The Small Nucleolar Host Gene 14 (SNHG14) is a host gene for small non-coding RNAs,
including the SNORD116 small nucleolar C/D box RNA encoding locus. Large deletions of …

Prader–Willi syndrome (PWS), a rare epigenetic disease mapping the imprinted
chromosomal domain of 15q11. 2-q13. 3, manifests a regular neurodevelopmental trajectory …

Background Hyperphagia is a key symptom in patients with monogenic obesity, but the
assessment is challenging. Objectives We aimed to investigate the applicability of Dykens' …

Severe hypotonia during infancy is a hallmark feature of Prader Willi syndrome (PWS).
Despite its transient expression, moto development is delayed and deficiencies in motor …

Prader-Willi syndrome (PWS) is a complex, genetic disorder characterized by multisystem
involvement, including hyperphagia, maladaptive behaviors and endocrinological …

Abstract Individuals with Prader–Willi syndrome (PWS) exhibit complex behavioral
characteristics, including hyperphagia, autistic features, and subsequent age-related …

Ultra-high field magnetic resonance imaging (MRI) has been introduced for use in pediatric
developmental neurology. While higher magnetic fields have certain advantages, optimized …

We compared body composition, biochemical parameters, motor function, and brain neural
activation in 27 adults with Prader–Willi syndrome and growth-hormone deficiency versus …

Abstract Purpose Prader-Willi syndrome (PWS) suffers from brain functional reorganization
and developmental delays during childhood, but the underlying neurodevelopmental …

Introduction: Prader-Willi syndrome (PWS) is a multisystem genetic imprinting disorder
mainly characterized by hyperphagia and childhood obesity. Extensive structural alterations …