Neurogenetics

Contributing journals to this collection:
JAMA & Archives Journals

Citations 201-210 of 623 total displayed.

Past content

Observations
Dissociation of Neuropathologic Findings and Cognition: Case Report of an Apolipoprotein E 2/2 Genotype

Daniel J. Berlau; Kristin Kahle-Wrobleski; Elizabeth Head; Matthew Goodus; Ronald Kim; Claudia Kawas
Arch Neurol 2007; 64: 1193-1196. [Abstract] [Full text] [PDF]  

Editorials
Dwindling Indications for Sural Nerve Biopsy

David E. Pleasure
Arch Neurol 2007; 64: 935-936. [Extract] [Full text] [PDF]  

Neurological Reviews
The New Neurobiology of Autism: Cortex, Connectivity, and Neuronal Organization

Nancy J. Minshew; Diane L. Williams
Arch Neurol 2007; 64: 945-950. [Abstract] [Full text] [PDF]  

Original Contributions
Clinical and Electrophysiological Features in Charcot-Marie-Tooth Disease With Mutations in the NEFL Gene

Gabriel Miltenberger-Miltenyi; Andreas R. Janecke; Julia V. Wanschitz; Vincent Timmerman; Christian Windpassinger; Michaela Auer-Grumbach; Wolfgang N. Löscher
Arch Neurol 2007; 64: 966-970. [Abstract] [Full text] [PDF]  

Original Contributions
Stoichiometric Alteration of PMP22 Protein Determines the Phenotype of Hereditary Neuropathy With Liability to Pressure Palsies

Jun Li; Khaled Ghandour; Danijela Radovanovic; Rosemary R. Shy; Karen M. Krajewski; Michael E. Shy; Garth A. Nicholson
Arch Neurol 2007; 64: 974-978. [Abstract] [Full text] [PDF]  

Original Contributions
Familial Parkinsonism and Ophthalmoplegia From a Mutation in the Mitochondrial DNA Helicase Twinkle

Robert H. Baloh; Ezequiel Salavaggione; Jeffrey Milbrandt; Alan Pestronk
Arch Neurol 2007; 64: 998-1000. [Abstract] [Full text] [PDF]  

Original Contributions
Screen for Excess FMR1 Premutation Alleles Among Males With Parkinsonism

Jeremy Kraff; Hiu-Tung Tang; Roberto Cilia; Margherita Canesi; Gianni Pezzoli; Stefano Goldwurm; Paul J. Hagerman; Flora Tassone
Arch Neurol 2007; 64: 1002-1006. [Abstract] [Full text] [PDF]  

Observations
Limb-Girdle Muscular Dystrophy Due to Emerin Gene Mutations

Shigehisa Ura; Yukiko K. Hayashi; Kanako Goto; Mina Nolasco Astejada; Terumi Murakami; Masako Nagato; Shigeru Ohta; Yasuhisa Daimon; Hidehiro Takekawa; Koichi Hirata; Ikuya Nonaka; Satoru Noguchi; Ichizo Nishino
Arch Neurol 2007; 64: 1038-1041. [Abstract] [Full text] [PDF]  

Observations
Mitochondrial Complex I Gene Variant Associated With Early Age at Onset in Spinocerebellar Ataxia Type 2

David K. Simon; Kangni Zheng; Luis Velázquez; Nieves Santos; Luis Almaguer; K. Pattie Figueroa; Stefan-M. Pulst
Arch Neurol 2007; 64: 1042-1044. [Abstract] [Full text] [PDF]  

Research Letters
Glucocerebrosidase Mutations and Risk of Parkinson Disease in Chinese Patients

Eng-King Tan; Justina Tong; Stephanie Fook-Chong; Yuen Yih; Meng-Cheong Wong; Ratnagopal Pavanni; Yi Zhao
Arch Neurol 2007; 64: 1056-1058. [Extract] [Full text] [PDF]  

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