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Neurogenetics
Citations 231-240 of 574 total displayed.
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Past content
(since May 1998):
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- Observations
A Novel Mitochondrial Transfer RNAAsn Mutation Causing Multiorgan Failure
- Ann Meulemans; Sara Seneca; Lieven Lagae; Willy Lissens; Boel De Paepe; Joél Smet; Rudy Van Coster; Linda De Meirleir
Arch Neurol 2006; 63: 1194-1198.
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- Corrections
Errors in Table in: The G93C Mutation in Superoxide Dismutase 1: Clinicopathologic Phenotype and Prognosis
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Arch Neurol 2006; 63: 963.
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- Original Contributions
Influence of Homozygosity for Methionine at Codon 129 of the Human Prion Gene on the Onset of Neurological and Hepatic Symptoms in Wilson Disease
- Uta Merle; Wolfgang Stremmel; Reinhard Geßner
Arch Neurol 2006; 63: 982-985.
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- Original Contributions
At Risk for Huntington Disease: The PHAROS (Prospective Huntington At Risk Observational Study) Cohort Enrolled
- The Huntington Study Group PHAROS Investigators
Arch Neurol 2006; 63: 991-996.
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- Original Contributions
Type 1 Diabetes and Multiple Sclerosis: A Danish Population-Based Cohort Study
- Nete M. Nielsen; Tine Westergaard; Morten Frisch; Klaus Rostgaard; Jan Wohlfahrt; Nils Koch-Henriksen; Mads Melbye; Henrik Hjalgrim
Arch Neurol 2006; 63: 1001-1004.
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- Observations
Childhood Onset in Familial Prion Disease With a Novel Mutation in the PRNP Gene
- Ekaterina Rogaeva; Cindy Zadikoff; Jonathan Ponesse; Gerold Schmitt-Ulms; Toshitaka Kawarai; Christine Sato; Shabnam Salehi-Rad; Peter St. George-Hyslop; Anthony E. Lang
Arch Neurol 2006; 63: 1016-1021.
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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
Influence of Heterozygosity for Parkin Mutation on Onset Age in Familial Parkinson Disease: The GenePD Study
- Mei Sun; Jeanne C. Latourelle; G. Frederick Wooten; Mark F. Lew; Christine Klein; Holly A. Shill; Lawrence I. Golbe; Margery H. Mark; Brad A. Racette; Joel S. Perlmutter; Abbas Parsian; Mark Guttman; Garth Nicholson; Gang Xu; Jemma B. Wilk; Marie H. Saint-Hilaire; Anita L. DeStefano; Ranjana Prakash; Sally Williamson; Oksana Suchowersky; Nancy Labelle; John H. Growdon; Carlos Singer; Ray L. Watts; Stefano Goldwurm; Gianni Pezzoli; Kenneth B. Baker; Peter P. Pramstaller; David J. Burn; Patrick F. Chinnery; Scott Sherman; Peter Vieregge; Irene Litvan; Tammy Gillis; Marcy E. MacDonald; Richard H. Myers; James F. Gusella
Arch Neurol 2006; 63: 826-832.
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- Original Contributions
Clinical Spectrum of Homozygous and Heterozygous PINK1 Mutations in a Large German Family With Parkinson Disease: Role of a Single Hit?
- Katja Hedrich; Johann Hagenah; Ana Djarmati; Anja Hiller; Thora Lohnau; Kathrin Lasek; Anne Grünewald; Rüdiger Hilker; Susanne Steinlechner; Heather Boston; Norman Kock; Christiane Schneider-Gold; Wolfram Kress; Hartwig Siebner; Ferdinand Binkofski; Rebekka Lencer; Alexander Münchau; Christine Klein
Arch Neurol 2006; 63: 833-838.
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- Observations
Novel Mitochondrial Transfer RNAPhe Gene Mutation Associated With Late-Onset Neuromuscular Disease
- Marcus Deschauer; Helen Swalwell; Maria Strauss; Stephan Zierz; Robert W. Taylor
Arch Neurol 2006; 63: 902-905.
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