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Neurogenetics
Citations 51-60 of 574 total displayed.
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Past content
(since May 1998):
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- Original Contributions
Modification of Multiple Sclerosis Phenotypes by African Ancestry at HLA
- Bruce A. C. Cree; David E. Reich; Omar Khan; Philip L. De Jager; Ichiro Nakashima; Toshiyuki Takahashi; Amit Bar-Or; Christine Tong; Stephen L. Hauser; Jorge R. Oksenberg
Arch Neurol 2009; 66: 226-233.
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- Original Contributions
SEPT9 Mutations and a Conserved 17q25 Sequence in Sporadic and Hereditary Brachial Plexus Neuropathy
- Christopher J. Klein; Yanhong Wu; Julie M. Cunningham; Anthony J. Windebank; P. James B. Dyck; Scott M. Friedenberg; Diane M. Klein; Peter J. Dyck
Arch Neurol 2009; 66: 238-243.
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- Original Contributions
Screening for the Presence of FMR1 Premutation Alleles in Women With Parkinsonism
- Roberto Cilia; Jeremy Kraff; Margherita Canesi; Gianni Pezzoli; Stefano Goldwurm; Khalid Amiri; Hiu-Tung Tang; Ruiqin Pan; Paul J. Hagerman; Flora Tassone
Arch Neurol 2009; 66: 244-249.
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- Original Contributions
GAB2 as an Alzheimer Disease Susceptibility Gene: Follow-up of Genomewide Association Results
- Brit-Maren M. Schjeide; Basavaraj Hooli; Michele Parkinson; Meghan F. Hogan; Jason DiVito; Kristina Mullin; Deborah Blacker; Rudolph E. Tanzi; Lars Bertram
Arch Neurol 2009; 66: 250-254.
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- Research Letters
Genetic Polymorphism at Codon 129 of the Prion Protein Gene Is Not Associated With Multiple Sclerosis
- Olaf Stüve; Carsten Korth; Pablo Gabatto; Elizabeth M. Cameron; Wei Hu; Todd N. Eagar; Nancy L. Monson; Elliot M. Frohman; Michael K. Racke; Cyrus P. Zabetian; Jorge R. Oksenberg
Arch Neurol 2009; 66: 280-281.
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- Research Letters
No TARDBP Mutations in a French Canadian Population of Patients With Parkinson Disease
- Edor Kabashi; Hussein Daoud; Jean-Baptiste Rivière; Paul N. Valdamanis; Patrick Bourgouin; Pierre Provencher; Emmanuelle Pourcher; Patrick Dion; Nicolas Dupré; Guy A. Rouleau
Arch Neurol 2009; 66: 281-282.
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- Neurological Reviews
Translational Research in Epilepsy Genetics: Sodium Channels in Man to Interneuronopathy in Mouse
- Saul A. Mullen; Ingrid E. Scheffer
Arch Neurol 2009; 66: 21-26.
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- Original Contributions
Protean Phenotypic Features of the A3243G Mitochondrial DNA Mutation
- Petra Kaufmann; Kristin Engelstad; Ying Wei; Romana Kulikova; Maryam Oskoui; Vanessa Battista; Dorcas Y. Koenigsberger; Juan M. Pascual; Mary Sano; Michio Hirano; Salvatore DiMauro; Dikoma C. Shungu; Xiangling Mao; Darryl C. De Vivo
Arch Neurol 2009; 66: 85-91.
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- Original Contributions
Episodic Ataxia Associated With EAAT1 Mutation C186S Affecting Glutamate Reuptake
- Boukje de Vries; Hafsa Mamsa; Anine H. Stam; Jijun Wan; Stef L. M. Bakker; Kaate R. J. Vanmolkot; Joost Haan; Gisela M. Terwindt; Elles M. J. Boon; Bruce D. Howard; Rune R. Frants; Robert W. Baloh; Michel D. Ferrari; Joanna C. Jen; Arn M. J. M. van den Maagdenberg
Arch Neurol 2009; 66: 97-101.
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- Original Contributions
 -Synuclein Gene Rearrangements in Dominantly Inherited Parkinsonism: Frequency, Phenotype, and Mechanisms
- Pablo Ibáñez; Suzanne Lesage; Sabine Janin; Ebba Lohmann; Frank Durif; Alain Destée; Anne-Marie Bonnet; Christine Brefel-Courbon; Simon Heath; Diana Zelenika; Yves Agid; Alexandra Dürr; Alexis Brice; for the French Parkinson's Disease Genetics Study Group
Arch Neurol 2009; 66: 102-108.
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