• A Multicenter Pilot Study of Biliary Atresia Screening Using Digital Stool Color Imaging
• A Pilot Study for Biliary Atresia Diagnosis: Fluorescent Imaging of Indocyanine Green in Stool
• A Rare Case of Biliary Atresia with Biliary Ascites on a (Hepatobiliary Iminodiacetic Acid) HIDA Scan
• Abnormally Low Alanine Aminotransferase Ameliorated by a Living Donor Liver Transplantation: A Case Report
• Alkaline Phosphatase > 2000 U/L in an Infant With Stool Changes: A Case Report
• Amniotic fluid gamma-glutamyl transferase for prediction of biliary atresia in cases of non-visualisation of the fetal gallbladder: a retrospective study using a validated analytical platform and local reference range
• Analysis of gut microecological characteristics and differences between children with biliary atresia and non-biliary atresia in infantile cholestasis
• Analysis of the effect of hormone therapy on native liver survival after Kasai procedure in biliary atresia: A systematic review and meta-analysis of randomized controlled trials
• Animal and organoid models to elucidate the anti-fibrotic effect of steroid on biliary atresia
• Application of a quality threshold to improve liver shear wave elastography measurements in free-breathing pediatric patients
• Are Medical Students and Primary Health-care Professionals Aware of Neonatal Cholestasis and Acholic Stool
• Assessment of the utility of two-dimensional shear wave elastography and superb microvascular imaging in postoperative patients with biliary atresia
• Bile lakes in patients with biliary atresia who presented with jaundice-free native liver survival indicating the risk of subsequent liver transplantation due to various factors
• Biliary atresia
• Biliary atresia and cholestasis plasma non-targeted metabolomics unravels perturbed metabolic pathways and unveils a diagnostic model for biliary atresia
• Biliary atresia in a 3-month-old infant (case report)
• Biliary atresia in children (analytical literature review and review of own observation)
• Biliary atresia-splenic malformation (BASM) syndrome: A case report
• Biliary atresia: insights into mechanisms using a toxic model of the disease including Wnt and Hippo signaling pathways and microtubules
• Biliary atresia: the role of gut microbiome, and microbial metabolites
• Booster administration of Tc-99m PMT for delayed static imaging in patients with biliary atresia
• Ceftazidime-Avibactam Use in a Case Series of Difficult-to-Treat or Recurrent Infections in Pediatric Patients with Complex Chronic Conditions: Effectiveness and Absence of Resistance Development
• Cholestasis after Kasai operation predicts portal hypertension in native liver survivors of biliary atresia: a multicenter study
• Cholestasis alters polarization and suppressor function of hepatic regulatory T cells
• Cognitive function of children with biliary atresia after primary living donor liver transplantation
• Combination of Pirfenidone and Andrographolide Ameliorates Hepatic Stellate Cell Activation and Liver Fibrosis by Mediating TGF-<em>β</em>/Smad Signaling Pathway
• Combined Predictors of Long-Term Outcomes of Kasai Surgery in Infants with Biliary Atresia
• Comparing animal well-being between bile duct ligation models
• Comparison for the diagnostic performance of early diagnostic methods for biliary atresia: a systematic review and network meta-analysis
• Comparison of Long-Term Outcomes Achieved With Live Donor and Split Deceased Donor Liver Grafts in Pediatric Liver Transplantation
• Comparison of Mir122 expression in children with biliary atresia and healthy group
• Considerable differences in management of cytomegalovirus infection in patients with biliary atresia
• CTHRC1 serves as an indicator in biliary atresia for evaluating the stage of liver fibrosis and predicting prognosis
• Delphi Method Analysis and Consensus of Prevalent Distinctive Practices for Biliary Atresia Management after Kasai Portoenterostomy
• Determining the minimally clinically important difference for the pediatric liver transplant quality of life questionnaire
• Development of a diagnostic model for biliary atresia based on MMP7 and serological tests using machine learning
• Does amyloid beta precursor protein gene expression have a role in diagnosis of biliary atresia?
