Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what?
Identifieur interne : 004F67 ( PubMed/Checkpoint ); précédent : 004F66; suivant : 004F68Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what?
Auteurs : A E Harding [Royaume-Uni]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 1989.
English descriptors
- KwdEn :
- MESH :
- diagnosis : Cerebellar Ataxia, Epilepsies, Myoclonic, Myoclonic Cerebellar Dyssynergia.
- genetics : Myoclonic Cerebellar Dyssynergia.
- Diagnosis, Differential, Humans.
DOI: 10.1002/mds.870040105
PubMed: 2494437
Affiliations:
Links toward previous steps (curation, corpus...)
Links to Exploration step
pubmed:2494437Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what?</title>
<author><name sortKey="Harding, A E" sort="Harding, A E" uniqKey="Harding A" first="A E" last="Harding">A E Harding</name>
<affiliation wicri:level="2"><nlm:affiliation>Institute of Neurology, Queen Square, London, England.</nlm:affiliation>
<country>Royaume-Uni</country>
<placeName><region type="country">Angleterre</region>
</placeName>
<wicri:cityArea>Institute of Neurology, Queen Square, London</wicri:cityArea>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="1989">1989</date>
<idno type="RBID">pubmed:2494437</idno>
<idno type="pmid">2494437</idno>
<idno type="doi">10.1002/mds.870040105</idno>
<idno type="wicri:Area/PubMed/Corpus">005006</idno>
<idno type="wicri:Area/PubMed/Curation">005006</idno>
<idno type="wicri:Area/PubMed/Checkpoint">004F67</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what?</title>
<author><name sortKey="Harding, A E" sort="Harding, A E" uniqKey="Harding A" first="A E" last="Harding">A E Harding</name>
<affiliation wicri:level="2"><nlm:affiliation>Institute of Neurology, Queen Square, London, England.</nlm:affiliation>
<country>Royaume-Uni</country>
<placeName><region type="country">Angleterre</region>
</placeName>
<wicri:cityArea>Institute of Neurology, Queen Square, London</wicri:cityArea>
</affiliation>
</author>
</analytic>
<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="1989" type="published">1989</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cerebellar Ataxia (diagnosis)</term>
<term>Diagnosis, Differential</term>
<term>Epilepsies, Myoclonic (diagnosis)</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>Epilepsies, Myoclonic</term>
<term>Myoclonic Cerebellar Dyssynergia</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Myoclonic Cerebellar Dyssynergia</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Diagnosis, Differential</term>
<term>Humans</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
</TEI>
<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">2494437</PMID>
<DateCreated><Year>1989</Year>
<Month>05</Month>
<Day>03</Day>
</DateCreated>
<DateCompleted><Year>1989</Year>
<Month>05</Month>
<Day>03</Day>
</DateCompleted>
<DateRevised><Year>2004</Year>
<Month>11</Month>
<Day>17</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0885-3185</ISSN>
<JournalIssue CitedMedium="Print"><Volume>4</Volume>
<Issue>1</Issue>
<PubDate><Year>1989</Year>
</PubDate>
</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what?</ArticleTitle>
<Pagination><MedlinePgn>18-9</MedlinePgn>
</Pagination>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Harding</LastName>
<ForeName>A E</ForeName>
<Initials>AE</Initials>
<AffiliationInfo><Affiliation>Institute of Neurology, Queen Square, London, England.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
</Article>
<MedlineJournalInfo><Country>UNITED STATES</Country>
<MedlineTA>Mov Disord</MedlineTA>
<NlmUniqueID>8610688</NlmUniqueID>
<ISSNLinking>0885-3185</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D002524">Cerebellar Ataxia</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000175">diagnosis</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D003937">Diagnosis, Differential</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D004831">Epilepsies, Myoclonic</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000175">diagnosis</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D002527">Myoclonic Cerebellar Dyssynergia</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000175">diagnosis</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1989</Year>
<Month>1</Month>
<Day>1</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>1989</Year>
<Month>1</Month>
<Day>1</Day>
<Hour>0</Hour>
<Minute>1</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>1989</Year>
<Month>1</Month>
<Day>1</Day>
<Hour>0</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">2494437</ArticleId>
<ArticleId IdType="doi">10.1002/mds.870040105</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations><list><country><li>Royaume-Uni</li>
</country>
<region><li>Angleterre</li>
</region>
</list>
<tree><country name="Royaume-Uni"><region name="Angleterre"><name sortKey="Harding, A E" sort="Harding, A E" uniqKey="Harding A" first="A E" last="Harding">A E Harding</name>
</region>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/PubMed/Checkpoint
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 004F67 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd -nk 004F67 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= MovDisordV3 |flux= PubMed |étape= Checkpoint |type= RBID |clé= pubmed:2494437 |texte= Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what? }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/RBID.i -Sk "pubmed:2494437" \ | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd \ | NlmPubMed2Wicri -a MovDisordV3
This area was generated with Dilib version V0.6.23. |