Contains fulltext : 98113.pdf (publisher's version ) (Closed access)Motor problems in Prader-Willi syndrome (PWS) are presumably related to abnormal body composition and certain neuromuscular abnormalities. The authors reviewed the literature to evaluate the extent to which body composition is affected and gathered all findings on neuromuscular functioning in PWS. A systematic review was conducted in four databases (1956-2010). The methodological quality of each included article was evaluated. Thirty-eight papers were included: body composition (9 studies), neuromuscular functioning (7) and growth hormone (GH) effect studies (23). Increased fat mass and decreased lean body mass are characteristics of PWS. As a result, musc...
The aim of this systematic review was to summarize evidence on the acute responses of individuals wi...
Prader-Willi syndrome (PWS) is characterized by hyperphagia, obesity if food intake is not strictly ...
textabstractThe first patient with Prader-Willi syndrome (PWS), described in 1887 by Langdon-Down1 (...
Motor problems in Prader-Willi syndrome (PWS) are presumably related to abnormal body composition an...
AbstractMotor problems in Prader–Willi syndrome (PWS) are presumably related to abnormal body compos...
Item does not contain fulltextAlthough motor problems in Prader-Willi syndrome (PWS) are prominent i...
Children and adults with Prader-Willi syndrome are usually overweight, if not obese. Nevertheless, i...
This review is aiming to review and analysis the Prader -Willi Syndrome. The present review was cond...
OBJECTIVE: To investigate the effect of physical training combined with growth hormone (GH) on muscl...
We compared body composition, biochemical parameters, motor function, and brain neural activation in...
Although severe motor problems in infants with Prader-Willi syndrome (PWS) are striking, motor devel...
BACKGROUND: Prader-Willi syndrome (PWS) is associated with an inappropriate proportion of fat mass (...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
OBJECTIVE: To study the relationship of fat mass, extracellular-to-intracellular-water ratio, and bo...
Contains fulltext : 234058.pdf (Publisher’s version ) (Open Access)Prader-Labhart-...
The aim of this systematic review was to summarize evidence on the acute responses of individuals wi...
Prader-Willi syndrome (PWS) is characterized by hyperphagia, obesity if food intake is not strictly ...
textabstractThe first patient with Prader-Willi syndrome (PWS), described in 1887 by Langdon-Down1 (...
Motor problems in Prader-Willi syndrome (PWS) are presumably related to abnormal body composition an...
AbstractMotor problems in Prader–Willi syndrome (PWS) are presumably related to abnormal body compos...
Item does not contain fulltextAlthough motor problems in Prader-Willi syndrome (PWS) are prominent i...
Children and adults with Prader-Willi syndrome are usually overweight, if not obese. Nevertheless, i...
This review is aiming to review and analysis the Prader -Willi Syndrome. The present review was cond...
OBJECTIVE: To investigate the effect of physical training combined with growth hormone (GH) on muscl...
We compared body composition, biochemical parameters, motor function, and brain neural activation in...
Although severe motor problems in infants with Prader-Willi syndrome (PWS) are striking, motor devel...
BACKGROUND: Prader-Willi syndrome (PWS) is associated with an inappropriate proportion of fat mass (...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
OBJECTIVE: To study the relationship of fat mass, extracellular-to-intracellular-water ratio, and bo...
Contains fulltext : 234058.pdf (Publisher’s version ) (Open Access)Prader-Labhart-...
The aim of this systematic review was to summarize evidence on the acute responses of individuals wi...
Prader-Willi syndrome (PWS) is characterized by hyperphagia, obesity if food intake is not strictly ...
textabstractThe first patient with Prader-Willi syndrome (PWS), described in 1887 by Langdon-Down1 (...