{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,17]],"date-time":"2026-04-17T14:01:03Z","timestamp":1776434463591,"version":"3.51.2"},"reference-count":28,"publisher":"Baskent University","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Exp Clin Transplant"],"published-print":{"date-parts":[[2026,3]]},"DOI":"10.6002\/ect.2025.0201","type":"journal-issue","created":{"date-parts":[[2026,4,17]],"date-time":"2026-04-17T12:51:14Z","timestamp":1776430274000},"source":"Crossref","is-referenced-by-count":0,"title":[],"prefix":"10.6002","volume":"24","member":"4021","reference":[{"key":"ref0","doi-asserted-by":"publisher","unstructured":"1. Nio M, Wada M, Sasaki H, Kazama T, Tanaka H, Kudo H. Technical standardization of Kasai portoenterostomy for biliary atresia. J Pediatr Surg. 2016;51(12):2105-2108. doi:10.1016\/j.jpedsurg.2016.09.047","DOI":"10.1016\/j.jpedsurg.2016.09.047"},{"key":"ref1","doi-asserted-by":"publisher","unstructured":"2. Raia S, Nery JR, Mies S. Liver transplantation from live donors. Lancet. 1989;2(8661):497. doi:10.1016\/s0140-6736(89)92101-6","DOI":"10.1016\/S0140-6736(89)92101-6"},{"key":"ref2","doi-asserted-by":"publisher","unstructured":"3. Inomata Y, Oike F, Okamoto S, et al. Impact of the development of a liver transplant program on the treatment of biliary atresia in an institution in Japan. J Pediatr Surg. 1997;32(8):1201-1205. doi:10.1016\/s0022-3468(97)90682-5","DOI":"10.1016\/S0022-3468(97)90682-5"},{"key":"ref3","doi-asserted-by":"publisher","unstructured":"4. Kasahara M, Umeshita K, Sakamoto S, et al. Living donor liver transplantation for biliary atresia: an analysis of 2085 cases in the registry of the Japanese Liver Transplantation Society. Am J Transplant. 2018;18:659-668. doi:10.1111\/ajt.14489","DOI":"10.1111\/ajt.14489"},{"key":"ref4","unstructured":"5. Ohi R, Ibrahim M. Biliary atresia. Semin Pediatr Surg. 1992;1:115-124."},{"key":"ref5","doi-asserted-by":"publisher","unstructured":"6. Ichida F, Tsuji T, Omata M, et al. New Inuyama classification; new criteria for histological assessment of chronic hepatitis. Int Hepatol Commun. 1996;6(2):112-119. doi:10.1016\/S0928-4346(96)00325-8","DOI":"10.1016\/S0928-4346(96)00325-8"},{"key":"ref6","doi-asserted-by":"publisher","unstructured":"7. Nio M. Japanese biliary atresia registry. Pediatr Surg Int. 2017;33(12):1319-1325. doi:10.1007\/s00383-017-4160-x","DOI":"10.1007\/s00383-017-4160-x"},{"key":"ref7","doi-asserted-by":"publisher","unstructured":"8. Serinet MO, Brou\u00e9 P, Jacquemin E, et al. Management of patients with biliary atresia in France: results of a decentralized policy 1986-2002. Hepatology. 2006;44(1):75-84. doi:10.1002\/hep.21219","DOI":"10.1002\/hep.21219"},{"key":"ref8","doi-asserted-by":"publisher","unstructured":"9. Shneider BL, Brown MB, Haber B, et al. A multicenter study of the outcome of biliary atresia in the United States, 1997 to 2000. J Pediatr. 2006;148(4):467-474. doi:10.1016\/j.jpeds.2005.12.054","DOI":"10.1016\/j.jpeds.2005.12.054"},{"key":"ref9","doi-asserted-by":"publisher","unstructured":"10. Davenport M, Ong E, Sharif K, et al. Biliary atresia in England and Wales: results of centralization and new benchmark. J Pediatr Surg. 2011;46(9):1689-1694. doi:10.1016\/j.jpedsurg.2011.04.013","DOI":"10.1016\/j.jpedsurg.2011.04.013"},{"key":"ref10","doi-asserted-by":"publisher","unstructured":"11. Lampela H, Kosola S, Heikkil\u00e4 P, Lohi J, Jalanko H, Pakarinen MP. Native liver histology after successful portoenterostomy in biliary atresia. J Clin Gastroenterol. 