Epidemiology and Genetics of Essential Tremor
Identifieur interne : 001205 ( Istex/Curation ); précédent : 001204; suivant : 001206Epidemiology and Genetics of Essential Tremor
Auteurs : Mitchell F. Brin [États-Unis] ; William Koller [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 1998.
Descripteurs français
- Wicri :
- topic : épidémiologie, Génétique.
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Abstract
Essential tremor (ET) is one of the most common movement disorders. However, the etiology and pathogenesis are as yet unknown. Continued research will give us clues to understanding the impact on society, identifying genetic and environmental contributors to the disease, understanding the significance of a sporadic case, the phenotypic spectrum and timing of presentation, and the relationship with other neurologic disorders. Because the condition is both clinically and genetically heterogeneous and there is overlap with these other disorders, such as dystonia, parkinsonism, peripheral neuropathy. and migraine, the definition of phenotype plagues research in this area. Advances in understanding the genetic and molecular underpinnings of tremor should provide additional tools to unravel the clinical phenotype (including physiology), genotype‐phenotype relationships, and the epidemiology of tremor.
Url:
DOI: 10.1002/mds.870131310
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Brin</name><affiliation wicri:level="2"><mods:affiliation>Movement Disorder Program, Mount Sinai Medical Center, Department of Neurology, New York, NY</mods:affiliation><country xml:lang="fr">États-Unis</country><placeName><region type="state">État de New York</region></placeName><wicri:cityArea>Movement Disorder Program, Mount Sinai Medical Center, Department of Neurology, New York</wicri:cityArea></affiliation></author><author><name sortKey="Koller, William" sort="Koller, William" uniqKey="Koller W" first="William" last="Koller">William Koller</name><affiliation wicri:level="1"><mods:affiliation>Departntent of Neurology, University of Kansas Medical Center, Kansas City, Kansas, U.S.A.</mods:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Departntent of Neurology, University of Kansas Medical Center, Kansas City, Kansas</wicri:regionArea></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:D4A4EA64BCBFABB106A5DB5D82E8C256E0A959B5</idno><date when="1998" year="1998">1998</date><idno type="doi">10.1002/mds.870131310</idno><idno type="url">https://api.istex.fr/document/D4A4EA64BCBFABB106A5DB5D82E8C256E0A959B5/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">001205</idno><idno type="wicri:Area/Istex/Curation">001205</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Epidemiology and Genetics of Essential Tremor</title><author><name sortKey="Brin, Mitchell F" sort="Brin, Mitchell F" uniqKey="Brin M" first="Mitchell F." last="Brin">Mitchell F. Brin</name><affiliation wicri:level="2"><mods:affiliation>Movement Disorder Program, Mount Sinai Medical Center, Department of Neurology, New York, NY</mods:affiliation><country xml:lang="fr">États-Unis</country><placeName><region type="state">État de New York</region></placeName><wicri:cityArea>Movement Disorder Program, Mount Sinai Medical Center, Department of Neurology, New York</wicri:cityArea></affiliation></author><author><name sortKey="Koller, William" sort="Koller, William" uniqKey="Koller W" first="William" last="Koller">William Koller</name><affiliation wicri:level="1"><mods:affiliation>Departntent of Neurology, University of Kansas Medical Center, Kansas City, Kansas, U.S.A.</mods:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Departntent of Neurology, University of Kansas Medical Center, Kansas City, Kansas</wicri:regionArea></affiliation></author></analytic><monogr></monogr><series><title level="j">Movement Disorders</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="1998">1998</date><biblScope unit="vol">13</biblScope><biblScope unit="issue">S3</biblScope><biblScope unit="page" from="55">55</biblScope><biblScope unit="page" to="63">63</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">D4A4EA64BCBFABB106A5DB5D82E8C256E0A959B5</idno><idno type="DOI">10.1002/mds.870131310</idno><idno type="ArticleID">MDS870131310</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Epidemiology</term><term>Essential tremor</term><term>Genetics</term><term>Hereditary tremor</term></keywords><keywords scheme="Wicri" type="topic" xml:lang="fr"><term>épidémiologie</term><term>Génétique</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Essential tremor (ET) is one of the most common movement disorders. However, the etiology and pathogenesis are as yet unknown. Continued research will give us clues to understanding the impact on society, identifying genetic and environmental contributors to the disease, understanding the significance of a sporadic case, the phenotypic spectrum and timing of presentation, and the relationship with other neurologic disorders. Because the condition is both clinically and genetically heterogeneous and there is overlap with these other disorders, such as dystonia, parkinsonism, peripheral neuropathy. and migraine, the definition of phenotype plagues research in this area. Advances in understanding the genetic and molecular underpinnings of tremor should provide additional tools to unravel the clinical phenotype (including physiology), genotype‐phenotype relationships, and the epidemiology of tremor.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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