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Autor:
Véronique Chirouze, Alexandre Lapillonne, Alain Lachaux, Michelle Chambon, Valérie Mamoux, Vincent Fournier, Christine Hakme
Publikováno v:
Journal of Pediatric Gastroenterology and Nutrition. 30:528-532
BACKGROUND The long-chain polyunsaturated fatty acid (LC-PUFA) status of infants with untreated biliary atresia (BA) is known to be poor and is correlated to the severity of the liver disease. Liver transplantation (LT) markedly increases survival of