Young-onset Parkinson's disease: a clinical pathologic description of two siblings.
Identifieur interne : 003F33 ( PubMed/Curation ); précédent : 003F32; suivant : 003F34Young-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
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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>
<wicri:regionArea>Memorial Hospital of Rhode Island, Brown University School of Medicine, Pawtucket 02860</wicri:regionArea>
</affiliation>
</author>
<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>
</author>
<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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<sourceDesc><biblStruct><analytic><title xml:lang="en">Young-onset Parkinson's disease: a clinical pathologic description of two siblings.</title>
<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>
<wicri:regionArea>Memorial Hospital of Rhode Island, Brown University School of Medicine, Pawtucket 02860</wicri:regionArea>
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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>
</author>
<author><name sortKey="Friedman, J H" sort="Friedman, J H" uniqKey="Friedman J" first="J H" last="Friedman">J H Friedman</name>
</author>
<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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</analytic>
<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="2000" type="published">2000</date>
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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>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Cerebral Cortex</term>
<term>Lewy Bodies</term>
<term>Parkinson Disease</term>
<term>Substantia Nigra</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>DNA Mutational Analysis</term>
<term>Female</term>
<term>Humans</term>
<term>Neurologic Examination</term>
</keywords>
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<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">10928592</PMID>
<DateCreated><Year>2001</Year>
<Month>01</Month>
<Day>11</Day>
</DateCreated>
<DateCompleted><Year>2001</Year>
<Month>01</Month>
<Day>11</Day>
</DateCompleted>
<DateRevised><Year>2004</Year>
<Month>11</Month>
<Day>17</Day>
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<Article PubModel="Print"><Journal><ISSN IssnType="Print">0885-3185</ISSN>
<JournalIssue CitedMedium="Print"><Volume>15</Volume>
<Issue>4</Issue>
<PubDate><Year>2000</Year>
<Month>Jul</Month>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Young-onset Parkinson's disease: a clinical pathologic description of two siblings.</ArticleTitle>
<Pagination><MedlinePgn>744-6</MedlinePgn>
</Pagination>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Tabamo</LastName>
<ForeName>R E</ForeName>
<Initials>RE</Initials>
<AffiliationInfo><Affiliation>Memorial Hospital of Rhode Island, Brown University School of Medicine, Pawtucket 02860, USA.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Fernandez</LastName>
<ForeName>H H</ForeName>
<Initials>HH</Initials>
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<Author ValidYN="Y"><LastName>Friedman</LastName>
<ForeName>J H</ForeName>
<Initials>JH</Initials>
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<Author ValidYN="Y"><LastName>Simon</LastName>
<ForeName>D K</ForeName>
<Initials>DK</Initials>
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<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType>
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<MedlineJournalInfo><Country>UNITED STATES</Country>
<MedlineTA>Mov Disord</MedlineTA>
<NlmUniqueID>8610688</NlmUniqueID>
<ISSNLinking>0885-3185</ISSNLinking>
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<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D000328">Adult</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D004252">DNA Mutational Analysis</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005260">Female</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D016631">Lewy Bodies</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D009460">Neurologic Examination</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D010300">Parkinson Disease</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000175">diagnosis</QualifierName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D013378">Substantia Nigra</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2000</Year>
<Month>8</Month>
<Day>6</Day>
<Hour>11</Hour>
<Minute>0</Minute>
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<PubMedPubDate PubStatus="medline"><Year>2001</Year>
<Month>2</Month>
<Day>28</Day>
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<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">10928592</ArticleId>
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