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Autor:
Mikhail A. Firsov, Pavel A. Simonov, Daria A. Duntz, Elena V. Shalamay, Ekaterina A. Alekseeva, Eugene A. Bezrukov, Sergey V. Sorsunov
Publikováno v:
Consilium Medicum, Vol 25, Iss 7, Pp 456-460 (2023)
Background. According to foreign and domestic authors, autosomal dominant polycystic kidney disease (ADPKD) is a disease accompanied by a progressive deterioration in the functional state of the kidneys and occupies a significant contribution to the
Externí odkaz:
https://doaj.org/article/186a70b36161474c870091b6a449ec66