• <em>Ret</em> deficiency decreases neural crest progenitor proliferation and restricts fate potential during enteric nervous system development
• <em>RET</em> S409Y Germline Mutation and Associated Medullary Thyroid Carcinoma
• A homozygous MITF mutation leads to familial Waardenburg syndrome type 4
• A national analysis of operative treatment of adult patients with Hirschsprung's disease
• A novel case of concurrent occurrence of demyelinating-polyneuropathy-causing PMP22 duplication and SOX10 gene mutation producing severe hypertrophic neuropathy
• A primer on the genetics of medullary thyroid cancer
• A Rare Case Report on Postoperative Rehabilitation in Hirschsprung Disease
• Anal sphincter botulinum toxin injection in children with functional anorectal and colonic disorders: A large institutional study and review of the literature focusing on complications
• Application of enhanced recovery after surgery during the perioperative period in infants with Hirschsprung's disease - A multi-center randomized clinical trial
• Assessment of Quality of Life and Functional Outcomes of Operated Cases of Hirschsprung Disease in a Developing Country
• Botulinum toxin injection for internal anal sphincter achalasia after pull-through surgery in Hirschsprung disease
• Botulinum toxin injections after surgery for Hirschsprung disease: Systematic review and meta-analysis
• Bridging the Gap: A Systematic Review on Reporting Baseline Characteristics, Process, and Outcome Parameters in Rectosigmoid Hirschsprung's Disease
• Calretinin immunohistochemical staining in Hirschsprung's disease: An institutional experience
• Central venous catheter-associated bloodstream infections in children diagnosed with intestinal failure in Southern Israel
• Clinical and genetic approach in the characterization of newborns with anorectal malformation
• Clinical features of children with Haddad syndrome: A single-center experience
• Clinical features of epilepsy in 5 children with Mowat-Wilson syndrome
• Clinical Insights Into Waardenburg-Shah Syndrome: A Case Series and Literature Review
• Decreased expression of β1 integrin in enteric neural crest cells of the endothelin receptor B null mouse model
• Demographic Study and Management of Colonic Atresia: Single-Center Experience with Review of Literature
• Determining the Correct Resection Level in Patients with Hirschsprung Disease Using Contrast Enema and Full Thickness Biopsies: Can the Diagnostic Accuracy be Improved by Examining Submucosal Nerve Fiber Thickness?
• Diet and bowel function in children with Hirschsprung's disease: development and content validation of a patient-reported questionnaire
• Downregulation of Protein Tyrosine Phosphatase Receptor Type R Accounts for the Progression of Hirschsprung Disease
• Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humans
• Elevated basal serum levels of calcitonin and simultaneous surgery of MEN2A-specific tumors
• Endothelin B Receptor Immunodynamics in Pulmonary Arterial Hypertension
• Enema-Induced spastic left colon syndrome: An unintended consequence of chronic enema use
• Enteric Nervous System Striped Patterning and Disease: Unexplored Pathophysiology
• Factors influencing the incidence of Hirschsprung associated enterocolitis (HAEC)
• Features and choice of surgical strategy in patients with gastrointestinal fistulas
• Forty-Year Experience Alleviating Postoperative Hirschsprung-Associated Enterocolitis by Complete Full-Thickness Posterior Rectal Cuff Excision. The Anorectal Line Eliminates Problematic Anastomoses
• Gene- and tissue-level interactions in normal gastrointestinal development and Hirschsprung disease
• General versus general anaesthesia combined with caudal block in laparoscopic-assisted Soave pull-through of Hirschsprung disease: a retrospective study
• Health-related quality of life in children with Hirschsprung disease and children with functional constipation: Parent-child variability
• High intestinal vascular permeability in a murine model for Hirschsprung's disease: implications for postoperative Hirschsprung-associated enterocolitis
• Hirschsprung disease and anorectal malformations - An uncommon association
• Hirschsprung disease and other gastrointestinal motility disorders in patients with CCHS
• Hirschsprung disease outcomes
• Hirschsprung-Associated Enterocolitis at a Referral Institution: A Retrospective Review
• Hirschsprung-associated enterocolitis in children treated at US children's hospitals
• Home and Ambulatory Artificial Nutrition (NADYA) Group report: home parenteral nutrition in Spain, 2019
• Home and Ambulatory Artificial Nutrition (NADYA) Group Report. Home parenteral nutrition in Spain, 2018
• Home and Ambulatory Artificial Nutrition (NADYA) Report. Home Parenteral Nutrition in Spain, 2017
• Innervation of the entire internal anal sphincter in a mouse model of Hirschsprung's disease: a first report
• Inpatient management of Hirschsprung's associated enterocolitis treatment: the benefits of standardized care
• Intermediate and long-term outcomes of a bowel management program for children with severe constipation or fecal incontinence
• Laparoscopic-Assisted Colonic Derotation in Patients With Hirschsprung Disease
• Levator ani asymmetry and deviation in high-type anorectal malformation evaluated by magnetic resonance imaging
