MovDisordV3, Ncbi, Merge, bibRecord, 000B31

Myoclonus in spinal dysraphism.

Identifieur interne : 000B31 ( Ncbi/Merge ); précédent : 000B30; suivant : 000B32

Myoclonus in spinal dysraphism.

Auteurs : Jane E. Warren [Australie] ; Marie Vidailhet ; Christopher S. Kneebone ; Niall P. Quinn ; Philip D. Thompson

Source :

Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2003.

RBID : pubmed:12889092

English descriptors

KwdEn :
- Adolescent, Child, Preschool, Electromyography (instrumentation), Female, Humans, Magnetic Resonance Imaging, Myoclonus (diagnosis), Myoclonus (etiology), Severity of Illness Index, Spinal Cord (pathology), Spinal Dysraphism (complications), Spinal Dysraphism (diagnosis), Spine (pathology).
MESH :
- complications : Spinal Dysraphism.
- diagnosis : Myoclonus, Spinal Dysraphism.
- etiology : Myoclonus.
- instrumentation : Electromyography.
- pathology : Spinal Cord, Spine.
- Adolescent, Child, Preschool, Female, Humans, Magnetic Resonance Imaging, Severity of Illness Index.

Abstract

Two cases of segmental myoclonus occurring in association with spinal dysraphism are described. In one, myoclonus of paralysed legs arose below a region of spinal cord lacking any normal function, illustrating the capacity of the isolated spinal cord to generate and maintain rhythmic activity independent of supraspinal influences.

DOI: 10.1002/mds.10469
PubMed: 12889092

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to stream PubMed, to step Corpus: 003720
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pubmed:12889092

