Stereotypies in wilson's disease
Identifieur interne : 005253 ( Main/Exploration ); précédent : 005252; suivant : 005254Stereotypies in wilson's disease
Auteurs : Alberto A. Yorio [Argentine] ; Jacobo C. Mesri [Argentine] ; Miguel A. Pagano [Argentine] ; Lera [Argentine]Source :
- Movement Disorders [ 0885-3185 ] ; 1997-07.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Adult, Basal Ganglia (pathology), Case study, Chelating Agents (therapeutic use), Electromyography, Enzymopathy, Exploration, Female, Foot, Hepatolenticular Degeneration (complications), Hepatolenticular Degeneration (drug therapy), Hepatolenticular Degeneration (pathology), Hepatolenticular Degeneration (physiopathology), Human, Humans, Magnetic Resonance Imaging, Movement Disorders (drug therapy), Movement Disorders (etiology), Movement Disorders (pathology), Movement Disorders (physiopathology), Nuclear magnetic resonance imaging, Penicillamine (therapeutic use), Stereotyped Behavior (drug effects), Stereotypy, Video recording, Wilson disease.
- MESH :
- chemical , therapeutic use : Chelating Agents, Penicillamine.
- complications : Hepatolenticular Degeneration.
- drug effects : Stereotyped Behavior.
- drug therapy : Hepatolenticular Degeneration, Movement Disorders.
- etiology : Movement Disorders.
- pathology : Basal Ganglia, Hepatolenticular Degeneration, Movement Disorders.
- physiopathology : Hepatolenticular Degeneration, Movement Disorders.
- Adult, Female, Foot, Humans, Magnetic Resonance Imaging.
Url:
DOI: 10.1002/mds.870120427
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 003B49
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- to stream PubMed, to step Corpus: 004623
- to stream PubMed, to step Curation: 004623
- to stream PubMed, to step Checkpoint: 004567
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- to stream Ncbi, to step Curation: 004D60
- to stream Ncbi, to step Checkpoint: 004D60
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- to stream PascalFrancis, to step Curation: 003599
- to stream PascalFrancis, to step Checkpoint: 003145
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- to stream Main, to step Curation: 005253
Le document en format XML
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<term>Electromyography</term>
<term>Enzymopathy</term>
<term>Exploration</term>
<term>Female</term>
<term>Foot</term>
<term>Hepatolenticular Degeneration (complications)</term>
<term>Hepatolenticular Degeneration (drug therapy)</term>
<term>Hepatolenticular Degeneration (pathology)</term>
<term>Hepatolenticular Degeneration (physiopathology)</term>
<term>Human</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Movement Disorders (drug therapy)</term>
<term>Movement Disorders (etiology)</term>
<term>Movement Disorders (pathology)</term>
<term>Movement Disorders (physiopathology)</term>
<term>Nuclear magnetic resonance imaging</term>
<term>Penicillamine (therapeutic use)</term>
<term>Stereotyped Behavior (drug effects)</term>
<term>Stereotypy</term>
<term>Video recording</term>
<term>Wilson disease</term>
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<term>Penicillamine</term>
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<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Stereotyped Behavior</term>
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<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Hepatolenticular Degeneration</term>
<term>Movement Disorders</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Basal Ganglia</term>
<term>Hepatolenticular Degeneration</term>
<term>Movement Disorders</term>
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<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Hepatolenticular Degeneration</term>
<term>Movement Disorders</term>
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<term>Female</term>
<term>Foot</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
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<term>Enregistrement vidéo</term>
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<term>Exploration</term>
<term>Femelle</term>
<term>Homme</term>
<term>Imagerie RMN</term>
<term>Stéréotypie</term>
<term>Wilson maladie</term>
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