Disease: Prader-Willi syndrome
- "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 14-year-old male patient with diagnosis of Prader-Willi syndrome in Ethiopia: a case report
- A call for trauma-informed dental care for individuals with intellectual disabilities
- A comprehensive review of genetic causes of obesity
- A supervised learning method for classifying methylation disorders
- AAV-BDNF gene therapy ameliorates a hypothalamic neuroinflammatory signature in the <em>Magel2</em>-null model of Prader-Willi syndrome
- Aberrant brain intra- and internetwork functional connectivity in children with Prader-Willi syndrome
- 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 of diagnosis for children with chromosome 15q syndromes
- An Atypical 15q11.2 Microdeletion Not Involving <em>SNORD116</em> Resulting in Prader-Willi Syndrome
- Analysis of Hyperphagia Questionnaire for Clinical Trials (HQ-CT) scores in typically developing individuals and those with Prader-Willi syndrome
- Analysis of the Diet Quality and Nutritional State of Children, Youth, and Young Adults with Prader-Willi Syndrome: A Polish Multiple Case Study
- Anti-Müllerian hormone, testicular descent and cryptorchidism
- Appetite- and weight-regulating neuroendocrine circuitry in hypothalamic obesity
- Bardet-Biedl syndrome: A clinical overview focusing on diagnosis, outcomes and best-practice management
- Bariatric surgery for the adolescent with Prader-Willi syndrome: A literature review
- Behavioral Changes in Patients With Prader-Willi Syndrome Can Mask Severe Physical Illness
- Body Fat Distribution Contributes to Defining the Relationship between Insulin Resistance and Obesity in Human Diseases
- 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
- Chromosomal Aberrations in Pediatric Patients With Moderate/Severe Developmental Delay/Intellectual Disability With Abundant Phenotypic Heterogeneities: A Single-Center Study
- 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
- Corrigendum: Kidney disease in adults with Prader-Willi syndrome: international cohort study and systematic literature review
- Current and future state of pharmacological management of pediatric obesity
- Diazoxide choline extended-release tablet in people with Prader-Willi syndrome: results from long-term open-label study
- Differences in spinal postures and mobility among adults with Prader-Willi syndrome, essential obesity, and normal-weight individuals
- 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
- Early psychomotor development and growth hormone therapy in children with Prader-Willi syndrome: a review
- Editorial: Genetic obesity
- Editorial: Innovative approaches and therapeutic perspectives for early-onset neurodevelopmental disorders: from bench to bedside
- Effect of non-pharmacological intervention on the nutritional status of patients with Prader Willi Syndrome
- Effect of semaglutide on weight loss and glycaemic control in patients with Prader-Willi Syndrome and type 2 diabetes
- Effectiveness of the Kaufman Brief Intelligence Test in people with Prader-Willi syndrome
- Efficacy of adenotonsillectomy on pediatric obstructive sleep apnea and related outcomes: A narrative review of current evidence
- Elexacaftor/tezacaftor/ivacaftor can rescue pancreatic function in F508del homozygous children
- Evaluating the effect of recombinant human growth hormone treatment on sleep-related breathing disorders in toddlers with Prader-Willi syndrome: a one-year retrospective cohort study
- 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
- Feeding tube use and complications in Prader-Willi syndrome: Data from the Global Prader-Willi Syndrome Registry
- Food cue reward salience does not explain Hyperphagia in adolescents with Prader-Willi syndrome
- Generation of isogenic models of Angelman syndrome and Prader-Willi syndrome in CRISPR/Cas9-engineered human embryonic stem cells
- Genotype-phenotype correlation in Prader-Willi syndrome: A large-sample analysis in China
- GNB1 and obesity: Evidence for a correlation between haploinsufficiency and syndromic obesity
- Gut microbiota, a potential cause of higher insulin sensitivity in children with Prader-Willi syndrome
- High-resolution genomic profiling and locus-specific FISH in subcutaneous and visceral adipose tissue of obese patients
- Hormonal Imbalances in Prader-Willi and Schaaf-Yang Syndromes Imply the Evolution of Specific Regulation of Hypothalamic Neuroendocrine Function in Mammals
- 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
- Hypoventilation in patients with Prader-Willi syndrome across the pediatric age
- Identifying key underlying regulatory networks and predicting targets of orphan C/D box <em>SNORD116</em> snoRNAs in Prader-Willi syndrome
- Impact of exenatide on weight loss and eating behavior in adults with craniopharyngioma-related obesity: the CRANIOEXE randomized placebo-controlled trial
- Imprinted small nucleolar RNAs: Missing link in development and disease?
