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Neural correlates of executive functions in healthy G2019S LRRK2 mutation carriers

Author
THALER, Avner1 2 ; MIRELMAN, Anat1 3 ; GILADI, Nir1 2 ; HENDLER, Talma2 5 ; HELMICH, Rick C4 ; VAN NUENEN, Bart F. L4 ; ROSENBERG-KATZ, Keren2 5 ; GUREVICH, Tanya1 2 ; ORR-URTREGER, Avi2 6 ; MARDER, Karen7 ; BRESSMAN, Susan8 ; BLOEM, Bastiaan R4
[1] Movement Disorders Unit, Department of Neurology, Tel-Aviv Sourasky Medical Center, Israel
[2] Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel
[3] School for Health Professional, Ben-Gurion University, Beer Sheba, Israel
[4] Radboud University Nijmegen Medical Centre, Donders Institute for Brain, Cognition and Behaviour, Department of Neurology, Nijmegen, Netherlands
[5] Functional Brain Center, Wohl Institute for Advanced Imaging, Tel-Aviv Sourasky Medical Center, Israel
[6] Genetic Institute, Tel Aviv Sourasky Medical Center, Israel
[7] Columbia University, Columbia University Medical Center, New York, NY, United States
[8] Beth Israel Medical Center, New York, NY, United States
LRRK2 Ashkenazi Jewish consortium
Source

Cortex (Testo stampato). 2013, Vol 49, Num 9, pp 2501-2511, 11 p ; ref : 1 p.3/4

CODEN
CRTXAZ
ISSN
0010-9452
Scientific domain
Neurology; Psychophysiology; Psychology, psychopathology, psychiatry
Publisher
Elsevier, Kidlington
Publication country
United Kingdom
Document type
Article
Language
English
Author keyword
Executive functions LRRK2 Parkinson's disease Stroop task
Keyword (fr)
Effet Stroop Etude expérimentale Fonction exécutive Gène Homme Individu sain Maladie de Parkinson Mutation Porteur Gène LRRK2 Cognition Déterminisme génétique Génétique Maladie dégénérative Pathologie de l'encéphale Pathologie du système nerveux central Pathologie du système nerveux Syndrome extrapyramidal
Keyword (en)
Stroop effect Experimental study Executive function Gene Human Healthy subject Parkinson disease Mutation Carrier Cognition Genetic determinism Genetics Degenerative disease Cerebral disorder Central nervous system disease Nervous system diseases Extrapyramidal syndrome
Keyword (es)
Efecto Stroop Estudio experimental Función ejecutiva Gen Hombre Individuo sano Parkinson enfermedad Mutación Portador Cognición Determinismo genético Genética Enfermedad degenerativa Encéfalo patología Sistema nervosio central patología Sistema nervioso patología Extrapiramidal síndrome
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17A Nervous system (semeiology, syndromes) / 002B17A01 Nervous system as a whole

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17G Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B18 Psychopathology. Psychiatry / 002B18C Adult and adolescent clinical studies / 002B18C13 Organic mental disorders. Neuropsychology

Francis
770 Psychology. Psychoanalysis. Psychiatry / 770-D Psychopathology. Psychiatry / 770-D03 Adult and adolescent clinical studies / 770-D03M Organic mental disorders. Neuropsychology

Discipline
Neurology Psychopathology. Psychiatry. Clinical psychology
Origin
Inist-CNRS
Database
FRANCIS ; PASCAL
INIST identifier
27868368

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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