Intellectual development of patients with biliary atresia who underwent living donor liver transplantation in infancy
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/s00383-021-05042-6.pdf
Reference34 articles.
1. Hartley JL, Davenport M, Kelly DA (2009) Biliary atresia. Lancet 374:1704–1713. https://doi.org/10.1016/S0140-6736(09)60946-6
2. Kasai M, Suzuki S (1959) A new operation for “non-correctable” biliary atresia: hepatic porto-enterostomy. Shujutsu 13:733 (in Japanese)
3. Starzl TE, Marchioro TL, Von Kaulla KN et al (1963) Homotransplantation of the liver in humans. Surg Gynecol Obstet 117:659–676
4. Kasahara M, Umeshita K, Sakamoto S et al (2018) Living donor liver transplantation for biliary atresia: an analysis of 2085 cases in the registry of the Japanese Liver Transplantation Society. Am J Transplant 18:659–668. https://doi.org/10.1111/ajt.14489
5. Mohammad S, Hormaza L, Neighbors K et al (2012) Health status in young adults two decades after pediatric liver transplantation. Am J Transplant 12:1486–1495. https://doi.org/10.1111/j.1600-6143.2012.04080.x
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1. The Adolescent Transplant Recipient: An Overview of Neurocognitive Functioning and Implications for Long‐Term Outcomes;Pediatric Transplantation;2024-08-16
2. Cognitive function of children with biliary atresia after primary living donor liver transplantation;BMC Pediatrics;2024-06-01
3. Cognitive function of children with biliary atresia after primary living donor liver transplantation;2023-12-05
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