Zobrazeno 1 - 2
of 2
pro vyhledávání: '"O. A. Krogh-Jensen"'
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8f302dcc548d9f8486c888235e6094b
https://doi.org/10.21508/1027-4065-2020-65-5-73-82
https://doi.org/10.21508/1027-4065-2020-65-5-73-82
Autor:
I. V. Nikitina, A. E. Donnikov, O. A. Krogh-Jensen, A. A. Lenyushkina, N. D. Degtyareva, А. V. Degtyareva
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 65, Iss 4, Pp 16-26 (2020)
It is a common fact that children are less susceptible to COVID-19 than adults, and they usually have milder forms often without symptoms, due to the age-related characteristics of their immune response and the features of the renin-angiotensin syste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99ba4e0162b8cc2aec37bdba00ca4c72
https://doi.org/10.21508/1027-4065-2020-65-4-16-26
https://doi.org/10.21508/1027-4065-2020-65-4-16-26