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Neurogenetics
Citations 151-160 of 574 total displayed.
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Past content
(since May 1998):
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- Original Contributions
Asian Origin for the Worldwide-Spread Mutational Event in Machado-Joseph Disease
- Sandra Martins; Francesc Calafell; Claudia Gaspar; Virginia C. N. Wong; Isabel Silveira; Garth A. Nicholson; Ewout R. Brunt; Lisbeth Tranebjaerg; Giovanni Stevanin; Mingli Hsieh; Bing-wen Soong; Leal Loureiro; Alexandra Dürr; Shoji Tsuji; Mitsunori Watanabe; Laura B. Jardim; Paola Giunti; Olaf Riess; Laura P. W. Ranum; Alexis Brice; Guy A. Rouleau; Paula Coutinho; António Amorim; Jorge Sequeiros
Arch Neurol 2007; 64: 1502-1508.
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- Original Contributions
Importance of Low-Range CAG Expansion and CAA Interruption in SCA2 Parkinsonism
- Jong-Min Kim; Susie Hong; Gyoung Pyoung Kim; Yoon Jae Choi; Yu Kyeong Kim; Sung Sup Park; Sang Eun Kim; Beom S. Jeon
Arch Neurol 2007; 64: 1510-1518.
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- Observations
Familial Early-Onset Dementia With Tau Intron 10 + 16 Mutation With Clinical Features Similar to Those of Alzheimer Disease
- Mark Doran; Daniel G. du Plessis; Eric J. Ghadiali; David M. A. Mann; Stuart Pickering-Brown; Andrew J. Larner
Arch Neurol 2007; 64: 1535-1539.
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- Corrections
Error in Byline in: Stoichiometric Alteration of PMP22 Protein Determines the Phenotype of Hereditary Neuropathy With Liability to Pressure Palsies
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Arch Neurol 2007; 64: 1547.
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- Original Contributions
Cognitive Domain Decline in Healthy Apolipoprotein E  4 Homozygotes Before the Diagnosis of Mild Cognitive Impairment
- Richard J. Caselli; Eric M. Reiman; Dona E. C. Locke; Michael L. Hutton; Joseph G. Hentz; Charlene Hoffman-Snyder; Bryan K. Woodruff; Gene E. Alexander; David Osborne
Arch Neurol 2007; 64: 1306-1311.
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- Observations
Congenital Myopathy With Nemaline Rods and Cap Structures Caused by a Mutation in the  -Tropomyosin Gene (TPM2)
- Homa Tajsharghi; Monica Ohlsson; Christopher Lindberg; Anders Oldfors
Arch Neurol 2007; 64: 1334-1338.
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- Observations
Two Novel Mitochondrial DNA Mutations in Muscle Tissue of a Patient With Limb-Girdle Myopathy
- Ann Meulemans; Boel De Paepe; Jan De Bleecker; Joél Smet; Willy Lissens; Rudy Van Coster; Linda De Meirleir; Sara Seneca
Arch Neurol 2007; 64: 1339-1343.
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- Original Contributions
Clinical, Genetic, and Pathologic Characteristics of Patients With Frontotemporal Dementia and Progranulin Mutations
- Vivianna M. Van Deerlin; Elisabeth McCarty Wood; Peachie Moore; Wuxing Yuan; Mark S. Forman; Christopher M. Clark; Manuela Neumann; Linda K. Kwong; John Q. Trojanowski; Virginia M.-Y. Lee; Murray Grossman
Arch Neurol 2007; 64: 1148-1153.
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- Original Contributions
Phenotypic Study in 40 Patients With Dysferlin Gene Mutations: High Frequency of Atypical Phenotypes
- Karine Nguyen; Guillaume Bassez; Martin Krahn; Rafaelle Bernard; Pascal Laforêt; Véronique Labelle; Jon Andoni Urtizberea; Dominique Figarella-Branger; Norma Romero; Shahram Attarian; France Leturcq; Jean Pouget; Nicolas Lévy; Bruno Eymard
Arch Neurol 2007; 64: 1176-1182.
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- Observations
Neuromyelitis Optica in a Mother and Daughter
- Tiffany Braley; Daniel D. Mikol
Arch Neurol 2007; 64: 1189-1192.
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