Improved survival in biliary atresia patients in the present era of liver transplantation
- 31 March 1993
- journal article
- Published by Elsevier in Journal of Pediatric Surgery
- Vol. 28 (3) , 382-386
- https://doi.org/10.1016/0022-3468(93)90236-e
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Segmental orthotopic hepatic transplantation as a means to improve patient survival and diminish waiting-list mortalityJournal of Pediatric Surgery, 1991
- Long-term outcome after surgery for biliary atresiaGastroenterology, 1990
- Biliary atresia registry, 1976 to 1989Journal of Pediatric Surgery, 1990
- Long-term survival after Kasai's operation for biliary atresiaPediatric Surgery International, 1990
- The therapy of biliary atresia combining the Kasai portoenterostomy with liver transplantation: A single center experienceJournal of Pediatric Surgery, 1990
- Optimal therapy for patients with biliary atresia: Portoenterostomy (“Kasai” procedures) versus primary transplantationJournal of Pediatric Surgery, 1990
- Long-Term Follow-Up Study of Patients with Cholangitis after Successful Kasai Operation in Biliary AtresiaJournal of Pediatric Gastroenterology and Nutrition, 1989
- Liver transplantation and kasai operation in the first year of life: Therapeutic dilemma in biliary atresiaThe Journal of Pediatrics, 1987
- Results of re-operations for correction of extrahepatic biliary atresiaJournal of Pediatric Surgery, 1979
- Prognosis of uncorrected biliary atresia: An updateJournal of Pediatric Surgery, 1978