Gallengangatresie und angeborene Cholestasesyndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Internal Medicine
Link
http://link.springer.com/article/10.1007/s00108-018-0506-2/fulltext.html
Reference32 articles.
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3. Chardot C, Buet C, Serinet MO et al (2013) Improving outcomes of biliary atresia: French national series 1986–2009. J Hepatol 58(6):1209–1217. https://doi.org/10.1016/j.jhep.2013.01.040
4. de Vries W, de Langen ZJ, Groen H et al (2012) Biliary atresia in the Netherlands: outcome of patients diagnosed between 1987 and 2008. J Pediatr 160(4):638–644.e2. https://doi.org/10.1016/j.jpeds.2011.09.061
5. 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(4):443–450
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