The startle syndrome.
Identifieur interne : 003B42 ( PubMed/Curation ); précédent : 003B41; suivant : 003B43The startle syndrome.
Auteurs : Peter Brown [Royaume-Uni]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2002.
English descriptors
- KwdEn :
- MESH :
- drug therapy : Nervous System Diseases.
- genetics : Nervous System Diseases, Reflex, Abnormal, Reflex, Startle.
- physiopathology : Nervous System Diseases.
- Animals, Electromyography, Humans, Syndrome.
PubMed: 11836762
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pubmed:11836762Le document en format XML
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<author><name sortKey="Brown, Peter" sort="Brown, Peter" uniqKey="Brown P" first="Peter" last="Brown">Peter Brown</name>
<affiliation wicri:level="1"><nlm:affiliation>Sobell Department of Neurophysiology, Institute of Neurology, London, United Kingdom. p.brown@ion.ucl.ac.uk</nlm:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Sobell Department of Neurophysiology, Institute of Neurology, London</wicri:regionArea>
</affiliation>
</author>
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<publicationStmt><idno type="wicri:source">PubMed</idno>
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<author><name sortKey="Brown, Peter" sort="Brown, Peter" uniqKey="Brown P" first="Peter" last="Brown">Peter Brown</name>
<affiliation wicri:level="1"><nlm:affiliation>Sobell Department of Neurophysiology, Institute of Neurology, London, United Kingdom. p.brown@ion.ucl.ac.uk</nlm:affiliation>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Sobell Department of Neurophysiology, Institute of Neurology, London</wicri:regionArea>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<imprint><date when="2002" type="published">2002</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term>
<term>Electromyography</term>
<term>Humans</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>Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Nervous System Diseases</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Nervous System Diseases</term>
<term>Reflex, Abnormal</term>
<term>Reflex, Startle</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Nervous System Diseases</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Electromyography</term>
<term>Humans</term>
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<Month>02</Month>
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<DateCompleted><Year>2003</Year>
<Month>08</Month>
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<DateRevised><Year>2014</Year>
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<JournalIssue CitedMedium="Print"><Volume>17 Suppl 2</Volume>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
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<ArticleTitle>The startle syndrome.</ArticleTitle>
<Pagination><MedlinePgn>S79-82</MedlinePgn>
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<ForeName>Peter</ForeName>
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<QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName>
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<NumberOfReferences>16</NumberOfReferences>
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<ArticleId IdType="pii">10.1002/mds.10066</ArticleId>
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