Natural history of Huntington disease.
Identifieur interne : 000112 ( Main/Merge ); précédent : 000111; suivant : 000113Natural history of Huntington disease.
Auteurs : E Dorsey [États-Unis] ; Christopher. Beck [États-Unis] ; Kristin Darwin [États-Unis] ; Paige Nichols [États-Unis] ; Alicia. Brocht [États-Unis] ; Kevin. Biglan [États-Unis] ; Ira Shoulson [États-Unis]Source :
- JAMA neurology ; 2013.
Descripteurs français
- Wicri :
- geographic : Australie, Canada, États-Unis.
English descriptors
- KwdEn :
- Adult, Aged, Australia, Canada, Cognition Disorders (etiology), Cohort Studies, Disability Evaluation, Disease Progression, Female, Humans, 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.
- geographic : Australia, Canada, United States.
- complications : Huntington Disease.
- etiology : Cognition Disorders, Mental Disorders, Movement Disorders.
- genetics : Trinucleotide Repeats.
- Adult, Aged, Cohort Studies, Disability Evaluation, Disease Progression, Female, Humans, Male, Middle Aged, Retrospective Studies, Severity of Illness Index.
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
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pubmed:24126537Le document en format XML
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<author><name sortKey="Dorsey, E Ray" sort="Dorsey, E Ray" uniqKey="Dorsey E" first="E" last="Dorsey">E Dorsey</name>
<affiliation wicri:level="2"><nlm:affiliation>Department of Neurology, Johns Hopkins Medicine, Baltimore, Maryland6now with the University of Rochester Medical Center, Rochester, New York.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<placeName><region type="state">État de New York</region>
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<wicri:cityArea>Department of Neurology, Johns Hopkins Medicine, Baltimore, Maryland6now with the University of Rochester Medical Center, Rochester</wicri:cityArea>
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<author><name sortKey="Beck, Christopher A" sort="Beck, Christopher A" uniqKey="Beck C" first="Christopher" last="Beck">Christopher. Beck</name>
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<series><title level="j">JAMA neurology</title>
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<term>Cohort Studies</term>
<term>Disability Evaluation</term>
<term>Disease Progression</term>
<term>Female</term>
<term>Humans</term>
<term>Huntington Disease (complications)</term>
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<term>Mental Disorders (etiology)</term>
<term>Middle Aged</term>
<term>Movement Disorders (etiology)</term>
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<term>Retrospective Studies</term>
<term>Severity of Illness Index</term>
<term>Trinucleotide Repeats (genetics)</term>
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<term>Canada</term>
<term>United States</term>
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<term>Aged</term>
<term>Cohort Studies</term>
<term>Disability Evaluation</term>
<term>Disease Progression</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Retrospective Studies</term>
<term>Severity of Illness Index</term>
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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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