• 'Triangular Cord' Sign in Biliary Atresia
• A curatively resectable case of cholangiocarcinoma 52 years after cholecystoduodenostomy for biliary atresia
• A fetal wound healing program after intrauterine bile duct injury may contribute to biliary atresia
• A Mouse Model of Chronic Liver Fibrosis for the Study of Biliary Atresia
• A pilot study of the value of a stool color card as a diagnostic tool for extrahepatic biliary atresia at a single tertiary referral center in a low/middle income country
• A ZFYVE19 gene mutation associated with neonatal cholestasis and cilia dysfunction: case report with a novel pathogenic variant
• Acute-on-chronic liver failure before liver transplantation does not impact post-transplant survival in children with biliary atresia
• Advances in understanding of biliary atresia pathogenesis and progression - a riddle wrapped in a mystery inside an enigma
• Alterations of gut microbiota in infants with biliary atresia identified by 16S rRNA-sequencing
• An Unusual Cause of Cholestasis in an Infant: Biliary Atresia Type IIB
• Anatomical patterns of biliary atresia including hepatic radicles at the porta hepatis influence short- and long-term prognoses
• Association analysis and functional follow-up identified common variants of JAG1 accounting for risk to biliary atresia
• Association between mitochondrial and nuclear DNA damages and cellular senescence in the patients with biliary atresia undergoing Kasai portoenterostomy and liver transplantation
• Biliary Atresia
• Biliary atresia
• Biliary atresia & choledochal malformation--Embryological and anatomical considerations
• Biliary atresia and congenital disorders of the extrahepatic bile ducts
• Biliary Atresia and Rare Concurrent Cystic Fibrosis Variant: Case Report and Management Considerations
• Biliary atresia in a 3-month-old infant (case report)
• Biliary Atresia With Extrahepatic Cyst: A Diagnostic Dilemma
• Biliary atresia: the development, pathological features, and classification of the bile duct
• Biliary atresia: the role of gut microbiome, and microbial metabolites
• Biliary Disorders, Anomalies, and Malignancies in Children
• Biliatresone induces cholangiopathy in C57BL/6J neonates
• Case Report: Kasai Operation in Biliary Atresia After Extensive Bowel Resection
• Cholecysto-hepatic duct serving as the only drainage pathway of bile from the intrahepatic to the extrahepatic biliary system in an infant: a case report
• Complete Absence of the Extrahepatic Biliary Tree in a Newborn With Pigmented Stools
• Congenital anomalies of the gastrointestinal tract: the liver, extrahepatic biliary tree and pancreas
• Congenital biliary atresia is correlated with disrupted cell junctions and polarity caused by Cdc42 insufficiency in the liver
• Conjugated Hyperbilirubinemia in Infants: Is There Still a Role for ERCP?
• Controversies in Choledochal Malformation in Children: An International Survey among Pediatric Hepatobiliary Surgeons and Gastroenterologists
• Correlation of endoscopic findings with Doppler ultrasound in portal hypertension in children
• Current status and future directions of liver transplantation for metabolic liver disease in children
• De novo HBV Hepatitis in a Child with Liver Transplantation
• Delphi Method Analysis and Consensus of Prevalent Distinctive Practices for Biliary Atresia Management after Kasai Portoenterostomy
• Development of liver inflammatory injury in biliary atresia: from basic to clinical research
• Developmental histology of the portal plate in biliary atresia: observations and implications
• Diminution of the Primary Cilia From the Intrahepatic Cholangiocytes in a Pediatric Choledochal Cyst
• Etiology, Clinical Presentations, and Short-Term Treatment Outcomes of Extrahepatic Obstructive Jaundice in South-Western Uganda
• Event-free survival of maralixibat-treated patients with Alagille syndrome compared to a real-world cohort from GALA
• Extrahepatic Bile Duct and Gall Bladder Dissection in Nine-Day-Old Mouse Neonates
• Extrahepatic biliary atresia in a premature neonate with congenital cytomegalovirus infection
• Feasibility and outcomes of transjugular intrahepatic portosystemic shunts in infants
• Feasibility of Immunoadsorption plasmapheresis in an infant for ABO-incompatible solid organ transplant-A reality
• Frequency of Causes of Portal Hypertension in Children
• Glial Cell Line-Derived Neurotrophic Factor, S-100 Protein and Synaptophysin Expression in Biliary Atresia Gallbladder Tissue
• Gut Bifidobacterium longum is associated with better native liver survival in patients with biliary atresia
• Hypoplasia of Extrahepatic Biliary Tree and Intrahepatic Cholangiolopathy in Cystic Fibrosis Imperfectly Mimic Biliary Atresia in 4 Infants With Cystic Fibrosis and Kasai Portoenterostomy
• Identification of diagnostic biomarkers and potential therapeutic targets for biliary atresia via WGCNA and machine learning methods
• IL13 and periostin in active fibrogenic areas of the extrahepatic bile ducts in biliary atresia patients
• Imaging in Pediatric Obstructive Jaundice
• Immune Characteristics in Biliary Atresia Based on Immune Genes and Immune Cell Infiltration