• Does cytomegalovirus infection and antiviral therapy affect prognosis of biliary atresia? A real-world retrospective cohort study
• Duodenal atresia and biliary atresia combined with anterior duodenal portal vein: A case report
• Effectiveness of Cord blood as a Strategy to rule out Conjugated Hyperbilirubinemia
• Effectiveness of oral methylprednisolone as adjuvant therapy for clinical improvement, biochemical markers, and inflammation in infants with cholestasis
• Eicosapentaenoic acid administration ameliorates the progression of liver fibrosis after laparoscopic Kasai portoenterostomy
• Exploring causality with biliary atresia at different levels: two-sample Mendelian randomization study
• Factors predicting the need for liver transplantation in biliary atresia patients after 18 years of age
• Forward genetics combined with unsupervised classifications identified zebrafish mutants affecting biliary system formation
• Gastric sleeve as an extra-anatomical roux for biliary reconstruction in a pediatric third liver transplant
• Global research trends and hotspots for leukocyte cell-derived chemotaxin-2 from the past to 2023: a combined bibliometric review
• Gut Bifidobacterium longum is associated with better native liver survival in patients with biliary atresia
• Herbal and dietary supplement induced liver injury leading to hepatitis-associated severe aplastic anemia: A case report
• Heritable Chronic Cholestatic Liver Diseases: A Review
• Hsa_circ_0009096/miR-370-3p modulates hepatic stellate cell proliferation and fibrosis during biliary atresia pathogenesis
• Hyaline cartilage at the portal plate and gallbladder in biliary atresia
• Identification of diagnostic biomarkers and potential therapeutic targets for biliary atresia via WGCNA and machine learning methods
• Impact of gallbladder hypoplasia on hilar hepatic ducts in biliary atresia
• In Utero Extrahepatic Bile Duct Damage and Repair: Implications for Biliary Atresia
• Incidence, causative organisms, and risk factors of bloodstream infections in pediatric liver transplant patients: a systematic review
• Inflammation patterns in early post-operative cholangitis predict long-term outcomes in biliary atresia: a potential role of non-suppurative cholangitis
• Inhibition of Notch3/Hey1 ameliorates peribiliary hypoxia by preventing hypertrophic hepatic arteriopathy in biliary atresia progression
• Integrative single-cell and spatial transcriptomic analyses identify a pathogenic cholangiocyte niche and TNFRSF12A as therapeutic target for biliary atresia
• Kasai Portoenterostomy, Successful Liver Transplantation, and Immunosuppressive Therapy for Biliary Atresia in a Female Baby: A Case Report
• Key postnatal magnetic resonance characteristics for differentiating cystic biliary atresia from choledochal cyst
• Lack of differences in outcomes between three immunosuppression protocols in the first year post pediatric liver transplantation. A multicenter study
• Liver transplantation for pediatric genetic and metabolic disorders
• Liver Transplantation Profile Among Teenagers in the United States
• LncRNA MEG9 Promotes Inflammation and Liver Fibrosis Through S100A9 in Biliary Atresia
• Lymphangiogenesis in the liver of biliary atresia
• Machine Learning in Biliary Atresia: Taking a Cautious Step into the Future
• Major surgical conditions of childhood and their lifelong implications: comprehensive review
• Mesocolic hernia, a case series
• Molecular Pathways and Animal Models of Defects in Situs
• Mucosal-associated invariant T cells promote ductular reaction through amphiregulin in biliary atresia
• Navigating cholestasis: identifying inborn errors of bile acid metabolism for precision diagnosis
• Normalization of C1 Inhibitor in a Patient with Hereditary Angioedema
• Patterns and unique features of infantile cholestasis among Arabs
• Performance of Baveno VII criteria for the screening of varices needing treatment in patients with biliary atresia
• Porta hepatis lymph nodes on US: not only identify biliary atresia but also predict outcomes after Kasai portoenterostomy surgery
• Porta hepatis lymphnode mimicking biliary atresia: A case report
• Portal vein hypoplasia is present in patients with biliary atresia at the time of diagnosis
• Post liver transplantation complications in pediatric patients in a third level hospital, Lima-Peru, 2016-2020
• Postoperative hypoalbuminemia and outcomes of pediatric liver transplantation
• Postoperative outcomes of acute-on-chronic liver failure in infants and children with biliary atresia
• Predictive modeling for early detection of biliary atresia in infants with cholestasis: Insights from a machine learning study
• Quantitative Liver Imaging in Children
• Retrospective analysis of the standardized BARD criteria for acute cholangitis in biliary atresia patients
• Role of indocyanine green-guided near-infrared fluorescence imaging in identification of the cause of neonatal cholestasis
• Scrub typhus in pregnancy: A report of two cases
• Serum matrix metalloproteinase-7 for discriminating biliary atresia: a diagnostic accuracy and validation study
• Simple biliary atresia score-a validated diagnostic aid for infantile cholestasis
• Specific binding sites on Rhesus rotavirus capsid protein dictate the method of endocytosis inducing the murine model of biliary atresia
• Specific binding sites on Rhesus rotavirus capsid protein dictates the method of endocytosis inducing the murine model of biliary atresia
• Stable two- and three-dimensional cholangiocyte culture systems from extrahepatic bile ducts of biliary atresia patients: use of structural and functional bile duct epithelium models for in vitro analyses
• Successful management of an Iatrogenic portal vein and hepatic artery injury in a 4-month-old female patient: A case report and literature review
• Systematic review of the mechanism and assessment of liver fibrosis in biliary atresia
• The paediatric liver transplant experience in Johannesburg, South Africa: A broad overview and update
• The systemic immune-inflammation index at kasai portoenterostomy: related to clinical outcomes
• Timing of Kasai Procedure for Biliary Atresia: An Analysis of the Pediatric National Surgical Quality Improvement Program Database
• Transplant with prior Kasai procedure vs. primary liver transplantation for biliary atresia: A systematic review and meta-analysis
• Transplanting Livers in Young Children - Looking Back at 100 Cases
• Use of stool color card as screening tool for biliary atresia in resource-constraint country
• Youngest Living Donor Liver Transplant for End-Stage Liver Disease in a 6-Month-Old With a Novel Aggressive Mutation in KIF12 Gene