adrenal axis and its relationship with central respiratory dysfunction in children with Prader-Willi syndrom
Contains fulltext : 81198.pdf (publisher's version ) (Closed access)BACKGROUND: Th...
Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement. The literatur...
This thesis presents a detailed description of several studies on growth, metabolism, psychomotor de...
Background: Children with Prader-Willi Syndrome (PWS) have been considered at risk for central adren...
Purpose: Prader Willi syndrome (PWS) is a rare genetic condition that has concurrent endocrinologica...
Purpose: Prader Willi syndrome (PWS) is a rare genetic condition that has concurrent endocrinologica...
Introduction: It has been postulated that central adrenal insufficiency (CAI), resulting from hypoth...
OBJECTIVE: A recent study evidenced by metyrapone test a central adrenal insufficiency (CAI) in 60% ...
textabstractBackground: Prader-Willi syndrome (PWS) is a complex neurodevelopmental disorder, charac...
Background: Children with Prader Willi syndrome (PWS) are at risk of sleep disordered breathing invo...
Prader-Willi syndrome is a complex endocrinological and developmental disorder characterized by hype...
International audiencePrader-Willi syndrome is a rare genetic neurodevelopmental disorder resulting ...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
Context: Prader-Willi syndrome (PWS) is characterized by hypothalamic dysfunction. In children with ...
Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement. The literatur...
Contains fulltext : 81198.pdf (publisher's version ) (Closed access)BACKGROUND: Th...
Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement. The literatur...
This thesis presents a detailed description of several studies on growth, metabolism, psychomotor de...
Background: Children with Prader-Willi Syndrome (PWS) have been considered at risk for central adren...
Purpose: Prader Willi syndrome (PWS) is a rare genetic condition that has concurrent endocrinologica...
Purpose: Prader Willi syndrome (PWS) is a rare genetic condition that has concurrent endocrinologica...
Introduction: It has been postulated that central adrenal insufficiency (CAI), resulting from hypoth...
OBJECTIVE: A recent study evidenced by metyrapone test a central adrenal insufficiency (CAI) in 60% ...
textabstractBackground: Prader-Willi syndrome (PWS) is a complex neurodevelopmental disorder, charac...
Background: Children with Prader Willi syndrome (PWS) are at risk of sleep disordered breathing invo...
Prader-Willi syndrome is a complex endocrinological and developmental disorder characterized by hype...
International audiencePrader-Willi syndrome is a rare genetic neurodevelopmental disorder resulting ...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
Context: Prader-Willi syndrome (PWS) is characterized by hypothalamic dysfunction. In children with ...
Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement. The literatur...
Contains fulltext : 81198.pdf (publisher's version ) (Closed access)BACKGROUND: Th...
Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement. The literatur...
This thesis presents a detailed description of several studies on growth, metabolism, psychomotor de...