Caffeine improved paroxysmal dyskinesia caused by the PRRT2 mutation.
Identifieur interne : 000964 ( PubMed/Corpus ); précédent : 000963; suivant : 000965Caffeine improved paroxysmal dyskinesia caused by the PRRT2 mutation.
Auteurs : Virginie Lambrecq ; Florence Riant ; Elisabeth Tournier-Lasserve ; Véronique Michel ; Pierre BurbaudSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2013.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Membrane Proteins, Nerve Tissue Proteins.
- chemical , therapeutic use : Caffeine, Phosphodiesterase Inhibitors.
- drug therapy : Chorea.
- genetics : Chorea, Mutation.
- Female, Humans, Young Adult.
DOI: 10.1002/mds.25450
PubMed: 23536488
Links to Exploration step
pubmed:23536488Le document en format XML
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<author><name sortKey="Lambrecq, Virginie" sort="Lambrecq, Virginie" uniqKey="Lambrecq V" first="Virginie" last="Lambrecq">Virginie Lambrecq</name>
</author>
<author><name sortKey="Riant, Florence" sort="Riant, Florence" uniqKey="Riant F" first="Florence" last="Riant">Florence Riant</name>
</author>
<author><name sortKey="Tournier Lasserve, Elisabeth" sort="Tournier Lasserve, Elisabeth" uniqKey="Tournier Lasserve E" first="Elisabeth" last="Tournier-Lasserve">Elisabeth Tournier-Lasserve</name>
</author>
<author><name sortKey="Michel, Veronique" sort="Michel, Veronique" uniqKey="Michel V" first="Véronique" last="Michel">Véronique Michel</name>
</author>
<author><name sortKey="Burbaud, Pierre" sort="Burbaud, Pierre" uniqKey="Burbaud P" first="Pierre" last="Burbaud">Pierre Burbaud</name>
</author>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Caffeine improved paroxysmal dyskinesia caused by the PRRT2 mutation.</title>
<author><name sortKey="Lambrecq, Virginie" sort="Lambrecq, Virginie" uniqKey="Lambrecq V" first="Virginie" last="Lambrecq">Virginie Lambrecq</name>
</author>
<author><name sortKey="Riant, Florence" sort="Riant, Florence" uniqKey="Riant F" first="Florence" last="Riant">Florence Riant</name>
</author>
<author><name sortKey="Tournier Lasserve, Elisabeth" sort="Tournier Lasserve, Elisabeth" uniqKey="Tournier Lasserve E" first="Elisabeth" last="Tournier-Lasserve">Elisabeth Tournier-Lasserve</name>
</author>
<author><name sortKey="Michel, Veronique" sort="Michel, Veronique" uniqKey="Michel V" first="Véronique" last="Michel">Véronique Michel</name>
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<author><name sortKey="Burbaud, Pierre" sort="Burbaud, Pierre" uniqKey="Burbaud P" first="Pierre" last="Burbaud">Pierre Burbaud</name>
</author>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="eISSN">1531-8257</idno>
<imprint><date when="2013" type="published">2013</date>
</imprint>
</series>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Caffeine (therapeutic use)</term>
<term>Chorea (drug therapy)</term>
<term>Chorea (genetics)</term>
<term>Female</term>
<term>Humans</term>
<term>Membrane Proteins (genetics)</term>
<term>Mutation (genetics)</term>
<term>Nerve Tissue Proteins (genetics)</term>
<term>Phosphodiesterase Inhibitors (therapeutic use)</term>
<term>Young Adult</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Membrane Proteins</term>
<term>Nerve Tissue Proteins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Caffeine</term>
<term>Phosphodiesterase Inhibitors</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Chorea</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Chorea</term>
<term>Mutation</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Female</term>
<term>Humans</term>
<term>Young Adult</term>
</keywords>
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<DateCreated><Year>2013</Year>
<Month>05</Month>
<Day>16</Day>
</DateCreated>
<DateCompleted><Year>2014</Year>
<Month>01</Month>
<Day>02</Day>
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<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1531-8257</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>28</Volume>
<Issue>5</Issue>
<PubDate><Year>2013</Year>
<Month>May</Month>
</PubDate>
</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Caffeine improved paroxysmal dyskinesia caused by the PRRT2 mutation.</ArticleTitle>
<Pagination><MedlinePgn>683</MedlinePgn>
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<ELocationID EIdType="doi" ValidYN="Y">10.1002/mds.25450</ELocationID>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Lambrecq</LastName>
<ForeName>Virginie</ForeName>
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<Author ValidYN="Y"><LastName>Riant</LastName>
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<Author ValidYN="Y"><LastName>Tournier-Lasserve</LastName>
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<Author ValidYN="Y"><LastName>Michel</LastName>
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<Author ValidYN="Y"><LastName>Burbaud</LastName>
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<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016422">Letter</PublicationType>
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<ArticleDate DateType="Electronic"><Year>2013</Year>
<Month>03</Month>
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<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Mov Disord</MedlineTA>
<NlmUniqueID>8610688</NlmUniqueID>
<ISSNLinking>0885-3185</ISSNLinking>
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<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D002819">Chorea</DescriptorName>
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<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D010726">Phosphodiesterase Inhibitors</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D055815">Young Adult</DescriptorName>
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</MeshHeadingList>
</MedlineCitation>
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<Day>30</Day>
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<PubMedPubDate PubStatus="revised"><Year>2013</Year>
<Month>1</Month>
<Day>15</Day>
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<PubMedPubDate PubStatus="accepted"><Year>2013</Year>
<Month>2</Month>
<Day>1</Day>
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<PubMedPubDate PubStatus="aheadofprint"><Year>2013</Year>
<Month>3</Month>
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<PublicationStatus>ppublish</PublicationStatus>
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