Le document en format XML

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<author><name sortKey="Warren, Jane E" sort="Warren, Jane E" uniqKey="Warren J" first="Jane E" last="Warren">Jane E. Warren</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Neurology, Royal Adelaide Hospital, Adelaide, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Department of Neurology, Royal Adelaide Hospital, Adelaide</wicri:regionArea>
<wicri:noRegion>Adelaide</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Vidailhet, Marie" sort="Vidailhet, Marie" uniqKey="Vidailhet M" first="Marie" last="Vidailhet">Marie Vidailhet</name>
</author>
<author><name sortKey="Kneebone, Christopher S" sort="Kneebone, Christopher S" uniqKey="Kneebone C" first="Christopher S" last="Kneebone">Christopher S. Kneebone</name>
</author>
<author><name sortKey="Quinn, Niall P" sort="Quinn, Niall P" uniqKey="Quinn N" first="Niall P" last="Quinn">Niall P. Quinn</name>
</author>
<author><name sortKey="Thompson, Philip D" sort="Thompson, Philip D" uniqKey="Thompson P" first="Philip D" last="Thompson">Philip D. Thompson</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Myoclonus in spinal dysraphism.</title>
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<affiliation wicri:level="1"><nlm:affiliation>Department of Neurology, Royal Adelaide Hospital, Adelaide, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Department of Neurology, Royal Adelaide Hospital, Adelaide</wicri:regionArea>
<wicri:noRegion>Adelaide</wicri:noRegion>
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</author>
<author><name sortKey="Kneebone, Christopher S" sort="Kneebone, Christopher S" uniqKey="Kneebone C" first="Christopher S" last="Kneebone">Christopher S. Kneebone</name>
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<author><name sortKey="Quinn, Niall P" sort="Quinn, Niall P" uniqKey="Quinn N" first="Niall P" last="Quinn">Niall P. Quinn</name>
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<author><name sortKey="Thompson, Philip D" sort="Thompson, Philip D" uniqKey="Thompson P" first="Philip D" last="Thompson">Philip D. Thompson</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<imprint><date when="2003" type="published">2003</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term>
<term>Child, Preschool</term>
<term>Electromyography (instrumentation)</term>
<term>Female</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Myoclonus (diagnosis)</term>
<term>Myoclonus (etiology)</term>
<term>Severity of Illness Index</term>
<term>Spinal Cord (pathology)</term>
<term>Spinal Dysraphism (complications)</term>
<term>Spinal Dysraphism (diagnosis)</term>
<term>Spine (pathology)</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Spinal Dysraphism</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Myoclonus</term>
<term>Spinal Dysraphism</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Myoclonus</term>
</keywords>
<keywords scheme="MESH" qualifier="instrumentation" xml:lang="en"><term>Electromyography</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Spinal Cord</term>
<term>Spine</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Child, Preschool</term>
<term>Female</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Severity of Illness Index</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Two cases of segmental myoclonus occurring in association with spinal dysraphism are described. In one, myoclonus of paralysed legs arose below a region of spinal cord lacking any normal function, illustrating the capacity of the isolated spinal cord to generate and maintain rhythmic activity independent of supraspinal influences.</div>
</front>
</TEI>
<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">12889092</PMID>
<DateCreated><Year>2003</Year>
<Month>07</Month>
<Day>30</Day>
</DateCreated>
<DateCompleted><Year>2004</Year>
<Month>01</Month>
<Day>28</Day>
</DateCompleted>
<DateRevised><Year>2004</Year>
<Month>11</Month>
<Day>17</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0885-3185</ISSN>
<JournalIssue CitedMedium="Print"><Volume>18</Volume>
<Issue>8</Issue>
<PubDate><Year>2003</Year>
<Month>Aug</Month>
</PubDate>
</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Myoclonus in spinal dysraphism.</ArticleTitle>
<Pagination><MedlinePgn>961-4</MedlinePgn>
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<Abstract><AbstractText>Two cases of segmental myoclonus occurring in association with spinal dysraphism are described. In one, myoclonus of paralysed legs arose below a region of spinal cord lacking any normal function, illustrating the capacity of the isolated spinal cord to generate and maintain rhythmic activity independent of supraspinal influences.</AbstractText>
<CopyrightInformation>Copyright 2003 Movement Disorder Society</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Warren</LastName>
<ForeName>Jane E</ForeName>
<Initials>JE</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, Royal Adelaide Hospital, Adelaide, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Vidailhet</LastName>
<ForeName>Marie</ForeName>
<Initials>M</Initials>
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<Author ValidYN="Y"><LastName>Kneebone</LastName>
<ForeName>Christopher S</ForeName>
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<Author ValidYN="Y"><LastName>Quinn</LastName>
<ForeName>Niall P</ForeName>
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<Author ValidYN="Y"><LastName>Thompson</LastName>
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<MedlineJournalInfo><Country>United States</Country>
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<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D000293">Adolescent</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D002675">Child, Preschool</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D004576">Electromyography</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005260">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008279">Magnetic Resonance Imaging</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D009207">Myoclonus</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000175">diagnosis</QualifierName>
<QualifierName MajorTopicYN="Y" UI="Q000209">etiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D012720">Severity of Illness Index</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D013116">Spinal Cord</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D016135">Spinal Dysraphism</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000150">complications</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000175">diagnosis</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D013131">Spine</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2003</Year>
<Month>7</Month>
<Day>31</Day>
<Hour>5</Hour>
<Minute>0</Minute>
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<PubMedPubDate PubStatus="medline"><Year>2004</Year>
<Month>1</Month>
<Day>30</Day>
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<PublicationStatus>ppublish</PublicationStatus>
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<affiliations><list><country><li>Australie</li>
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<tree><noCountry><name sortKey="Kneebone, Christopher S" sort="Kneebone, Christopher S" uniqKey="Kneebone C" first="Christopher S" last="Kneebone">Christopher S. Kneebone</name>
<name sortKey="Quinn, Niall P" sort="Quinn, Niall P" uniqKey="Quinn N" first="Niall P" last="Quinn">Niall P. Quinn</name>
<name sortKey="Thompson, Philip D" sort="Thompson, Philip D" uniqKey="Thompson P" first="Philip D" last="Thompson">Philip D. Thompson</name>
<name sortKey="Vidailhet, Marie" sort="Vidailhet, Marie" uniqKey="Vidailhet M" first="Marie" last="Vidailhet">Marie Vidailhet</name>
</noCountry>
<country name="Australie"><noRegion><name sortKey="Warren, Jane E" sort="Warren, Jane E" uniqKey="Warren J" first="Jane E" last="Warren">Jane E. Warren</name>
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</record>

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	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.

Movement Disorders (revue)

Myoclonus in spinal dysraphism.

Myoclonus in spinal dysraphism.

Source :

English descriptors

Abstract

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