2014;48(8):721-728. doi:10.1097\/MCG.0000000000000013","DOI":"10.1097\/MCG.0000000000000013"},{"key":"ref11","doi-asserted-by":"publisher","unstructured":"12. Kerola A, Lampela H, Lohi J, et al. Molecular signature of active fibrogenesis prevails in biliary atresia after successful portoenterostomy. Surgery. 2017;162(3):548-556. doi:10.1016\/j.surg.2017.04.013","DOI":"10.1016\/j.surg.2017.04.013"},{"key":"ref12","doi-asserted-by":"publisher","unstructured":"13. Jain V, Burford C, Alexander EC, et al. Prognostic markers at adolescence in patients requiring liver transplantation for biliary atresia in adulthood. J Hepatol. 2019;71(1):71-77. doi:10.1016\/j.jhep.2019.03.005","DOI":"10.1016\/j.jhep.2019.03.005"},{"key":"ref13","doi-asserted-by":"publisher","unstructured":"14. Bessho K. Complications and quality of life in long-term survivors of biliary atresia with their native livers. J Pediatr. 2015;167(6):1202-1206. doi:10.1016\/j.jpeds.2015.08.041","DOI":"10.1016\/j.jpeds.2015.08.041"},{"key":"ref14","doi-asserted-by":"publisher","unstructured":"15. Uchida Y, Kasahara M, Egawa H, et al. Long-term outcome of adult-to-adult living donor liver transplantation for post-Kasai biliary atresia. Am J Transplant. 2006;6(10):2443-2448. doi:10.1111\/j.1600-6143.2006.01487.x","DOI":"10.1111\/j.1600-6143.2006.01487.x"},{"key":"ref15","doi-asserted-by":"publisher","unstructured":"16. Okamoto T, Okajima H, Ogawa E, et al. Progress in living donor liver transplantation for biliary atresia and challenges faced: a thirty-year single institutional experience. J Pediatr Surg. 2022;57(11):649-655. doi:10.1016\/j.jpedsurg.2022.03.009","DOI":"10.1016\/j.jpedsurg.2022.03.009"},{"key":"ref16","doi-asserted-by":"publisher","unstructured":"17. Sanada Y, Sakuma Y, Onishi Y, et al. Long-term outcomes in pediatric patients who underwent living donor liver transplantation for biliary atresia. Surgery. 2022;171(6):1671-1676. doi:10.1016\/j.surg.2021.11.027","DOI":"10.1016\/j.surg.2021.11.027"},{"key":"ref17","doi-asserted-by":"publisher","unstructured":"18. Udagawa D, Hasegawa Y, Obara H, et al. Risk assessment of liver transplantation after Kasai portoenterostomy in children and adults. J Surg Res. 2023;290:109-115. doi:10.1016\/j.jss.2023.04.014","DOI":"10.1016\/j.jss.2023.04.014"},{"key":"ref18","doi-asserted-by":"publisher","unstructured":"19. Nio M, Sasaki H, Tanaka H, et al. Redo surgery for biliary atresia. Pediatr Surg Int. 2013;29(10):989-993. doi:10.1007\/s00383-013-3396-3.","DOI":"10.1007\/s00383-013-3396-3"},{"key":"ref19","doi-asserted-by":"publisher","unstructured":"20. Nakamura H, Kawano T, Yoshizawa K, et al. Long-term follow-up for anicteric survival with native liver after redo Kasai: a first report. J Pediatr Surg. 2016;51(12):2109-2112. doi:10.1016\/j.jpedsurg.2016.09.049","DOI":"10.1016\/j.jpedsurg.2016.09.049"},{"key":"ref20","doi-asserted-by":"publisher","unstructured":"21. Barshes NR, Lee TC, Balkrishnan R, Karpen SJ, Carter BA, Goss JA. Orthotopic liver transplantation for biliary atresia: the U.S. experience. Liver Transpl. 