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Neurogenetics
Citations 351-360 of 574 total displayed.
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Past content
(since May 1998):
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- Correspondence
Haplotype-Phenotype Correlations in Kindreds With the N279K Mutation in the Tau Gene
- Bryan K. Woodruff; Yasuhiko Baba; Michael L. Hutton; Zbigniew K. Wszolek; Yoshio Tsuboi; Tomonori Kobayashi; Bernardino Ghetti; Kunimasa Arima; Minoru Yasuda; Olivier Rascol
Arch Neurol 2004; 61: 1327.
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- Editorials
Genes for Movement
- Roger N. Rosenberg
Arch Neurol 2004; 61: 1006.
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- Editorials
Perspectives on Shared Genetic Contributions for Parkinson Disease and Alzheimer Disease
- Walter A. Kukull
Arch Neurol 2004; 61: 1007-1008.
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- Original Contributions
Myofibrillogenesis Regulator 1 Gene Mutations Cause Paroxysmal Dystonic Choreoathetosis
- Shirley Rainier; Donald Thomas; Debra Tokarz; Lei Ming; Melanie Bui; Erin Plein; Xinping Zhao; Rosemary Lemons; Roger Albin; Colin Delaney; David Alvarado; John K. Fink
Arch Neurol 2004; 61: 1025-1029.
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- Original Contributions
Lack of Familial Aggregation of Parkinson Disease and Alzheimer Disease
- Gilberto Levy; Elan D. Louis; Helen Mejia-Santana; Lucien Côté; Howard Andrews; Juliette Harris; Cheryl Waters; Blair Ford; Steven Frucht; Stanley Fahn; Ruth Ottman; Karen Marder
Arch Neurol 2004; 61: 1033-1039.
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- Observations
A New Rare Mutation (691delCC/insAAA) in Exon 17 of the PYGM Gene Causing McArdle Disease
- Beatriz Quintans; Amalia Sanchez-Andrade; Susana Teijeira; Roberto Fernandez-Hojas; Eloy Rivas; María José López; Carmen Navarro
Arch Neurol 2004; 61: 1108-1110.
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- Editorials
Hereditary Spastic Paraplegia: Spastin Phenotype and Function
- John K. Fink; Shirley Rainier
Arch Neurol 2004; 61: 830-833.
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- Original Contributions
Hereditary Spastic Paraplegia: Clinical Genetic Study of 15 Families
- Antonio Orlacchio; Toshitaka Kawarai; Antonio Totaro; Alessia Errico; Peter H. St George-Hyslop; Elena I. Rugarli; Giorgio Bernardi
Arch Neurol 2004; 61: 849-855.
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- Original Contributions
Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
- Corrine O. Smith; Hillary P. Lipe; Thomas D. Bird
Arch Neurol 2004; 61: 875-880.
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- Original Contributions
CTG Repeat Number at the Myotonic Dystrophy Locus in Healthy Kuwaiti Individuals: Possible Explanation of Why Myotonic Dystrophy Is Rare in Kuwait
- Suad Alfadhli; Alaa E. Elshafey; Lailá Bastaki; Sadeqa Al-Awadi
Arch Neurol 2004; 61: 895-898.
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