Zobrazeno 1 - 6 of 6 pro vyhledávání: '"T. Yu. Abaseeva"'
1
Akademický článek
SOLUBLE ADHESION MOLECULES IN CHILDREN WITH HEMOLYTIC UREMIC SYNDROME
Autor: T. E. Pankratenko, O. V. Moskalets, T. Yu. Abaseeva
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
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2
Akademický článek
THE CAUSES AND THE COURSE OF CHRONIC KIDNEY DISEASE IN CHILDREN OF PRESCHOOL AGE
Autor: T. Yu. Abaseeva, T. E. Pankratenko, A. A. Burov, Kh. M. Emirova, A. L. Muzurov
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
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4
SOLUBLE ADHESION MOLECULES IN CHILDREN WITH HEMOLYTIC UREMIC SYNDROME
Autor: O. V. Moskalets, T. Yu. Abaseeva, T.E. Pankratenko
Publikováno v: Medicinskaâ Immunologiâ, 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://explore.openaire.eu/search/publication?articleId=doi_dedup___::7756ccf835ce265db385513de7ff6493
https://www.mimmun.ru/mimmun/article/view/1672
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Plný text Recenzováno Digitální knihovna AV ČR
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