Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan.
Identifieur interne : 003E85 ( PubMed/Curation ); précédent : 003E84; suivant : 003E86Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan.
Auteurs : S N Illarioshkin [Russie] ; I A Ivanova-Smolenskaya ; R A Rahmonov ; E D Markova ; G. Stevanin ; A. BriceSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2000.
Descripteurs français
- Wicri :
- geographic : Tadjikistan.
English descriptors
- KwdEn :
- MESH :
- chemical : Genetic Markers.
- geographic : Tajikistan.
- genetics : Chromosomes, Human, Pair 3, Essential Tremor.
- Adult, Age of Onset, Aged, Anticipation, Genetic, Genetic Linkage, Genotype, Haplotypes, Humans, Lod Score, Middle Aged, Mutation, Pedigree, Phenotype, Severity of Illness Index.
PubMed: 11009220
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<author><name sortKey="Illarioshkin, S N" sort="Illarioshkin, S N" uniqKey="Illarioshkin S" first="S N" last="Illarioshkin">S N Illarioshkin</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Neurogenetics, Institute of Neurology, Russian Academy of Medical Sciences, Moscow.</nlm:affiliation>
<country>Russie</country>
<placeName><settlement type="city">Moscou</settlement>
<region>District fédéral central</region>
</placeName>
<wicri:orgArea>Department of Neurogenetics, Institute of Neurology, Russian Academy of Medical Sciences</wicri:orgArea>
</affiliation>
</author>
<author><name sortKey="Ivanova Smolenskaya, I A" sort="Ivanova Smolenskaya, I A" uniqKey="Ivanova Smolenskaya I" first="I A" last="Ivanova-Smolenskaya">I A Ivanova-Smolenskaya</name>
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<author><name sortKey="Rahmonov, R A" sort="Rahmonov, R A" uniqKey="Rahmonov R" first="R A" last="Rahmonov">R A Rahmonov</name>
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<author><name sortKey="Markova, E D" sort="Markova, E D" uniqKey="Markova E" first="E D" last="Markova">E D Markova</name>
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<author><name sortKey="Stevanin, G" sort="Stevanin, G" uniqKey="Stevanin G" first="G" last="Stevanin">G. Stevanin</name>
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<author><name sortKey="Brice, A" sort="Brice, A" uniqKey="Brice A" first="A" last="Brice">A. Brice</name>
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<author><name sortKey="Illarioshkin, S N" sort="Illarioshkin, S N" uniqKey="Illarioshkin S" first="S N" last="Illarioshkin">S N Illarioshkin</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Neurogenetics, Institute of Neurology, Russian Academy of Medical Sciences, Moscow.</nlm:affiliation>
<country>Russie</country>
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<region>District fédéral central</region>
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<author><name sortKey="Rahmonov, R A" sort="Rahmonov, R A" uniqKey="Rahmonov R" first="R A" last="Rahmonov">R A Rahmonov</name>
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<author><name sortKey="Markova, E D" sort="Markova, E D" uniqKey="Markova E" first="E D" last="Markova">E D Markova</name>
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<author><name sortKey="Stevanin, G" sort="Stevanin, G" uniqKey="Stevanin G" first="G" last="Stevanin">G. Stevanin</name>
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<author><name sortKey="Brice, A" sort="Brice, A" uniqKey="Brice A" first="A" last="Brice">A. Brice</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<term>Age of Onset</term>
<term>Aged</term>
<term>Anticipation, Genetic</term>
<term>Chromosomes, Human, Pair 3 (genetics)</term>
<term>Essential Tremor (genetics)</term>
<term>Genetic Linkage</term>
<term>Genetic Markers</term>
<term>Genotype</term>
<term>Haplotypes</term>
<term>Humans</term>
<term>Lod Score</term>
<term>Middle Aged</term>
<term>Mutation</term>
<term>Pedigree</term>
<term>Phenotype</term>
<term>Severity of Illness Index</term>
<term>Tajikistan</term>
</keywords>
<keywords scheme="MESH" type="chemical" xml:lang="en"><term>Genetic Markers</term>
</keywords>
<keywords scheme="MESH" type="geographic" xml:lang="en"><term>Tajikistan</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Chromosomes, Human, Pair 3</term>
<term>Essential Tremor</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Age of Onset</term>
<term>Aged</term>
<term>Anticipation, Genetic</term>
<term>Genetic Linkage</term>
<term>Genotype</term>
<term>Haplotypes</term>
<term>Humans</term>
<term>Lod Score</term>
<term>Middle Aged</term>
<term>Mutation</term>
<term>Pedigree</term>
<term>Phenotype</term>
<term>Severity of Illness Index</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr"><term>Tadjikistan</term>
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<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">11009220</PMID>
<DateCreated><Year>2001</Year>
<Month>01</Month>
<Day>09</Day>
</DateCreated>
<DateCompleted><Year>2001</Year>
<Month>01</Month>
<Day>09</Day>
</DateCompleted>
<DateRevised><Year>2010</Year>
<Month>11</Month>
<Day>18</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0885-3185</ISSN>
<JournalIssue CitedMedium="Print"><Volume>15</Volume>
<Issue>5</Issue>
<PubDate><Year>2000</Year>
<Month>Sep</Month>
</PubDate>
</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan.</ArticleTitle>
<Pagination><MedlinePgn>1020-3</MedlinePgn>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Illarioshkin</LastName>
<ForeName>S N</ForeName>
<Initials>SN</Initials>
<AffiliationInfo><Affiliation>Department of Neurogenetics, Institute of Neurology, Russian Academy of Medical Sciences, Moscow.</Affiliation>
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<Author ValidYN="Y"><LastName>Ivanova-Smolenskaya</LastName>
<ForeName>I A</ForeName>
<Initials>IA</Initials>
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<Author ValidYN="Y"><LastName>Rahmonov</LastName>
<ForeName>R A</ForeName>
<Initials>RA</Initials>
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<Author ValidYN="Y"><LastName>Markova</LastName>
<ForeName>E D</ForeName>
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<Author ValidYN="Y"><LastName>Stevanin</LastName>
<ForeName>G</ForeName>
<Initials>G</Initials>
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<Author ValidYN="Y"><LastName>Brice</LastName>
<ForeName>A</ForeName>
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<MedlineJournalInfo><Country>UNITED STATES</Country>
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<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D000328">Adult</DescriptorName>
</MeshHeading>
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</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D000368">Aged</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="Y" UI="D020132">Anticipation, Genetic</DescriptorName>
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<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D020329">Essential Tremor</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008040">Genetic Linkage</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="Y" UI="D005819">Genetic Markers</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005838">Genotype</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006239">Haplotypes</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008126">Lod Score</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008875">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="Y" UI="D009154">Mutation</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D010375">Pedigree</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D010641">Phenotype</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D012720">Severity of Illness Index</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" Type="Geographic" UI="D013620">Tajikistan</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
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