The Ramsay Hunt syndrome is no longer a useful diagnostic category
Identifieur interne : 006425 ( Main/Exploration ); précédent : 006424; suivant : 006426The Ramsay Hunt syndrome is no longer a useful diagnostic category
Auteurs : Andermann [Canada] ; Samuel Berkovic [Canada] ; Stirling Carpenter [Canada] ; Eva Andermann [Canada]Source :
- Movement Disorders [ 0885-3185 ] ; 1989.
English descriptors
- KwdEn :
- MESH :
- diagnosis : Cerebellar Ataxia, Myoclonic Cerebellar Dyssynergia.
- genetics : Epilepsies, Myoclonic, Myoclonic Cerebellar Dyssynergia.
- Diagnosis, Differential, Humans.
Url:
DOI: 10.1002/mds.870040104
Affiliations:
Links toward previous steps (curation, corpus...)
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Le document en format XML
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<author><name sortKey="Berkovic, Samuel" sort="Berkovic, Samuel" uniqKey="Berkovic S" first="Samuel" last="Berkovic">Samuel Berkovic</name>
</author>
<author><name sortKey="Carpenter, Stirling" sort="Carpenter, Stirling" uniqKey="Carpenter S" first="Stirling" last="Carpenter">Stirling Carpenter</name>
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<author><name sortKey="Andermann, Eva" sort="Andermann, Eva" uniqKey="Andermann E" first="Eva" last="Andermann">Eva Andermann</name>
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<author><name sortKey="Berkovic, Samuel" sort="Berkovic, Samuel" uniqKey="Berkovic S" first="Samuel" last="Berkovic">Samuel Berkovic</name>
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<author><name sortKey="Carpenter, Stirling" sort="Carpenter, Stirling" uniqKey="Carpenter S" first="Stirling" last="Carpenter">Stirling Carpenter</name>
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<author><name sortKey="Andermann, Eva" sort="Andermann, Eva" uniqKey="Andermann E" first="Eva" last="Andermann">Eva Andermann</name>
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<monogr></monogr>
<series><title level="j">Movement Disorders</title>
<title level="j" type="sub">Official Journal of the Movement Disorder Society</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="1989">1989</date>
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<term>Epilepsies, Myoclonic (genetics)</term>
<term>Humans</term>
<term>Myoclonic Cerebellar Dyssynergia (diagnosis)</term>
<term>Myoclonic Cerebellar Dyssynergia (genetics)</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Cerebellar Ataxia</term>
<term>Myoclonic Cerebellar Dyssynergia</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Epilepsies, Myoclonic</term>
<term>Myoclonic Cerebellar Dyssynergia</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Diagnosis, Differential</term>
<term>Humans</term>
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<region><li>Québec</li>
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<name sortKey="Carpenter, Stirling" sort="Carpenter, Stirling" uniqKey="Carpenter S" first="Stirling" last="Carpenter">Stirling Carpenter</name>
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