Motor progression of Parkinson's disease with the leucine-rich repeat kinase 2 G2019S mutation.
Identifieur interne : 000514 ( Main/Exploration ); précédent : 000513; suivant : 000515Motor progression of Parkinson's disease with the leucine-rich repeat kinase 2 G2019S mutation.
Auteurs : Gilad Yahalom [Israël] ; Yael Orlev ; Oren S. Cohen ; Evgenia Kozlova ; Eitan Friedman ; Rivka Inzelberg ; Sharon Hassin-BaerSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2014.
English descriptors
- KwdEn :
- Aged, Disease Progression, Female, Gene Frequency, Genetic Predisposition to Disease (genetics), Genotype, Glycine (genetics), Humans, Jews (genetics), Male, Middle Aged, Mutation (genetics), Parkinson Disease (ethnology), Parkinson Disease (genetics), Parkinson Disease (physiopathology), Protein-Serine-Threonine Kinases (genetics), Retrospective Studies.
- MESH :
- chemical , genetics : Glycine, Protein-Serine-Threonine Kinases.
- ethnology : Parkinson Disease.
- genetics : Genetic Predisposition to Disease, Jews, Mutation, Parkinson Disease.
- physiopathology : Parkinson Disease.
- Aged, Disease Progression, Female, Gene Frequency, Genotype, Humans, Male, Middle Aged, Retrospective Studies.
Abstract
In this retrospective study, we compared motor disease progression in Ashkenazi-Jewish (AJ) Parkinson's disease (PD) patients carrying the LRRK2*G2019S mutation with that of noncarriers.
DOI: 10.1002/mds.25931
PubMed: 24903616
Affiliations:
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Le document en format XML
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Cohen</name></author><author><name sortKey="Kozlova, Evgenia" sort="Kozlova, Evgenia" uniqKey="Kozlova E" first="Evgenia" last="Kozlova">Evgenia Kozlova</name></author><author><name sortKey="Friedman, Eitan" sort="Friedman, Eitan" uniqKey="Friedman E" first="Eitan" last="Friedman">Eitan Friedman</name></author><author><name sortKey="Inzelberg, Rivka" sort="Inzelberg, Rivka" uniqKey="Inzelberg R" first="Rivka" last="Inzelberg">Rivka Inzelberg</name></author><author><name sortKey="Hassin Baer, Sharon" sort="Hassin Baer, Sharon" uniqKey="Hassin Baer S" first="Sharon" last="Hassin-Baer">Sharon Hassin-Baer</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2014">2014</date><idno type="RBID">pubmed:24903616</idno><idno type="pmid">24903616</idno><idno type="doi">10.1002/mds.25931</idno><idno type="wicri:Area/PubMed/Corpus">000485</idno><idno type="wicri:Area/PubMed/Curation">000485</idno><idno type="wicri:Area/PubMed/Checkpoint">000522</idno><idno type="wicri:Area/Ncbi/Merge">004014</idno><idno type="wicri:Area/Ncbi/Curation">004014</idno><idno type="wicri:Area/Ncbi/Checkpoint">004014</idno><idno type="wicri:Area/Main/Merge">000514</idno><idno type="wicri:Area/Main/Curation">000514</idno><idno type="wicri:Area/Main/Exploration">000514</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Motor progression of Parkinson's disease with the leucine-rich repeat kinase 2 G2019S mutation.</title><author><name sortKey="Yahalom, Gilad" sort="Yahalom, Gilad" uniqKey="Yahalom G" first="Gilad" last="Yahalom">Gilad Yahalom</name><affiliation wicri:level="1"><nlm:affiliation>The Parkinson Disease and Movement Disorders Clinic, Department of Neurology and Sagol Neuroscience Center, Tel Aviv University, Tel Aviv, Israel; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.