State of the art review: Molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis
Identifieur interne : 000446 ( France/Analysis ); précédent : 000445; suivant : 000447State of the art review: Molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis
Auteurs : Thomas Gasser [Allemagne] ; Susan Bressman [États-Unis] ; Alexandra Dürr [France] ; Joseph Higgins [États-Unis] ; Thomas Klockgether [Allemagne] ; Richard H. Myers [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2003-01.
English descriptors
- KwdEn :
- Chromosome Mapping, DNA Mutational Analysis, Genetic Testing, Humans, Huntington's disease, Molecular Diagnostic Techniques, Movement Disorders (diagnosis), Movement Disorders (genetics), Parkinson's disease, Wilson disease, autosomal dominant cerebellar ataxias, autosomal recessive ataxias, essential tremor, genetic testing, parkinsonism, primary torsion dystonia.
- MESH :
- diagnosis : Movement Disorders.
- genetics : Movement Disorders.
- Chromosome Mapping, DNA Mutational Analysis, Genetic Testing, Humans, Molecular Diagnostic Techniques.
Abstract
This review is designed to provide practical help for the clinical neurologist to make appropriate use of the possibilities of molecular diagnosis of inherited movement disorders. Huntington's disease, Parkinson's disease and parkinsonian syndromes, ataxias, Wilson disease, essential tremor, dystonias, and other genetic diseases associated with a variety of movement disorders are considered separately.
Url:
DOI: 10.1002/mds.10338
Affiliations:
- Allemagne, France, États-Unis
- Bade-Wurtemberg, Bavière, District de Cologne, District de Haute-Bavière, District de Tübingen, Massachusetts, Rhénanie-du-Nord-Westphalie, État de New York
- Bonn, Munich, Paris, Tübingen
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Links to Exploration step
ISTEX:E7438BC544B20E799CD986B35BC8601738B60757Le document en format XML
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