Prader-Willi syndrome (PWS) is a rare and complex genetic disorder with multiple effects on the metabolic, endocrine, and neurological systems, as well as behavioral and intellectual difficulties. Despite advances in understanding the genetic basis of obesity in PWS, there are conflicting data on its management. Therefore, the present manuscript aims to provide an update on the nutritional treatment and pharmacological approach in adult patients with PWS
Prader-Willi syndrome (PWS) is a complex, genetic, neurodevelopmental disorder. PWS has three molecu...
In early childhood, individuals with Prader-Willi syndrome (PWS) experience excess weight gain and s...
Prader Willi syndrome (PWS) is a complex multi system genetic disorder, including severe neonatal hy...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
Prader-Willi Syndrome (PWS) is a rare genetic disorder characterized by physical, psychological and ...
Prader-Willi syndrome (PWS) is a genetic disorder that people inherit from their parents. It can be ...
Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement. The literatur...
This review is aiming to review and analysis the Prader -Willi Syndrome. The present review was cond...
Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement. The literatur...
Antonino Crinò,1 Danilo Fintini,2 Sarah Bocchini,1 Graziano Grugni3 1Autoimmune Endocrine Dis...
Prader-Willi Syndrome (PWS) is a genetic disorder caused by a lack of the 11q-13q segment of the pat...
Prader-Willi Syndrome (PWS) is a genetic imprinting disorder mainly caused by the absence of paterna...
Prader-Willi syndrome (PWS) is the leading genetic cause of obesity, caused by the loss of expressio...
Prader-Willi syndrome (PWS) is characterized by hyperphagia, obesity if food intake is not strictly ...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by the absence of paternally exp...
Prader-Willi syndrome (PWS) is a complex, genetic, neurodevelopmental disorder. PWS has three molecu...
In early childhood, individuals with Prader-Willi syndrome (PWS) experience excess weight gain and s...
Prader Willi syndrome (PWS) is a complex multi system genetic disorder, including severe neonatal hy...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
Prader-Willi Syndrome (PWS) is a rare genetic disorder characterized by physical, psychological and ...
Prader-Willi syndrome (PWS) is a genetic disorder that people inherit from their parents. It can be ...
Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement. The literatur...
This review is aiming to review and analysis the Prader -Willi Syndrome. The present review was cond...
Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement. The literatur...
Antonino Crinò,1 Danilo Fintini,2 Sarah Bocchini,1 Graziano Grugni3 1Autoimmune Endocrine Dis...
Prader-Willi Syndrome (PWS) is a genetic disorder caused by a lack of the 11q-13q segment of the pat...
Prader-Willi Syndrome (PWS) is a genetic imprinting disorder mainly caused by the absence of paterna...
Prader-Willi syndrome (PWS) is the leading genetic cause of obesity, caused by the loss of expressio...
Prader-Willi syndrome (PWS) is characterized by hyperphagia, obesity if food intake is not strictly ...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by the absence of paternally exp...
Prader-Willi syndrome (PWS) is a complex, genetic, neurodevelopmental disorder. PWS has three molecu...
In early childhood, individuals with Prader-Willi syndrome (PWS) experience excess weight gain and s...
Prader Willi syndrome (PWS) is a complex multi system genetic disorder, including severe neonatal hy...