Objective: Paternal deletion and maternal uniparental disomy are the principal genetic subtypes associated with Prader-Willi syndrome (PWS). Recent clinical findings suggest differences in phenotype between these subtypes. The present experimental study addresses this issue using a cognitive psycho-physiological setup. Methods: Behaviour and event-related brain activity (ERP) was recorded by a continuous performance response inhibition task (CPT-AX) in adults with paternal deletion PWS (n = 11), maternal uniparental disomy PWS (n= 11) and normal controls (n = 11). The dependent behavioural variables of the CPT-AX task were reaction time and correct scores. For the ERPs the N200 and P300 components were included which are related to early mo...
Abstract Background Prader-Willi syndrome (PWS) is a complex disorder caused by impaired paternally ...
Background: Prader-Willi Syndrome (PWS) is a complex neurogenetic disorder with symptoms involving n...
Background and Objectives: Several studies have suggested a difference in clinical features of intel...
Objective: Paternal deletion and maternal uniparental disomy are the principal genetic subtypes asso...
Prader Willi Syndrome (PWS) is a neuro-genetic disorder. It has been reported that cases due to pate...
ABSTRACT. Objective. To determine whether pheno-typic differences exist among individuals with Prade...
Prader-Willi syndrome (PWS) is caused by a deficiency of imprinted genes in the 15q11-q13 region and...
A number of developmental disorders of genetic origin show atypical aspects of face processing. Howe...
A number of developmental disorders of genetic origin show atypical aspects of face processing. Howe...
Background: Prader-Willi syndrome (PWS) is a genetic disorder caused by the absence of expression ...
Here we describe the genetic studies performed in 53 patients with the suspected diagnosis of Prader...
BACKGROUND: Behavioural phenotypes associated with genetic syndromes have been extensively investiga...
Previous work has suggested that there are specific deficits in dorsal stream processing in a variet...
textabstractBackground: Prader-Willi Syndrome (PWS) is a complex neurogenetic disorder with symptoms...
Prader-Willi syndrome (PWS) is a rare disorder caused by the loss of expression of genes on the pate...
Abstract Background Prader-Willi syndrome (PWS) is a complex disorder caused by impaired paternally ...
Background: Prader-Willi Syndrome (PWS) is a complex neurogenetic disorder with symptoms involving n...
Background and Objectives: Several studies have suggested a difference in clinical features of intel...
Objective: Paternal deletion and maternal uniparental disomy are the principal genetic subtypes asso...
Prader Willi Syndrome (PWS) is a neuro-genetic disorder. It has been reported that cases due to pate...
ABSTRACT. Objective. To determine whether pheno-typic differences exist among individuals with Prade...
Prader-Willi syndrome (PWS) is caused by a deficiency of imprinted genes in the 15q11-q13 region and...
A number of developmental disorders of genetic origin show atypical aspects of face processing. Howe...
A number of developmental disorders of genetic origin show atypical aspects of face processing. Howe...
Background: Prader-Willi syndrome (PWS) is a genetic disorder caused by the absence of expression ...
Here we describe the genetic studies performed in 53 patients with the suspected diagnosis of Prader...
BACKGROUND: Behavioural phenotypes associated with genetic syndromes have been extensively investiga...
Previous work has suggested that there are specific deficits in dorsal stream processing in a variet...
textabstractBackground: Prader-Willi Syndrome (PWS) is a complex neurogenetic disorder with symptoms...
Prader-Willi syndrome (PWS) is a rare disorder caused by the loss of expression of genes on the pate...
Abstract Background Prader-Willi syndrome (PWS) is a complex disorder caused by impaired paternally ...
Background: Prader-Willi Syndrome (PWS) is a complex neurogenetic disorder with symptoms involving n...
Background and Objectives: Several studies have suggested a difference in clinical features of intel...