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Autor:
Irina V. Ul’yankina, Evgenij S. Nevirovich, Oleg N. Reznik, Aleksej N. Anan’ev, Vasilij S. Dajneko
Publikováno v:
Urologicheskie vedomosti. 9:17-22
Introduction. Autosomal dominant polycystic kidney disease (PKD) is one of the most common hereditary diseases leading to the development of end-stage renal failure. According to modern concepts, nephrectomy of polycystic-altered kidneys in such pati