Ataxia and cerebellar atrophy--a novel manifestation of neuro-Behçet disease?
Identifieur interne : 001F33 ( Ncbi/Curation ); précédent : 001F32; suivant : 001F34Ataxia and cerebellar atrophy--a novel manifestation of neuro-Behçet disease?
Auteurs : Raquel C. Gardner ; Jeremy D. SchmahmannSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2008.
English descriptors
- KwdEn :
- MESH :
- complications : Behcet Syndrome.
- etiology : Ataxia.
- methods : Magnetic Resonance Imaging.
- pathology : Behcet Syndrome, Cerebellum.
- Adolescent, Atrophy, Female, Humans.
DOI: 10.1002/mds.21834
PubMed: 18044705
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pubmed:18044705Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Ataxia and cerebellar atrophy--a novel manifestation of neuro-Behçet disease?</title>
<author><name sortKey="Gardner, Raquel C" sort="Gardner, Raquel C" uniqKey="Gardner R" first="Raquel C" last="Gardner">Raquel C. Gardner</name>
</author>
<author><name sortKey="Schmahmann, Jeremy D" sort="Schmahmann, Jeremy D" uniqKey="Schmahmann J" first="Jeremy D" last="Schmahmann">Jeremy D. Schmahmann</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Ataxia and cerebellar atrophy--a novel manifestation of neuro-Behçet disease?</title>
<author><name sortKey="Gardner, Raquel C" sort="Gardner, Raquel C" uniqKey="Gardner R" first="Raquel C" last="Gardner">Raquel C. Gardner</name>
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<author><name sortKey="Schmahmann, Jeremy D" sort="Schmahmann, Jeremy D" uniqKey="Schmahmann J" first="Jeremy D" last="Schmahmann">Jeremy D. Schmahmann</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>
<imprint><date when="2008" type="published">2008</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term>
<term>Ataxia (etiology)</term>
<term>Atrophy</term>
<term>Behcet Syndrome (complications)</term>
<term>Behcet Syndrome (pathology)</term>
<term>Cerebellum (pathology)</term>
<term>Female</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging (methods)</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Behcet Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Ataxia</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Magnetic Resonance Imaging</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Behcet Syndrome</term>
<term>Cerebellum</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Atrophy</term>
<term>Female</term>
<term>Humans</term>
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