Long-term native liver survival in infants with biliary atresia and use of a stool color card: Case-control study
Author:
Affiliation:
1. Department of Hygiene and Public Health; Osaka Medical College; Osaka Japan
2. Department of Hepatology; National Medical Center for Children and Mothers; National Center for Child Health and Development; Tokyo Japan
Funder
National Center for Child Health and Development
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ped.13360/fullpdf
Reference16 articles.
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2. A new operation for non-correctable biliary atresia: Hepatic portoenterostomy;Kasai;Shujutsu,1959
3. 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;Kasahara;Am. J. Transplant.,2013
4. Impact of age at Kasai operation on its results in late childhood and adolescence: A rational basis for biliary atresia screening;Serinet;Pediatrics,2009
5. Early surgical outcomes and pathological scoring values of older infants (≥ 90 d old) with biliary atresia;Chen;J. Pediatr. Surg.,2012
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