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Genetic Counseling/ Testing/ Therapy

Citations 41-50 of 122 total displayed.

Past content (since May 1998):

Editorials
Genes for Movement
Roger N. Rosenberg
Arch Neurol 2004; 61: 1006. [Extract] [Full text] [PDF]  

Original Contributions
Myofibrillogenesis Regulator 1 Gene Mutations Cause Paroxysmal Dystonic Choreoathetosis
Shirley Rainier; Donald Thomas; Debra Tokarz; Lei Ming; Melanie Bui; Erin Plein; Xinping Zhao; Rosemary Lemons; Roger Albin; Colin Delaney; David Alvarado; John K. Fink
Arch Neurol 2004; 61: 1025-1029. [Abstract] [Full text] [PDF]  

Original Contributions
Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
Corrine O. Smith; Hillary P. Lipe; Thomas D. Bird
Arch Neurol 2004; 61: 875-880. [Abstract] [Full text] [PDF]  

Original Contributions
Molecular Genetics of Hereditary Spinocerebellar Ataxia: Mutation Analysis of Spinocerebellar Ataxia Genes and CAG/CTG Repeat Expansion Detection in 225 Italian Families
Alfredo Brusco; Cinzia Gellera; Claudia Cagnoli; Alessandro Saluto; Alessia Castucci; Chiara Michielotto; Vincenza Fetoni; Caterina Mariotti; Nicola Migone; Stefano Di Donato; Franco Taroni
Arch Neurol 2004; 61: 727-733. [Abstract] [Full text] [PDF]  

Basic Science Seminars in Neurology
Molecular Basis of Inherited Epilepsy
Alfred L. George Jr
Arch Neurol 2004; 61: 473-478. [Extract] [Full text] [PDF]  

Original Contributions
Brief Presence of Varicella-zoster Viral DNA in Mononuclear Cells During Relapses of Multiple Sclerosis
Graciela Ordoñez; Benjamin Pineda; Roberto Garcia-Navarrete; Julio Sotelo
Arch Neurol 2004; 61: 529-532. [Abstract] [Full text] [PDF]  

Editorials
Spinocerebellar Ataxia Type 17: Latest Member of Polyglutamine Disease Group Highlights Unanswered Questions
Shoji Tsuji
Arch Neurol 2004; 61: 183-184. [Extract] [Full text] [PDF]  

Observations
Revelation of a New Mitochondrial DNA Mutation (G12147A) in a MELAS/MERFF Phenotype
Mariarosa A. B. Melone; Alessandra Tessa; Stefania Petrini; Giacomo Lus; Simone Sampaolo; Giuseppe di Fede; Filippo M. Santorelli; Roberto Cotrufo
Arch Neurol 2004; 61: 269-272. [Abstract] [Full text] [PDF]  

Original Contributions
Mutation Screening of the ALS2 Gene in Sporadic and Familial Amyotrophic Lateral Sclerosis
Collette K. Hand; Rebecca S. Devon; Francois Gros-Louis; Daniel Rochefort; Jawad Khoris; Vincent Meininger; Jean-Pierre Bouchard; William Camu; Michael R. Hayden; Guy A. Rouleau
Arch Neurol 2003; 60: 1768-1771. [Abstract] [Full text] [PDF]  

Corrections
Frequency Analysis and Clinical Characterization of Spinocerebellar Ataxia Types 1, 2, 3, 6, and 7 in Korean Patients—Correction
Arch Neurol 2003; 60: 1256. [Full text] [PDF]  

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