Neurogenetics

Contributing journals to this collection:
JAMA & Archives Journals

Citations 361-370 of 623 total displayed.

Past content

Original Contributions
A Rare Truncating Mutation in ADH1C (G78Stop) Shows Significant Association With Parkinson Disease in a Large International Sample

Silvia Buervenich; Andrea Carmine; Dagmar Galter; Haydeh N. Shahabi; Bo Johnels; Björn Holmberg; Jarl Ahlberg; Hans Nissbrandt; Johanna Eerola; Olli Hellström; Pentti J. Tienari; Tohru Matsuura; Tetsuo Ashizawa; Ullrich Wüllner; Thomas Klockgether; Alexander Zimprich; Thomas Gasser; Melissa Hanson; Shamaila Waseem; Andrew Singleton; Francis J. McMahon; Maria Anvret; Olof Sydow; Lars Olson
Arch Neurol 2005; 62: 74-78. [Abstract] [Full text] [PDF]  

Original Contributions
Parkin Mutations and Early-Onset Parkinsonism in a Taiwanese Cohort

Ruey-Meei Wu; Rebecca Bounds; Sarah Lincoln; Mary Hulihan; Chin-Hsien Lin; Wuh-Liang Hwu; Judy Chen; Katrina Gwinn-Hardy; Matt Farrer
Arch Neurol 2005; 62: 82-87. [Abstract] [Full text] [PDF]  

Original Contributions
Failure to Find -Synuclein Gene Dosage Changes in 190 Patients With Familial Parkinson Disease

Suzana Gispert; Claudia Trenkwalder; Luisa Mota-Vieira; Vladimir Kostic; Georg Auburger
Arch Neurol 2005; 62: 96-98. [Abstract] [Full text] [PDF]  

Original Contributions
A Clinical, Magnetic Resonance Imaging, and Survival Motor Neuron Gene Deletion Study of Hirayama Disease

U. K. Misra; J. Kalita; V. N. Mishra; A. Kesari; B. Mittal
Arch Neurol 2005; 62: 120-123. [Abstract] [Full text] [PDF]  

Observations
Familial Periodic Paralysis and Charcot-Marie-Tooth Disease in a 7-Generation Family

Fuki M. Hisama
Arch Neurol 2005; 62: 135-138. [Abstract] [Full text] [PDF]  

Letters to the Editor
Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders: Where is the Evidence?—Reply

Corrine O. Smith; Hillary P. Lipe; Thomas D. Bird
Arch Neurol 2005; 62: 164-a. [Extract] [Full text] [PDF]  

Letters to the Editor
Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders: Where is the Evidence?

A. Cecile J. W. Janssens
Arch Neurol 2005; 62: 164. [Extract] [Full text] [PDF]  

Editorials
Beginning to Understand Hereditary Spastic Paraplegia Atlastin

Jeffrey L. Elliott
Arch Neurol 2004; 61: 1842-1843. [Extract] [Full text] [PDF]  

Original Contributions
Atlastin1 Mutations Are Frequent in Young-Onset Autosomal Dominant Spastic Paraplegia

Alexandra Dürr; Agnès Camuzat; Emilie Colin; Chantal Tallaksen; Didier Hannequin; Paula Coutinho; Bertrand Fontaine; Annick Rossi; Roger Gil; Christophe Rousselle; Merle Ruberg; Giovanni Stevanin; Alexis Brice
Arch Neurol 2004; 61: 1867-1872. [Abstract] [Full text] [PDF]  

Original Contributions
Genome-Wide Analysis of the Parkinsonism-Dementia Complex of Guam

Huw R. Morris; John C. Steele; Richard Crook; Fabienne Wavrant-De Vrièze; Luisa Onstead-Cardinale; Katrina Gwinn-Hardy; Nick W. Wood; Matthew Farrer; Andrew J. Lees; P. L. McGeer; Teepu Siddique; John Hardy; Jordi Perez-Tur
Arch Neurol 2004; 61: 1889-1897. [Abstract] [Full text] [PDF]  

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