Contains fulltext : 89221.pdf (publisher's version ) (Closed access)Background Individuals with Prader-Willi syndrome (PWS) are at risk of sleep disturbances, such as excessive daytime sleepiness (EDS) and sleep apnoea, and behavioural problems. Sleep disturbances and their relationship with other variables had not been researched extensively in adults with PWS. Method Sleep disturbances and behavioural problems were investigated in adults with genetically confirmed PWS using standardised questionnaires. Results of adults with paternal deletion (n = 45) were compared with those of adults with maternal uniparental disomy (n = 33). Results Eleven adults with PWS (i.e. 15%) had a current sleep problem, mostly night waking pro...
Prader-Willi syndrome (PWS) is an imprinted genetic disorder conferred by loss of paternal gene expr...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
textabstractObjective: The objective of the study was to provide recommendations for the diagnosis a...
Background Individuals with Prader-Willi syndrome (PWS) are at risk of sleep disturbances, such as e...
Study Objectives: Excessive sleepiness is a common symptom in Prader–Willi syndrome (PWS), and it ne...
To assess whether sleep abnormalities are related to the genetic abnormalities in Prader-Willi Syndr...
Prader–Willi syndrome (PWS) is a rare, genetic, multisymptomatic, neurodevelopmental disease commonl...
Prader Willi Syndrome (PWS) is a rare genetic disorder characterized by a range of physical, psychol...
Background: Children with Prader Willi syndrome (PWS) are at risk of sleep disordered breathing invo...
Prader–Willi syndrome (PWS) is a rare, genetic, multisymptomatic, neurodevelopmental disease commonl...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, mental retardation...
Objectives To determine the prevalence and type of sleep-disordered breathing among patients with Pr...
Contains fulltext : 77351.pdf (publisher's version ) (Closed access
Contains fulltext : 81198.pdf (publisher's version ) (Closed access)BACKGROUND: Th...
Purpose of review Although several studies in the last years have evaluated obesity, obstructive sle...
Prader-Willi syndrome (PWS) is an imprinted genetic disorder conferred by loss of paternal gene expr...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
textabstractObjective: The objective of the study was to provide recommendations for the diagnosis a...
Background Individuals with Prader-Willi syndrome (PWS) are at risk of sleep disturbances, such as e...
Study Objectives: Excessive sleepiness is a common symptom in Prader–Willi syndrome (PWS), and it ne...
To assess whether sleep abnormalities are related to the genetic abnormalities in Prader-Willi Syndr...
Prader–Willi syndrome (PWS) is a rare, genetic, multisymptomatic, neurodevelopmental disease commonl...
Prader Willi Syndrome (PWS) is a rare genetic disorder characterized by a range of physical, psychol...
Background: Children with Prader Willi syndrome (PWS) are at risk of sleep disordered breathing invo...
Prader–Willi syndrome (PWS) is a rare, genetic, multisymptomatic, neurodevelopmental disease commonl...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, mental retardation...
Objectives To determine the prevalence and type of sleep-disordered breathing among patients with Pr...
Contains fulltext : 77351.pdf (publisher's version ) (Closed access
Contains fulltext : 81198.pdf (publisher's version ) (Closed access)BACKGROUND: Th...
Purpose of review Although several studies in the last years have evaluated obesity, obstructive sle...
Prader-Willi syndrome (PWS) is an imprinted genetic disorder conferred by loss of paternal gene expr...
Prader-Willi syndrome (PWS) is a genetic disorder characterized by short stature, low lean body mass...
textabstractObjective: The objective of the study was to provide recommendations for the diagnosis a...