Zobrazeno 1 - 10
of 37
pro vyhledávání: '"A. E. Pashkova"'
Autor:
R. M. Kurabekova, O. E. Gichkun, O. M. Tsirulnikova, I. E. Pashkova, E. A. Vakurova, O. P. Shevchenko, S. V. Gautier
Publikováno v:
Вестник трансплантологии и искусственных органов, Vol 26, Iss 3, Pp 168-175 (2024)
Objective: to evaluate the occurrence of single nucleotide polymorphisms (SNPs) in transforming growth factor beta 1 (TGFB1) – rs1800469, rs1800470, rs1800471 – and their haplotypes in children with biliary atresia (BA).Materials and methods. We
Externí odkaz:
https://doaj.org/article/ff796dccbc324299b50a2c6f4ec32d65
Autor:
Inga V. Anisimova, Marina B. Albegova, Madlena E. Bagaeva, Galina V. Baidakova, Aleksandr A. Baranov, Nato D. Vashakmadze, Elena A. Vishneva, Olga S. Gundobina, Anna V. Degtiareva, Marat V. Ezhov, Maria S. Zharkova, Nataliia V. Zhurkova, Ekaterina Yu. Zaharova, Vladimir T. Ivashkin, Elena A. Kamenets, Sergey I. Kutzev, Alla E. Lavrova, Irina A. Matinian, Svetlana V. Mikhailova, Leyla S. Namazova-Baranova, Irina E. Pashkova, Elena E. Petriaykina, Tatiana M. Pervunina, Nataliia L. Pechatnikova, Nelia S. Pogosian, Svetlana A. Repina, Lilia R. Selimzianova, Tamara A. Skvortsova, Tatiana V. Strokova, Dmitriy M. Subbotin, Andrey N. Surkov, Elena L. Tumanova, Ekaterina G. Tzimbalova
Publikováno v:
Педиатрическая фармакология, Vol 20, Iss 4, Pp 337-354 (2023)
Lysosomal acid lipase deficiency is s a rare hereditary enzymopathy. The article presents epidemiological data and features of etiopathogenesis of two phenotypic forms of lysosomal acid lipase deficiency — Wolman disease and cholesterol ester stora
Externí odkaz:
https://doaj.org/article/bbadc6c645734812b65cf6da590af630
Autor:
R. M. Kurabekova, O. V. Silina, O. M. Tsirulnikova, I. E. Pashkova, O. E. Gichkun, G. A. Olefirenko, S. Yu. Oleshkevich, A. R. Monakhov, O. P. Shevchenko
Publikováno v:
Вестник трансплантологии и искусственных органов, Vol 25, Iss 2, Pp 140-147 (2023)
Growth hormone (GH) plays a leading role in the regulation of cell and tissue metabolism and growth. Its effects are mediated through the so-called somatomedins, among which the most important is the liver-produced insulinlike growth factor 1 (IGF-1)
Externí odkaz:
https://doaj.org/article/6ab49f7f00574d498dbc851125c62526
Autor:
N. L. Pulnova, T. N. Rybalkina, N. V. Karazhas, R. E. Bosh’ian, M. N. Kornienko, O. F. Kabikova, N. I. Gabrielyan, I. E. Pashkova, O. V. Silina
Publikováno v:
Детские инфекции (Москва), Vol 21, Iss 4, Pp 21-26 (2022)
Infections occupy one of the central places among the complications of transplants. The frequency of fatal infectious complications during the first twelve months after transplantation ranges from 2.6 to 51.7%. Identifying markers of opportunistic in
Externí odkaz:
https://doaj.org/article/4b20141318fe46afb60cbf08d642bea8
Publikováno v:
Вестник трансплантологии и искусственных органов, Vol 24, Iss 2, Pp 65-70 (2022)
Growth hormone (GH) and insulin-like growth factor 1 (IGF-1) are the most important regulators of growth, regeneration and metabolism. The influence of GH and IGF-1 on pediatric liver transplant outcomes is mediated through growth and body weight reg
Externí odkaz:
https://doaj.org/article/f39d49eaa2d8424499f399d49d1425a9
Autor:
A. V. Syrkina, O. M. Tsirulnikova, I. E. Pashkova, O. V. Silina, E. V. Chekletsova, S. Yu. Oleshkevich
Publikováno v:
Вестник трансплантологии и искусственных органов, Vol 23, Iss 4, Pp 8-12 (2022)
Background. Liver cirrhosis occurring before 1 year of age can affect a child’s development. Liver transplantation is the only radical treatment for decompensated cirrhosis. In biliary atresia, cirrhosis develops during the first months of life. Th
Externí odkaz:
https://doaj.org/article/52075dd3256b4f55a24c7e490bfea9ab
Publikováno v:
Вестник трансплантологии и искусственных органов, Vol 23, Iss 4, Pp 13-18 (2022)
Cytomegalovirus (CMV) infection is the most severe viral infection in renal transplant recipients, which can occur in the post-transplant period in both adult and pediatric recipients. Developing and applying an effective prevention and treatment str
Externí odkaz:
https://doaj.org/article/850ebcd6deab4294bf5234a3d1e45327
Autor:
A. V. Syrkina, I. E. Pashkova, A. R. Monakhov, O. V. Silina, E. V. Chekletsova, S. Yu. Oleshkevich, I. B. Komarova, O. M. Tsirulnikova
Publikováno v:
Вестник трансплантологии и искусственных органов, Vol 23, Iss 3, Pp 66-72 (2021)
Background. In young children, the most common liver disease leading to transplantation is biliary atresia. Liver transplantation has fundamentally improved the survival rate of children with biliary atresia. Studies on developmental outcomes in chil
Externí odkaz:
https://doaj.org/article/22a8e5d9020b4fc8b0358c6fc66e78d6
Autor:
I. A. Miloserdov, V. S. Bogdanov, P. M. Gadzhieva, D. A. Saydulaev, A. A. Kartashev, E. G. Kulikova, I. E. Pashkova
Publikováno v:
Вестник трансплантологии и искусственных органов, Vol 23, Iss 2, Pp 60-66 (2021)
Background. Focal segmental glomerulosclerosis (FSGS) of the graft in kidney recipients is a rare and difficultto-diagnose post-kidney transplant complication, which can lead to graft loss and death of the recipient. A unified protocol is required fo
Externí odkaz:
https://doaj.org/article/005fb9db92134b36a2040f8dc9d56e66
Autor:
R. M. Kurabekova, O. M. Tsirulnikova, O. E. Gichkun, G. A. Olefirenko, I. E. Pashkova, A. A. Belchenkov, O. P. Shevchenko
Publikováno v:
Вестник трансплантологии и искусственных органов, Vol 23, Iss 2, Pp 13-20 (2021)
Introduction. To prevent post-transplant complications associated with unbalanced immunosuppression, objective indicators reflecting the state of the immune system and associated with the immunosuppressant dose are required. In pediatric liver transp
Externí odkaz:
https://doaj.org/article/997f16983d9d4093922b5f7dfab84660