yonas E. Geda; David S. Knopman; David A. Mrazek; Gregory A. Jicha; Glenn E. Smith; Selamawit Negash; Bradley F. Boeve; Robert J. Ivnik; Ronald C. Petersen; V. Shane Pankratz; Walter A. Rocca
Arch Neurol 2006; 63: 435-440.
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- Neurological Reviews
Apolipoprotein E and Dementia in Parkinson Disease: A Meta-analysis
- Xuemei Huang; Peter Chen; Daniel I. Kaufer; Alexander I. Tröster; Charles Poole
Arch Neurol 2006; 63: 189-193.
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- Original Contributions
Heterogeneous Phenotype in a Family With Compound Heterozygous Parkin Gene Mutations
- Hao Deng; Wei-Dong Le; Christine B. Hunter; William G. Ondo; Yi Guo; Wen-Jie Xie; Joseph Jankovic
Arch Neurol 2006; 63: 273-277.
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- Original Contributions
Phenotypic Variability Among Adult Siblings With Sjögren-Larsson Syndrome
- Alexander Lossos; Moona Khoury; William B. Rizzo; John M. Gomori; Eyal Banin; Abraham Zlotogorski; Saleh Jaber; Oded Abramsky; Zohar Argov; Hanna Rosenmann
Arch Neurol 2006; 63: 278-280.
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- Observations
A Missense Mutation in the Coiled-Coil Domain of the KIF5A Gene and Late-Onset Hereditary Spastic Paraplegia
- Mariangela Lo Giudice; Marcella Neri; Michele Falco; Maurizio Sturnio; Elisa Calzolari; Daniela Di Benedetto; Marco Fichera
Arch Neurol 2006; 63: 284-287.
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