</nlm:affiliation><country xml:lang="fr">Israël</country><wicri:regionArea>The Parkinson Disease and Movement Disorders Clinic, Department of Neurology and Sagol Neuroscience Center, Tel Aviv University, Tel Aviv, Israel; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv</wicri:regionArea><wicri:noRegion>Tel Aviv</wicri:noRegion></affiliation></author><author><name sortKey="Orlev, Yael" sort="Orlev, Yael" uniqKey="Orlev Y" first="Yael" last="Orlev">Yael Orlev</name></author><author><name sortKey="Cohen, Oren S" sort="Cohen, Oren S" uniqKey="Cohen O" first="Oren S" last="Cohen">Oren S. Cohen</name></author><author><name sortKey="Kozlova, Evgenia" sort="Kozlova, Evgenia" uniqKey="Kozlova E" first="Evgenia" last="Kozlova">Evgenia Kozlova</name></author><author><name sortKey="Friedman, Eitan" sort="Friedman, Eitan" uniqKey="Friedman E" first="Eitan" last="Friedman">Eitan Friedman</name></author><author><name sortKey="Inzelberg, Rivka" sort="Inzelberg, Rivka" uniqKey="Inzelberg R" first="Rivka" last="Inzelberg">Rivka Inzelberg</name></author><author><name sortKey="Hassin Baer, Sharon" sort="Hassin Baer, Sharon" uniqKey="Hassin Baer S" first="Sharon" last="Hassin-Baer">Sharon Hassin-Baer</name></author></analytic><series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title><idno type="eISSN">1531-8257</idno><imprint><date when="2014" type="published">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Disease Progression</term><term>Female</term><term>Gene Frequency</term><term>Genetic Predisposition to Disease (genetics)</term><term>Genotype</term><term>Glycine (genetics)</term><term>Humans</term><term>Jews (genetics)</term><term>Male</term><term>Middle Aged</term><term>Mutation (genetics)</term><term>Parkinson Disease (ethnology)</term><term>Parkinson Disease (genetics)</term><term>Parkinson Disease (physiopathology)</term><term>Protein-Serine-Threonine Kinases (genetics)</term><term>Retrospective Studies</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Glycine</term><term>Protein-Serine-Threonine Kinases</term></keywords><keywords scheme="MESH" qualifier="ethnology" xml:lang="en"><term>Parkinson Disease</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Genetic Predisposition to Disease</term><term>Jews</term><term>Mutation</term><term>Parkinson Disease</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Parkinson Disease</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Disease Progression</term><term>Female</term><term>Gene Frequency</term><term>Genotype</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Retrospective Studies</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">In this retrospective study, we compared motor disease progression in Ashkenazi-Jewish (AJ) Parkinson's disease (PD) patients carrying the LRRK2*G2019S mutation with that of noncarriers.</div></front></TEI><affiliations><list><country><li>Israël</li></country></list><tree><noCountry><name sortKey="Cohen, Oren S" sort="Cohen, Oren S" uniqKey="Cohen O" first="Oren S" last="Cohen">Oren S. Cohen</name><name sortKey="Friedman, Eitan" sort="Friedman, Eitan" uniqKey="Friedman E" first="Eitan" last="Friedman">Eitan Friedman</name><name sortKey="Hassin Baer, Sharon" sort="Hassin Baer, Sharon" uniqKey="Hassin Baer S" first="Sharon" last="Hassin-Baer">Sharon Hassin-Baer</name><name sortKey="Inzelberg, Rivka" sort="Inzelberg, Rivka" uniqKey="Inzelberg R" first="Rivka" last="Inzelberg">Rivka Inzelberg</name><name sortKey="Kozlova, Evgenia" sort="Kozlova, Evgenia" uniqKey="Kozlova E" first="Evgenia" last="Kozlova">Evgenia Kozlova</name><name sortKey="Orlev, Yael" sort="Orlev, Yael" uniqKey="Orlev Y" first="Yael" last="Orlev">Yael Orlev</name></noCountry><country name="Israël"><noRegion><name sortKey="Yahalom, Gilad" sort="Yahalom, Gilad" uniqKey="Yahalom G" first="Gilad" last="Yahalom">Gilad Yahalom</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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