Background: Prader-Willi syndrome (PWS) is a complex developmental genetic disorder associated with intellectual disability and deficits in executive functions which result in disorganisation and poor personal autonomy. Aims: This study aimed to determine impairments in planning skills of adults with PWS, in relation with their intellectual disabilities, as well as the influence of food compulsions on their performance. Methods and procedures: A modified version of the Zoo Map from the Behavioural Assessment of the Dysexecutive Syndrome was used in three groups: a group of adults with PWS in comparison with two groups both matched on chronological age, one with typical development (TD) and one with intellectual disability (ID). Ou...
The purpose of this paper is to present an overview of the psychological characteristics associated ...
BACKGROUND: Individuals with Prader-Willi syndrome (PWS) have been shown to demonstrate a particular...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder of genomic imprinting, presenting with ...
Background: Prader-Willi syndrome (PWS) is a genetic disorder caused by the absence of expression ...
Background: Prader-Willi syndrome (PWS) is a neurodevelopmental genetic disorder involving executive...
Prader-Willi Syndrome (PWS) is a neurodevelopmental genetic disorder with executive deficits. Planni...
Le Syndrome de Prader-Willi (SPW) est une maladie neuro-développementale rare d’origine génétique as...
Background: Maladaptive behavior has been reported as a phenotypical feature in Prader–Willi syndrom...
The aim of this study was to support the growing evidence suggesting that Prader-Willi Syndrome (PWS...
Individuals with Prader-Willi syndrome (PWS) are at risk for psychopathology due to their maladaptiv...
We present a mini-review of cognition in Prader-Willi syndrome. Studies cited include findings on ge...
Background The goal of the current study was to determine if the Dementia Rating Scale-2 (DRS-2) is ...
© 2018 International Strategic Management Association. All rights reserved. Aim: The article is devo...
Le syndrome de Prader-Willi (SPW) est une maladieneurodéveloppementale rare d’origine génétique dont...
Background: Prader-Willi Syndrome (PWS) is a complex neurogenetic disorder with symptoms involving n...
The purpose of this paper is to present an overview of the psychological characteristics associated ...
BACKGROUND: Individuals with Prader-Willi syndrome (PWS) have been shown to demonstrate a particular...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder of genomic imprinting, presenting with ...
Background: Prader-Willi syndrome (PWS) is a genetic disorder caused by the absence of expression ...
Background: Prader-Willi syndrome (PWS) is a neurodevelopmental genetic disorder involving executive...
Prader-Willi Syndrome (PWS) is a neurodevelopmental genetic disorder with executive deficits. Planni...
Le Syndrome de Prader-Willi (SPW) est une maladie neuro-développementale rare d’origine génétique as...
Background: Maladaptive behavior has been reported as a phenotypical feature in Prader–Willi syndrom...
The aim of this study was to support the growing evidence suggesting that Prader-Willi Syndrome (PWS...
Individuals with Prader-Willi syndrome (PWS) are at risk for psychopathology due to their maladaptiv...
We present a mini-review of cognition in Prader-Willi syndrome. Studies cited include findings on ge...
Background The goal of the current study was to determine if the Dementia Rating Scale-2 (DRS-2) is ...
© 2018 International Strategic Management Association. All rights reserved. Aim: The article is devo...
Le syndrome de Prader-Willi (SPW) est une maladieneurodéveloppementale rare d’origine génétique dont...
Background: Prader-Willi Syndrome (PWS) is a complex neurogenetic disorder with symptoms involving n...
The purpose of this paper is to present an overview of the psychological characteristics associated ...
BACKGROUND: Individuals with Prader-Willi syndrome (PWS) have been shown to demonstrate a particular...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder of genomic imprinting, presenting with ...