• A case of eighteen intestinal and colonic atresias in a patient treated with staged surgery
• A Novel Homozygous <em>TTC7A</em> Missense Mutation Results in Familial Multiple Intestinal Atresia and Combined Immunodeficiency
• A Novel Homozygous TTC7A Missense Mutation Results in Familial Multiple Intestinal Atresia and Combined Immunodeficiency
• A rare case of jejunal atresia
• A rare occurrence of multiple intestinal atresias, with successful one-procedure resection and primary anastomosis
• An Atypical Variant of Apple Peel Atresia: Reporting a Rare Case
• Analysis of the clinical diagnosis and treatment of fetal meconium peritonitis
• Appearance of fetal intestinal obstruction on fetal MRI
• Apple-peel jejunal atresia associated with multiple ileal atresias in a preterm newborn: A rare congenital anomaly
• Biallelic PI4KA variants cause neurological, intestinal and immunological disease
• Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes
• Biliatresone: progress in biliary atresia study
• Bovine congenital defects recorded by veterinary practitioners
• Case Report: Jejunoileal Atresia With Persistent Poor Bowel Function Can Occur After Surgical Correction for Hirschsprung Disease
• Case report: Neonatal pancreatitis, chromosomal abnormality and duodenal stenosis in a newborn. A new syndrome?
• Challenging management of a baby with congenital multiple intestinal atresia, trisomy 18 and extremely low birth weight: a case report
• Chromosomal abnormalities associated with fetal megacystis
• Chronic Intestinal Pseudo-Obstruction and Lymphoproliferative Syndrome as a Novel Phenotype Associated With Tetratricopeptide Repeat Domain 7A Deficiency
• Clinical outcome of pregnancies with the prenatal double bubble sign - a five-year experience from one single centre in mainland China
• Collateral Damage From Fetal Interventions: Increasing the Complexity of Complex Patients
• Combined Immunodeficiency With Inflammatory Bowel Disease in a Patient With TTC7A Deficiency
• Comparing levocardia and dextrocardia in fetuses with heterotaxy syndrome: prenatal features, clinical significance and outcomes
• Complex gastroschisis: a new indication for fetal surgery?
• Complicated Gastroschisis Is Associated with Greater Intestinal Morbidity than Gastroschisis or Intestinal Atresia Alone
• Comprehensive Analysis of Gut Microbiota and Fecal Bile Acid Profiles in Children With Biliary Atresia
• Congenital Acinar Cystic Transformation of the Pancreas with Proximal Jejunal Atresia and Hepatic Iron Overload: An Autopsy Case
• Congenital anomalies of the tubular gastrointestinal tract
• Congenital intestinal atresias with multiple episodes of sepsis: A case report and review of literature
• Congenital multiple colonic atresias with intestinal malrotation: a case report
• Congenital sodium diarrhoea caused by rare de novo activating guanylate cyclase mutation
• Consecutive siblings, each with two separate small bowel atresias
• Correctable biliary atresia and cholangiocarcinoma: a case report of a 63-year-old patient
• Delayed Presentation of Jejunal Atresia with Multiple Enteric Fistula: A Case Report and Review of Literature
• Differential Diagnosis of Polyhydramnios in a Patient with Gestational Diabetes and Structurally Abnormal Fetus
• Drug Screen Identifies Leflunomide for Treatment of Inflammatory Bowel Disease Caused by TTC7A Deficiency
• Duodenal atresia and associated intestinal atresia: a cohort study and review of the literature
• Effect of previous abdominal surgery and gallbladder appearance on biliary atresia outcomes
• European Pediatric Surgeon' Association Survey on the Management of Short-Bowel Syndrome
• Exencephaly-Anencephaly Sequence Associated with Maxillary Brachygnathia, Spinal Defects, and Palatoschisis in a Male Domestic Cat
• Experience in the Management of Complex Apple Peel Intestinal Atresia in a Limited-Resource Health Center in Mexico
• Fetal megacystis: a lot more than LUTO
• FOXA2 gene mutation in a patient with congenital complex pituitary hormone deficiency
• Ganglioneuromatosis intestinal difusa a lo largo del tubo digestivo
• Gastrointestinal Duplications: A Decade's Experience
• Hereditary Multiple Intestinal Atresia: A Case Report and Review of the Literature
• High Rates of Positive Severe Combined Immunodeficiency Screening Among Newborns with Severe Intestinal Failure
• How can we improve perinatal care in isolated multiple intestinal atresia? A retrospective study with a 30-year literature review
• Ileal Atresia
• Ileal Atresia
• Ileal Atresia in a 10-day-old male baby: A case report
• Ileal lengthening through internal distraction: A novel procedure for ultrashort bowel syndrome
• Immune function and infectious complications in children with jejunoileal atresia
• Incidence of late severe intestinal complications after bowel atresia/stenosis
• Intestinal Atresias: A Ten-Year Evaluation of Outcomes
• Jejunal Atresia With a Rare Association: A Case Report and Literature Review
• Long-term surgical outcomes of apple-peel atresia
• Maximal Segmental Score Method for Localizing Recessive Disease Variants Based on Sequence Data
• Meconium peritonitis in multiple intestinal atresia with combined immune deficiency caused by a TTC7A mutation: A case report
• Miro-dependent mitochondrial pool of CENP-F and its farnesylated C-terminal domain are dispensable for normal development in mice
• Missense mutation of TTC7A mimicking tricho-hepato-enteric (SD/THE) syndrome in a patient with very-early onset inflammatory bowel disease
• Molecular Pathways and Animal Models of Defects in Situs
• Multiple Small Bowel Atresia: Resection or Conservation?
