Background: Prader-Willi syndrome (PWS) is known for hyperphagia with impaired satiety and a specific behavioural phenotype with stubbornness, temper tantrums, manipulative and controlling behaviour and obsessive
Temper outbursts are a persistent cause of morbidity for people with Prader-Willi syndrome (PWS), fo...
Obesity is the most common cause of metabolic complications and poor quality of life in Prader–Willi...
Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients wi...
textabstractBackground: Prader-Willi syndrome (PWS) is known for hyperphagia with impaired satiety a...
Context: Prader-Willi syndrome (PWS) is characterized by hypothalamic dysfunction, hyperphagia and a...
Prader-Willi syndrome (PWS) is a rare, complex multisystem genetic disorder which includes hypothala...
International audienceBACKGROUND: Prader-Willi syndrome (PWS) is a complex neurodevelopmental geneti...
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...
Background Prader-Willi Syndrome (PWS) is a complex genetic syndrome associated with hyperphagia ...
BackgroundOxytocin and vasopressin systems are altered in Prader Willi syndrome (PWS). However, inve...
Prader-Willi syndrome (PWS) is a rare genetic syndrome affecting around 1 in 20,000 births in France...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by the absence of paternally exp...
The role of endogenous oxytocin as neuromodulator of birth, lactation and social behaviors is well-r...
Prader-Willi syndrome (PWS) is a complex, genetic, neurodevelopmental disorder. PWS has three molecu...
Temper outbursts are a persistent cause of morbidity for people with Prader-Willi syndrome (PWS), fo...
Obesity is the most common cause of metabolic complications and poor quality of life in Prader–Willi...
Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients wi...
textabstractBackground: Prader-Willi syndrome (PWS) is known for hyperphagia with impaired satiety a...
Context: Prader-Willi syndrome (PWS) is characterized by hypothalamic dysfunction, hyperphagia and a...
Prader-Willi syndrome (PWS) is a rare, complex multisystem genetic disorder which includes hypothala...
International audienceBACKGROUND: Prader-Willi syndrome (PWS) is a complex neurodevelopmental geneti...
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...
Background Prader-Willi Syndrome (PWS) is a complex genetic syndrome associated with hyperphagia ...
BackgroundOxytocin and vasopressin systems are altered in Prader Willi syndrome (PWS). However, inve...
Prader-Willi syndrome (PWS) is a rare genetic syndrome affecting around 1 in 20,000 births in France...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by the absence of paternally exp...
The role of endogenous oxytocin as neuromodulator of birth, lactation and social behaviors is well-r...
Prader-Willi syndrome (PWS) is a complex, genetic, neurodevelopmental disorder. PWS has three molecu...
Temper outbursts are a persistent cause of morbidity for people with Prader-Willi syndrome (PWS), fo...
Obesity is the most common cause of metabolic complications and poor quality of life in Prader–Willi...
Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients wi...