Tandem gait performance in essential tremor.
Identifieur interne : 003047 ( Ncbi/Curation ); précédent : 003046; suivant : 003048Tandem 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
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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>
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<date when="2011">2011</date>
<idno type="doi">10.1002/mds.23569</idno>
<idno type="RBID">pubmed: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>
</imprint>
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</biblStruct>
</sourceDesc>
</fileDesc>
<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>
</textClass>
</profileDesc>
</teiHeader>
</TEI>
</record>
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