• Multiple-center study of laparoscopic and open treatment of duodenal atresia
• Neonatal Intestinal Anastomosis Using a 5 mm Laparoscopic Stapler
• Neonatal intestinal obstruction associated with situs inversus totalis: two case reports and a review of the literature
• New features of aplasia cutis congenita type 5 - Skin atrophy associated with respiratory insufficiency and multiple intestinal atresia caused by the early death of twin fetus
• Novel Exonic Deletions in TTC7A in a Newborn with Multiple Intestinal Atresia and Combined Immunodeficiency
• Novel Mutations of the <em>Tetratricopeptide Repeat Domain 7A</em> Gene and Phenotype/Genotype Comparison
• Nutritional role of amniotic fluid: clues from infants with congenital obstruction of the digestive tract
• Pancake kidney and jejunal atresia: An uncommon dual anomaly detected prenatally-A case report
• Pediatric Gastrointestinal Histopathology in Patients With Tetratricopeptide Repeat Domain 7A (TTC7A) Germline Mutations: A Rare Condition Leading to Multiple Intestinal Atresias, Severe Combined Immunodeficiency, and Congenital Enteropathy
• Phenotypic expansion in Zhu-Tokita-Takenouchi-Kim syndrome caused by de novo variants in the SON gene
• Postoperative Enteral Nutrition Guidelines Reduce the Risk of Intestinal Failure-Associated Liver Disease in Surgical Infants
• Prominent Follicular Keratosis in Multiple Intestinal Atresia with Combined Immune Deficiency Caused by a TTC7A Homozygous Mutation
• Pyloric atresia and Down's syndrome: prenatal double bubble false sign
• Quadruple bubble-a sign of three concomitant malformations
• Rare case report of anorectal malformation and intestinal atresia
• Recurrent Intestinal Perforation After Cessation of Immunosuppression in Posttransplant Lymphoproliferative Disease in Pediatric Liver Transplant Recipient
• Refractory pruritus responds to dupilumab in a patient with TTC7A mutation
• Renal and extra-renal phenotypes in a fetus with a de novo pathogenic variant in the HNF1B gene
• Renal involvement and Strømme syndrome
• RFX6 regulates human intestinal patterning and function upstream of PDX1
• Risk factors of blood loss during liver transplantation in children with biliary atresia and its influence on prognosis
• Serum bile acids profiling by liquid chromatography-tandem mass spectrometry (LC-MS/MS) and its application on pediatric liver and intestinal diseases
• SPINT2 (HAI-2) missense variants identified in congenital sodium diarrhea/tufting enteropathy affect the ability of HAI-2 to inhibit prostasin but not matriptase
• Successful staged repair of pulmonary atresia, ventricular septal defect, and major aortopulmonary collateral arteries in an extremely low birth weight infant
• Syndromic and single gene disorders associated with fetal megacystis (I): Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS)
• Systematic review of phenotypes and genotypes of patients with gastrointestinal defects and immunodeficiency syndrome-1 (GIDID1) (related to TTC7A)
• T-tube enterostomy in the management of apple-peel atresia: A case series from a single center
• Tethered Cord Syndrome in the United States Cluster Analysis of Presenting Anomalies and Associated
• The multivariate cox regression model for complete enteral nutrition after primary anastomosis in neonates with intestinal atresia
• Total Intestinal Atresia: Revisiting the Pathogenesis of Congenital Atresias
• Transanastomotic tube in intestinal atresia: How beneficial are they?
• Troubleshooting Tips for Diagnosing Complex Fetal Genitourinary Malformations
• TTC7A mutation must be considered in patients with repeated intestinal atresia associated with early inflammatory bowel disease: Two new case reports and a literature review
• TTC7A: Steward of Intestinal Health
• Tubular intestinal duplication extending from the stomach to the ileum associated with multiple intestinal atresia and situs inversus: a case report
• Type II Congenital Pyloric Atresia with Desquamative Enteropathy Diagnosed Postoperatively: A Case Report
• Ultrasound and Fetal MRI Complementary Contributions to Appropriate Counseling in Small Bowel Obstruction
• Umbilical Cord Ulcer and Intrauterine Death in Fetal Intestinal Atresia