Hemiparkinsonism–hemiatrophy syndrome may mimic early‐stage cortical–basal ganglionic degeneration
Identifieur interne : 006012 ( Main/Exploration ); précédent : 006011; suivant : 006013Hemiparkinsonism–hemiatrophy syndrome may mimic early‐stage cortical–basal ganglionic degeneration
Auteurs : Nir Giladi [États-Unis] ; Stanley Fahn [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 1992.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Adult, Atrophy, Basal Ganglia (pathology), Basal Ganglia Diseases (diagnosis), Basal Ganglia Diseases (pathology), Basal ganglion, Brain (vertebrata), Cerebral Cortex (pathology), Degeneration, Diagnosis, Diagnosis, Differential, Functional Laterality (physiology), Hemiatrophy, Human, 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.
Url:
DOI: 10.1002/mds.870070419
Affiliations:
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Le document en format XML
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<series><title level="j">Movement Disorders</title>
<title level="j" type="sub">Official Journal of the Movement Disorder Society</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
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<pubPlace>Hoboken</pubPlace>
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<term>Atrophy</term>
<term>Basal Ganglia (pathology)</term>
<term>Basal Ganglia Diseases (diagnosis)</term>
<term>Basal Ganglia Diseases (pathology)</term>
<term>Basal ganglion</term>
<term>Brain (vertebrata)</term>
<term>Cerebral Cortex (pathology)</term>
<term>Degeneration</term>
<term>Diagnosis</term>
<term>Diagnosis, Differential</term>
<term>Functional Laterality (physiology)</term>
<term>Hemiatrophy</term>
<term>Human</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>
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<term>Muscular Atrophy</term>
<term>Parkinson Disease, Secondary</term>
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<term>Basal Ganglia Diseases</term>
<term>Cerebral Cortex</term>
<term>Muscular Atrophy</term>
<term>Parkinson Disease, Secondary</term>
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<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Functional Laterality</term>
<term>Nerve Degeneration</term>
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<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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<keywords scheme="Pascal" xml:lang="fr"><term>Diagnostic</term>
<term>Dégénérescence</term>
<term>Encéphale</term>
<term>Homme</term>
<term>Hémiatrophie</term>
<term>Noyau gris central</term>
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<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term>
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