Young-onset Parkinson's disease: a clinical pathologic description of two siblings.
Identifieur interne : 006F74 ( Main/Merge ); précédent : 006F73; suivant : 006F75Young-onset Parkinson's disease: a clinical pathologic description of two siblings.
Auteurs : R E Tabamo [États-Unis] ; H H Fernandez ; J H Friedman ; D K SimonSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2000.
English descriptors
- KwdEn :
- MESH :
- diagnosis : Parkinson Disease.
- genetics : Parkinson Disease.
- pathology : Cerebral Cortex, Lewy Bodies, Parkinson Disease, Substantia Nigra.
- Adult, DNA Mutational Analysis, Female, Humans, Neurologic Examination.
PubMed: 10928592
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 003F33
- to stream PubMed, to step Curation: 003F33
- to stream PubMed, to step Checkpoint: 003E31
- to stream Ncbi, to step Merge: 000318
- to stream Ncbi, to step Curation: 000318
- to stream Ncbi, to step Checkpoint: 000318
Links to Exploration step
pubmed:10928592Le document en format XML
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<author><name sortKey="Tabamo, R E" sort="Tabamo, R E" uniqKey="Tabamo R" first="R E" last="Tabamo">R E Tabamo</name>
<affiliation wicri:level="1"><nlm:affiliation>Memorial Hospital of Rhode Island, Brown University School of Medicine, Pawtucket 02860, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
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<author><name sortKey="Fernandez, H H" sort="Fernandez, H H" uniqKey="Fernandez H" first="H H" last="Fernandez">H H Fernandez</name>
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<author><name sortKey="Friedman, J H" sort="Friedman, J H" uniqKey="Friedman J" first="J H" last="Friedman">J H Friedman</name>
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<author><name sortKey="Simon, D K" sort="Simon, D K" uniqKey="Simon D" first="D K" last="Simon">D K Simon</name>
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<author><name sortKey="Tabamo, R E" sort="Tabamo, R E" uniqKey="Tabamo R" first="R E" last="Tabamo">R E Tabamo</name>
<affiliation wicri:level="1"><nlm:affiliation>Memorial Hospital of Rhode Island, Brown University School of Medicine, Pawtucket 02860, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
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<author><name sortKey="Fernandez, H H" sort="Fernandez, H H" uniqKey="Fernandez H" first="H H" last="Fernandez">H H Fernandez</name>
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<author><name sortKey="Friedman, J H" sort="Friedman, J H" uniqKey="Friedman J" first="J H" last="Friedman">J H Friedman</name>
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<author><name sortKey="Simon, D K" sort="Simon, D K" uniqKey="Simon D" first="D K" last="Simon">D K Simon</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Cerebral Cortex (pathology)</term>
<term>DNA Mutational Analysis</term>
<term>Female</term>
<term>Humans</term>
<term>Lewy Bodies (pathology)</term>
<term>Neurologic Examination</term>
<term>Parkinson Disease (diagnosis)</term>
<term>Parkinson Disease (genetics)</term>
<term>Parkinson Disease (pathology)</term>
<term>Substantia Nigra (pathology)</term>
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<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Parkinson Disease</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Parkinson Disease</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Cerebral Cortex</term>
<term>Lewy Bodies</term>
<term>Parkinson Disease</term>
<term>Substantia Nigra</term>
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<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>DNA Mutational Analysis</term>
<term>Female</term>
<term>Humans</term>
<term>Neurologic Examination</term>
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