JankovicV1, Ncbi, Merge, bibRecord, 000092

Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation.

Identifieur interne : 000092 ( Ncbi/Merge ); précédent : 000091; suivant : 000093

Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation.

Auteurs : Hao Deng ; Weidong Le ; Yi Guo ; Christine. Hunter ; Wenjie Xie ; Joseph Jankovic [États-Unis]

Source :

Annals of neurology [ 0364-5134 ] ; 2005.

RBID : pubmed:15929036

English descriptors

KwdEn :
- Aged, Female, Humans, Male, Middle Aged, North America, Parkinson Disease (genetics), Point Mutation, Protein-Serine-Threonine Kinases (genetics).
MESH :
- chemical , genetics : Protein-Serine-Threonine Kinases.
- geographic : North America.
- genetics : Parkinson Disease.
- Aged, Female, Humans, Male, Middle Aged, Point Mutation.

DOI: 10.1002/ana.20510
PubMed: 15929036

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pubmed:15929036

Le document en format XML

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<author><name sortKey="Deng, Hao" sort="Deng, Hao" uniqKey="Deng H" first="Hao" last="Deng">Hao Deng</name>
</author>
<author><name sortKey="Le, Weidong" sort="Le, Weidong" uniqKey="Le W" first="Weidong" last="Le">Weidong Le</name>
</author>
<author><name sortKey="Guo, Yi" sort="Guo, Yi" uniqKey="Guo Y" first="Yi" last="Guo">Yi Guo</name>
</author>
<author><name sortKey="Hunter, Christine B" sort="Hunter, Christine B" uniqKey="Hunter C" first="Christine" last="Hunter">Christine. Hunter</name>
</author>
<author><name sortKey="Xie, Wenjie" sort="Xie, Wenjie" uniqKey="Xie W" first="Wenjie" last="Xie">Wenjie Xie</name>
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<author><name sortKey="Jankovic, Joseph" sort="Jankovic, Joseph" uniqKey="Jankovic J" first="Joseph" last="Jankovic">Joseph Jankovic</name>
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<term>Parkinson Disease (genetics)</term>
<term>Point Mutation</term>
<term>Protein-Serine-Threonine Kinases (genetics)</term>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Protein-Serine-Threonine Kinases</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Parkinson Disease</term>
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<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Point Mutation</term>
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<Month>06</Month>
<Day>06</Day>
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<DateCompleted><Year>2005</Year>
<Month>07</Month>
<Day>26</Day>
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<DateRevised><Year>2012</Year>
<Month>06</Month>
<Day>25</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0364-5134</ISSN>
<JournalIssue CitedMedium="Print"><Volume>57</Volume>
<Issue>6</Issue>
<PubDate><Year>2005</Year>
<Month>Jun</Month>
</PubDate>
</JournalIssue>
<Title>Annals of neurology</Title>
<ISOAbbreviation>Ann. Neurol.</ISOAbbreviation>
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<ArticleTitle>Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation.</ArticleTitle>
<Pagination><MedlinePgn>933-4</MedlinePgn>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Deng</LastName>
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<Language>eng</Language>
<GrantList CompleteYN="Y"><Grant><GrantID>NS 043567</GrantID>
<Acronym>NS</Acronym>
<Agency>NINDS NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant><GrantID>NS 40370</GrantID>
<Acronym>NS</Acronym>
<Agency>NINDS NIH HHS</Agency>
<Country>United States</Country>
</Grant>
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<ChemicalList><Chemical><RegistryNumber>EC 2.7.11.1</RegistryNumber>
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<MeshHeading><DescriptorName MajorTopicYN="Y" UI="D017354">Point Mutation</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D017346">Protein-Serine-Threonine Kinases</DescriptorName>
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<affiliations><list><country><li>États-Unis</li>
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<region><li>Texas</li>
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<settlement><li>Houston</li>
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<tree><noCountry><name sortKey="Deng, Hao" sort="Deng, Hao" uniqKey="Deng H" first="Hao" last="Deng">Hao Deng</name>
<name sortKey="Guo, Yi" sort="Guo, Yi" uniqKey="Guo Y" first="Yi" last="Guo">Yi Guo</name>
<name sortKey="Hunter, Christine B" sort="Hunter, Christine B" uniqKey="Hunter C" first="Christine" last="Hunter">Christine. Hunter</name>
<name sortKey="Le, Weidong" sort="Le, Weidong" uniqKey="Le W" first="Weidong" last="Le">Weidong Le</name>
<name sortKey="Xie, Wenjie" sort="Xie, Wenjie" uniqKey="Xie W" first="Wenjie" last="Xie">Wenjie Xie</name>
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<country name="États-Unis"><region name="Texas"><name sortKey="Jankovic, Joseph" sort="Jankovic, Joseph" uniqKey="Jankovic J" first="Joseph" last="Jankovic">Joseph Jankovic</name>
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Serveur d'exploration autour de Joseph Jankovic

Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation.

Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation.

Source :

English descriptors

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki