Disease Onset in Huntington's Disease: When Is the Conversion?-Reference-Cited by-同舟云学术

Disease Onset in Huntington's Disease: When Is the Conversion?

Published:2021-01-31 Issue:3 Volume:8 Page:352-360
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Mov Disord Clin Pract

Author:

Oosterloo Mayke¹²,Greef Bianca T.A.¹³,Bijlsma Emilia K.⁴,Durr Alexandra⁵,Tabrizi Sarah J.⁶^ORCID,Estevez‐Fraga Carlos⁶,Die‐Smulders Christine E.M.⁷⁸,Roos Raymund A.C.²

Affiliation:

1. Department of Neurology Maastricht University Medical Center Maastricht The Netherlands

2. Department of Neurology Leiden University Medical Center Leiden The Netherlands

3. Department of Clinical Epidemiology and Medical Technology Assessment Maastricht University Medical Center Maastricht The Netherlands

4. Department of Clinical Genetics Leiden University Medical Center Leiden The Netherlands

5. Institut du Cerveau et de la Moelle épinière (ICM), AP‐HP, Inserm, CNRS, Sorbonne Université University Hospital Pitié‐Salpêtrière Paris France

6. Department of Neurodegenerative Disease, Huntington's Disease Centre, UCL Queen Square Institute of Neurology University College London London United Kingdom

7. Department of Clinical Genetics Maastricht University Medical Center Maastricht The Netherlands

8. GROW Research Institute for Oncology and Developmental Biology Maastricht University Maastricht The Netherlands

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.13148

Reference24 articles.

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

2. Unified Huntington's disease rating scale: Reliability and consistency

3. Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline data

4. Subtle involuntary movements are not reliable indicators of incipient Huntington's disease

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