Neurogenetics

Contributing journals to this collection:
JAMA & Archives Journals

Citations 241-250 of 623 total displayed.

Past content

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]  

Correspondence
Fragile X Syndrome vs Fragile X–Associated Tremor/Ataxia Syndrome—Reply

Elena Cellini; Paolo Forleo; Andrea Ginestroni; Benedetta Nacmias; Andrea Tedde; Silvia Bagnoli; Silvia Piacentini; Mario Mascalchi; Sandro Sorbi
Arch Neurol 2007; 64: 289-a-290-a. [Extract] [Full text] [PDF]  

Correspondence
Fragile X Syndrome vs Fragile X–Associated Tremor/Ataxia Syndrome

Maureen A. Leehey; Randi J. Hagerman; Paul J. Hagerman
Arch Neurol 2007; 64: 289. [Extract] [Full text] [PDF]  

Editorials
Progranulin and Tau Gene Mutations Both as Cause for Dementia: 17q21 Finally Defined

Roger N. Rosenberg
Arch Neurol 2007; 64: 18-19. [Extract] [Full text] [PDF]  

Original Contributions
Progranulin Mutations in Primary Progressive Aphasia: The PPA1 and PPA3 Families

Marsel Mesulam; Nancy Johnson; Thomas A. Krefft; Jennifer M. Gass; Ashley D. Cannon; Jennifer L. Adamson; Eileen H. Bigio; Sandra Weintraub; Dennis W. Dickson; Michael L. Hutton; Neill R. Graff-Radford
Arch Neurol 2007; 64: 43-47. [Abstract] [Full text] [PDF]  

Original Contributions
The Association Between H63D Mutations in HFE and Amyotrophic Lateral Sclerosis in a Dutch Population

Nadia A. Sutedja; Richard J. Sinke; Paul W. J. Van Vught; Michiel W. Van der Linden; John H. J. Wokke; Cornelia M. Van Duijn; Omer T. Njajou; Yvonne T. Van der Schouw; Jan H. Veldink; Leonard H. Van den Berg
Arch Neurol 2007; 64: 63-67. [Abstract] [Full text] [PDF]  

Original Contributions
Specific Psychiatric Manifestations Among Preclinical Huntington Disease Mutation Carriers

Jeanine Marshall; Kerry White; Marjorie Weaver; Leah Flury Wetherill; Siu Hui; Julie C. Stout; Shannon A. Johnson; Xabier Beristain; Jacqueline Gray; Joanne Wojcieszek; Tatiana Foroud
Arch Neurol 2007; 64: 116-121. [Abstract] [Full text] [PDF]  

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