Viewpoints on the Ramsay Hunt syndrome. III: Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what?
Identifieur interne : 006488 ( Main/Exploration ); précédent : 006487; suivant : 006489Viewpoints on the Ramsay Hunt syndrome. III: Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what?
Auteurs : A. E. HardingSource :
- Movement disorders [ 0885-3185 ] ; 1989.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PascalFrancis, to step Corpus: 003981
- to stream PascalFrancis, to step Curation: 002E44
- to stream PascalFrancis, to step Checkpoint: 003979
- to stream Main, to step Merge: 009841
- to stream Main, to step Curation: 006488
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Viewpoints on the Ramsay Hunt syndrome. III: 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>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">90-0192170</idno>
<date when="1989">1989</date>
<idno type="stanalyst">PASCAL 90-0192170 INIST</idno>
<idno type="RBID">Pascal:90-0192170</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">003981</idno>
<idno type="wicri:Area/PascalFrancis/Curation">002E44</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">003979</idno>
<idno type="wicri:doubleKey">0885-3185:1989:Harding A:viewpoints:on:the</idno>
<idno type="wicri:Area/Main/Merge">009841</idno>
<idno type="wicri:Area/Main/Curation">006488</idno>
<idno type="wicri:Area/Main/Exploration">006488</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Viewpoints on the Ramsay Hunt syndrome. III: 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>
</author>
</analytic>
<series><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="1989">1989</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Ataxia</term>
<term>Degenerative disease</term>
<term>Differential diagnostic</term>
<term>Dyssynergia cerebellia myoclonica</term>
<term>Epilepsy</term>
<term>Genetic disease</term>
<term>Human</term>
<term>Myoclonus</term>
<term>Nervous system diseases</term>
<term>Progressive myoclonus epilepsy</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Dyssynergie cérébelleuse myoclonique Hunt</term>
<term>Epilepsie myoclonique familiale Unverricht Lundborg</term>
<term>Ataxie</term>
<term>Myoclonie</term>
<term>Epilepsie</term>
<term>Maladie dégénérative</term>
<term>Maladie héréditaire</term>
<term>Système nerveux pathologie</term>
<term>Diagnostic différentiel</term>
<term>Homme</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
</TEI>
<affiliations><list></list>
<tree><noCountry><name sortKey="Harding, A E" sort="Harding, A E" uniqKey="Harding A" first="A. E." last="Harding">A. E. Harding</name>
</noCountry>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 006488 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 006488 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= MovDisordV3 |flux= Main |étape= Exploration |type= RBID |clé= Pascal:90-0192170 |texte= Viewpoints on the Ramsay Hunt syndrome. III: Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what? }}
This area was generated with Dilib version V0.6.23. |