MovDisordV3, PubMed, Corpus, bibRecord, 000E17

Identical twins with Leucine rich repeat kinase type 2 mutations discordant for Parkinson's disease.

Identifieur interne : 000E17 ( PubMed/Corpus ); précédent : 000E16; suivant : 000E18

Identical twins with Leucine rich repeat kinase type 2 mutations discordant for Parkinson's disease.

Auteurs : Georgia Xiromerisiou ; Henry Houlden ; Anna Sailer ; Laura Silveira-Moriyama ; John Hardy ; Andrew J. Lees

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2012.

RBID : pubmed:22488887

English descriptors

KwdEn :
- Aged, Humans, Male, Mutation (genetics), Parkinson Disease (genetics), Protein-Serine-Threonine Kinases (genetics), Twins, Monozygotic (genetics).
MESH :
- chemical , genetics : Protein-Serine-Threonine Kinases.
- genetics : Mutation, Parkinson Disease, Twins, Monozygotic.
- Aged, Humans, Male.

DOI: 10.1002/mds.24924
PubMed: 22488887

Links to Exploration step

pubmed:22488887

Le document en format XML

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<author><name sortKey="Xiromerisiou, Georgia" sort="Xiromerisiou, Georgia" uniqKey="Xiromerisiou G" first="Georgia" last="Xiromerisiou">Georgia Xiromerisiou</name>
</author>
<author><name sortKey="Houlden, Henry" sort="Houlden, Henry" uniqKey="Houlden H" first="Henry" last="Houlden">Henry Houlden</name>
</author>
<author><name sortKey="Sailer, Anna" sort="Sailer, Anna" uniqKey="Sailer A" first="Anna" last="Sailer">Anna Sailer</name>
</author>
<author><name sortKey="Silveira Moriyama, Laura" sort="Silveira Moriyama, Laura" uniqKey="Silveira Moriyama L" first="Laura" last="Silveira-Moriyama">Laura Silveira-Moriyama</name>
</author>
<author><name sortKey="Hardy, John" sort="Hardy, John" uniqKey="Hardy J" first="John" last="Hardy">John Hardy</name>
</author>
<author><name sortKey="Lees, Andrew J" sort="Lees, Andrew J" uniqKey="Lees A" first="Andrew J" last="Lees">Andrew J. Lees</name>
</author>
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<author><name sortKey="Xiromerisiou, Georgia" sort="Xiromerisiou, Georgia" uniqKey="Xiromerisiou G" first="Georgia" last="Xiromerisiou">Georgia Xiromerisiou</name>
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<author><name sortKey="Houlden, Henry" sort="Houlden, Henry" uniqKey="Houlden H" first="Henry" last="Houlden">Henry Houlden</name>
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<author><name sortKey="Sailer, Anna" sort="Sailer, Anna" uniqKey="Sailer A" first="Anna" last="Sailer">Anna Sailer</name>
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<author><name sortKey="Silveira Moriyama, Laura" sort="Silveira Moriyama, Laura" uniqKey="Silveira Moriyama L" first="Laura" last="Silveira-Moriyama">Laura Silveira-Moriyama</name>
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<author><name sortKey="Hardy, John" sort="Hardy, John" uniqKey="Hardy J" first="John" last="Hardy">John Hardy</name>
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<author><name sortKey="Lees, Andrew J" sort="Lees, Andrew J" uniqKey="Lees A" first="Andrew J" last="Lees">Andrew J. Lees</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<term>Humans</term>
<term>Male</term>
<term>Mutation (genetics)</term>
<term>Parkinson Disease (genetics)</term>
<term>Protein-Serine-Threonine Kinases (genetics)</term>
<term>Twins, Monozygotic (genetics)</term>
</keywords>
<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>Mutation</term>
<term>Parkinson Disease</term>
<term>Twins, Monozygotic</term>
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<DateCreated><Year>2012</Year>
<Month>09</Month>
<Day>14</Day>
</DateCreated>
<DateCompleted><Year>2013</Year>
<Month>02</Month>
<Day>14</Day>
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<DateRevised><Year>2015</Year>
<Month>01</Month>
<Day>14</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1531-8257</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>27</Volume>
<Issue>10</Issue>
<PubDate><Year>2012</Year>
<Month>Sep</Month>
<Day>1</Day>
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</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
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<ArticleTitle>Identical twins with Leucine rich repeat kinase type 2 mutations discordant for Parkinson's disease.</ArticleTitle>
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<ForeName>Georgia</ForeName>
<Initials>G</Initials>
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<Author ValidYN="Y"><LastName>Houlden</LastName>
