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Autor:
R. Piotrowski, Karl-Heinz Herzig, Dorota Sands, A. Nowakowska, Jarosław Walkowiak, Katarzyna Zybert, Andrzej Milanowski
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 40(2)
BACKGROUND Most cystic fibrosis (CF) patients develop steatorrhea and require pancreatic enzyme replacement therapy. However, there are few data regarding the decline of exocrine pancreatic function within the first years of life in relation to CF ge