Natural history of Huntington disease.
Identifieur interne : 000D24 ( Main/Exploration ); précédent : 000D23; suivant : 000D25Natural history of Huntington disease.
Auteurs : E Ray Dorsey [États-Unis] ; Christopher A. Beck [États-Unis] ; Kristin Darwin [États-Unis] ; Paige Nichols [États-Unis] ; Alicia F D. Brocht [États-Unis] ; Kevin M. Biglan [États-Unis] ; Ira Shoulson [États-Unis]Source :
- JAMA neurology [ 2168-6157 ] ; 2013.
English descriptors
- KwdEn :
- Adult, Aged, Australia, Canada, Cognition Disorders (etiology), Cohort Studies, Disability Evaluation, Disease Progression, Female, Humans, Huntingtin Protein, Huntington Disease (complications), Male, Mental Disorders (etiology), Middle Aged, Movement Disorders (etiology), Nerve Tissue Proteins (genetics), Retrospective Studies, Severity of Illness Index, Trinucleotide Repeats (genetics), United States.
- MESH :
- chemical , genetics : Nerve Tissue Proteins.
- chemical : Huntingtin Protein.
- complications : Huntington Disease.
- etiology : Cognition Disorders, Mental Disorders, Movement Disorders.
- genetics : Trinucleotide Repeats.
- Adult, Aged, Australia, Canada, Cohort Studies, Disability Evaluation, Disease Progression, Female, Humans, Male, Middle Aged, Retrospective Studies, Severity of Illness Index, United States.
Abstract
Understanding the natural history of Huntington disease will inform patients and clinicians on the disease course and researchers on the design of clinical trials.
DOI: 10.1001/jamaneurol.2013.4408
PubMed: 24126537
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Understanding the natural history of Huntington disease will inform patients and clinicians on the disease course and researchers on the design of clinical trials.</div>
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