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Association of DRD3 and GRIN2B with Impulse Control and Related Behaviors in Parkinson's Disease

Autor
LEE, Jee-Young1 ; EUN KYUNG LEE2 ; SUNG SUP PARK2 3 ; LIM, Ji-Yeon2 ; HEE JIN KIM2 4 ; JI SUN KIM5 ; JEON, Beom S2 4 6
[1] Department of Neurology, Inje University Ilsan Paik Hospital, Goyang, Korea, Republic of
[2] Clinical Research Institute and Movement Disorders Center, Seoul National University Hospital, Seoul, Korea, Republic of
[3] Department of Laboratory Medicine, Seoul National University Hospital, Seoul, Korea, Republic of
[4] Department of Neurology, Seoul National University Hospital, Seoul, Korea, Republic of
[5] Department of Neurology, Seoul National University Bundang Hospital, Seongnam, Korea, Republic of
[6] Neuroscience Research Institute, College of Medicine, Seoul National University, Seoul, Korea, Republic of
Fuente

Movement disorders. 2009, Vol 24, Num 12, pp 1803-1810, 8 p ; ref : 37 ref

ISSN
0885-3185
Campo Científico
Neurology
Editor
Wiley, Hoboken, NJ
País de la publicación
United States
Tipo de documento
Article
Idioma
English
Palabra clave de autor
Parkinson's disease dopamine receptor genetic association glutamate NMDA receptor type 2B impulse control and related behavior serotonin transporter
Palabra clave (fr)
Comportement Maladie de Parkinson Pathologie du système nerveux Récepteur NMDA Récepteur dopaminergique Récepteur glutamate Transporteur sérotonine Maladie dégénérative Pathologie de l'encéphale Pathologie du système nerveux central Syndrome extrapyramidal
Palabra clave (in)
Behavior Parkinson disease Nervous system diseases NMDA receptor Dopamine receptor Glutamate receptor Serotonin transporter Degenerative disease Cerebral disorder Central nervous system disease Extrapyramidal syndrome
Palabra clave (es)
Conducta Parkinson enfermedad Sistema nervioso patología Receptor NMDA Receptor dopaminérgico Receptor glutámato Enfermedad degenerativa Encéfalo patología Sistema nervosio central patología Extrapiramidal síndrome
Clasificación
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17G Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases

Disciplina
Neurology
Procedencia
Inist-CNRS
Base de datos
PASCAL
Identificador INIST
22005674

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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