MovDisordV3, PubMed, Checkpoint, bibRecord, 001212

Myoclonus-dystonia in 18p deletion syndrome.

Identifieur interne : 001212 ( PubMed/Checkpoint ); précédent : 001211; suivant : 001213

Myoclonus-dystonia in 18p deletion syndrome.

Auteurs : Markus C. Kowarik ; Sabine Langer ; Corinna Keri ; Bernhard Hemmer ; Konrad Oexle ; Juliane Winkelmann

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2011.

RBID : pubmed:21462265

English descriptors

KwdEn :
- Adult, Chromosome Deletion, Chromosome Disorders (complications), Chromosomes, Human, Pair 18, Dystonia (etiology), Female, Humans, Karyotyping (methods), Magnetic Resonance Imaging (methods), Myoclonus (etiology).
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

Affiliations:

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pubmed:21462265

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Myoclonus-dystonia in 18p deletion syndrome.</title>
<author><name sortKey="Kowarik, Markus C" sort="Kowarik, Markus C" uniqKey="Kowarik M" first="Markus C" last="Kowarik">Markus C. Kowarik</name>
</author>
<author><name sortKey="Langer, Sabine" sort="Langer, Sabine" uniqKey="Langer S" first="Sabine" last="Langer">Sabine Langer</name>
</author>
<author><name sortKey="Keri, Corinna" sort="Keri, Corinna" uniqKey="Keri C" first="Corinna" last="Keri">Corinna Keri</name>
</author>
<author><name sortKey="Hemmer, Bernhard" sort="Hemmer, Bernhard" uniqKey="Hemmer B" first="Bernhard" last="Hemmer">Bernhard Hemmer</name>
</author>
<author><name sortKey="Oexle, Konrad" sort="Oexle, Konrad" uniqKey="Oexle K" first="Konrad" last="Oexle">Konrad Oexle</name>
</author>
<author><name sortKey="Winkelmann, Juliane" sort="Winkelmann, Juliane" uniqKey="Winkelmann J" first="Juliane" last="Winkelmann">Juliane Winkelmann</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Myoclonus-dystonia in 18p deletion syndrome.</title>
<author><name sortKey="Kowarik, Markus C" sort="Kowarik, Markus C" uniqKey="Kowarik M" first="Markus C" last="Kowarik">Markus C. Kowarik</name>
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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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<author><name sortKey="Winkelmann, Juliane" sort="Winkelmann, Juliane" uniqKey="Winkelmann J" first="Juliane" last="Winkelmann">Juliane Winkelmann</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="eISSN">1531-8257</idno>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Chromosome Deletion</term>
<term>Chromosome Disorders (complications)</term>
<term>Chromosomes, Human, Pair 18</term>
<term>Dystonia (etiology)</term>
<term>Female</term>
<term>Humans</term>
<term>Karyotyping (methods)</term>
<term>Magnetic Resonance Imaging (methods)</term>
<term>Myoclonus (etiology)</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Chromosome Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Dystonia</term>
<term>Myoclonus</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Karyotyping</term>
<term>Magnetic Resonance Imaging</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Chromosome Deletion</term>
<term>Chromosomes, Human, Pair 18</term>
<term>Female</term>
<term>Humans</term>
</keywords>
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<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">21462265</PMID>
<DateCreated><Year>2011</Year>
<Month>04</Month>
<Day>04</Day>
</DateCreated>
<DateCompleted><Year>2011</Year>
<Month>07</Month>
<Day>29</Day>
</DateCompleted>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1531-8257</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>26</Volume>
<Issue>3</Issue>
<PubDate><Year>2011</Year>
<Month>Feb</Month>
<Day>15</Day>
</PubDate>
</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Myoclonus-dystonia in 18p deletion syndrome.</ArticleTitle>
<Pagination><MedlinePgn>560-1</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1002/mds.23446</ELocationID>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Kowarik</LastName>
<ForeName>Markus C</ForeName>
<Initials>MC</Initials>
</Author>
<Author ValidYN="Y"><LastName>Langer</LastName>
<ForeName>Sabine</ForeName>
<Initials>S</Initials>
</Author>
<Author ValidYN="Y"><LastName>Keri</LastName>
<ForeName>Corinna</ForeName>
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<Author ValidYN="Y"><LastName>Hemmer</LastName>
<ForeName>Bernhard</ForeName>
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<Author ValidYN="Y"><LastName>Oexle</LastName>
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<Author ValidYN="Y"><LastName>Winkelmann</LastName>
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<Initials>J</Initials>
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<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType>
<PublicationType UI="D016422">Letter</PublicationType>
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<ArticleDate DateType="Electronic"><Year>2010</Year>
<Month>12</Month>
<Day>13</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Mov Disord</MedlineTA>
<NlmUniqueID>8610688</NlmUniqueID>
<ISSNLinking>0885-3185</ISSNLinking>
</MedlineJournalInfo>
<SupplMeshList><SupplMeshName Type="Disease" UI="C538309">Chromosome 18p deletion syndrome</SupplMeshName>
</SupplMeshList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D000328">Adult</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D002872">Chromosome Deletion</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D025063">Chromosome Disorders</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000150">complications</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D002887">Chromosomes, Human, Pair 18</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D004421">Dystonia</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000209">etiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005260">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D007621">Karyotyping</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000379">methods</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008279">Magnetic Resonance Imaging</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000379">methods</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D009207">Myoclonus</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000209">etiology</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="aheadofprint"><Year>2010</Year>
<Month>12</Month>
<Day>13</Day>
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<PubMedPubDate PubStatus="entrez"><Year>2011</Year>
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<PubMedPubDate PubStatus="medline"><Year>2011</Year>
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<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="doi">10.1002/mds.23446</ArticleId>
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<affiliations><list></list>
<tree><noCountry><name sortKey="Hemmer, Bernhard" sort="Hemmer, Bernhard" uniqKey="Hemmer B" first="Bernhard" last="Hemmer">Bernhard Hemmer</name>
<name sortKey="Keri, Corinna" sort="Keri, Corinna" uniqKey="Keri C" first="Corinna" last="Keri">Corinna Keri</name>
<name sortKey="Kowarik, Markus C" sort="Kowarik, Markus C" uniqKey="Kowarik M" first="Markus C" last="Kowarik">Markus C. Kowarik</name>
<name sortKey="Langer, Sabine" sort="Langer, Sabine" uniqKey="Langer S" first="Sabine" last="Langer">Sabine Langer</name>
<name sortKey="Oexle, Konrad" sort="Oexle, Konrad" uniqKey="Oexle K" first="Konrad" last="Oexle">Konrad Oexle</name>
<name sortKey="Winkelmann, Juliane" sort="Winkelmann, Juliane" uniqKey="Winkelmann J" first="Juliane" last="Winkelmann">Juliane Winkelmann</name>
</noCountry>
</tree>
</affiliations>
</record>

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	Movement Disorders (revue)
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Movement Disorders (revue)

Myoclonus-dystonia in 18p deletion syndrome.

Myoclonus-dystonia in 18p deletion syndrome.

Source :

English descriptors

Links toward previous steps (curation, corpus...)

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