Myoclonus-dystonia in 18p deletion syndrome.
Identifieur interne : 001331 ( PubMed/Curation ); précédent : 001330; suivant : 001332Myoclonus-dystonia in 18p deletion syndrome.
Auteurs : Markus C. Kowarik ; Sabine Langer ; Corinna Keri ; Bernhard Hemmer ; Konrad Oexle ; Juliane WinkelmannSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2011.
English descriptors
- KwdEn :
- MESH :
- complications : Chromosome Disorders.
- etiology : Dystonia, Myoclonus.
- methods : Karyotyping, Magnetic Resonance Imaging.
- Adult, Chromosome Deletion, Chromosomes, Human, Pair 18, Female, Humans.
DOI: 10.1002/mds.23446
PubMed: 21462265
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pubmed:21462265Le document en format XML
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<author><name sortKey="Langer, Sabine" sort="Langer, Sabine" uniqKey="Langer S" first="Sabine" last="Langer">Sabine Langer</name>
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<author><name sortKey="Keri, Corinna" sort="Keri, Corinna" uniqKey="Keri C" first="Corinna" last="Keri">Corinna Keri</name>
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<author><name sortKey="Hemmer, Bernhard" sort="Hemmer, Bernhard" uniqKey="Hemmer B" first="Bernhard" last="Hemmer">Bernhard Hemmer</name>
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<author><name sortKey="Oexle, Konrad" sort="Oexle, Konrad" uniqKey="Oexle K" first="Konrad" last="Oexle">Konrad Oexle</name>
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<term>Dystonia (etiology)</term>
<term>Female</term>
<term>Humans</term>
<term>Karyotyping (methods)</term>
<term>Magnetic Resonance Imaging (methods)</term>
<term>Myoclonus (etiology)</term>
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<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Chromosome Disorders</term>
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<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Dystonia</term>
<term>Myoclonus</term>
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<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Karyotyping</term>
<term>Magnetic Resonance Imaging</term>
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<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
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<ArticleTitle>Myoclonus-dystonia in 18p deletion syndrome.</ArticleTitle>
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