• <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 5-year follow-up study of neonates with Hirschsprung's disease undergoing transanal Soave or Swenson surgery
• A comparative observational study on intrasphincteric injections with Botulinum toxin vs. enteral neuromodulation in chronic refractory constipation
• A Long-Term Follow-Up of a New Surgery Method: Laparoscope-Assisted Heart-Shaped Anastomosis for Hirschsprung's Disease
• 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 Co-occurrence of Intestinal Malrotation and Hirschsprung's Disease in a Neonate with 13q21.31q33.1 Interstitial Deletion Including the <em>EDNRB</em> Gene
• A Rare Co-occurrence of Intestinal Malrotation and Hirschsprung's Disease in a Neonate with 13q21.31q33.1 Interstitial Deletion Including the EDNRB Gene
• Anorectal malformation & Hirschsprung's disease: A cross-sectional comparison of quality of life and bowel function to healthy controls
• Application of enhanced recovery after surgery during the perioperative period in infants with Hirschsprung's disease - A multi-center randomized clinical trial
• B-lymphocyte-intrinsic and -extrinsic defects in secretory immunoglobulin A production in the neural crest-conditional deletion of endothelin receptor B model of Hirschsprung-associated enterocolitis
• Bioavailability of rectal acetaminophen in children following anorectal surgery
• Botulinum toxin injection for internal anal sphincter achalasia after pull-through surgery in Hirschsprung disease
• Calretinin immunohistochemical staining in Hirschsprung's disease: An institutional experience
• Case of Waardenburg Shah syndrome in a family with review of literature
• Case Report: A novel <em>PHOX2B</em> p.Ala248_Ala266dup variant causing congenital central hypoventilation syndrome
• Central venous catheter-associated bloodstream infections in children diagnosed with intestinal failure in Southern Israel
• Characterizing the use of botulinum toxin in patients with Hirschsprung disease treated at referral institutions for pediatric colorectal surgery
• Clinical and genetic approach in the characterization of newborns with anorectal malformation
• Clinical characteristics and validation of diagnosis in individuals with Hirschsprung disease and inflammatory bowel disease
• Clinical Evaluation of Laparoscopic Surgery for Hirschsprung Disease Combined with Colorectal Anastomosis with a Stapling Technique in Infants
• Clinical features of children with Haddad syndrome: A single-center experience
• Clinical features of epilepsy in 5 children with Mowat-Wilson syndrome
• Colonic tubular duplication combined with congenital megacolon: A case report
• 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
• Dental pulp stem cells as a therapy for congenital entero-neuropathy
• Does Length of Extended Resection Beyond Transition Zone Change Clinical Outcome for Hirschsprung Pull-Through?
• Duhamel operation vs. transanal endorectal pull-through procedure for Hirschsprung disease: A systematic review and meta-analysis
• Dysmorphic Neurofilament-Positive Ganglion Cells in the Myenteric Plexus at the Proximal Resection Margin Indicate Worse Postoperative Prognosis in Hirschsprung's Disease
• Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humans
• Early prenatal presentation of the cartilage-hair hypoplasia / anauxetic dysplasia spectrum of disorders mimicking recurrent thanatophoric dysplasia
• Elevated basal serum levels of calcitonin and simultaneous surgery of MEN2A-specific tumors
• Enterostomy-related complications in Hirschsprung's disease in a single cohort
• Evaluation of Post-neonatal Intensive Care Unit Home Irrigations Prior to Pull-through: Implications for Hirschsprung Disease Management
• 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
• Glial Cell-Derived Neurotrophic Factor Induces Enteric Neurogenesis and Improves Colon Structure and Function in Mouse Models of Hirschsprung Disease
• Health-related quality of life in children with Hirschsprung disease and children with functional constipation: Parent-child variability
• Hirschsprung disease - integrating basic science and clinical medicine to improve outcomes
• Hirschsprung disease and anorectal malformations - An uncommon association
• Hirschsprung disease in Down syndrome: An opportunity for improvement
• Hirschsprung Disease: The Rise of Structured Transition and Long-term Care
• Hirschsprung-associated enterocolitis in children treated at US children's hospitals
• Home and Ambulatory Artificial Nutrition (NADYA) Group Report - Home parenteral nutrition in Spain, 2016
• 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
• Ileal pouch-anal anastomosis in paediatric age group: perioperative period, functional outcome and patient satisfaction
• Incidence of medullary thyroid carcinoma and Hirschsprung disease based on the cosmos database
• Increased enteric neural crest cell differentiation after transplantation into aganglionic mouse gut
• Innervation of the entire internal anal sphincter in a mouse model of Hirschsprung's disease: a first report
• Intermediate and long-term outcomes of a bowel management program for children with severe constipation or fecal incontinence
• Intestinal Obstruction in Early Neonatal Period: A 3-Year Review Of Admitted Cases from a Tertiary Hospital in Ethiopia
• Isolated intestinal neuronal dysplasia- type B of ileum: A rare occurrence
• Levator ani asymmetry and deviation in high-type anorectal malformation evaluated by magnetic resonance imaging
• 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
• Neurostimulation-guided Anal Intrasphincteric Botulinum Toxin Injection in Children With Hirschsprung Disease
• OBLIQUE VS. CIRCULAR ANASTOMOSIS IN THE CHILDREN UNDERWENT SOAVE'S PULL-THROUGH SURGERY FOR THE TREATMENT OF HIRSCHSPRUNG'S DISEASE: WHICH IS THE BEST?
• Optimal time for single-stage pull-through colectomy in infants with short-segment Hirschsprung disease
• 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
• Patient-reported urinary outcomes in adult males with congenital colorectal conditions
• PATTERN AND OUTCOME OF NEONATAL SURGICAL CASES AT TIKUR ANBESSA UNIVERSITY TEACHING HOSPITAL, ADDIS ABABA, ETHIOPIA
• Pediatric Home Parenteral Nutrition in France: A six years national survey
• 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
• Prevention and management of recurrent postoperative Hirschsprung's disease obstructive symptoms and enterocolitis: Systematic review and meta-analysis
• Pull-through procedure in children with Hirschsprung disease: A nationwide analysis on postoperative outcomes
• 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 receptor signaling: Function in development, metabolic disease, and cancer
• 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
• Should we look for Hirschsprung disease in all children with meconium plug syndrome?
• Structural and functional differences in PHOX2B frameshift mutations underlie isolated or syndromic congenital central hypoventilation syndrome
• Surgical management of functional constipation: An intermediate report of a new approach using a laparoscopic sigmoid resection combined with malone appendicostomy
• The bowel function and quality of life of Hirschsprung disease patients who have reached 18 years of age or older - the long-term outcomes after undergoing the transabdominal soave procedure
• The impact of NRG1 expressions and methylation on multifactorial Hirschsprung disease
• 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 utility of the 24-h delayed film of barium enema for detecting the dysganglionic bowel segment in Hirschsprung's disease
• Timely diagnosis of multiple endocrine neoplasia 2B by identification of intestinal ganglioneuromatosis: a case series
• 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
• 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
• Waardenburg Syndrome
• Waardenburg Syndrome
• Waardenburg Syndrome: The Contribution of Next-Generation Sequencing to the Identification of Novel Causative Variants
• What is the appropriate aganglionic bowel length on contrast enema for attempting single stage transanal endorectal pull-through in Hirschsprung disease?
• Windsock or Cobra Head Sign: A Distinctive Imaging Sign to Differentiate Type 1 Colonic Atresia From Hirschsprung's Disease