Neurogenetics

Contributing journals to this collection:
JAMA & Archives Journals

Citations 291-300 of 623 total displayed.

Past content

Neurological Reviews
Implications of Genetics on the Diagnosis and Care of Patients With Parkinson Disease

Christine Klein
Arch Neurol 2006; 63: 328-334. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

Original Contributions
LRRK2 Mutations in Spanish Patients With Parkinson Disease: Frequency, Clinical Features, and Incomplete Penetrance

Carles Gaig; Mario Ezquerra; Maria Jose Marti; Esteban Muñoz; Francesc Valldeoriola; Eduardo Tolosa
Arch Neurol 2006; 63: 377-382. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

Observations
De Novo Occurrence of Novel SPG3A/Atlastin Mutation Presenting as Cerebral Palsy

Shirley Rainier; Carron Sher; Orit Reish; Donald Thomas; John K. Fink
Arch Neurol 2006; 63: 445-447. [Abstract] [Full text] [PDF]  

Observations
Familial Creutzfeldt-Jakob Disease With an R208H-129V Haplotype and Kuru Plaques

Céline Basset-Leobon; Emmanuelle Uro-Coste; Katell Peoc’h; Stéphane Haik; Véronique Sazdovitch; Mathieu Rigal; Olivier Andreoletti; Jean-Jacques Hauw; Marie-Bernadette Delisle
Arch Neurol 2006; 63: 449-452. [Abstract] [Full text] [PDF]  

Original Contributions
Spectrum of Brain Changes in Patients With Congenital Muscular Dystrophy and FKRP Gene Mutations

Eugenio Mercuri; Haluk Topaloglu; Martin Brockington; Angela Berardinelli; Anna Pichiecchio; Filippo Santorelli; Mary Rutherford; Beril Talim; Enzo Ricci; Thomas Voit; Francesco Muntoni
Arch Neurol 2006; 63: 251-257. [Abstract] [Full text] [PDF]  

Original Contributions
The G93C Mutation in Superoxide Dismutase 1: Clinicopathologic Phenotype and Prognosis

Luc Régal; Ludo Vanopdenbosch; Petra Tilkin; Ludo Van Den Bosch; Vincent Thijs; Rafael Sciot; Wim Robberecht
Arch Neurol 2006; 63: 262-267. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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