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Neurogenetics
Contributing journals to this collection:
JAMA & Archives Journals
Citations 161-170 of 623 total displayed.
- Original Contributions
Interferon Gamma Allelic Variants: Sex-Biased Multiple Sclerosis Susceptibility and Gene Expression
- Orhun H. Kantarci; David D. Hebrink; Janet Schaefer-Klein; Yulong Sun; Sara Achenbach; Elizabeth J. Atkinson; Shirley Heggarty; Anne C. Cotleur; Mariza de Andrade; Koen Vandenbroeck; Clara M. Pelfrey; Brian G. Weinshenker
Arch Neurol 2008; 65: 349-357.
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- Original Contributions
Cortical Brain Malformations: Effect of Clinical, Neuroradiological, and Modern Genetic Classification
- Marie Claire Yvette de Wit; Maarten H. Lequin; Ireneaus F. M. de Coo; Esther Brusse; Dicky J. J. Halley; Raoul van de Graaf; Rachel Schot; Frans W. Verheijen; Grazia M. S. Mancini
Arch Neurol 2008; 65: 358-366.
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- Original Contributions
The G13513A Mutation in the ND5 Gene of Mitochondrial DNA as a Common Cause of MELAS or Leigh Syndrome: Evidence From 12 Cases
- Sara Shanske; Jorida Coku; Jiesheng Lu; Jaya Ganesh; Sindu Krishna; Kurenai Tanji; Eduardo Bonilla; Ali B. Naini; Michio Hirano; Salvatore DiMauro
Arch Neurol 2008; 65: 368-372.
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- Original Contributions
Conjugal Alzheimer Disease: Risk in Children When Both Parents Have Alzheimer Disease
- Suman Jayadev; Ellen J. Steinbart; Yueh-Yun Chi; Walter A. Kukull; Gerard D. Schellenberg; Thomas D. Bird
Arch Neurol 2008; 65: 373-378.
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- Original Contributions
Glucocerebrosidase Gene Mutations: A Risk Factor for Lewy Body Disorders
- Ignacio F. Mata; Ali Samii; Seth H. Schneer; John W. Roberts; Alida Griffith; Berta C. Leis; Gerard D. Schellenberg; Ellen Sidransky; Thomas D. Bird; James B. Leverenz; Debby Tsuang; Cyrus P. Zabetian
Arch Neurol 2008; 65: 379-382.
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- Original Contributions
A Locus for Primary Lateral Sclerosis on Chromosome 4ptel-4p16.1
- Paul N. Valdmanis; Nicolas Dupré; Guy A. Rouleau
Arch Neurol 2008; 65: 383-386.
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- Original Contributions
Long-term Follow-up of Taiwanese Chinese Patients Treated Early for 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency
- Kai-Ming Liu; Tze-Tze Liu; Ni-Chung Lee; Ling-Yee Cheng; Kwang-Jen Hsiao; Dau-Ming Niu
Arch Neurol 2008; 65: 387-392.
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- Original Contributions
Hereditary Spastic Paraplegia With Mental Impairment and Thin Corpus Callosum in Tunisia: SPG11, SPG15, and Further Genetic Heterogeneity
- Amir Boukhris; Giovanni Stevanin; Imed Feki; Elodie Denis; Nizar Elleuch; Mohamed Imed Miladi; Jérémy Truchetto; Paola Denora; Samir Belal; Chokri Mhiri; Alexis Brice
Arch Neurol 2008; 65: 393-402.
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- Observations
Amyotrophic Lateral Sclerosis With Ragged-Red Fibers
- Michio Hirano; Corrado Angelini; Pasquale Montagna; Arthur P. Hays; Kurenai Tanji; Hiroshi Mitsumoto; Paul H. Gordon; Ali B. Naini; Salvatore DiMauro; Lewis P. Rowland
Arch Neurol 2008; 65: 403-406.
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- Observations
Altered Cerebral Glucose Metabolism in a Family With Clinical Features Resembling Mitochondrial Neurogastrointestinal Encephalomyopathy Syndrome in Association With Multiple Mitochondrial DNA Deletions
- Fritz-Georg Lehnhardt; Rita Horvath; Roland Ullrich; Lutz Kracht; Jan Sobesky; Walter Möller-Hartmann; Andreas H. Jacobs; Walter F. Haupt
Arch Neurol 2008; 65: 407-411.
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