Prader-Willi syndrome (PWS) is a complex hypothalamic disorder. Features of PWS include hyperphagia, hypotonia, intellectual disability, and pituitary hormone deficiencies. The combination of growth hormone treatment and multidisciplinary care (GHMDc) has greatly improved the health of children with PWS. Little is known about the effects of childhood GHMDc on health outcomes in adulthood. We retrospectively collected clinical data of 109 adults with PWS. Thirty-nine had received GHMDc during childhood and adolescence (GHMDc+ group) and sixty-three had never received growth hormone treatment (GHt) nor multidisciplinary care (GHMDc− group). Our systematic screening revealed fewer undetected health problems in the GHMDc+ group (10%) than in th...
Introduction: Prader-Willi syndrome (PWS) is a complex disorder resulting from the failure of expres...
Introduction and objective: Prader-Willi syndrome (PWS) is a severe genetic disorder being manifeste...
textabstractThe first patient with Prader-Willi syndrome (PWS), described in 1887 by Langdon-Down1 (...
Prader-Willi syndrome (PWS) is a complex hypothalamic disorder. Features of PWS include hyperphagia,...
Prader Willi syndrome (PWS) is a complex multi system genetic disorder, including severe neonatal hy...
Prader-Willi syndrome (PWS) is characterized by hyperphagia, obesity if food intake is not strictly ...
Abstract Growth hormone treatment for children with Prader Willi syndrome (PWS) has shown proven ben...
Background: In children with Prader-Willi syndrome (PWS), the benefits of growth hormone treatment a...
Prader-Willi syndrome (PWS) is the most common cause of morbid obesity in childhood. It is the conse...
Prader Willi Syndrome (PWS) is a complex genetic disorder characterized by muscular hypotonia, hyper...
OBJECTIVE: Since limited data exist on adults with Prader-Willi syndrome (PWS) and growth hormone (G...
Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement. The literatur...
Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement. The literatur...
OBJECTIVE: Some features of subjects with Prader-Willi syndrome (PWS) resemble those seen in growth ...
Prader-Willi syndrome (PWS) is a complex, multi-system, neurodevelopmental disorder characterised by...
Introduction: Prader-Willi syndrome (PWS) is a complex disorder resulting from the failure of expres...
Introduction and objective: Prader-Willi syndrome (PWS) is a severe genetic disorder being manifeste...
textabstractThe first patient with Prader-Willi syndrome (PWS), described in 1887 by Langdon-Down1 (...
Prader-Willi syndrome (PWS) is a complex hypothalamic disorder. Features of PWS include hyperphagia,...
Prader Willi syndrome (PWS) is a complex multi system genetic disorder, including severe neonatal hy...
Prader-Willi syndrome (PWS) is characterized by hyperphagia, obesity if food intake is not strictly ...
Abstract Growth hormone treatment for children with Prader Willi syndrome (PWS) has shown proven ben...
Background: In children with Prader-Willi syndrome (PWS), the benefits of growth hormone treatment a...
Prader-Willi syndrome (PWS) is the most common cause of morbid obesity in childhood. It is the conse...
Prader Willi Syndrome (PWS) is a complex genetic disorder characterized by muscular hypotonia, hyper...
OBJECTIVE: Since limited data exist on adults with Prader-Willi syndrome (PWS) and growth hormone (G...
Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement. The literatur...
Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement. The literatur...
OBJECTIVE: Some features of subjects with Prader-Willi syndrome (PWS) resemble those seen in growth ...
Prader-Willi syndrome (PWS) is a complex, multi-system, neurodevelopmental disorder characterised by...
Introduction: Prader-Willi syndrome (PWS) is a complex disorder resulting from the failure of expres...
Introduction and objective: Prader-Willi syndrome (PWS) is a severe genetic disorder being manifeste...
textabstractThe first patient with Prader-Willi syndrome (PWS), described in 1887 by Langdon-Down1 (...