Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder involving nutritional, endocrine /metabolic, emotional and behavior dimensions. There is evidence for impaired hypothalamic development and function in PWS, involving oxytocin and ghrelin, which can account for the typical PWS phenotype. Hyperphagia with addiction-like behavior is one of the common features of PWS and is a consequence of the hypothalamic dysfunction. In this study, we hypothesized that brain regions associated with compulsive eating behavior would be abnormally activated by food-related odors in PWS, as these can stimulate the appetite and induce hunger-related behavior
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder of genomic imprinting, presenting with ...
Prader-Willi syndrome (PWS) is a genetic imprinting disorder that is mainly characterized by hyperph...
Prader-Willi syndrome (PWS) is the leading genetic cause of obesity, caused by the loss of expressio...
Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder involving nutritional, end...
Prader-Willi syndrome is a rare neurodevelopmental genetic disorder characterized by various endocri...
To investigate, based on a putative abnormal neural processing of disgusting signals in Prader Willi...
This study focused on genetic and behavioural aspects of one important component of the motivation t...
(1) Background: Prader-Willi syndrome (PWS) is characterized by hyperphagia, resulting in morbid obe...
Hyperphagia and the associated interest in food is a characteristic feature of Prader-Willi syndrome...
Hyperphagia is one of the main problems of patients with Prader-Willi syndrome (PWS) to cope with ev...
Hyperphagia is one of the main problems of patients with Prader-Willi syndrome (PWS) to cope with ev...
Obesity is the most common cause of metabolic complications and poor quality of life in Prader-Willi...
(1) Background: Prader–Willi syndrome (PWS) is characterized by hyperphagia, resulting in morbid obe...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by the absence of paternally exp...
Prader-Willi Syndrome (PWS) is a rare and incurable congenital neurodevelopmental disorder, resultin...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder of genomic imprinting, presenting with ...
Prader-Willi syndrome (PWS) is a genetic imprinting disorder that is mainly characterized by hyperph...
Prader-Willi syndrome (PWS) is the leading genetic cause of obesity, caused by the loss of expressio...
Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder involving nutritional, end...
Prader-Willi syndrome is a rare neurodevelopmental genetic disorder characterized by various endocri...
To investigate, based on a putative abnormal neural processing of disgusting signals in Prader Willi...
This study focused on genetic and behavioural aspects of one important component of the motivation t...
(1) Background: Prader-Willi syndrome (PWS) is characterized by hyperphagia, resulting in morbid obe...
Hyperphagia and the associated interest in food is a characteristic feature of Prader-Willi syndrome...
Hyperphagia is one of the main problems of patients with Prader-Willi syndrome (PWS) to cope with ev...
Hyperphagia is one of the main problems of patients with Prader-Willi syndrome (PWS) to cope with ev...
Obesity is the most common cause of metabolic complications and poor quality of life in Prader-Willi...
(1) Background: Prader–Willi syndrome (PWS) is characterized by hyperphagia, resulting in morbid obe...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by the absence of paternally exp...
Prader-Willi Syndrome (PWS) is a rare and incurable congenital neurodevelopmental disorder, resultin...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder of genomic imprinting, presenting with ...
Prader-Willi syndrome (PWS) is a genetic imprinting disorder that is mainly characterized by hyperph...
Prader-Willi syndrome (PWS) is the leading genetic cause of obesity, caused by the loss of expressio...