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Neurogenetics
Citations 321-330 of 574 total displayed.
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Past content
(since May 1998):
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- Editorials
Beginning to Understand Hereditary Spastic Paraplegia Atlastin
- Jeffrey L. Elliott
Arch Neurol 2004; 61: 1842-1843.
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- Original Contributions
Atlastin1 Mutations Are Frequent in Young-Onset Autosomal Dominant Spastic Paraplegia
- Alexandra Dürr; Agnès Camuzat; Emilie Colin; Chantal Tallaksen; Didier Hannequin; Paula Coutinho; Bertrand Fontaine; Annick Rossi; Roger Gil; Christophe Rousselle; Merle Ruberg; Giovanni Stevanin; Alexis Brice
Arch Neurol 2004; 61: 1867-1872.
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- Original Contributions
Genome-Wide Analysis of the Parkinsonism-Dementia Complex of Guam
- Huw R. Morris; John C. Steele; Richard Crook; Fabienne Wavrant-De Vrièze; Luisa Onstead-Cardinale; Katrina Gwinn-Hardy; Nick W. Wood; Matthew Farrer; Andrew J. Lees; P. L. McGeer; Teepu Siddique; John Hardy; Jordi Perez-Tur
Arch Neurol 2004; 61: 1889-1897.
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- Original Contributions
Analysis of the PINK1 Gene in a Large Cohort of Cases With Parkinson Disease
- Ekaterina Rogaeva; Janel Johnson; Anthony E. Lang; Cindy Gulick; Katrina Gwinn-Hardy; Toshitaka Kawarai; Christine Sato; Angharad Morgan; John Werner; Robert Nussbaum; Agnes Petit; Michael S. Okun; Aideen McInerney; Ronald Mandel; Justus L. Groen; Hubert H. Fernandez; Ron Postuma; Kelly D. Foote; Shabnam Salehi-Rad; Yan Liang; Sharon Reimsnider; Anurag Tandon; John Hardy; Peter St George-Hyslop; Andrew B. Singleton
Arch Neurol 2004; 61: 1898-1904.
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- Original Contributions
APOE Genotype, Family History of Dementia, and Alzheimer Disease Risk: A 6-Year Follow-up Study
- Wenyong Huang; Chengxuan Qiu; Eva von Strauss; Bengt Winblad; Laura Fratiglioni
Arch Neurol 2004; 61: 1930-1934.
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- Original Contributions
Studies of COX16, COX19, and PET191 in Human Cytochrome-c Oxidase Deficiency
- Stacey K. H. Tay; Claudia Nesti; Michelangelo Mancuso; Eric A. Schon; Sara Shanske; Eduardo Bonilla; Mercy M. Davidson; Salvatore DiMauro
Arch Neurol 2004; 61: 1935-1937.
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- Original Contributions
Characterization of the Pattern of Cognitive Impairment in Myotonic Dystrophy Type 1
- Anna Modoni; Gabriella Silvestri; Maria Grazia Pomponi; Fortunato Mangiola; Pietro A. Tonali; Camillo Marra
Arch Neurol 2004; 61: 1943-1947.
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- Editorials
Tales From the Neural Genome: The Lessons of Homozygous Porphyria
- Golder N. Wilson
Arch Neurol 2004; 61: 1650-1651.
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- Neurological Reviews
Meta-analysis of Genetic Studies in Ischemic Stroke: Thirty-two Genes Involving Approximately 18 000 Cases and 58 000 Controls
- Juan P. Casas; Aroon D. Hingorani; Leonelo E. Bautista; Pankaj Sharma
Arch Neurol 2004; 61: 1652-1661.
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- Original Contributions
Cognitive Impairments in Machado-Joseph Disease
- Yoshinari Kawai; Akinori Takeda; Yuji Abe; Yukihiko Washimi; Fumiaki Tanaka; Gen Sobue
Arch Neurol 2004; 61: 1757-1760.
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