• "Unable to Feed My Hungry Child": Experiences of Mothers Caring for Children With Prader-Willi Syndrome
• 14 and 6 Hz like spike wave activity is a common finding in in young patients with Prader-Willi syndrome
• A Case Report of Acute Saddle Pulmonary Embolism in Prader-Willi Syndrome
• A genetic condition that spans both extremes of the nutritional spectrum
• A supervised learning method for classifying methylation disorders
• Aberrant behavior checklist in youth with Prader-Willi syndrome: Preliminary study of cross-sectional and longitudinal behavior characterization
• Acquiring social safety engages oxytocin neurons in the supraoptic nucleus - role of Magel2 deficiency
• Activation of the imprinted Prader-Willi Syndrome locus by CRISPR-based epigenome editing
• Age-Related Blood Levels of Creatine Kinase-MM in Newborns and Patients with Duchenne Muscular Dystrophy: Considerations for the Development of Newborn Screening Algorithms
• Anti-Müllerian hormone, testicular descent and cryptorchidism
• Bardet-Biedl syndrome: A clinical overview focusing on diagnosis, outcomes and best-practice management
• Behavioral changes in patients with Prader-Willi syndrome receiving diazoxide choline extended-release tablets compared to the PATH for PWS natural history study
• Body weight, behaviours of concern, and social contact in adults and adolescents with Prader-Willi syndrome in full-time care services: Findings from pooled international archival data
• Case Report: Plummer's adenoma in Prader-Willi syndrome
• Comparative analysis of emotional facial expression recognition and empathy in children with prader-willi syndrome and autism spectrum disorder
• Complex Cardiovascular Morbidities in Prader-Willi Syndrome: A Multidisciplinary Approach
• Congenital Central Hypoventilation Syndrome and Disorders of Control of Ventilation
• Correction notice: Growth hormone treatment in Prader-Willi syndrome patients: systematic review and meta-analysis
• Corrigendum: Kidney disease in adults with Prader-Willi syndrome: international cohort study and systematic literature review
• Cyclogram-based evaluation of inter-limb gait symmetry in Prader-Willi Syndrome
• Deficiency in Prader-Willi syndrome gene necdin leads to attenuated cardiac contractility
• Diagnosis and management of children and adult craniopharyngiomas: a French Endocrine Society/French Society for Paediatric Endocrinology & Diabetes Consensus Statement
• Diagnosis of Two Unrelated Syndromes of Prader-Willi and Calpainopathy: Insight from Trio Whole Genome Analysis and Isodisomy Mapping
• Differential DNA methylation in iPSC-derived dopaminergic neurons: a step forward on the role of SNORD116 microdeletion in the pathophysiology of addictive behavior in Prader-Willi syndrome
• Disengagement of somatostatin neurons from lateral septum circuitry by oxytocin and vasopressin restores social-fear extinction and suppresses aggression outbursts in Prader-Willi syndrome model
• Early onset stage III diabetic nephropathy in a child with Prader-Willi syndrome treated with dulaglutide: a case report
• Editorial: Innovative approaches and therapeutic perspectives for early-onset neurodevelopmental disorders: from bench to bedside
• Effect of semaglutide on weight loss and glycaemic control in patients with Prader-Willi Syndrome and type 2 diabetes
• Efficacy of a Remote Play-Based Intervention for Children With Prader-Willi Syndrome
• Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation
• Epigenetics in rare neurological diseases
• Establishing a Standardized DNA Extraction Method Using NaCl from Oral Mucosa Cells for Its Application in Imprinting Diseases Such as Prader-Willi and Angelman Syndromes: A Preliminary Investigation
• Examination of sensory reception and integration abilities in children with and without Prader-Willi syndrome
• Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11-q13 imprinting region
• Exploring the Complex Interplay of Obesity, Allergic Diseases, and Sleep-Disordered Breathing in Children
• Exploring the Diagnostic Complexity of Diabetes Subtypes in Pediatric Obesity: A Case Report of an Adolescent With Prader-Willi Phenotype and Literature Review
• Feasibility, safety, and efficacy of dietary or lifestyle interventions for hypothalamic obesity: A systematic review
• Genotype-phenotype characteristics of 57 patients with Prader-Willi syndrome: a single-center experience from Turkey
• GNB1 and obesity: Evidence for a correlation between haploinsufficiency and syndromic obesity
• Herlyn-Werner-Wunderlinch: An unusual presentation in a patient with Prader-Willi syndrome
• High-resolution genomic profiling and locus-specific FISH in subcutaneous and visceral adipose tissue of obese patients
• Hyperphagia and impulsivity: use of self-administered Dykens' and in-house impulsivity questionnaires to characterize eating behaviors in children with severe and early-onset obesity
• Impact of exenatide on weight loss and eating behavior in adults with craniopharyngioma-related obesity: the CRANIOEXE randomized placebo-controlled trial
• Implication of locus coeruleus dysfunction in Prader-Willi syndrome: Insights from a mouse model
• Imprinting disorders in children conceived with assisted reproductive technology in Sweden
• Integration of CTCF Loops, Methylome, and Transcriptome in Differentiating LUHMES as a Model for Imprinting Dynamics of the 15q11-q13 Locus in Human Neurons
• Integration of CTCF loops, methylome, and transcriptome in differentiating LUHMES as a model for imprinting dynamics of the 15q11-q13 locus in human neurons
