Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: the 12-month longitudinal analysis-Reference-Cited by-同舟云学术

Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: the 12-month longitudinal analysis

Published:2011-01 Issue:1 Volume:10 Page:31-42
ISSN:1474-4422
Container-title:The Lancet Neurology
language:en
Short-container-title:The Lancet Neurology

Author:

Tabrizi Sarah J,Scahill Rachael I,Durr Alexandra,Roos Raymund AC,Leavitt Blair R,Jones Rebecca,Landwehrmeyer G Bernhard,Fox Nick C,Johnson Hans,Hicks Stephen L,Kennard Christopher,Craufurd David,Frost Chris,Langbehn Douglas R,Reilmann Ralf,Stout Julie C

Publisher

Elsevier BV

Subject

Neurology (clinical)

Reference40 articles.

1. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes;Cell,1993

2. A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length;Langbehn;Clin Genet,2004

3. Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset;Swami;Hum Mol Genet,2009

4. Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline data;Tabrizi;Lancet Neurol,2009

5. Detection of Huntington's disease decades before diagnosis: the Predict-HD study;Paulsen;J Neurol Neurosurg Psychiatry,2008

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