Intrafamilial heterogeneity of facial hyperkinesias: chance association of tics, cranial dystonia, and Huntington's disease?
Identifieur interne : 000491 ( Ncbi/Checkpoint ); précédent : 000490; suivant : 000492Intrafamilial heterogeneity of facial hyperkinesias: chance association of tics, cranial dystonia, and Huntington's disease?
Auteurs : J. Müller [Autriche] ; G K Wenning ; J. Wissel ; Werner Poewe [Autriche]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2001.
English descriptors
- KwdEn :
- Adult, Atrophy (pathology), Caudate Nucleus (metabolism), Caudate Nucleus (pathology), Cognition Disorders (diagnosis), Cognition Disorders (etiology), Corpus Striatum (metabolism), Corpus Striatum (pathology), Dopamine (metabolism), Dystonic Disorders (complications), Dystonic Disorders (genetics), Facial Muscles (physiopathology), Humans, Huntington Disease (complications), Huntington Disease (diagnosis), Huntington Disease (genetics), Hyperkinesis (genetics), Hyperkinesis (physiopathology), Magnetic Resonance Imaging, Male, Middle Aged, Neuropsychological Tests, Skull, Tic Disorders (complications), Tic Disorders (genetics), Tomography, Emission-Computed, Single-Photon, Trinucleotide Repeats (genetics).
- MESH :
- chemical , metabolism : Dopamine.
- complications : Dystonic Disorders, Huntington Disease, Tic Disorders.
- diagnosis : Cognition Disorders, Huntington Disease.
- etiology : Cognition Disorders.
- genetics : Dystonic Disorders, Huntington Disease, Hyperkinesis, Tic Disorders, Trinucleotide Repeats.
- metabolism : Caudate Nucleus, Corpus Striatum.
- pathology : Atrophy, Caudate Nucleus, Corpus Striatum.
- physiopathology : Facial Muscles, Hyperkinesis.
- Adult, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Neuropsychological Tests, Skull, Tomography, Emission-Computed, Single-Photon.
PubMed: 11295801
Affiliations:
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pubmed:11295801Le document en format XML
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Wissel</name></author><author><name sortKey="Poewe, W" sort="Poewe, W" uniqKey="Poewe W" first="W" last="Poewe">Werner Poewe</name><affiliation><country>Autriche</country><placeName><settlement type="city">Innsbruck</settlement><region nuts="2" type="region">Tyrol (Land)</region></placeName><orgName type="university">Université de médecine d'Innsbruck</orgName></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2001">2001</date><idno type="RBID">pubmed:11295801</idno><idno type="pmid">11295801</idno><idno type="wicri:Area/PubMed/Corpus">003D60</idno><idno type="wicri:Area/PubMed/Curation">003D60</idno><idno type="wicri:Area/PubMed/Checkpoint">003D20</idno><idno type="wicri:Area/Ncbi/Merge">000491</idno><idno type="wicri:Area/Ncbi/Curation">000491</idno><idno type="wicri:Area/Ncbi/Checkpoint">000491</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Intrafamilial heterogeneity of facial hyperkinesias: chance association of tics, cranial dystonia, and Huntington's disease?</title><author><name sortKey="Muller, J" sort="Muller, J" uniqKey="Muller J" first="J" last="Müller">J. Müller</name><affiliation wicri:level="1"><nlm:affiliation>Department of Neurology, University Hospital Innsbruck, Innsbruck, Austria. joerg.mueller@uibk.ac.at</nlm:affiliation><country xml:lang="fr">Autriche</country><wicri:regionArea>Department of Neurology, University Hospital Innsbruck, Innsbruck</wicri:regionArea><wicri:noRegion>Innsbruck</wicri:noRegion></affiliation></author><author><name sortKey="Wenning, G K" sort="Wenning, G K" uniqKey="Wenning G" first="G K" last="Wenning">G K Wenning</name></author><author><name sortKey="Wissel, J" sort="Wissel, J" uniqKey="Wissel J" first="J" last="Wissel">J. Wissel</name></author><author><name sortKey="Poewe, W" sort="Poewe, W" uniqKey="Poewe W" first="W" last="Poewe">Werner Poewe</name><affiliation><country>Autriche</country><placeName><settlement type="city">Innsbruck</settlement><region nuts="2" type="region">Tyrol (Land)</region></placeName><orgName type="university">Université de médecine d'Innsbruck</orgName></affiliation></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="2001" type="published">2001</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Atrophy (pathology)</term><term>Caudate Nucleus (metabolism)</term><term>Caudate Nucleus (pathology)</term><term>Cognition Disorders (diagnosis)</term><term>Cognition Disorders (etiology)</term><term>Corpus Striatum (metabolism)</term><term>Corpus Striatum (pathology)</term><term>Dopamine (metabolism)</term><term>Dystonic Disorders (complications)</term><term>Dystonic Disorders (genetics)</term><term>Facial Muscles (physiopathology)</term><term>Humans</term><term>Huntington Disease (complications)</term><term>Huntington Disease (diagnosis)</term><term>Huntington Disease (genetics)</term><term>Hyperkinesis (genetics)</term><term>Hyperkinesis (physiopathology)</term><term>Magnetic Resonance Imaging</term><term>Male</term><term>Middle Aged</term><term>Neuropsychological Tests</term><term>Skull</term><term>Tic Disorders (complications)</term><term>Tic Disorders (genetics)</term><term>Tomography, Emission-Computed, Single-Photon</term><term>Trinucleotide Repeats (genetics)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Dopamine</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Dystonic Disorders</term><term>Huntington Disease</term><term>Tic Disorders</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Cognition Disorders</term><term>Huntington Disease</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Cognition Disorders</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Dystonic Disorders</term><term>Huntington Disease</term><term>Hyperkinesis</term><term>Tic Disorders</term><term>Trinucleotide Repeats</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Caudate Nucleus</term><term>Corpus Striatum</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Atrophy</term><term>Caudate Nucleus</term><term>Corpus Striatum</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Facial Muscles</term><term>Hyperkinesis</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Humans</term><term>Magnetic Resonance Imaging</term><term>Male</term><term>Middle Aged</term><term>Neuropsychological Tests</term><term>Skull</term><term>Tomography, Emission-Computed, Single-Photon</term></keywords></textClass></profileDesc></teiHeader></TEI><affiliations><list><country><li>Autriche</li></country><region><li>Tyrol (Land)</li></region><settlement><li>Innsbruck</li></settlement><orgName><li>Université de médecine d'Innsbruck</li></orgName></list><tree><noCountry><name sortKey="Wenning, G K" sort="Wenning, G K" uniqKey="Wenning G" first="G K" last="Wenning">G K Wenning</name><name sortKey="Wissel, J" sort="Wissel, J" uniqKey="Wissel J" first="J" last="Wissel">J. Wissel</name></noCountry><country name="Autriche"><noRegion><name sortKey="Muller, J" sort="Muller, J" uniqKey="Muller J" first="J" last="Müller">J. Müller</name></noRegion><name sortKey="Poewe, W" sort="Poewe, W" uniqKey="Poewe W" first="W" last="Poewe">Werner Poewe</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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