The Startle syndrome
Identifieur interne : 004263 ( Main/Exploration ); précédent : 004262; suivant : 004264The Startle syndrome
Auteurs : Peter Brown [Royaume-Uni]Source :
- Movement Disorders [ 0885-3185 ] ; 2002-01-31.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Animals, Electromyography, Etiology, Human, Humans, Hyperekplexia, Nervous System Diseases (drug therapy), Nervous System Diseases (genetics), Nervous System Diseases (physiopathology), Reflex, Abnormal (genetics), Reflex, Startle (genetics), Sporadic, Startle epilepsy, Startle reflex, Syndrome, brainstem, familial hyperekplexia, hyperekplexia, startle response.
- MESH :
- drug therapy : Nervous System Diseases.
- genetics : Nervous System Diseases, Reflex, Abnormal, Reflex, Startle.
- physiopathology : Nervous System Diseases.
- Animals, Electromyography, Humans, Syndrome.
Url:
DOI: 10.1002/mds.10066
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 003B59
- to stream Istex, to step Curation: 003B59
- to stream Istex, to step Checkpoint: 002B54
- to stream Main, to step Merge: 006268
- to stream PascalFrancis, to step Corpus: 002876
- to stream PascalFrancis, to step Curation: 000445
- to stream PascalFrancis, to step Checkpoint: 002580
- to stream Main, to step Merge: 006619
- to stream PubMed, to step Corpus: 003B42
- to stream PubMed, to step Curation: 003B42
- to stream PubMed, to step Checkpoint: 003903
- to stream Ncbi, to step Merge: 000709
- to stream Ncbi, to step Curation: 000709
- to stream Ncbi, to step Checkpoint: 000709
- to stream Main, to step Merge: 006112
- to stream Main, to step Curation: 004263
Le document en format XML
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<series><title level="j">Movement Disorders</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint><publisher>John Wiley & Sons, Inc.</publisher>
<pubPlace>New York</pubPlace>
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<term>Electromyography</term>
<term>Etiology</term>
<term>Human</term>
<term>Humans</term>
<term>Hyperekplexia</term>
<term>Nervous System Diseases (drug therapy)</term>
<term>Nervous System Diseases (genetics)</term>
<term>Nervous System Diseases (physiopathology)</term>
<term>Reflex, Abnormal (genetics)</term>
<term>Reflex, Startle (genetics)</term>
<term>Sporadic</term>
<term>Startle epilepsy</term>
<term>Startle reflex</term>
<term>Syndrome</term>
<term>brainstem</term>
<term>familial hyperekplexia</term>
<term>hyperekplexia</term>
<term>startle response</term>
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<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Nervous System Diseases</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Nervous System Diseases</term>
<term>Reflex, Abnormal</term>
<term>Reflex, Startle</term>
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<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Electromyography</term>
<term>Humans</term>
<term>Syndrome</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Electromyographie</term>
<term>Epilepsie sursaut</term>
<term>Etiologie</term>
<term>Homme</term>
<term>Hyperekplexie</term>
<term>Réflexe sursaut</term>
<term>Sporadique</term>
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