Educational content from recorded physician discussions — not medical advice. Always talk to your child's care team about your child's situation.
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Underestimating and Underdiagnosing Biliary Atresia: We Can Do Better
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Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society · 2022
article · Oct 2026
Primary Kasai Portoenterostomy1 item
Customized Postoperative Therapy Improves Bile Drainage in Biliary Atresia: A Single Center Preliminary Report
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Controversies in management of biliary atresia (BA) after hepatoportoenterostomy (HPE) lead to variable treatment protocols. We implemented standardized medical management after HPE, customizing the use of antibiotics and corticosteroids ba
article · Oct 2026
Revision Kasai Procedures2 items
Revision Kasai portoenterostomy: A review of indications and outcomes
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The Kasai portoenterostomy (KPE) can provide a surgical cure for children with biliary atresia (BA), without the need for a liver transplant (OLTxp). Revision KPE can be attempted following a failed initial KPE where biliary clearance is no
article · Oct 2026
The beneficial impact of revision of Kasai portoenterostomy for biliary atresia: an institutional study
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Objective: To determine whether portoenterostomy (PE) revision in patients afflicted with biliary atresia (BA) is a viable treatment option and, if so, identify which patients may benefit. Background: BA, the most common cause of neonatal l
article · Oct 2026
Rotavirus-Induced Models7 items
Specific binding sites on Rhesus rotavirus capsid protein dictate the method of endocytosis inducing the murine model of biliary atresia
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Biliary atresia (BA) is the leading indication for pediatric liver transplantation. Rhesus rotavirus (RRV)-induced murine BA develops an obstructive cholangiopathy that mirrors the human disease. We have previously demonstrated the "SRL" mo
article · Oct 2026
Rotavirus Reassortant-Induced Murine Model of Liver Fibrosis Parallels Human Biliary Atresia
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Background And Aims: Biliary atresia (BA) is a devastating neonatal cholangiopathy that progresses to fibrosis and end-stage liver disease by 2 years of age. Portoenterostomy may reestablish biliary drainage, but, despite drainage, virtuall
article · Oct 2026
Rotavirus replication in the cholangiocyte mediates the temporal dependence of murine biliary atresia
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Biliary atresia (BA) is a neonatal disease that results in obliteration of the biliary tree. The murine model of BA, which mirrors the human disease, is based upon infection of newborn mice with rhesus rotavirus (RRV), leading to an obstruc
article · Oct 2026
The rhesus rotavirus gene encoding VP4 is a major determinant in the pathogenesis of biliary atresia in newborn mice
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Biliary atresia (BA) is a devastating disease of childhood for which increasing evidence supports a viral component in pathogenesis. The murine model of BA is induced by perinatal infection with rhesus rotavirus (RRV) but not with other str
article · Oct 2026
Prevention of the murine model of biliary atresia after live rotavirus vaccination of dams
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Maternal vaccination against RRV can prevent the rotavirus-induced murine model of BA in newborn mouse pups.
article · Oct 2026
Cholangiocyte secretion of chemokines in experimental biliary atresia
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Unlabelled: Biliary atresia (BA) is a disease of the newborn that results in obstruction of the biliary tree. The cause of BA remains unknown; however, recent studies using the murine model of biliary atresia have found that rotavirus infec
article · Oct 2026
Cholangiocyte expression of alpha2beta1-integrin confers susceptibility to rotavirus-induced experimental biliary atresia
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Inoculation of BALB/c mice with rhesus rotavirus (RRV) in the newborn period results in biliary epithelial cell (cholangiocyte) infection and the murine model of biliary atresia. Rotavirus infection of a cell requires attachment, which is g
article · Oct 2026
Immune Mechanisms1 item
T-Bet Deficiency Attenuates Bile Duct Injury in Experimental Biliary Atresia
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Biliary atresia (BA) is an obstructive neonatal cholangiopathy leading to liver cirrhosis and end stage liver disease. A Kasai portoenterostomy may restore biliary drainage, but most patients ultimately require liver transplantation for sur
article · Oct 2026
Extracorporeal Membrane Oxygenation in a Patient with Biliary Atresia: Case and Review of Extracorporeal Life Support Organization Data
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Biliary atresia is a newborn cholangiopathy that may lead to portopulmonary hypertension and cirrhosis-induced cardiomyopathy while awaiting liver transplantation. Extracorporeal life support and hepatic toxin filtration are life-saving int
article · Oct 2026
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