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Neurogenetics
Citations 281-290 of 574 total displayed.
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Past content
(since May 1998):
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- Original Contributions
Mutation Analysis of the Small Heat Shock Protein 27 Gene in Chinese Patients With Charcot-Marie-Tooth Disease
- Beisha Tang; Xiaomin Liu; Guohua Zhao; Wei Luo; Kun Xia; Qian Pan; Fang Cai; Zhengmao Hu; Cheng Zhang; Biao Chen; Fufeng Zhang; Lu Shen; Ruxu Zhang; Hong Jiang
Arch Neurol 2005; 62: 1201-1207.
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- Original Contributions
Identification of a Novel Founder Mutation in the DYSF Gene Causing Clinical Variability in the Spanish Population
- Juan J. Vilchez; Pia Gallano; Eduard Gallardo; Adriana Lasa; Ricardo Rojas-García; Alba Freixas; Noemí De Luna; Francesc Calafell; Teresa Sevilla; Fernando Mayordomo; Montserrat Baiget; Isabel Illa
Arch Neurol 2005; 62: 1256-1259.
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- Original Contributions
Prognosis of Parkinson Disease: Risk of Dementia and Mortality: The Rotterdam Study
- Lonneke M. L. de Lau; C. Maarten A. Schipper; Albert Hofman; Peter J. Koudstaal; Monique M. B. Breteler
Arch Neurol 2005; 62: 1265-1269.
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- Original Contributions
Dopamine Transporter Positron Emission Tomography in Spinocerebellar Ataxias Type 1, 2, 3, and 6
- Ullrich Wüllner; Michael Reimold; Michael Abele; Katrin Bürk; Martina Minnerop; Bernd-Michael Dohmen; Hans-Juergen Machulla; Roland Bares; Thomas Klockgether
Arch Neurol 2005; 62: 1280-1285.
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- Editorials
Lorenzo’s Oil: Advances in the Treatment of Neurometabolic Disorders
- Raymond Ferri; Phillip F. Chance
Arch Neurol 2005; 62: 1045-1046.
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- Original Contributions
Spectrum of Mutations in Biopsy-Proven CADASIL: Implications for Diagnostic Strategies
- Nils Peters; Christian Opherk; Tanja Bergmann; Mirna Castro; Jürgen Herzog; Martin Dichgans
Arch Neurol 2005; 62: 1091-1094.
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- Original Contributions
Sporadic and Familial Dementia With Ubiquitin-Positive Tau-Negative Inclusions: Clinical Features of One Histopathological Abnormality Underlying Frontotemporal Lobar Degeneration
- Alison K. Godbolt; Keith A. Josephs; Tamas Revesz; Elizabeth K. Warrington; Peter Lantos; Andrew King; Nick C. Fox; Safa Al Sarraj; Janice Holton; Lisa Cipolotti; M. Nadeem Khan; Martin N. Rossor
Arch Neurol 2005; 62: 1097-1101.
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- Original Contributions
Mutation Analysis of SPG4 and SPG3A Genes and Its Implication in Molecular Diagnosis of Korean Patients With Hereditary Spastic Paraplegia
- Su-Yon Park; Chang-Seok Ki; Hee-Jin Kim; Jong-Won Kim; Duk Hyun Sung; Byoung Joon Kim; Won Yong Lee
Arch Neurol 2005; 62: 1118-1121.
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- Observations
Moyamoya Syndrome With Intraventricular Hemorrhage in an Adult With Factor V Leiden Mutation
- Rosette Jabbour; Ali Taher; Ali Shamseddine; Samir F. Atweh
Arch Neurol 2005; 62: 1144-1146.
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- Original Contributions
Expression Profiling of Substantia Nigra in Parkinson Disease, Progressive Supranuclear Palsy, and Frontotemporal Dementia With Parkinsonism
- Michael A. Hauser; Yi-Ju Li; Hong Xu; Maher A. Noureddine; Yujun S. Shao; Steven R. Gullans; Clemens R. Scherzer; Roderick V. Jensen; Adam C. McLaurin; Jason R. Gibson; Burton L. Scott; Rita M. Jewett; Judith E. Stenger; Donald E. Schmechel; Christine M. Hulette; Jeffery M. Vance
Arch Neurol 2005; 62: 917-921.
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