Outcomes of adult native liver survivors with biliary atresia: the current situation in Japan
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Surgery,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00383-023-05551-6.pdf
Reference25 articles.
1. Shinkai M, Ohhama Y, Take H et al (2009) Long-term outcome of children with biliary atresia who were not transplanted after the Kasai operation: >20-year experience at a Children’s Hospital. J Pediatr Gastroenterol Nutr 48:443–450. https://doi.org/10.1097/mpg.0b013e318189f2d5
2. Parolini F, Boroni G, Milianti S et al (2019) Biliary atresia: 20–40-year follow-up with native liver in an Italian centre. J Pediatr Surg 54:1440–1444. https://doi.org/10.1016/j.jpedsurg.2018.10.060
3. Nio M, Wada M, Sasaki H et al (2012) Risk factors affecting late-presenting liver failure in adult patients with biliary atresia. J Pediatr Surg 47:2179–2183. https://doi.org/10.1016/j.jpedsurg.2012.09.003
4. International registry of organ donation and transplantation (IRODaT). https://www.irodat.org/?p=database. Donation and Transplantation Institute, Barcelona; c2022 Accessed 1 Dec 2022
5. Japan Organ Transplant Network. (JOTN). https://www.jotnw.or.jp/. JOTN, Tokyo; c2022. Accessed 1 Dec 2022
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