Liver transplantation in infants with biliary atresia: comparison of primary versus temporary abdominal closure
Author:
Publisher
Springer Science and Business Media LLC
Subject
Surgery
Link
http://link.springer.com/content/pdf/10.1007/s00423-016-1525-x.pdf
Reference17 articles.
1. Broering DC, Kim JS, Mueller T, Fischer L, Ganschow R, Bicak T et al (2004) One hundred thirty-two consecutive pediatric liver transplants without hospital mortality: lessons learned and outlook for the future. Ann Surg 240:1002–1012
2. Lee S, Park H, Moon SB, Jung SM, Kim JM, Kwon CH et al (2013) Long-term results of biliary atresia in the era of liver transplantation. Pediatr Surg Int 29:1297–1301
3. Sasaki H, Tanaka H, Wada M, Kazama T, Nishi K, Nakamura M et al (2014) Liver transplantation following the Kasai procedure in treatment of biliary atresia: a single institution analysis. Pediatr Surg Int 30:871–875
4. Schukfeh N, Lenz V, Metzelder ML, Paul A, Mathe Z, Kathemann S et al (2015) First case studies of successful ABO-incompatible living-related liver transplantation in infants in Germany. Eur J Pediatr Surg 25:77–81
5. Schukfeh N, Doerner JM (2014) Heintschel von Heinegg E, Steinmann J, Metzelder ML, Kathemann S et al. Spectrum of pathogens in native liver, bile, and blood during pediatric liver transplantation. Pediatr Transplant 18:266–271
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