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Neurogenetics

Citations 191-200 of 574 total displayed.

Past content (since May 1998):

Clinical Trials
Effects of Methylphenidate on Response to Oral Levodopa: A Double-blind Clinical Trial
John G. Nutt; Julie H. Carter; Nichole E. Carlson
Arch Neurol 2007; 64: 319-323. [Abstract] [Full text] [PDF]  

Neurological Reviews
New Ideas in Epilepsy Genetics: Novel Epilepsy Genes, Copy Number Alterations, and Gene Regulation
Christina A. Gurnett; Peter Hedera
Arch Neurol 2007; 64: 324-328. [Abstract] [Full text] [PDF]  

Original Contributions
Voxel-Based Morphometry in Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions With and Without Progranulin Mutations
Jennifer L. Whitwell; Clifford R. Jack Jr; Matthew Baker; Rosa Rademakers; Jennifer Adamson; Bradley F. Boeve; David S. Knopman; Joseph F. Parisi; Ronald C. Petersen; Dennis W. Dickson; Michael L. Hutton; Keith A. Josephs
Arch Neurol 2007; 64: 371-376. [Abstract] [Full text] [PDF]  

Original Contributions
A Family With Parkinson Disease, Essential Tremor, Bell Palsy, and Parkin Mutations
Hao Deng; Wei-Dong Le; Christine B. Hunter; Nicte Mejia; Wen-Jie Xie; Joseph Jankovic
Arch Neurol 2007; 64: 421-424. [Abstract] [Full text] [PDF]  

Original Contributions
LRRK2 Exon 41 Mutations in Sporadic Parkinson Disease in Europeans
Suzanne Lesage; Sabine Janin; Ebba Lohmann; Anne-Louise Leutenegger; Laurence Leclere; François Viallet; Pierre Pollak; Franck Durif; Stéphane Thobois; Valérie Layet; Marie Vidailhet; Yves Agid; Alexandra Dürr; Alexis Brice; for the French Parkinson's Disease Genetics Study Group
Arch Neurol 2007; 64: 425-430. [Abstract] [Full text] [PDF]  

Original Contributions
Two Novel Epilepsy-Linked Mutations Leading to a Loss of Function of LGI1
Elodie Chabrol; Cyprian Popescu; Isabelle Gourfinkel-An; Oriane Trouillard; Christel Depienne; Kristen Senechal; Michel Baulac; Eric LeGuern; Stéphanie Baulac
Arch Neurol 2007; 64: 217-222. [Abstract] [Full text] [PDF]  

Original Contributions
Molecular Analysis and Prenatal Prediction of Spinal Muscular Atrophy in Chinese Patients by the Combination of Restriction Fragment Length Polymorphism Analysis, Denaturing High-Performance Liquid Chromatography, and Linkage Analysis
Wan-Jin Chen; Zhi-Ying Wu; Min-Ting Lin; Jun-Feng Su; Yu Lin; Shen-Xing Murong; Ning Wang
Arch Neurol 2007; 64: 225-231. [Abstract] [Full text] [PDF]  

Original Contributions
Three Families With Amyotrophic Lateral Sclerosis and Frontotemporal Dementia With Evidence of Linkage to Chromosome 9p
Paul N. Valdmanis; Nicolas Dupre; Jean-Pierre Bouchard; William Camu; François Salachas; Vincent Meininger; Michael Strong; Guy A. Rouleau
Arch Neurol 2007; 64: 240-245. [Abstract] [Full text] [PDF]  

Original Contributions
Apolipoprotein E Gene Polymorphism, Total Plasma Cholesterol Level, and Parkinson Disease Dementia
Barbara Jasinska-Myga; Grzegorz Opala; Christopher G. Goetz; Jerzy Tustanowski; Stanislaw Ochudlo; Agnieszka Gorzkowska; Jadwiga Tyrpa
Arch Neurol 2007; 64: 261-265. [Abstract] [Full text] [PDF]  

Observations
X-linked Hyper-IgM Syndrome Associated With a Rapid Course of Multifocal Leukoencephalopathy
Zsuzsanna Aschermann; Eva Gomori; Gabor G. Kovacs; Endre Pal; Gabor Simon; Samuel Komoly; Laszlo Marodi; Zsolt Illes
Arch Neurol 2007; 64: 273-276. [Abstract] [Full text] [PDF]  

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