Tandem gait performance in essential tremor.
Identifieur interne : 001377 ( PubMed/Corpus ); précédent : 001376; suivant : 001378Tandem gait performance in essential tremor.
Auteurs : Renato P. Munhoz ; Hélio A G. TeiveSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2011.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Fragile X Mental Retardation Protein.
- complications : Essential Tremor.
- etiology : Gait Disorders, Neurologic.
- genetics : Essential Tremor, Gait Disorders, Neurologic, Trinucleotide Repeat Expansion.
- Aged, Aged, 80 and over, Female, Humans, Male, Middle Aged.
DOI: 10.1002/mds.23569
PubMed: 21425336
Links to Exploration step
pubmed:21425336Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Tandem gait performance in essential tremor.</title>
<author><name sortKey="Munhoz, Renato P" sort="Munhoz, Renato P" uniqKey="Munhoz R" first="Renato P" last="Munhoz">Renato P. Munhoz</name>
</author>
<author><name sortKey="Teive, Helio A G" sort="Teive, Helio A G" uniqKey="Teive H" first="Hélio A G" last="Teive">Hélio A G. Teive</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2011">2011</date>
<idno type="doi">10.1002/mds.23569</idno>
<idno type="RBID">pubmed:21425336</idno>
<idno type="pmid">21425336</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Tandem gait performance in essential tremor.</title>
<author><name sortKey="Munhoz, Renato P" sort="Munhoz, Renato P" uniqKey="Munhoz R" first="Renato P" last="Munhoz">Renato P. Munhoz</name>
</author>
<author><name sortKey="Teive, Helio A G" sort="Teive, Helio A G" uniqKey="Teive H" first="Hélio A G" last="Teive">Hélio A G. Teive</name>
</author>
</analytic>
<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="eISSN">1531-8257</idno>
<imprint><date when="2011" type="published">2011</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term>
<term>Aged, 80 and over</term>
<term>Essential Tremor (complications)</term>
<term>Essential Tremor (genetics)</term>
<term>Female</term>
<term>Fragile X Mental Retardation Protein (genetics)</term>
<term>Gait Disorders, Neurologic (etiology)</term>
<term>Gait Disorders, Neurologic (genetics)</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Trinucleotide Repeat Expansion (genetics)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Fragile X Mental Retardation Protein</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Essential Tremor</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Gait Disorders, Neurologic</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Essential Tremor</term>
<term>Gait Disorders, Neurologic</term>
<term>Trinucleotide Repeat Expansion</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Aged, 80 and over</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
</keywords>
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<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">21425336</PMID>
<DateCreated><Year>2011</Year>
<Month>04</Month>
<Day>26</Day>
</DateCreated>
<DateCompleted><Year>2011</Year>
<Month>08</Month>
<Day>24</Day>
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<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1531-8257</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>26</Volume>
<Issue>5</Issue>
<PubDate><Year>2011</Year>
<Month>Apr</Month>
</PubDate>
</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Tandem gait performance in essential tremor.</ArticleTitle>
<Pagination><MedlinePgn>932; author reply 933</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1002/mds.23569</ELocationID>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Munhoz</LastName>
<ForeName>Renato P</ForeName>
<Initials>RP</Initials>
</Author>
<Author ValidYN="Y"><LastName>Teive</LastName>
<ForeName>Hélio A G</ForeName>
<Initials>HA</Initials>
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<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016420">Comment</PublicationType>
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<ArticleDate DateType="Electronic"><Year>2011</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>
<NameOfSubstance UI="C497683">FMR1 protein, human</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>139135-51-6</RegistryNumber>
<NameOfSubstance UI="D051860">Fragile X Mental Retardation Protein</NameOfSubstance>
</Chemical>
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<CitationSubset>IM</CitationSubset>
<CommentsCorrectionsList><CommentsCorrections RefType="CommentOn"><RefSource>Mov Disord. 2010 Aug 15;25(11):1633-8</RefSource>
<PMID Version="1">20629168</PMID>
</CommentsCorrections>
</CommentsCorrectionsList>
<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D000368">Aged</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D000369">Aged, 80 and over</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D020329">Essential Tremor</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000150">complications</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005260">Female</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D051860">Fragile X Mental Retardation Protein</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D020233">Gait Disorders, Neurologic</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000209">etiology</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008875">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D019680">Trinucleotide Repeat Expansion</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="received"><Year>2010</Year>
<Month>10</Month>
<Day>15</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted"><Year>2010</Year>
<Month>11</Month>
<Day>11</Day>
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<PubMedPubDate PubStatus="aheadofprint"><Year>2011</Year>
<Month>3</Month>
<Day>21</Day>
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<PubMedPubDate PubStatus="entrez"><Year>2011</Year>
<Month>3</Month>
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<PubMedPubDate PubStatus="medline"><Year>2011</Year>
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<PublicationStatus>ppublish</PublicationStatus>
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