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Neurogenetics
Citations 201-210 of 574 total displayed.
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Past content
(since May 1998):
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- 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.
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- 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.
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- Editorials
Progranulin and Tau Gene Mutations Both as Cause for Dementia: 17q21 Finally Defined
- Roger N. Rosenberg
Arch Neurol 2007; 64: 18-19.
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- 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.
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- 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.
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- 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.
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- 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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