Indexing disease progression at study entry with individuals at-risk for Huntington disease-Reference-Cited by-同舟云学术

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Indexing disease progression at study entry with individuals at-risk for Huntington disease

Published:2011-08-19 Issue:7 Volume:156 Page:751-763
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Zhang Ying,Long Jeffrey D.,Mills James A.,Warner John H.,Lu Wenjing,Paulsen Jane S.,

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics(clinical)

Reference55 articles.

1. Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds;Andresen;J Med Genet,2007a

2. The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset;Andresen;Ann Hum Genet,2007b

3. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease;Andrew;Nat Genet,1993

4. Longitudinal change in regional brain volumes in prodromal Huntington disease;Aylward;J Neurol Neurosurg Psychiatry,2010

5. Obsessive and compulsive symptoms in prediagnosed Huntington's disease;Beglinger;J Clin Psychiatry,2008

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1. Sleep fragmentation despite intact rest-activity patterns in premanifest Huntington's disease: An actigraphy study;Sleep Medicine;2024-12

2. White Matter Microstructure Changes Revealed by Diffusion Kurtosis and Diffusion Tensor Imaging in Mutant Huntingtin Gene Carriers;Journal of Huntington's Disease;2024-09-10

3. Structural MRI Correlates of Anosognosia in Huntington’s Disease;Journal of Huntington's Disease;2024-09-10

4. Time to Functional Loss as an Endpoint in Huntington's Disease Trials: Enrichment and Sample Size;Movement Disorders;2024-08-05

5. Multimodal, Longitudinal Profiling of SCA1 Identifies Predictors of Disease Severity and Progression;Annals of Neurology;2024-08-03

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