ParkinsonFranceV1, PubMed, Corpus, bibRecord, 000C48

Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

Identifieur interne : 000C48 ( PubMed/Corpus ); précédent : 000C47; suivant : 000C49

Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

Auteurs : S. Lesage ; S. Belarbi ; A. Troiano ; C. Condroyer ; N. Hecham ; P. Pollak ; E. Lohman ; T. Benhassine ; F. Ysmail-Dahlouk ; A. Dürr ; M. Tazir ; A. Brice

Source :

Neurology [ 1526-632X ] ; 2008.

RBID : pubmed:18981379

English descriptors

KwdEn :
- Adolescent, Adult, Africa, Northern, Aged, Aged, 80 and over, Child, Dyskinesias (genetics), Female, Humans, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Male, Middle Aged, Parkinson Disease (genetics), Parkinson Disease (physiopathology), Point Mutation, Protein-Serine-Threonine Kinases (genetics).
MESH :
- chemical , genetics : Protein-Serine-Threonine Kinases.
- chemical : Leucine-Rich Repeat Serine-Threonine Protein Kinase-2.
- genetics : Dyskinesias, Parkinson Disease.
- physiopathology : Parkinson Disease.
- Adolescent, Adult, Africa, Northern, Aged, Aged, 80 and over, Child, Female, Humans, Male, Middle Aged, Point Mutation.

DOI: 10.1212/01.wnl.0000338460.89796.06
PubMed: 18981379

Links to Exploration step

pubmed:18981379

Le document en format XML

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<affiliation><nlm:affiliation>INSERM UMR 679 (former U289), Hôpital de la Salpêtrière, Paris Cedex 13, France.</nlm:affiliation>
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<author><name sortKey="Belarbi, S" sort="Belarbi, S" uniqKey="Belarbi S" first="S" last="Belarbi">S. Belarbi</name>
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<author><name sortKey="Troiano, A" sort="Troiano, A" uniqKey="Troiano A" first="A" last="Troiano">A. Troiano</name>
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<author><name sortKey="Condroyer, C" sort="Condroyer, C" uniqKey="Condroyer C" first="C" last="Condroyer">C. Condroyer</name>
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<author><name sortKey="Hecham, N" sort="Hecham, N" uniqKey="Hecham N" first="N" last="Hecham">N. Hecham</name>
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<author><name sortKey="Pollak, P" sort="Pollak, P" uniqKey="Pollak P" first="P" last="Pollak">P. Pollak</name>
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<author><name sortKey="Lohman, E" sort="Lohman, E" uniqKey="Lohman E" first="E" last="Lohman">E. Lohman</name>
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<author><name sortKey="Benhassine, T" sort="Benhassine, T" uniqKey="Benhassine T" first="T" last="Benhassine">T. Benhassine</name>
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<author><name sortKey="Ysmail Dahlouk, F" sort="Ysmail Dahlouk, F" uniqKey="Ysmail Dahlouk F" first="F" last="Ysmail-Dahlouk">F. Ysmail-Dahlouk</name>
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<author><name sortKey="Durr, A" sort="Durr, A" uniqKey="Durr A" first="A" last="Dürr">A. Dürr</name>
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<author><name sortKey="Tazir, M" sort="Tazir, M" uniqKey="Tazir M" first="M" last="Tazir">M. Tazir</name>
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<author><name sortKey="Brice, A" sort="Brice, A" uniqKey="Brice A" first="A" last="Brice">A. Brice</name>
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<author><name sortKey="Ysmail Dahlouk, F" sort="Ysmail Dahlouk, F" uniqKey="Ysmail Dahlouk F" first="F" last="Ysmail-Dahlouk">F. Ysmail-Dahlouk</name>
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<author><name sortKey="Durr, A" sort="Durr, A" uniqKey="Durr A" first="A" last="Dürr">A. Dürr</name>
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<author><name sortKey="Tazir, M" sort="Tazir, M" uniqKey="Tazir M" first="M" last="Tazir">M. Tazir</name>
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<author><name sortKey="Brice, A" sort="Brice, A" uniqKey="Brice A" first="A" last="Brice">A. Brice</name>
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<term>Dyskinesias (genetics)</term>
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<term>Parkinson Disease (physiopathology)</term>
<term>Point Mutation</term>
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<term>Parkinson Disease</term>
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<term>Adult</term>
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<term>Aged, 80 and over</term>
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	La maladie de Parkinson en France (serveur d'exploration)
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La maladie de Parkinson en France (serveur d'exploration)

Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson 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