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Genetic Disorders
Citations 21-30 of 396 total displayed.
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Past content
(since Jan 1998):
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- Corrections
Error in Byline and Author Contributions in: No TARDBP Mutations in a French Canadian Population of Patients With Parkinson Disease
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Arch Neurol 2009; 66: 432.
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- Original Contributions
Reduction of SorLA/LR11, a Sorting Protein Limiting β-Amyloid Production, in Alzheimer Disease Cerebrospinal Fluid
- Qiu-Lan Ma; Douglas R. Galasko; John M. Ringman; Harry V. Vinters; Steven D. Edland; Justine Pomakian; Oliver J. Ubeda; Emily R. Rosario; Bruce Teter; Sally A. Frautschy; Greg M. Cole
Arch Neurol 2009; 66: 448-457.
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- Corrections
Omission of Participating Site Investigators/Coordinators in: Randomized Controlled Trial of Ethyl-Eicosapentaenoic Acid in Huntington Disease: The TREND-HD Study
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Arch Neurol 2009; 66: 305.
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- Observations
Muscle Phosphoglycerate Mutase Deficiency Revisited
- Ali Naini; Antonio Toscano; Olimpia Musumeci; John Vissing; Hasan O. Akman; Salvatore DiMauro
Arch Neurol 2009; 66: 394-398.
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- Editorials
200 Years After Darwin
- Roger N. Rosenberg; Olaf Stüve; Todd Eagar
Arch Neurol 2009; 66: 153-155.
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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
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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