• Immune-mediated cholangiopathies in children: the need to better understand the pathophysiology for finding the future possible treatment targets
• Impact of gallbladder hypoplasia on hilar hepatic ducts in biliary atresia
• In Utero Extrahepatic Bile Duct Damage and Repair: Implications for Biliary Atresia
• Inflammation patterns in early post-operative cholangitis predict long-term outcomes in biliary atresia: a potential role of non-suppurative cholangitis
• Intrahepatic Cholangiolitis in Cystic Fibrosis (ICCF): An Under-Appreciated Cause of Persistent Cholestasis in Infancy
• Isolation and Culturing Primary Chaolangiocytes from Mouse Liver
• Jaundice in Young Children
• Kaposi sarcoma in three pediatric liver transplantation recipients
• Liver Explants of Biliary Atresia Patients Transplanted in Adulthood Show Features of Obliterative Portal Venopathy: Case Series and Guidelines for Pathologic Reporting of Adult Explants
• Liver transplantation for pediatric genetic and metabolic disorders
• Liver Transplantation in a Child with Kartagener Syndrome: A Case Report
• Liver Transplantation Profile Among Teenagers in the United States
• Maternal risk factors associated with offspring biliary atresia: population-based study
• Mesocolic hernia, a case series
• Metabolic regulation of cholestatic liver injury by D-2-hydroxyglutarate with the modulation of hepatic microenvironment and the mammalian target of rapamycin signaling
• Microcystin-RR is a biliary toxin selective for neonatal cholangiocytes
• Missing the main actor: Intra-operative diagnosis of agenesis of the gallbladder - When late is not 'too' late
• Multiple organ involvement and ICU considerations for the care of acute liver failure (ALF) and acute on chronic liver failure (ACLF) in children
• Necroptosis in biliary atresia of the liver
• Necroptosis of macrophage is a key pathological feature in biliary atresia via GDCA/S1PR2/ZBP1/p-MLKL axis
• Oral findings in children with congenital cholestatic disease: A systematic review of case reports and case series
• Overview of Biliary Atresia
• Pathological role of methionine in the initiation and progression of biliary atresia
• Pediatric liver cirrhosis interventional procedures: from biopsy to transjugular intrahepatic portosystemic shunt
• Periductal bile acid exposure causes cholangiocyte injury and fibrosis
• Pkd1l1-deficiency drives biliary atresia through ciliary dysfunction in biliary epithelial cells
• Portal Hypertension in Children: A Tertiary Center Experience in Turkey
• Portojejunostomy: A Salvage Technique for Extrahepatic Bile Ducts Surgery
• Postoperative outcomes of acute-on-chronic liver failure in infants and children with biliary atresia
• Practical approach for the diagnosis of biliary atresia on imaging, part 2: magnetic resonance cholecystopancreatography, hepatobiliary scintigraphy, percutaneous cholecysto-cholangiography, endoscopic retrograde cholangiopancreatography, percutaneous liv
• Preliminary exploration of the efficacy of laparoscopic fluorescence cholangiography (LFC) in the diagnosis of biliary atresia compared with intraoperative cholangiography (IOC)
• Protocols of Investigation of Neonatal Cholestasis-A Critical Appraisal
• Reduced peroxisome proliferator-activated receptor-alpha and bile acid nuclear receptor NR1H4/FXR may affect the hepatic immune microenvironment of biliary atresia
• Regulatory T Cell (Treg) Cytotoxic T Lymphocyte-associated Antigen-4 Deficits in Biliary Atresia (BA) and Disease Rescue With Treg Augmentation in Murine BA
• Rhesus rotavirus receptor-binding site affects high mobility group box 1 release, altering the pathogenesis of experimental biliary atresia
• Robotic monosegment donor hepatectomy for pediatric liver transplantation: First report
• Role of indocyanine green-guided near-infrared fluorescence imaging in identification of the cause of neonatal cholestasis
• Serum Matrix Metalloproteinase 7 as a Diagnostic and Prognostic Biomarker for Extrahepatic Biliary Atresia
• Small Intestinal Adenocarcinoma Arising at the Anastomotic Site after Kasai Operation for Biliary Atresia: A Case Report and Literature Review
• 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
• Study of Intrahepatic Biliary Architecture in Patients Operated for Extrahepatic Biliary Atresia using Magnetic Resonance Cholangiopancreatography
• T-Bet Deficiency Attenuates Bile Duct Injury in Experimental Biliary Atresia
• The clinical impact of macrophage polarity after Kasai portoenterostomy in biliary atresia
• The morphological and histopathological assessment of Alagille syndrome with extrahepatic bile duct obstruction: the importance of the differential diagnosis with subgroup "o" biliary atresia
• The Utility of Gallbladder Absence on Ultrasound for Children With Biliary Atresia
• Use of stool color card as screening tool for biliary atresia in resource-constraint country
• Von Willebrand factor and esophageal varices in children with chronic liver diseases
• What to measure in biliary atresia research: study protocol for developing a core outcome set