Prader-Willi syndrome (PWS) is a rare, complex multisystem genetic disorder which includes hypothalamic dysfunction, hyperphagia, cognitive and behavioral problems, increased anxiety, and compulsive behaviors. Individuals with PWS have a deficit of oxytocin producing neurons in the paraventricular nucleus of the hypothalamus. Oxytocin plays a role in regulation of feeding behaviors, social interactions, and emotional reactivity, which are all issues that significantly affect the quality of life for individuals with this syndrome. We performed a double-blind, placebo-controlled, crossover study in 24 children with PWS at three academic institutions using 5 days of intranasal oxytocin (IN-OT) or 5 days of intranasal placebo spray, followed by...
Prader-Willi Syndrome (PWS) is a genetic imprinting disorder mainly caused by the absence of paterna...
Prader-Willi syndrome (PWS) is a rare neurodevelopmental genetic disorder associated with a characte...
INTRODUCTION:Prader-Willi syndrome (PWS) is a complex genetic condition characterized by hyperphagia...
textabstractBackground: Prader-Willi syndrome (PWS) is known for hyperphagia with impaired satiety a...
International audienceBACKGROUND: Prader-Willi syndrome (PWS) is a complex neurodevelopmental geneti...
Context: Prader-Willi syndrome (PWS) is characterized by hypothalamic dysfunction, hyperphagia and a...
BACKGROUND AND OBJECTIVES: Patients with Prader–Willi syndrome (PWS) display poor feeding and social...
OBJECTIVE: The objective of this selective EBM review is to determine whether or not intranasal oxyt...
Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients wi...
International audienceAbstract The prosocial neuropeptide oxytocin is being developed as a potential...
Prader-Willi syndrome (PWS) is a complex, genetic, neurodevelopmental disorder. PWS has three molecu...
BackgroundOxytocin and vasopressin systems are altered in Prader Willi syndrome (PWS). However, inve...
Prader-Willi syndrome (PWS) is a complex genetic disorder with three genetic classes. Patients with ...
Temper outbursts are a persistent cause of morbidity for people with Prader-Willi syndrome (PWS), fo...
Abstract Background Phelan-McDermid syndrome (PMS) is a rare neurodevelopmental disorder caused by h...
Prader-Willi Syndrome (PWS) is a genetic imprinting disorder mainly caused by the absence of paterna...
Prader-Willi syndrome (PWS) is a rare neurodevelopmental genetic disorder associated with a characte...
INTRODUCTION:Prader-Willi syndrome (PWS) is a complex genetic condition characterized by hyperphagia...
textabstractBackground: Prader-Willi syndrome (PWS) is known for hyperphagia with impaired satiety a...
International audienceBACKGROUND: Prader-Willi syndrome (PWS) is a complex neurodevelopmental geneti...
Context: Prader-Willi syndrome (PWS) is characterized by hypothalamic dysfunction, hyperphagia and a...
BACKGROUND AND OBJECTIVES: Patients with Prader–Willi syndrome (PWS) display poor feeding and social...
OBJECTIVE: The objective of this selective EBM review is to determine whether or not intranasal oxyt...
Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients wi...
International audienceAbstract The prosocial neuropeptide oxytocin is being developed as a potential...
Prader-Willi syndrome (PWS) is a complex, genetic, neurodevelopmental disorder. PWS has three molecu...
BackgroundOxytocin and vasopressin systems are altered in Prader Willi syndrome (PWS). However, inve...
Prader-Willi syndrome (PWS) is a complex genetic disorder with three genetic classes. Patients with ...
Temper outbursts are a persistent cause of morbidity for people with Prader-Willi syndrome (PWS), fo...
Abstract Background Phelan-McDermid syndrome (PMS) is a rare neurodevelopmental disorder caused by h...
Prader-Willi Syndrome (PWS) is a genetic imprinting disorder mainly caused by the absence of paterna...
Prader-Willi syndrome (PWS) is a rare neurodevelopmental genetic disorder associated with a characte...
INTRODUCTION:Prader-Willi syndrome (PWS) is a complex genetic condition characterized by hyperphagia...