• Investigating the correlation between genotype and phenotype in Prader-Willi syndrome: a study of 45 cases from Brazil
• Laryngeal clefts in Prader-Willi syndrome: Feeding difficulties and aspiration not always caused by hypotonia
• Lessons from two patients with Prader-Willi syndrome attributed to heterodisomy and isodisomy
• Long-term effect of growth hormone on sleep-disordered breathing in Malaysian children with Prader-Willi syndrome: a retrospective study
• Loss-of-function G6PD variant moderated high fat diet-induced obesity, adipocyte hypertrophy, and fatty liver in male rats
• MAGEL2 (patho-)physiology and Schaaf-Yang syndrome
• Mechanism of EHMT2-mediated genomic imprinting associated with Prader-Willi syndrome
• Metabolomic profiling of Prader-Willi syndrome compared with essential obesity
• Methods of Determining Energy Expenditure in Individuals with Prader-Willi Syndrome: A Systematic Literature Review
• Microduplication and Microdeletion Syndromes Diagnosed Prenatally Using Single Nucleotide Polymorphism Array
• Microglial phagolysosome dysfunction and altered neural communication amplify phenotypic severity in Prader-Willi Syndrome with larger deletion
• NanoImprint: A DNA methylation tool for clinical interpretation and diagnosis of common imprinting disorders using nanopore long-read sequencing
• Neuromodulation for the treatment of Prader-Willi syndrome - A systematic review
• Neuropsychiatry of Histaminergic Circuits: Potential Role of Novel H3 Receptor Selective Antagonist/Inverse Agonist Pitolisant in Prader-Willi Syndrome
• Newly developed oral bioavailable EHMT2 inhibitor as a potential epigenetic therapy for Prader-Willi syndrome
• Orthopedic manifestations in children with Prader-Willi syndrome
• Outcomes of growth hormone treatment in children with Prader-Willi syndrome over a 30-year period: a single tertiary center experience
• Pathological analysis of Prader-Willi syndrome using adipocytes
• Pharmacogenomics for Prader-Willi syndrome: caregiver interest and planned utilization
• Population-Based Risk of Psychiatric Disorders Associated With Recurrent Copy Number Variants
• Postural-motor development, spinal range of movement and caregiver burden in Prader-Willi syndrome-associated scoliosis: an observational study
• Prader Willi syndrome, its psychiatric implications and their possible biological basis
• Prader-Willi Syndrome: guidance for children and transition into adulthood
• Prader-Willi Syndrome: The More We Know, the Less We Know
• Prediction of LncRNA-protein Interactions Using Auto-Encoder, SE-ResNet Models and Transfer Learning
• Premature pubarche in Prader-Willi syndrome: Risk factors and consequences
• Prevalence and genotypic associations of epilepsy in Prader-Willi Syndrome: A systematic review and meta-analysis
• Prostate-specific antigen (PSA) levels in men with Prader-Willi syndrome
• Psychiatric care for people with Prader-Willi syndrome-characteristics, needs and barriers
• Psychotic illness in people with Prader-Willi syndrome: a systematic review of clinical presentation, course and phenomenology
• Puberty in girls with Prader-Willi syndrome: cohort evaluation and clinical recommendations in a Latin American tertiary center
• Quality of Life for Adults with Prader-Willi Syndrome in Residential Group Homes
• Relationship of thyroid function with genetic subtypes and treatment with growth hormone in Prader-Willi syndrome
• Role of projective psychological tests in patients with Prader-Willi syndrome
• Scoliosis and rare diseases: our experience with the Prader-Willi syndrome
• Secondary diabetes due to different etiologies: Four case reports
• Should we routinely assess hypothalamic-pituitary-adrenal axis in pediatric patients with Prader-Willi syndrome?
• Similar metabolic pathways are affected in both Congenital Myasthenic Syndrome-22 and Prader-Willi Syndrome
• Specificity of Early Childhood Hyperphagia Profiles in Neurogenetic Conditions
• STAC3 disorder: a common cause of congenital hypotonia in Southern African patients
• Syndromic and Monogenic Obesity: New Opportunities Due to Genetic-Based Pharmacological Treatment
• The importance of early recognition of Prader-Willi syndrome
• The Multiple Odysseys in Research and Clinical Care for Neurogenetic Conditions
• The Pivotal Role of Oxytocin's Mechanism of Thermoregulation in Prader-Willi Syndrome, Schaaf-Yang Syndrome, and Autism Spectrum Disorder
• The Prader-Willi syndrome Profile: validation of a new measure of behavioral and emotional problems in Prader-Willi syndrome
• Thyroid hormone levels in children with Prader-Willi Syndrome: A randomized controlled Growth Hormone (GH)-trial and 10-year GH study
• Thyroid hormone levels in children with Prader-Willi syndrome: a randomized controlled growth hormone trial and 10-year growth hormone study
• Transcranial Direct Current Stimulation in neurogenetic syndromes: new treatment perspectives for Down syndrome?
• Transcutaneous auricular vagus nerve stimulation to acutely reduce emotional vulnerability and improve emotional regulation in borderline personality disorder (tVNS-BPD): study protocol for a randomized, single-blind, sham-controlled trial
• Truncated variants of MAGEL2 are involved in the etiologies of the Schaaf-Yang and Prader-Willi syndromes
• Variants of the GNAI1 gene manifest as Prader-Willi-like syndrome: Case report with literature review
• When they just don't sleep: differential impacts of reduced child sleep on depression, anxiety, and stress among caregivers of children with and without neurogenetic syndromes
• Whole exome sequencing reveals a dual diagnosis of BCAP31-related syndrome and glutaric aciduria III