Zobrazeno 1 - 4
of 4
pro vyhledávání: '"T E Pankratenko"'
Autor:
E. I. Prokopenko, S. A. Pasov, A. V. Vatazin, A. Ya. Tsalman, T. E. Pankratenko, G. A. Generalova
Publikováno v:
Вестник трансплантологии и искусственных органов, Vol 22, Iss 2, Pp 132-138 (2020)
Atypical hemolytic-uremic syndrome (aHUS) is an extremely rare complement-mediated disease that belongs to the group of thrombotic microangiopathies (TMA). It often reoccurs after kidney transplantation (KT). Previously, KT was considered contraindic
Externí odkaz:
https://doaj.org/article/d26de9c4ba89493b8b4ffe0e11adc5d4
Publikováno v:
Медицинская иммунология, Vol 20, Iss 6, Pp 871-876 (2018)
Atypical hemolytic uremic syndrom (aHUS) is a rare severe life-threatening form of thrombotic microangiopathy. aHUS is thought to be primarily mediated by dysfunctional complement regulation, due to mutations or genetic rearrangement of the complemen
Externí odkaz:
https://doaj.org/article/6ddb4f90dd4a4159bc6cbc00b2a66176
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 0, Iss 42, Pp 58-65 (2016)
Background: Data on etiology and clinical course of CKD stage 3 to 5 in children of preschool age could help obstetricians, pediatricians, and nephrologists with proper diagnostics and management of this condition and prediction of outcomes. Aim: To
Externí odkaz:
https://doaj.org/article/a1938c08b7e24b6c809a0262ed622304
Publikováno v:
Nephrology Dialysis Transplantation. 31:i337-i337
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::002348b60dd6892d0bf5aa6670cff4b9
https://doi.org/10.1093/ndt/gfw179.33
https://doi.org/10.1093/ndt/gfw179.33