Prader-Willi syndrome (PWS) is a complex neurobehavioral condition which has been classically described as having two nutritional stages: poor feeding, frequently with failure to thrive (FTT) in infancy (Stage 1), followed by hyperphagia leading to obesity in later childhood (Stage 2). We have longitudinally followed the feeding behaviors of individuals with PWS and found a much more gradual and complex progression of the nutritional phases than the traditional two stages described in the literature. Therefore, this study characterizes the growth, metabolic, and laboratory changes associated with the various nutritional phases of PWS in a large cohort of subjects. We have identified a total of seven different nutritional phases, with five m...
Prader-Willi syndrome (PWS) is an imprinting genetic disorder characterized by lack of expression of...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
Prader-Willi syndrome (PWS) is a disorder comprisingsevere neonatal hypotonia, hypogonadism, gross o...
Prader-Willi syndrome (PWS) is a complex neurobehavioral condition which has been classically descri...
Prader–Willi syndrome (PWS) is a complex neurobehavioral condition which has been classically descri...
Obesity is the most common cause of metabolic complications and poor quality of life in Prader-Willi...
Prader-Willi syndrome (PWS) is a genetic disorder that people inherit from their parents. It can be ...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by the absence of paternally exp...
Prader-Willi syndrome (PWS) is caused by a lack of expression of paternally-expressed imprinted gene...
Prader-Willi Syndrome (PWS) is a rare and incurable congenital neurodevelopmental disorder, resultin...
Hyperphagia is one of the main problems of patients with Prader-Willi syndrome (PWS) to cope with ev...
BACKGROUND: Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder with different...
Prader-Willi syndrome (PWS) is the leading genetic cause of obesity, caused by the loss of expressio...
Hyperphagia is one of the main problems of patients with Prader-Willi syndrome (PWS) to cope with ev...
Antonino Crinò,1 Danilo Fintini,2 Sarah Bocchini,1 Graziano Grugni3 1Autoimmune Endocrine Dis...
Prader-Willi syndrome (PWS) is an imprinting genetic disorder characterized by lack of expression of...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
Prader-Willi syndrome (PWS) is a disorder comprisingsevere neonatal hypotonia, hypogonadism, gross o...
Prader-Willi syndrome (PWS) is a complex neurobehavioral condition which has been classically descri...
Prader–Willi syndrome (PWS) is a complex neurobehavioral condition which has been classically descri...
Obesity is the most common cause of metabolic complications and poor quality of life in Prader-Willi...
Prader-Willi syndrome (PWS) is a genetic disorder that people inherit from their parents. It can be ...
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by the absence of paternally exp...
Prader-Willi syndrome (PWS) is caused by a lack of expression of paternally-expressed imprinted gene...
Prader-Willi Syndrome (PWS) is a rare and incurable congenital neurodevelopmental disorder, resultin...
Hyperphagia is one of the main problems of patients with Prader-Willi syndrome (PWS) to cope with ev...
BACKGROUND: Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder with different...
Prader-Willi syndrome (PWS) is the leading genetic cause of obesity, caused by the loss of expressio...
Hyperphagia is one of the main problems of patients with Prader-Willi syndrome (PWS) to cope with ev...
Antonino Crinò,1 Danilo Fintini,2 Sarah Bocchini,1 Graziano Grugni3 1Autoimmune Endocrine Dis...
Prader-Willi syndrome (PWS) is an imprinting genetic disorder characterized by lack of expression of...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
Prader-Willi syndrome (PWS) is a disorder comprisingsevere neonatal hypotonia, hypogonadism, gross o...