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Neurogenetics
Citations 211-220 of 574 total displayed.
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Past content
(since May 1998):
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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 George–Hyslop; 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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- Observations
T313M PINK1 Mutation in an Extended Highly Consanguineous Saudi Family With Early-Onset Parkinson Disease
- Muhammad A. Chishti; Saeed Bohlega; Maqbool Ahmed; Arslan Loualich; Pamela Carroll; Christine Sato; Peter St George-Hyslop; David Westaway; Ekaterina Rogaeva
Arch Neurol 2006; 63: 1483-1485.
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- Observations
POMGnT1 Mutations in Congenital Muscular Dystrophy: Genotype-Phenotype Correlation and Expanded Clinical Spectrum
- Roberta Biancheri; Enrico Bertini; Antonio Falace; Marina Pedemonte; Andrea Rossi; Adele D’Amico; Sara Scapolan; Laura Bergamino; Stefania Petrini; Denise Cassandrini; Paolo Broda; Mario Manfredi; Federico Zara; Filippo M. Santorelli; Carlo Minetti; Claudio Bruno
Arch Neurol 2006; 63: 1491-1495.
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- Editorials
The Importance of LRRK2 Mutations in Parkinson Disease
- Anthony H. V. Schapira
Arch Neurol 2006; 63: 1225-1228.
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- Neurological Reviews
Genetic Testing in Parkinson Disease: Promises and Pitfalls
- Eng-King Tan; Joseph Jankovic
Arch Neurol 2006; 63: 1232-1237.
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- Original Contributions
Clinical Heterogeneity of the LRRK2 G2019S Mutation
- Spiridon Papapetropoulos; Carlos Singer; Owen A. Ross; Mathias Toft; Joseph L. Johnson; Matthew J. Farrer; Deborah C. Mash
Arch Neurol 2006; 63: 1242-1246.
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