Essential tremor: the beginning of a new era.
Identifieur interne : 008236 ( Main/Merge ); précédent : 008235; suivant : 008237Essential tremor: the beginning of a new era.
Auteurs : W C KollerSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 1997.
English descriptors
- KwdEn :
- MESH :
PubMed: 9399204
Links toward previous steps (curation, corpus...)
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- to stream PubMed, to step Curation: 004577
- to stream PubMed, to step Checkpoint: 004664
- to stream Ncbi, to step Merge: 004E08
- to stream Ncbi, to step Curation: 004E08
- to stream Ncbi, to step Checkpoint: 004E08
Links to Exploration step
pubmed:9399204Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Essential tremor: the beginning of a new era.</title>
<author><name sortKey="Koller, W C" sort="Koller, W C" uniqKey="Koller W" first="W C" last="Koller">W C Koller</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="1997">1997</date>
<idno type="RBID">pubmed:9399204</idno>
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<idno type="wicri:Area/Ncbi/Merge">004E08</idno>
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<idno type="wicri:Area/Ncbi/Checkpoint">004E08</idno>
<idno type="wicri:doubleKey">0885-3185:1997:Koller W:essential:tremor:the</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Essential tremor: the beginning of a new era.</title>
<author><name sortKey="Koller, W C" sort="Koller, W C" uniqKey="Koller W" first="W C" last="Koller">W C Koller</name>
</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="1997" type="published">1997</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Chromosome Aberrations</term>
<term>Chromosome Disorders</term>
<term>Chromosomes, Human, Pair 2 (genetics)</term>
<term>Chromosomes, Human, Pair 3 (genetics)</term>
<term>Genetic Linkage (genetics)</term>
<term>Humans</term>
<term>Tremor (genetics)</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Chromosomes, Human, Pair 2</term>
<term>Chromosomes, Human, Pair 3</term>
<term>Genetic Linkage</term>
<term>Tremor</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Chromosome Aberrations</term>
<term>Chromosome Disorders</term>
<term>Humans</term>
</keywords>
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