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Neurogenetics
Contributing journals to this collection:
JAMA & Archives Journals
Citations 251-260 of 623 total displayed.
- Editorials
Pedaling From Genotype to Phenotype
- Salvatore DiMauro; Michio Hirano
Arch Neurol 2006; 63: 1679-1680.
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- Original Contributions
Muscle Phenotype and Mutation Load in 51 Persons With the 3243A>G Mitochondrial DNA Mutation
- Tina D. Jeppesen; Marianne Schwartz; Anja L. Frederiksen; Flemming Wibrand; David B. Olsen; John Vissing
Arch Neurol 2006; 63: 1701-1706.
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- Observations
Novel Mutation in the PYGM Gene Resulting in McArdle Disease
- Juan C. Rubio; Alejandro Lucia; Israel Fernández-Cadenas; Ana Cabello; Alberto Blázquez; Josep Gámez; Antoni L. Andreu; Miguel A. Martín; Joaquin Arenas
Arch Neurol 2006; 63: 1782-1784.
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- Observations
Effect of an R69C Mutation in the Myelin Protein Zero Gene on Myelination and Ion Channel Subtypes
- Yunhong Bai; Emilia Ianokova; Qin Pu; Khaled Ghandour; Rock Levinson; Jean-Jacques Martin; Chantal Ceuterick-de Groote; Radim Mazanec; Pavel Seeman; Michael E. Shy; Jun Li
Arch Neurol 2006; 63: 1787-1794.
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- Neurological Reviews
The Future of Genomic Profiling of Neurological Diseases Using Blood
- Frank R. Sharp; Huichun Xu; Lisa Lit; Wynn Walker; Michelle Apperson; Donald L. Gilbert; Tracy A. Glauser; Brenda Wong; Andrew Hershey; Da-Zhi Liu; Joseph Pinter; Xinhua Zhan; Xinshe Liu; Ruiqiong Ran
Arch Neurol 2006; 63: 1529-1536.
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- Original Contributions
Apolipoprotein E 4 and Age at Onset of Sporadic and Familial Alzheimer Disease in Caribbean Hispanics
- Lucia Olarte; Nicole Schupf; Joseph H. Lee; Ming-Xin Tang; Vincent Santana; Jennifer Williamson; Prashanthi Maramreddy; Benjamin Tycko; Richard Mayeux
Arch Neurol 2006; 63: 1586-1590.
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- Original Contributions
Expanded Genomewide Scan Implicates a Novel Locus at 3q28 Among Caribbean Hispanics With Familial Alzheimer Disease
- Joseph H. Lee; Rong Cheng; Vincent Santana; Jennifer Williamson; Rafael Lantigua; Martin Medrano; Alex Arriaga; Yaakov Stern; Benjamin Tycko; Ekaterina Rogaeva; Yosuke Wakutani; Toshitaka Kawarai; Peter St GeorgeHyslop; Richard Mayeux
Arch Neurol 2006; 63: 1591-1598.
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- Original Contributions
Novel Mutations in the Guanosine Triphosphate Cyclohydrolase 1 Gene Associated With DYT5 Dystonia
- Etsuro Ohta; Manabu Funayama; Hiroshi Ichinose; Itaru Toyoshima; Fumi Urano; Mitsuhiro Matsuo; Nishida Tomoko; Konishi Yukihiko; Syuji Yoshino; Hiroyuki Yokoyama; Hideki Shimazu; Koji Maeda; Kazuko Hasegawa; Fumiya Obata
Arch Neurol 2006; 63: 1605-1610.
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- Original Contributions
Cardiac and Pulmonary Investigations in Bethlem Myopathy
- Anneke J. van der Kooi; Willem G. de Voogt; Enrico Bertini; Luciano Merlini; F. Beril Talim; Rabah Ben Yaou; Andoni Urtziberea; Marianne de Visser
Arch Neurol 2006; 63: 1617-1621.
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- Original Contributions
Monoamine Transporter Gene Polymorphisms and Antidepressant Response in Koreans With Late-Life Depression
- Hyeran Kim; Shinn-Won Lim; Seonwoo Kim; Jong-Won Kim; Yun Hee Chang; Bernard J. Carroll; Doh Kwan Kim
JAMA 2006; 296: 1609-1618.
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