• Long-term functional outcomes of patients with Hirschsprung disease following pull-through
• Long-Term Male Sexual Function and Fecal Incontinence Outcomes for Adult Patients with Hirschsprung Disease or Anorectal Malformation
• Long-term Outcomes of Patients Surgically Treated for Hirschsprung Disease
• Medullary Thyroid Carcinoma and Associated Endocrinopathies in Slovenia from 1995 to 2021
• Molecular Diagnosis and Treatment of Multiple Endocrine Neoplasia Type 2B in Ethnic Han Chinese
• MPGES-1 derived PGE2 inhibits cell migration by regulating ARP2/3 in the pathogenesis of Hirschsprung disease
• Multiple endocrine neoplasia type 2B diagnosed after small intestinal volvulus with progressive megacolon in an adolescent
• Multiple Endocrine Neoplasias Type 2
• Multiple Endocrine Neoplasias Type 2
• Neurocristopathies: Enigmatic Appearances of Neural Crest Cell-derived Abnormalities
• Neuronal lineages derived from the nerve-associated Schwann cell precursors
• Null mutation of the endothelin receptor type B gene causes embryonic death in the GK rat
• Optimal time for single-stage pull-through colectomy in infants with short-segment Hirschsprung disease
• Outcomes after enterostomies in children with and without motility disorders: A description and comparison of postoperative complications
• Paediatric constipation for general paediatricians: Review using a case-based and evidence-based approach
• Parenteral support and micronutrient deficiencies in children with short bowel syndrome: A comprehensive retrospective study
• Pediatric Home Parenteral Nutrition in France: A six years national survey
• Postoperative enterocolitis assessment using two different cut-off values in the HAEC score in Hirschsprung patients undergoing Duhamel and Soave pull-through
• Prevalence of Hirschsprung-associated enterocolitis in patients with Hirschsprung disease
• Prevalence of Mental Health Disorders in Individuals With Gastrointestinal Congenital Surgical Anomalies: A Systematic Review and Meta-analysis
• Reaching adulthood with Hirschsprung's disease: Patient experiences and recommendations for transitional care
• Rectal Biopsy Technique for the Diagnosis of Hirschsprung Disease in Children: A Systematic Review and Meta-Analysis
• Rectourethral and rectovesical fistula as serious and rare complications after Hirschsprung disease operation: Experience in seven patients
• Remodeling of Rectal Innervation After Pullthrough Surgery for Hirschsprung Disease: Relevance to Criteria for the Determination of Retained Transition Zone
• RET in breast cancer: pathogenic implications and mechanisms of drug resistance
• RET receptor signaling: Function in development, metabolic disease, and cancer
• Role of ano rectal myomectomy in children with chronic refractory constipation
• Roles of the <em>RET</em> Proto-oncogene in Cancer and Development
• Should primary anastomosis be considered more? A retrospective analysis of anastomotic complications in young children
• SOX10: 20 years of phenotypic plurality and current understanding of its developmental function
• Suction Rectal Biopsy is Accurate in Late Preterm Infants with Suspected Hirschsprung Disease
• Susceptibility of <em>PCSK2</em> Polymorphism to Hirschsprung Disease in Southern Chinese Children
• Susceptibility of PCSK2 Polymorphism to Hirschsprung Disease in Southern Chinese Children
• The impact of NRG1 expressions and methylation on multifactorial Hirschsprung disease
• The important role of miR-770 as a novel potential diagnostic and therapeutic target for human cancer and other diseases
• The outcomes of transanal endorectal pull-through for Hirschsprung's disease according to the mucosectomy-commencing points: A study based on the results of a nationwide survey in Japan
• The RET C611Y mutation causes MEN 2A and associated cutaneous
• The role of stomas in the initial and long-term management of Hirschsprung disease
• The utility of the 24-h delayed film of barium enema for detecting the dysganglionic bowel segment in Hirschsprung's disease
• Transitional Care in Anorectal Malformation and Hirschsprung's Disease: A Systematic Review of Challenges and Solutions
• Transumbilical enterostomy for Hirschsprung's disease with a two-stage laparoscopy-assisted pull-through procedure
• Treatment of classic-type Hirschsprung's disease: rectoplasty with posterior triangular colonic flap versus transanal endorectal pull-through with rectoanal myotomy
• Urinary tract anomalies and urinary tract dysfunction in children with Hirschsprung disease-Is follow-up indicated?
• Variable phenotypes in congenital central hypoventilation syndrome with <em>PHOX2B</em> nonpolyalanine repeat mutations
• Variation in Practice Surrounding Antegrade Colonic Enema Channel Placement
• Waardenburg Syndrome
• Waardenburg Syndrome
• Waardenburg Syndrome: The Contribution of Next-Generation Sequencing to the Identification of Novel Causative Variants
• Waardenburg-Shah syndrome rare and challenging case report from Somalia
• What is the appropriate aganglionic bowel length on contrast enema for attempting single stage transanal endorectal pull-through in Hirschsprung disease?
• ZEB2, the Mowat-Wilson Syndrome Transcription Factor: Confirmations, Novel Functions, and Continuing Surprises