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Autor:
I. V. Nikitina, I. M. Amelin, I. Sh. Makhmudov, O. A. Krogh-Jensen, E. A. Tumasyan, А. A. Lenyushkina, A. V. Degtyareva, D. N. Degtyarev
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 65, Iss 5, Pp 73-82 (2020)
Galactosemia is a hereditary disease characterized by impaired galactose metabolism. A newborn fed by breast milk or an adapted infant formula quickly develop clinical manifestations of the disease associated with accumulation of galactose and its to
Externí odkaz:
https://doaj.org/article/f351c4565d584aacb0deb0a1c18a83a6