A tale of two factors: What determines the rate of progression in Huntington's disease? A longitudinal MRI study-Reference-Cited by-同舟云学术

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A tale of two factors: What determines the rate of progression in Huntington's disease? A longitudinal MRI study

Published:2011-05-24 Issue:9 Volume:26 Page:1691-1697
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Rosas H. Diana,Reuter Martin,Doros Gheorghe,Lee Stephanie Y.,Triggs Tyler,Malarick Keith,Fischl Bruce,Salat David H.,Hersch Steven M.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.23762/fullpdf

Reference26 articles.

1. Trinucleotide repeat length and progression of illness in Huntington's disease;Kieburtz;J Med Genet,1994

2. The relationship between CAG repeat length and clinical progression in Huntington's disease;Ravina;Mov Disord,2008

3. The association of CAG repeat length with clinical progression in Huntington disease;Rosenblatt;Neurology,2006

4. Unified Huntington's Disease Rating Scale: reliability and consistency. Huntington Study Group;Group;Mov Disord,1996

5. Cerebral cortex and the clinical expression of Huntington's disease: complexity and heterogeneity;Rosas;Brain,2008

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