What is it? Case 2, 1988. Congenital mental retardation and juvenile parkinsonism
Identifieur interne : 006518 ( Main/Exploration ); précédent : 006517; suivant : 006519What is it? Case 2, 1988. Congenital mental retardation and juvenile parkinsonism
Auteurs : Joseph Jankovic [États-Unis] ; Dawna Armstrong [États-Unis] ; Niels L. Low [États-Unis] ; Christopher G. Goetz [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 1988.
English descriptors
- KwdEn :
- Adolescent, Atrophy, Biopsy, Blindness (pathology), Brain (pathology), Child, Preschool, Dementia (pathology), Epilepsies, Myoclonic (pathology), Female, Humans, Intellectual Disability (congenital), Intellectual Disability (pathology), Male, Microscopy, Electron, Muscles (pathology), Neuronal Ceroid-Lipofuscinoses (pathology), Parkinson Disease (pathology), SSPE Virus (ultrastructure), Subacute Sclerosing Panencephalitis (pathology).
- MESH :
- congenital : Intellectual Disability.
- pathology : Blindness, Brain, Dementia, Epilepsies, Myoclonic, Intellectual Disability, Muscles, Neuronal Ceroid-Lipofuscinoses, Parkinson Disease, Subacute Sclerosing Panencephalitis.
- ultrastructure : SSPE Virus.
- Adolescent, Atrophy, Biopsy, Child, Preschool, Female, Humans, Male, Microscopy, Electron.
Url:
- https://api.istex.fr/document/922F437C9EA918E4DE44099A9717036E4A54F3E0/fulltext/pdf
- https://api.istex.fr/document/0CFAEEDB042545695D81B0668F5004B77BB14D53/fulltext/pdf
DOI: 10.1002/mds.870030413
Affiliations:
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Le document en format XML
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<placeName><region type="state">Texas</region>
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<wicri:cityArea>Department of Neurology, Baylor College of Medicine, Houston</wicri:cityArea>
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<author><name sortKey="Goetz, Christopher G" sort="Goetz, Christopher G" uniqKey="Goetz C" first="Christopher G." last="Goetz">Christopher G. Goetz</name>
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<series><title level="j">Movement Disorders</title>
<title level="j" type="sub">Official Journal of the Movement Disorder Society</title>
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<idno type="ISSN">0885-3185</idno>
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<term>Atrophy</term>
<term>Biopsy</term>
<term>Blindness (pathology)</term>
<term>Brain (pathology)</term>
<term>Child, Preschool</term>
<term>Dementia (pathology)</term>
<term>Epilepsies, Myoclonic (pathology)</term>
<term>Female</term>
<term>Humans</term>
<term>Intellectual Disability (congenital)</term>
<term>Intellectual Disability (pathology)</term>
<term>Male</term>
<term>Microscopy, Electron</term>
<term>Muscles (pathology)</term>
<term>Neuronal Ceroid-Lipofuscinoses (pathology)</term>
<term>Parkinson Disease (pathology)</term>
<term>SSPE Virus (ultrastructure)</term>
<term>Subacute Sclerosing Panencephalitis (pathology)</term>
</keywords>
<keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Intellectual Disability</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Blindness</term>
<term>Brain</term>
<term>Dementia</term>
<term>Epilepsies, Myoclonic</term>
<term>Intellectual Disability</term>
<term>Muscles</term>
<term>Neuronal Ceroid-Lipofuscinoses</term>
<term>Parkinson Disease</term>
<term>Subacute Sclerosing Panencephalitis</term>
</keywords>
<keywords scheme="MESH" qualifier="ultrastructure" xml:lang="en"><term>SSPE Virus</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
<term>Atrophy</term>
<term>Biopsy</term>
<term>Child, Preschool</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
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