Hereditary geniospasm: Two new families
Identifieur interne : 005639 ( Main/Exploration ); précédent : 005638; suivant : 005640Hereditary geniospasm: Two new families
Auteurs : Valerie L. Soland [Canada] ; Kailash P. Bhatia [Royaume-Uni] ; Geoffrey L. Sheean [Royaume-Uni] ; C. David Marsden [Royaume-Uni]Source :
- Movement Disorders [ 0885-3185 ] ; 1996-11.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- MESH :
- diagnosis : Spasm, Tremor.
- genetics : Chromosome Aberrations, Genes, Dominant, Spasm, Tremor.
- innervation : Chin.
- Adult, Chromosome Disorders, Female, Humans, Male, Pedigree.
Url:
DOI: 10.1002/mds.870110626
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 003B86
- to stream Istex, to step Curation: 003B86
- to stream Istex, to step Checkpoint: 003B41
- to stream PubMed, to step Corpus: 004747
- to stream PubMed, to step Curation: 004747
- to stream PubMed, to step Checkpoint: 004816
- to stream Ncbi, to step Merge: 004C35
- to stream Ncbi, to step Curation: 004C35
- to stream Ncbi, to step Checkpoint: 004C35
- to stream Main, to step Merge: 008745
- to stream PascalFrancis, to step Corpus: 003334
- to stream PascalFrancis, to step Curation: 003490
- to stream PascalFrancis, to step Checkpoint: 003363
- to stream Main, to step Merge: 008895
- to stream Main, to step Curation: 005639
Le document en format XML
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<author><name sortKey="Bhatia, Kailash P" sort="Bhatia, Kailash P" uniqKey="Bhatia K" first="Kailash P." last="Bhatia">Kailash P. Bhatia</name>
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<author><name sortKey="Sheean, Geoffrey L" sort="Sheean, Geoffrey L" uniqKey="Sheean G" first="Geoffrey L." last="Sheean">Geoffrey L. Sheean</name>
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<author><name sortKey="Marsden, C David" sort="Marsden, C David" uniqKey="Marsden C" first="C. David" last="Marsden">C. David Marsden</name>
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<idno type="doi">10.1002/mds.870110626</idno>
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<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Hereditary geniospasm: Two new families</title>
<author><name sortKey="Soland, Valerie L" sort="Soland, Valerie L" uniqKey="Soland V" first="Valerie L." last="Soland">Valerie L. Soland</name>
<affiliation wicri:level="1"><country xml:lang="fr">Canada</country>
<wicri:regionArea>Department of Neurology, Hôpital du Sacre‐Coeur de Montrel, Montreal, Québec</wicri:regionArea>
<wicri:noRegion>Québec</wicri:noRegion>
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<author><name sortKey="Bhatia, Kailash P" sort="Bhatia, Kailash P" uniqKey="Bhatia K" first="Kailash P." last="Bhatia">Kailash P. Bhatia</name>
<affiliation wicri:level="2"><country>Royaume-Uni</country>
<placeName><region type="country">Angleterre</region>
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<wicri:cityArea>University Department of Clinical Neurology, Institute of Neurology, London</wicri:cityArea>
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<author><name sortKey="Sheean, Geoffrey L" sort="Sheean, Geoffrey L" uniqKey="Sheean G" first="Geoffrey L." last="Sheean">Geoffrey L. Sheean</name>
<affiliation wicri:level="2"><country>Royaume-Uni</country>
<placeName><region type="country">Angleterre</region>
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<wicri:cityArea>University Department of Clinical Neurology, Institute of Neurology, London</wicri:cityArea>
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<author><name sortKey="Marsden, C David" sort="Marsden, C David" uniqKey="Marsden C" first="C. David" last="Marsden">C. David Marsden</name>
<affiliation wicri:level="2"><country>Royaume-Uni</country>
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<wicri:cityArea>University Department of Clinical Neurology, Institute of Neurology, London</wicri:cityArea>
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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="1996-11">1996-11</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Chin</term>
<term>Chin (innervation)</term>
<term>Chromosome Aberrations (genetics)</term>
<term>Chromosome Disorders</term>
<term>Diagnosis</term>
<term>Family study</term>
<term>Female</term>
<term>Genes, Dominant (genetics)</term>
<term>Human</term>
<term>Humans</term>
<term>Male</term>
<term>Pedigree</term>
<term>Spasm (diagnosis)</term>
<term>Spasm (genetics)</term>
<term>Tremor</term>
<term>Tremor (diagnosis)</term>
<term>Tremor (genetics)</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Spasm</term>
<term>Tremor</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Chromosome Aberrations</term>
<term>Genes, Dominant</term>
<term>Spasm</term>
<term>Tremor</term>
</keywords>
<keywords scheme="MESH" qualifier="innervation" xml:lang="en"><term>Chin</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Chromosome Disorders</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Pedigree</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Diagnostic</term>
<term>Etude familiale</term>
<term>Homme</term>
<term>Menton</term>
<term>Tremblement</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term>
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<affiliations><list><country><li>Canada</li>
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<region><li>Angleterre</li>
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<tree><country name="Canada"><noRegion><name sortKey="Soland, Valerie L" sort="Soland, Valerie L" uniqKey="Soland V" first="Valerie L." last="Soland">Valerie L. Soland</name>
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<name sortKey="Marsden, C David" sort="Marsden, C David" uniqKey="Marsden C" first="C. David" last="Marsden">C. David Marsden</name>
<name sortKey="Sheean, Geoffrey L" sort="Sheean, Geoffrey L" uniqKey="Sheean G" first="Geoffrey L." last="Sheean">Geoffrey L. Sheean</name>
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