MovDisordV3, France, Analysis, bibRecord, 000462

Molecular diagnosis of inherited movement disorders. Movement disorders Society Task Force on Molecular Diagnosis

Identifieur interne : 000462 ( France/Analysis ); précédent : 000461; suivant : 000463

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.

RBID : Pascal:03-0147173

Descripteurs français

Pascal (Inist)
- Parkinson maladie, Parkinsonisme, Chorée Huntington, Ataxie cérébelleuse, Dystonie, Tremblement, Essentiel, Wilson maladie, Conseil génétique, Déterminisme génétique, Biologie moléculaire, Diagnostic, Homme, Enzymopathie.
Wicri :
- topic : Homme.

English descriptors

KwdEn :
- Cerebellar ataxia, Diagnosis, Dystonia, Enzymopathy, Essential, Genetic counseling, Genetic determinism, Human, Huntington disease, Molecular biology, Parkinson disease, Parkinsonism, Tremor, Wilson disease.

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.

Affiliations:

Links toward previous steps (curation, corpus...)

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Pascal:03-0147173

Le document en format XML

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<orgName type="university">Université Louis-et-Maximilien de Munich</orgName>
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<affiliation wicri:level="3"><inist:fA14 i1="02"><s1>Center of Neurology, Department of Neurodegenerative Disorders and Hertie Institute of Clinical Brain Research, University of Tübingen</s1>
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<country>Allemagne</country>
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<author><name sortKey="Bressman, Susan" sort="Bressman, Susan" uniqKey="Bressman S" first="Susan" last="Bressman">Susan Bressman</name>
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<term>Dystonia</term>
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<term>Essential</term>
<term>Genetic counseling</term>
<term>Genetic determinism</term>
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<term>Ataxie cérébelleuse</term>
<term>Dystonie</term>
<term>Tremblement</term>
<term>Essentiel</term>
<term>Wilson maladie</term>
<term>Conseil génétique</term>
<term>Déterminisme génétique</term>
<term>Biologie moléculaire</term>
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<front><div type="abstract" xml:lang="en">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.</div>
</front>
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	Movement Disorders (revue)
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Movement Disorders (revue)

Molecular diagnosis of inherited movement disorders. Movement disorders Society Task Force on Molecular Diagnosis

Molecular diagnosis of inherited movement disorders. Movement disorders Society Task Force on Molecular Diagnosis

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri