Introductory comments—Special section
Plasma obestatin and ghrelin levels in subjects with Prader–Willi syndrome
Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader–Willi syndrome
Whole genome microarray analysis of gene expression in Prader–Willi syndrome
Two years of growth hormone therapy in young children with Prader–Willi syndrome
Energy expenditure and physical activity in Prader–Willi syndrome
Clinical-etiologic correlation in children with Prader-Willi syndrome (PWS)
X-chromosome inactivation patterns in females with Prader–Willi syndrome
Intracranial abnormalities detected by three-dimensional magnetic resonance imaging in Prader–Willi syndrome
Deaths due to choking in Prader–Willi syndrome
Thyroid function studies in Prader–Willi syndrome
001. NECDIN AND MAGEL2
002. BIOMARKERS FOR PEDIATRIC TYPE 2 DIABETES IN SUBJECTS WITH PRADER-WILLI SYNDROME
003. PSYCHIATRIC RESILIENCE AMONG INDIVIDUALS WITH PRADER-WILLI SYNDROME AND PRESUMED MATERNAL UNIPARENTAL DISOMY WARRANTING FURTHER GENETIC TESTING
004. AUTISTIC PHENOTYPE AND HYPERPHAGIA IN AN ADOLESCENT MALE WITH PATERNAL MICRODELETION OF GABRB3
005. PSYCHIATRIC PHENOMENOLOGY OF MOOD ACTIVATION IN PRADER-WILLI SYNDROME
006. PSYCHOPATHOLOGIC DISORDER IN PRADER-WILLI SYNDROME
007. COGNITIVE AND BEHAVIORAL FINDINGS IN PRADER-WILLI SYNDROME AND EARLY-ONSET MORBID OBESITY
008. THE USE OF PSYCHOTROPIC MEDICATIONS IN PRADER-WILLI SYNDROME
009. SLEEP IN PRADER-WILLI SYNDROME
010. STABILIZATION OF SCOLIOSIS IN SUBJECTS WITH PRADER-WILLI SYNDROME TREATED WITH GH-THERAPY
011. PRADER-WILLI SYNDROME ASSOCIATION (USA) DATABASE COLLECTION UNCOVER AREAS OF NEEDED RESEARCH
012. CAUSES OF DEATH IN PRADER-WILLI SYNDROME UTILIZING THE PRADER-WILLI SYNDROME ASSOCIATION USA BEREAVEMENT PROGRAM
013. ASSESSMENT OF ENERGY EXPENDITURE IN PRADER-WILLI SYNDROME
014. GROWTH HORMONE EFFECTS IN INFANTS AND TODDLERS WITH PRADER-WILLI SYNDROME
015. THE EXISTENCE AND EXPERIENCE OF BODY IMAGE IN INDIVIDUALS WITH PRADER-WILLI SYNDROME
016. LACK OF SATIETY
Book review
Phenotypic spectrum of mosaic trisomy 18
Trisomy 13 mosaicism in a phenotypically normal child