Cell Therapy for Biliary Atresia
Author:
Publisher
Springer Nature Singapore
Link
https://link.springer.com/content/pdf/10.1007/978-981-96-1261-1_14
Reference22 articles.
1. Antala, S., & Taylor, S. A. (2022). Biliary atresia in children: Update on disease mechanism, therapies, and patient outcomes. Clinics in Liver Disease, 26, 341–354. https://doi.org/10.1016/j.cld.2022.03.001
2. Chardot, C., Buet, C., Serinet, M. O., et al. (2013). Improving outcomes of biliary atresia: French national series 1986–2009. Journal of Hepatology, 58, 1209–1217. https://doi.org/10.1016/j.jhep.2013.01.040
3. Hopkins, P. C., Yazigi, N., & Nylund, C. M. (2017). Incidence of biliary atresia and timing of hepatoportoenterostomy in the United States. The Journal of Pediatrics, 187, 253–257. https://doi.org/10.1016/j.jpeds.2017.05.006
4. Chardot, C., Carton, M., Spire-Bendelac, N., et al. (1999). Epidemiology of biliary atresia in France: A national study 1986–96. Journal of Hepatology, 31, 1006–1013. https://doi.org/10.1016/s0168-8278(99)80312-2
5. Wada, H., Muraji, T., Yokoi, A., et al. (2007). Insignificant seasonal and geographical variation in incidence of biliary atresia in Japan: A regional survey of over 20 years. Journal of Pediatric Surgery, 42, 2090–2092. https://doi.org/10.1016/j.jpedsurg.2007.08.035
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