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<Author ValidYN="Y"><LastName>Sailer</LastName>
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<Author ValidYN="Y"><LastName>Silveira-Moriyama</LastName>
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<Author ValidYN="Y"><LastName>Hardy</LastName>
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<Initials>J</Initials>
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<Author ValidYN="Y"><LastName>Lees</LastName>
<ForeName>Andrew J</ForeName>
<Initials>AJ</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<GrantList CompleteYN="Y"><Grant><GrantID>089698</GrantID>
<Agency>Wellcome Trust</Agency>
<Country>United Kingdom</Country>
</Grant>
<Grant><GrantID>G-0907</GrantID>
<Agency>Parkinson's UK</Agency>
<Country>United Kingdom</Country>
</Grant>
<Grant><GrantID>G0701075</GrantID>
<Agency>Medical Research Council</Agency>
<Country>United Kingdom</Country>
</Grant>
<Grant><GrantID>G0802760</GrantID>
<Agency>Medical Research Council</Agency>
<Country>United Kingdom</Country>
</Grant>
<Grant><Agency>Medical Research Council</Agency>
<Country>United Kingdom</Country>
</Grant>
<Grant><Agency>Wellcome Trust</Agency>
<Country>United Kingdom</Country>
</Grant>
</GrantList>
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<PublicationType UI="D052061">Research Support, N.I.H., Extramural</PublicationType>
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<ArticleDate DateType="Electronic"><Year>2012</Year>
<Month>04</Month>
<Day>04</Day>
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<MedlineJournalInfo><Country>United States</Country>
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<NlmUniqueID>8610688</NlmUniqueID>
<ISSNLinking>0885-3185</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>EC 2.7.11.1</RegistryNumber>
<NameOfSubstance UI="C495280">LRRK2 protein, human</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>EC 2.7.11.1</RegistryNumber>
<NameOfSubstance UI="D017346">Protein-Serine-Threonine Kinases</NameOfSubstance>
</Chemical>
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<CitationSubset>IM</CitationSubset>
<CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Neuropathol Appl Neurobiol. 2009 Aug;35(4):427-32</RefSource>
<PMID Version="1">19207267</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Lancet. 2005 Jan 29-Feb 4;365(9457):415-6</RefSource>
<PMID Version="1">15680457</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141B(6):681</RefSource>
<PMID Version="1">16823802</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Lancet Neurol. 2008 Jul;7(7):583-90</RefSource>
<PMID Version="1">18539534</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Nat Rev Neurosci. 2008 Oct;9(10):741-5</RefSource>
<PMID Version="1">18769444</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Neuron. 2004 Nov 18;44(4):595-600</RefSource>
<PMID Version="1">15541308</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Neuron. 2004 Nov 18;44(4):601-7</RefSource>
<PMID Version="1">15541309</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>JAMA. 1999 Jan 27;281(4):341-6</RefSource>
<PMID Version="1">9929087</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Neurology. 2001 Apr 10;56(7):981-2</RefSource>
<PMID Version="1">11294946</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="CommentIn"><RefSource>Mov Disord. 2013 Apr;28(4):561-2</RefSource>
<PMID Version="1">23450721</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="CommentIn"><RefSource>Mov Disord. 2013 Apr;28(4):561</RefSource>
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<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D000368">Aged</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D009154">Mutation</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D010300">Parkinson Disease</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D017346">Protein-Serine-Threonine Kinases</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D014430">Twins, Monozygotic</DescriptorName>
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	Movement Disorders (revue)
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Movement Disorders (revue)

Identical twins with Leucine rich repeat kinase type 2 mutations discordant for Parkinson's disease.

Identical twins with Leucine rich repeat kinase type 2 mutations discordant for Parkinson's disease.

Source :

English descriptors

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