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 …

Objective: The objective of the study was to provide recommendations for the diagnosis and
management of Prader-Willi syndrome throughout the life span to guide clinical practice …

After sagittal division of the prosencephalon at 4.5 weeks of gestation, the early fetal
cerebral hemisphere bends or rotates posteroventrally from seven weeks of gestation. The …

In the chapter, we explore the relationship between the peptide hormone, oxytocin (OT), and
behavioral and metabolic disturbances observed in the genetic disorder Prader-Willi …

Despite behavioral differences between genetic subtypes of Prader–Willi syndrome (PWS),
no studies have been published characterizing brain structure in these subgroups. Our goal …

Prader–Willi syndrome (PWS) is a genetic imprinting disorder characterized mainly by
hyperphagia and early childhood obesity. Previous functional neuroimaging studies used …

Prader-Willi syndrome (PWS) is a neurodevelopmental disorder of genomic imprinting,
presenting with a behavioural phenotype encompassing hyperphagia, intellectual disability …

The planum temporale is a region on the posterior surface of the temporal lobe that exhibits
robust leftward structural asymmetry, which has been linked to verbal ability in children and …

Prader-Willi syndrome (PWS) is a relatively rare disorder that originates from paternally
inherited deletions and maternal disomy (mUPD) within the 15q11-q13 region or alterations …

Transcranial direct current stimulation (tDCS) is a non-invasive technique for brain
stimulation and it increasingly being used in the treatments of some neurological/psychiatric …