Genetic Counseling/ Testing/ Therapy

Contributing journals to this collection:
JAMA & Archives Journals

Citations 321-330 of 718 total displayed.

Past content

Observations
Adult Onset Metachromatic Leukodystrophy Without Electroclinical Peripheral Nervous System Involvement: A New Mutation in the ARSA Gene

Ana M. Marcão; Roland Wiest; Kaspar Schindler; Ulrich Wiesmann; Joachim Weis; Gerhard Schroth; Maria Clara S. Miranda; Matthias Sturzenegger; Volkmar Gieselmann
Arch Neurol 2005; 62: 309-313. [Abstract] [Full text] [PDF]  

Original Contributions
Sodium Channel Mutations and Susceptibility to Heart Failure and Atrial Fibrillation

Timothy M. Olson; Virginia V. Michels; Jeffrey D. Ballew; Sandra P. Reyna; Margaret L. Karst; Kathleen J. Herron; Steven C. Horton; Richard J. Rodeheffer; Jeffrey L. Anderson
JAMA 2005; 293: 447-454. [Abstract] [Full text] [PDF]  

Medical News & Perspectives
Down Syndrome Protein Deters Cancer: Scientists Reveal Molecular Mechanism

Tracy Hampton
JAMA 2005; 293: 284-285. [Extract] [Full text] [PDF]  

Letters
Premutation Alleles and Fragile X–Associated Tremor/Ataxia Syndrome—Reply

Hao Deng; Weidong Le; Joseph Jankovic
JAMA 2005; 293: 296-a-297-a. [Extract] [Full text] [PDF]  

Letters
Premutation Alleles and Fragile X–Associated Tremor/Ataxia Syndrome

Mathias Toft; Matthew Farrer
JAMA 2005; 293: 296. [Extract] [Full text] [PDF]  

Original Articles
Molecular Profiling of Tumor Progression in Head and Neck Cancer

Thomas J. Belbin; Bhuvanesh Singh; Richard V. Smith; Nicholas D. Socci; Volkert B. Wreesmann; Marta Sanchez-Carbayo; Jessica Masterson; Snehal Patel; Carlos Cordon-Cardo; Michael B. Prystowsky; Geoffrey Childs
Arch Otolaryngol Head Neck Surg 2005; 131: 10-18. [Abstract] [Full text] [PDF]  

Neurological Reviews
Muscle Carnitine Palmitoyltransferase II Deficiency: Clinical and Molecular Genetic Features and Diagnostic Aspects

Marcus Deschauer; Thomas Wieser; Stephan Zierz
Arch Neurol 2005; 62: 37-41. [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]  

Letters
Free Fetal DNA in Maternal Circulation—Reply

Ravinder Dhallan; Michael Cronin; Sarah Emche; Philip Bayliss; Marian Damewood
JAMA 2004; 292: 2835-a-2836-a. [Extract] [Full text] [PDF]  

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