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Neurogenetics
Citations 391-400 of 574 total displayed.
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Past content
(since May 1998):
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- Book Reviews
Genetics and Genomics of Neurobehavioral Disorders
- Thomas D. Bird
Arch Neurol 2004; 61: 154.
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- Original Contributions
Spinocerebellar Ataxia Type 14 Caused by a Mutation in Protein Kinase C 
- Ichiro Yabe; Hidenao Sasaki; Dong-Hui Chen; Wendy H. Raskind; Thomas D. Bird; Isao Yamashita; Shoji Tsuji; Seiji Kikuchi; Kunio Tashiro
Arch Neurol 2003; 60: 1749-1751.
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- Original Contributions
Mutation Screening of the ALS2 Gene in Sporadic and Familial Amyotrophic Lateral Sclerosis
- Collette K. Hand; Rebecca S. Devon; Francois Gros-Louis; Daniel Rochefort; Jawad Khoris; Vincent Meininger; Jean-Pierre Bouchard; William Camu; Michael R. Hayden; Guy A. Rouleau
Arch Neurol 2003; 60: 1768-1771.
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- Editorials
Alzheimer Disease Genes: Presenilin 2 Mutation Number 9 and Still Counting
- Gerard D. Schellenberg
Arch Neurol 2003; 60: 1521-1522.
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- Original Contributions
Identification of New Presenilin Gene Mutations in Early-Onset Familial Alzheimer Disease
- Andrea Tedde; Benedetta Nacmias; Monica Ciantelli; Paolo Forleo; Elena Cellini; Silvia Bagnoli; Carolina Piccini; Paolo Caffarra; Enrico Ghidoni; Marco Paganini; Laura Bracco; Sandro Sorbi
Arch Neurol 2003; 60: 1541-1544.
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- Original Contributions
Clinical and Neuroradiological Features of Patients With Spinocerebellar Ataxias From Korean Kindreds
- Oh Young Bang; Kyoon Huh; Phil Hyu Lee; Hyon J. Kim
Arch Neurol 2003; 60: 1566-1574.
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- Observations
A Korean Kindred With Autosomal Dominant Nocturnal Frontal Lobe Epilepsy and Mental Retardation
- Yong-Won Cho; Gholam K. Motamedi; Iris Laufenberg; Sung-Il Sohn; Jeong-Geun Lim; Hyung Lee; Sang-Doe Yi; Ju-Hwa Lee; Dae-Kwang Kim; Richard Reba; William D. Gaillard; William H. Theodore; Ronald P. Lesser; Ortrud K. Steinlein
Arch Neurol 2003; 60: 1625-1632.
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- Original Contributions
Atypical Phenotypes in Patients With Facioscapulohumeral Muscular Dystrophy 4q35 Deletion
- Michael Krasnianski; Katharina Eger; Stephan Neudecker; Sibylle Jakubiczka; Stephan Zierz
Arch Neurol 2003; 60: 1421-1425.
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- Observations
Muscle Glycogenosis and Mitochondrial Hepatopathy in an Infant With Mutations in Both the Myophosphorylase and Deoxyguanosine Kinase Genes
- Michelangelo Mancuso; Massimiliano Filosto; Seiichi Tsujino; Costanza Lamperti; Sara Shanske; Michéle Coquet; Claude Desnuelle; Salvatore DiMauro
Arch Neurol 2003; 60: 1445-1447.
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- Observations
A Case of Dementia Parkinsonism Resembling Progressive Supranuclear Palsy Due to Mutation in the Tau Protein Gene
- Paola Soliveri; Giacomina Rossi; Daniela Monza; Fabrizio Tagliavini; Sylvie Piacentini; Alberto Albanese; Orso Bugiani; Floriano Girotti
Arch Neurol 2003; 60: 1454-1456.
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