- Increased IGFBP proteolysis, IGF-I bioavailability and pappalysin levels in children with Prader-Willi syndrome
- Integration of CTCF Loops, Methylome, and Transcriptome in Differentiating LUHMES as a Model for Imprinting Dynamics of the 15q11-q13 Locus in Human Neurons
- Intranasal Oxytocin in Pediatric Populations: Exploring the Potential for Reducing Irritability and Modulating Neural Responses: A Mini Review
- Isolated polyhydramnios: Is a genetic evaluation of value?
- Ketonuria in an adult with Prader-Willi syndrome and diabetes mellitus: A case report
- Laryngeal clefts in Prader-Willi syndrome: Feeding difficulties and aspiration not always caused by hypotonia
- Long-term effect of growth hormone on sleep-disordered breathing in Malaysian children with Prader-Willi syndrome: a retrospective study
- Longitudinal changes in acylated versus unacylated ghrelin levels may be involved in the underlying mechanisms of the switch in nutritional phases in Prader-Willi syndrome
- m6A-Mediated Upregulation of Imprinted in Prader-Willi Syndrome Induces Aberrant Apical-Basal Polarization and Oxidative Damage in RPE Cells
- Management of Monogenic and Syndromic Obesity
- Mental health impact on primary and secondary Prader-Willi syndrome caregivers
- 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
- Morbidity and mortality in Schaaf-Yang syndrome
- Mothering a Child With Complexity and Rarity: A Narrative Inquiry Exploring Prader-Willi Syndrome
- Neuromodulation for the treatment of Prader-Willi syndrome - A systematic review
- Orthopedic manifestations in children with Prader-Willi syndrome
- Parental and familial factors related to participation in a home-based physical activity intervention in children with obesity or Prader-Willi syndrome
- Pharmacogenomics for Prader-Willi syndrome: caregiver interest and planned utilization
- Population-based Risk of Psychiatric Disorders Associated with Recurrent CNVs
- Postural-motor development, spinal range of movement and caregiver burden in Prader-Willi syndrome-associated scoliosis: an observational study
- Prader-Willi syndrome in a large sample from Spain: general features, obesity and regular use of psychotropic medication
- Prader-Willi syndrome: an update
- Prediction of LncRNA-protein Interactions Using Auto-Encoder, SE-ResNet Models and Transfer Learning
- Prevalence and genotypic associations of epilepsy in Prader-Willi Syndrome: A systematic review and meta-analysis
- Prevalence of Sleep-Disordered Breathing in Prader-Willi Syndrome
- Proteome profiling identifies circulating biomarkers associated with hepatic steatosis in subjects with Prader-Willi syndrome
- Psychotic illness in people with Prader-Willi syndrome: a systematic review of clinical presentation, course and phenomenology
- Register-based and genetic studies of Prader-Willi syndrome show a high frequency of gonadal tumors and a possible mechanism for tumorigenesis through imprinting relaxation
- Scoliosis and rare diseases: our experience with the Prader-Willi syndrome
- Serum Ghrelin and Glukagon-like Peptid 1 Levels in Children with Prader-Willi and Bardet-Biedl Syndromes
- Similar metabolic pathways are affected in both Congenital Myasthenic Syndrome-22 and Prader-Willi Syndrome
- Specificity of Early Childhood Hyperphagia Profiles in Neurogenetic Conditions
- Structural Variation Evolution at the 15q11-q13 Disease-Associated Locus
- Syndromic and Monogenic Obesity: New Opportunities Due to Genetic-Based Pharmacological Treatment
- The Exon 3-Deleted Growth Hormone Receptor (d3GHR) Polymorphism-A Favorable Backdoor Mechanism for the GHR Function
- The Impact of Growth Hormone Therapy on Sleep-Related Health Outcomes in Children with Prader-Willi Syndrome: A Review and Clinical Analysis
- The Multiple Odysseys in Research and Clinical Care for Neurogenetic Conditions
- The outcomes of growth hormone therapy in the obstructive sleep apnea parameters of Prader-Willi syndrome patients: a systematic review
- 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
- The Year in Growth and Short Stature
- Transcranial Direct Current Stimulation in neurogenetic syndromes: new treatment perspectives for Down syndrome?
- Use of the MS-MLPA assay in prenatal diagnosis of Prader-Willi syndrome with mosaic trisomy 15
- Variants of the GNAI1 gene manifest as Prader-Willi-like syndrome: Case report with literature review
- What is the Role for Pediatric Endocrinologists in the Management of Skeletal Dysplasias?
- World-Renowned "Swiss" Pediatricians, Their Syndromes, and Matching Imaging Findings: A Historical Perspective