The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study.
Identifieur interne : 004161 ( Ncbi/Curation ); précédent : 004160; suivant : 004162The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study.
Auteurs : Madeleine E. Sharp [États-Unis] ; Elise Caccappolo ; Helen Mejia-Santana ; Ming-X Tang ; Llency Rosado ; Martha Orbe Reilly ; Diana Ruiz ; Elan D. Louis ; Cynthia Comella ; Martha Nance ; Susan Bressman ; William K. Scott ; Caroline Tanner ; Cheryl Waters ; Stanley Fahn ; Lucien Cote ; Blair Ford ; Michael Rezak ; Kevin Novak ; Joseph H. Friedman ; Ronald Pfeiffer ; Haydeh Payami ; Eric Molho ; Stuart A. Factor ; John Nutt ; Carmen Serrano ; Maritza Arroyo ; Michael W. Pauciulo ; William C. Nichols ; Lorraine N. Clark ; Roy N. Alcalay ; Karen S. MarderSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2015.
English descriptors
- KwdEn :
- Adult, Age of Onset, Aged, Female, Genetic Predisposition to Disease, Genetic Testing, Genotype, Heterozygote, Humans, Male, Middle Aged, Mutation (genetics), Obsessive-Compulsive Disorder (etiology), Obsessive-Compulsive Disorder (genetics), Parkinson Disease (complications), Parkinson Disease (genetics), Ubiquitin-Protein Ligases (genetics).
- MESH :
- chemical , genetics : Ubiquitin-Protein Ligases.
- complications : Parkinson Disease.
- etiology : Obsessive-Compulsive Disorder.
- genetics : Mutation, Obsessive-Compulsive Disorder, Parkinson Disease.
- Adult, Age of Onset, Aged, Female, Genetic Predisposition to Disease, Genetic Testing, Genotype, Heterozygote, Humans, Male, Middle Aged.
Abstract
Few studies have systematically investigated the association between PARKIN genotype and psychiatric co-morbidities of Parkison's disease (PD). PARKIN-associated PD is characterized by severe nigral dopaminergic neuronal loss, a finding that may have implications for behaviors rooted in dopaminergic circuits such as obsessive-compulsive symptoms (OCS).
DOI: 10.1002/mds.26065
PubMed: 25393808
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pubmed:25393808Le document en format XML
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<term>Aged</term>
<term>Female</term>
<term>Genetic Predisposition to Disease</term>
<term>Genetic Testing</term>
<term>Genotype</term>
<term>Heterozygote</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Mutation (genetics)</term>
<term>Obsessive-Compulsive Disorder (etiology)</term>
<term>Obsessive-Compulsive Disorder (genetics)</term>
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<term>Obsessive-Compulsive Disorder</term>
<term>Parkinson Disease</term>
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<term>Age of Onset</term>
<term>Aged</term>
<term>Female</term>
<term>Genetic Predisposition to Disease</term>
<term>Genetic Testing</term>
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<front><div type="abstract" xml:lang="en">Few studies have systematically investigated the association between PARKIN genotype and psychiatric co-morbidities of Parkison's disease (PD). PARKIN-associated PD is characterized by severe nigral dopaminergic neuronal loss, a finding that may have implications for behaviors rooted in dopaminergic circuits such as obsessive-compulsive symptoms (OCS).</div>
</front>
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