MovDisordV3, PubMed, Corpus, bibRecord, 004B52

Variable onset of adult inherited focal dystonia: a problem for genetic studies.

Identifieur interne : 004B52 ( PubMed/Corpus ); précédent : 004B51; suivant : 004B53

Variable onset of adult inherited focal dystonia: a problem for genetic studies.

Auteurs : S. Micheli ; M. Fernández-Pardal ; P. Quesada ; T. Brannan ; J A Obeso

Source :

Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 1994.

RBID : pubmed:8139606

English descriptors

KwdEn :
- Adult, Aged, Aged, 80 and over, Blepharospasm (diagnosis), Blepharospasm (genetics), Chromosome Aberrations (diagnosis), Chromosome Aberrations (genetics), Chromosome Disorders, Dystonia Musculorum Deformans (diagnosis), Dystonia Musculorum Deformans (genetics), Female, Genes, Dominant (genetics), Humans, Male, Middle Aged, Neurologic Examination, Pedigree, Torticollis (diagnosis), Torticollis (genetics), Tremor (diagnosis), Tremor (genetics).
MESH :
- diagnosis : Blepharospasm, Chromosome Aberrations, Dystonia Musculorum Deformans, Torticollis, Tremor.
- genetics : Blepharospasm, Chromosome Aberrations, Dystonia Musculorum Deformans, Genes, Dominant, Torticollis, Tremor.
- Adult, Aged, Aged, 80 and over, Chromosome Disorders, Female, Humans, Male, Middle Aged, Neurologic Examination, Pedigree.

DOI: 10.1002/mds.870090110
PubMed: 8139606

Links to Exploration step

pubmed:8139606

Le document en format XML

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<author><name sortKey="Micheli, S" sort="Micheli, S" uniqKey="Micheli S" first="S" last="Micheli">S. Micheli</name>
<affiliation><nlm:affiliation>Sección de Enfermedades Extrapiramidales, Hospital de Clinicas, Facultad de Medicina, Universidad de Buenos Aires, Argentina.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Fernandez Pardal, M" sort="Fernandez Pardal, M" uniqKey="Fernandez Pardal M" first="M" last="Fernández-Pardal">M. Fernández-Pardal</name>
</author>
<author><name sortKey="Quesada, P" sort="Quesada, P" uniqKey="Quesada P" first="P" last="Quesada">P. Quesada</name>
</author>
<author><name sortKey="Brannan, T" sort="Brannan, T" uniqKey="Brannan T" first="T" last="Brannan">T. Brannan</name>
</author>
<author><name sortKey="Obeso, J A" sort="Obeso, J A" uniqKey="Obeso J" first="J A" last="Obeso">J A Obeso</name>
</author>
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<affiliation><nlm:affiliation>Sección de Enfermedades Extrapiramidales, Hospital de Clinicas, Facultad de Medicina, Universidad de Buenos Aires, Argentina.</nlm:affiliation>
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<author><name sortKey="Fernandez Pardal, M" sort="Fernandez Pardal, M" uniqKey="Fernandez Pardal M" first="M" last="Fernández-Pardal">M. Fernández-Pardal</name>
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<author><name sortKey="Quesada, P" sort="Quesada, P" uniqKey="Quesada P" first="P" last="Quesada">P. Quesada</name>
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<author><name sortKey="Brannan, T" sort="Brannan, T" uniqKey="Brannan T" first="T" last="Brannan">T. Brannan</name>
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<author><name sortKey="Obeso, J A" sort="Obeso, J A" uniqKey="Obeso J" first="J A" last="Obeso">J A Obeso</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Blepharospasm (diagnosis)</term>
<term>Blepharospasm (genetics)</term>
<term>Chromosome Aberrations (diagnosis)</term>
<term>Chromosome Aberrations (genetics)</term>
<term>Chromosome Disorders</term>
<term>Dystonia Musculorum Deformans (diagnosis)</term>
<term>Dystonia Musculorum Deformans (genetics)</term>
<term>Female</term>
<term>Genes, Dominant (genetics)</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Neurologic Examination</term>
<term>Pedigree</term>
<term>Torticollis (diagnosis)</term>
<term>Torticollis (genetics)</term>
<term>Tremor (diagnosis)</term>
<term>Tremor (genetics)</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Blepharospasm</term>
<term>Chromosome Aberrations</term>
<term>Dystonia Musculorum Deformans</term>
<term>Torticollis</term>
<term>Tremor</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Blepharospasm</term>
<term>Chromosome Aberrations</term>
<term>Dystonia Musculorum Deformans</term>
<term>Genes, Dominant</term>
<term>Torticollis</term>
<term>Tremor</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Chromosome Disorders</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Neurologic Examination</term>
<term>Pedigree</term>
</keywords>
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</profileDesc>
</teiHeader>
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<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">8139606</PMID>
<DateCreated><Year>1994</Year>
<Month>04</Month>
<Day>25</Day>
</DateCreated>
<DateCompleted><Year>1994</Year>
<Month>04</Month>
<Day>25</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>9</Volume>
<Issue>1</Issue>
<PubDate><Year>1994</Year>
<Month>Jan</Month>
</PubDate>
</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Variable onset of adult inherited focal dystonia: a problem for genetic studies.</ArticleTitle>
<Pagination><MedlinePgn>64-8</MedlinePgn>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Micheli</LastName>
<ForeName>S</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>Sección de Enfermedades Extrapiramidales, Hospital de Clinicas, Facultad de Medicina, Universidad de Buenos Aires, Argentina.</Affiliation>
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<Author ValidYN="Y"><LastName>Fernández-Pardal</LastName>
<ForeName>M</ForeName>
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<Author ValidYN="Y"><LastName>Quesada</LastName>
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<Author ValidYN="Y"><LastName>Brannan</LastName>
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<Author ValidYN="Y"><LastName>Obeso</LastName>
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<Language>eng</Language>
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<MedlineJournalInfo><Country>UNITED STATES</Country>
<MedlineTA>Mov Disord</MedlineTA>
<NlmUniqueID>8610688</NlmUniqueID>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D000369">Aged, 80 and over</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D001764">Blepharospasm</DescriptorName>
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<QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D002869">Chromosome Aberrations</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000175">diagnosis</QualifierName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D025063">Chromosome Disorders</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D004422">Dystonia Musculorum Deformans</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000175">diagnosis</QualifierName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005260">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005799">Genes, Dominant</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008875">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D009460">Neurologic Examination</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D010375">Pedigree</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D014103">Torticollis</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000175">diagnosis</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D014202">Tremor</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000175">diagnosis</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1994</Year>
<Month>1</Month>
<Day>1</Day>
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	Movement Disorders (revue)
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Movement Disorders (revue)

Variable onset of adult inherited focal dystonia: a problem for genetic studies.

Variable onset of adult inherited focal dystonia: a problem for genetic studies.

Source :

English descriptors

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki