Post-Transplant Disease Recurrence in Pediatric PSC
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology,General Medicine
Link
http://link.springer.com/article/10.1007/s11894-018-0649-2/fulltext.html
Reference62 articles.
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2. • Deneau M, Jensen MK, Holmen J, Williams MS, Book LS, Guthery SL. Primary sclerosing cholangitis, autoimmune hepatitis, and overlap in Utah children: epidemiology and natural history. Hepatology. 2013;58(4):1392–400. Population-based study of IBD and PSC epidemiology in children.
3. Squires RH, Ng V, Romero R, Ekong U, Hardikar W, Emre S, et al. Evaluation of the pediatric patient for liver transplantation: 2014 practice guideline by the American Association for the Study of Liver Diseases, American Society of Transplantation and the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. Hepatology. 2014;60(1):362–98.
4. •• Miloh T, Anand R, Yin W, Vos M, Kerkar N, Alonso E, et al. Pediatric liver transplantation for primary sclerosing cholangitis. Liver Transpl. 2011;17(8):925–33. The SPLIT database analysis of pediatric PSC post-LT outcomes.–33.
5. Luthold SC, Kaseje N, Jannot AS, Mentha G, Majno P, Toso C, et al. Risk factors for early and late biliary complications in pediatric liver transplantation. Pediatr Transplant. 2014;18(8):822–30.
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2. Recurrent Primary Sclerosing Cholangitis: Current Understanding, Management, and Future Directions;Seminars in Liver Disease;2021-06-28
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