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Autor:
Anastasiа A. Rogozhinа, Olga N. Ivanova, Larisа O. Minushkinа, Victotia A. Brazhnik, Ekaterina A. Zubova, Ludmila A. Ivanovа, Dmitry A. Zateyshchikov
Publikováno v:
Клиническая практика, Vol 14, Iss 2, Pp 36-43 (2023)
Background: The clinical phenotype of familial hypercholesterolemia (FH) combined with the classical genetic defects of this disease increase the risk of coronary artery disease (CAD) in the case of a high level of lipoprotein (a) (Lp(a)). Aim: To as
Externí odkaz:
https://doaj.org/article/f25df69e694a4c2cb9d4db1c5c0ea7f7