Hemiparkinsonism-hemiatrophy syndrome may mimic early-stage cortical-basal ganglionic degeneration.
Identifieur interne : 004D05 ( PubMed/Corpus ); précédent : 004D04; suivant : 004D06Hemiparkinsonism-hemiatrophy syndrome may mimic early-stage cortical-basal ganglionic degeneration.
Auteurs : N. Giladi ; S. FahnSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 1992.
English descriptors
- KwdEn :
- Adult, Atrophy, Basal Ganglia (pathology), Basal Ganglia Diseases (diagnosis), Basal Ganglia Diseases (pathology), Cerebral Cortex (pathology), Diagnosis, Differential, Functional Laterality (physiology), Humans, Magnetic Resonance Imaging, Male, Muscular Atrophy (diagnosis), Muscular Atrophy (pathology), Nerve Degeneration (physiology), Neurologic Examination, Parkinson Disease, Secondary (diagnosis), Parkinson Disease, Secondary (pathology).
- MESH :
- diagnosis : Basal Ganglia Diseases, Muscular Atrophy, Parkinson Disease, Secondary.
- pathology : Basal Ganglia, Basal Ganglia Diseases, Cerebral Cortex, Muscular Atrophy, Parkinson Disease, Secondary.
- physiology : Functional Laterality, Nerve Degeneration.
- Adult, Atrophy, Diagnosis, Differential, Humans, Magnetic Resonance Imaging, Male, Neurologic Examination.
DOI: 10.1002/mds.870070419
PubMed: 1484539
Links to Exploration step
pubmed:1484539Le document en format XML
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<author><name sortKey="Giladi, N" sort="Giladi, N" uniqKey="Giladi N" first="N" last="Giladi">N. Giladi</name>
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<author><name sortKey="Fahn, S" sort="Fahn, S" uniqKey="Fahn S" first="S" last="Fahn">S. Fahn</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Hemiparkinsonism-hemiatrophy syndrome may mimic early-stage cortical-basal ganglionic degeneration.</title>
<author><name sortKey="Giladi, N" sort="Giladi, N" uniqKey="Giladi N" first="N" last="Giladi">N. Giladi</name>
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<author><name sortKey="Fahn, S" sort="Fahn, S" uniqKey="Fahn S" first="S" last="Fahn">S. Fahn</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="ISSN">0885-3185</idno>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Atrophy</term>
<term>Basal Ganglia (pathology)</term>
<term>Basal Ganglia Diseases (diagnosis)</term>
<term>Basal Ganglia Diseases (pathology)</term>
<term>Cerebral Cortex (pathology)</term>
<term>Diagnosis, Differential</term>
<term>Functional Laterality (physiology)</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Muscular Atrophy (diagnosis)</term>
<term>Muscular Atrophy (pathology)</term>
<term>Nerve Degeneration (physiology)</term>
<term>Neurologic Examination</term>
<term>Parkinson Disease, Secondary (diagnosis)</term>
<term>Parkinson Disease, Secondary (pathology)</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Basal Ganglia Diseases</term>
<term>Muscular Atrophy</term>
<term>Parkinson Disease, Secondary</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Basal Ganglia</term>
<term>Basal Ganglia Diseases</term>
<term>Cerebral Cortex</term>
<term>Muscular Atrophy</term>
<term>Parkinson Disease, Secondary</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Functional Laterality</term>
<term>Nerve Degeneration</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Atrophy</term>
<term>Diagnosis, Differential</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Neurologic Examination</term>
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<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">1484539</PMID>
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<Month>02</Month>
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<DateCompleted><Year>1993</Year>
<Month>02</Month>
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<DateRevised><Year>2006</Year>
<Month>11</Month>
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<Issue>4</Issue>
<PubDate><Year>1992</Year>
<Month>Oct</Month>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
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<ArticleTitle>Hemiparkinsonism-hemiatrophy syndrome may mimic early-stage cortical-basal ganglionic degeneration.</ArticleTitle>
<Pagination><MedlinePgn>384-5</MedlinePgn>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Giladi</LastName>
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<Language>eng</Language>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D001479">Basal Ganglia</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D001480">Basal Ganglia Diseases</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D009133">Muscular Atrophy</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000175">diagnosis</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D009410">Nerve Degeneration</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000502">physiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D009460">Neurologic Examination</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D010302">Parkinson Disease, Secondary</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000175">diagnosis</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
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