We compared body composition, biochemical parameters, motor function, and brain neural activation in 27 adults with Prader–Willi syndrome and growth-hormone deficiency versus age-and sex-matched controls and baseline versus posttreatment values of these parameters after one year of recombinant human growth hormone (rhGH) treatment. To study body composition, we analyzed percentage of fat mass, percentage of lean mass, and muscle-mass surrogate variables from dual X-ray absorptiometry. Biochemical parameters analyzed included IGF-I, glucose metabolism, and myokines (myostatin, irisin, and IL6). To explore muscle function, we used dynamometer-measured handgrip strength, the Timed Up and Go (TUG) test, and the Berg Balance Scale (BBS). To stud...
Summary. The effects of 6 months of recombinant growth hormone (GH) treatment (0–5 IU kg‐1 per week)...
Pharmacological treatment of growth hormone deficiency (GHD) in adults began in clinical practice mo...
Prader Willi syndrome (PWS) is a complex multi system genetic disorder, including severe neonatal hy...
We compared body composition, biochemical parameters, motor function, and brain neural activation in...
Altres ajuts: Fundació Parc Taulí CIR2020/022We compared body composition, biochemical parameters, m...
Recombinant human growth hormone (rhGH) treatment is an established management in patients with Prad...
BACKGROUND: Prader-Willi syndrome (PWS) is associated with an inappropriate proportion of fat mass (...
OBJECTIVE: Since limited data exist on adults with Prader-Willi syndrome (PWS) and growth hormone (G...
Context:In adults with Prader-Willi syndrome (PWS), abnormal body composition with decreased lean bo...
Prader Willi Syndrome (PWS) is a complex genetic disorder characterized by muscular hypotonia, hyper...
AbstractMotor problems in Prader–Willi syndrome (PWS) are presumably related to abnormal body compos...
Prader-Willi syndrome (PWS) is characterized by hyperphagia, obesity if food intake is not strictly ...
Purpose: Early institution of GH therapy in children with Prader–Willi syndrome (PWS) yields benefic...
Background: In children with Prader-Willi syndrome (PWS), the benefits of growth hormone treatment a...
Objective: To assess the effects of growth hormone (GH) replacement in an individual who sustained m...
Summary. The effects of 6 months of recombinant growth hormone (GH) treatment (0–5 IU kg‐1 per week)...
Pharmacological treatment of growth hormone deficiency (GHD) in adults began in clinical practice mo...
Prader Willi syndrome (PWS) is a complex multi system genetic disorder, including severe neonatal hy...
We compared body composition, biochemical parameters, motor function, and brain neural activation in...
Altres ajuts: Fundació Parc Taulí CIR2020/022We compared body composition, biochemical parameters, m...
Recombinant human growth hormone (rhGH) treatment is an established management in patients with Prad...
BACKGROUND: Prader-Willi syndrome (PWS) is associated with an inappropriate proportion of fat mass (...
OBJECTIVE: Since limited data exist on adults with Prader-Willi syndrome (PWS) and growth hormone (G...
Context:In adults with Prader-Willi syndrome (PWS), abnormal body composition with decreased lean bo...
Prader Willi Syndrome (PWS) is a complex genetic disorder characterized by muscular hypotonia, hyper...
AbstractMotor problems in Prader–Willi syndrome (PWS) are presumably related to abnormal body compos...
Prader-Willi syndrome (PWS) is characterized by hyperphagia, obesity if food intake is not strictly ...
Purpose: Early institution of GH therapy in children with Prader–Willi syndrome (PWS) yields benefic...
Background: In children with Prader-Willi syndrome (PWS), the benefits of growth hormone treatment a...
Objective: To assess the effects of growth hormone (GH) replacement in an individual who sustained m...
Summary. The effects of 6 months of recombinant growth hormone (GH) treatment (0–5 IU kg‐1 per week)...
Pharmacological treatment of growth hormone deficiency (GHD) in adults began in clinical practice mo...
Prader Willi syndrome (PWS) is a complex multi system genetic disorder, including severe neonatal hy...