2005;11(10):1193-1200. doi:10.1002\/lt.20509","DOI":"10.1002\/lt.20509"},{"key":"ref21","doi-asserted-by":"publisher","unstructured":"22. Fouquet V, Alves A, Branchereau S, et al. Long-term outcome of pediatric liver transplantation for biliary atresia: a 10-year follow-up in a single center. Liver Transpl. 2005;11(2):152-160. doi:10.1002\/lt.20358","DOI":"10.1002\/lt.20358"},{"key":"ref22","doi-asserted-by":"publisher","unstructured":"23. Chen CL, Concejero A, Wang CC, et al. Living donor liver transplantation for biliary atresia: a single-center experience with first 100 cases. Am J Transplant. 2006;6(11):2672-2679. doi:10.1111\/j.1600-6143.2006.01528.x","DOI":"10.1111\/j.1600-6143.2006.01528.x"},{"key":"ref23","doi-asserted-by":"publisher","unstructured":"24. Arnon R, Annunziato RA, Willis A, et al. Liver transplantation for children with biliary atresia in the pediatric end-stage liver disease era: the role of insurance status. Liver Transpl. 2013;19(5):543-550. doi:10.1002\/lt.23607","DOI":"10.1002\/lt.23607"},{"key":"ref24","doi-asserted-by":"publisher","unstructured":"25. Kasahara M, Umeshita K, Inomata Y, Uemoto S; Japanese Liver Transplantation Society. Long-term outcomes of pediatric living donor liver transplantation in Japan: an analysis of more than 2200 cases listed in the registry of the Japanese Liver Transplantation Society. Am J Transplant. 2013;13(7):1830-1839. doi:10.1111\/ajt.12276","DOI":"10.1111\/ajt.12276"},{"key":"ref25","doi-asserted-by":"publisher","unstructured":"26. Neto JS, Feier FH, Bierrenbach AL, et al. Impact of Kasai portoenterostomy on liver transplantation outcomes: a retrospective cohort study of 347 children with biliary atresia. Liver Transpl. 2015;21(7):922-927. doi:10.1002\/lt.24132","DOI":"10.1002\/lt.24132"},{"key":"ref26","doi-asserted-by":"publisher","unstructured":"27. Kasahara M, Umeshita K, Eguchi S, et al. Outcomes of pediatric liver transplantation in Japan: a report from the registry of the Japanese Liver Transplantation Society. Transplantation. 2021;105(12):2587-2595. doi:10.1097\/TP.0000000000003610","DOI":"10.1097\/TP.0000000000003610"},{"key":"ref27","doi-asserted-by":"publisher","unstructured":"28. Harpavat S, Hawthorne K, Setchell KDR, et al.; for Childhood Liver Disease Research Network (ChiLDReN). Serum bile acids as a prognostic biomarker in biliary atresia following Kasai portoenterostomy. Hepatology. 2023;77(3):862-873. doi:10.1002\/hep.32800","DOI":"10.1002\/hep.32800"}],"container-title":["Experimental and Clinical Transplantation"],"original-title":[],"deposited":{"date-parts":[[2026,4,17]],"date-time":"2026-04-17T13:18:32Z","timestamp":1776431912000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ectrx.org\/detail\/archive\/2026\/24\/3\/0\/243\/0"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,3]]},"references-count":28,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2026,3]]}},"URL":"https:\/\/doi.org\/10.6002\/ect.2025.0201","relation":{},"ISSN":["1304-0855","2146-8427"],"issn-type":[{"value":"1304-0855","type":"print"},{"value":"2146-8427","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,3]]}}}