Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Y V SIDOROVA"'
Autor:
N G Chernova, Y V Sidorova, S Y Smirnova, N V Ryzhikova, E E Nikulina, A M Kovrigina, M N Sinitsyna, A B Sudarikov
Publikováno v:
Терапевтический архив, Vol 91, Iss 7, Pp 63-69 (2019)
Aim: to determine molecular diagnostics routine for different tissue samples in angioimmunoblastic T-cell lymphoma. Materials and methods. Molecular studies were performed for 84 primary AITL patients. The median age was 61 year (29-81); the male to
Externí odkaz:
https://doaj.org/article/ac72a42eedfd496684231e0083be1b9c
Autor:
N G CHERNOVA, E E ZVONKOV, D S BADMAZHAPOVA, M N SINITSYNA, L A GREBENYUK, Y V SIDOROVA, I E KOSTINA, A M KOVRIGINA, T N OBUKHOVA, A B SUDARIKOV, V G SAVCHENKO
Publikováno v:
Терапевтический архив, Vol 90, Iss 7, Pp 77-81 (2018)
Nodal anaplastic ALK-negative large cell lymphoma (nALCL, ALK-) is a Т-cell lymphoma that is characterized by aggressive clinical course and low sensitivity to СНОР (cyclophosphamide, doxorubicin, vincristine, prednisolone) and other chemotherap
Externí odkaz:
https://doaj.org/article/e9ba462d8d304be8a6be0d343c1661cf
Autor:
N G CHERNOVA, N P SOBOLEVA, S A MARIINA, Y V SIDOROVA, M N SINITSYNA, V N DVIRNYK, D S BADMAZHAPOVA, Y E VINOGRADOVA, E E ZVONKOV, V G SAVCHENKO
Publikováno v:
Терапевтический архив, Vol 90, Iss 7, Pp 51-56 (2018)
Contex. Angioimmunoblastic T-cell lymphoma (AITL) is a rare form of non-Hodgkins lymphoma, characterized by generalized lymphadenopathy, hepatosplenomegaly and dysproteinemia. Hypergammaglobulinaemia is revealed in 50-83% pts with AITL. However, the
Externí odkaz:
https://doaj.org/article/c60d2a7924bc4112967d0c4ce8a16e0d
Autor:
V R Gorodetsky, N A Probatova, O A Logvinenko, V I Vasiljev, Y V Sidorova, N V Ryzikova, N A Kupryshina, T T Kondratjeva, A I Pavlovskaya, E L Nasonov
Publikováno v:
Научно-практическая ревматология, Vol 47, Iss 3, Pp 94-101 (2009)
In the article is presented a detailed description of two rare cases of lymphoid neoplasia (αβT-cell large granular lymphocyte leukaemia and primary γδT-cell lymphoma of the spleen) in patients with rheumatoid arthritis. These examples illustrate
Externí odkaz:
https://doaj.org/article/67a2d329286b48618b290441eb0e08f8
Publikováno v:
Фармакокинетика и Фармакодинамика, Vol 0, Iss 1, Pp 18-24 (2020)
Background. Treatment of depression disorders is insufficiently effectively. It uses for increasing of treatment efficiency empirical selected combinations of antidepressants with preparations of lithium and certain others, which possess cerebroprote
Externí odkaz:
https://doaj.org/article/8ac4bc5c6ae54fb2b6e46dbb0432d5fa
Autor:
N. G. Chernova, D. S. Tihomirov, N. P. Soboleva, S. A. Mariina, Y. V. Sidorova, M. N. Sinitsyna, V. N. Dvirnyk, S. M. Kulikov, T. A. Tupoleva, E. E. Zvonkov
Publikováno v:
Вопросы вирусологии, Vol 63, Iss 4, Pp 171-176 (2018)
Introduction. Angioimmunoblastic T-cell lymphoma (AITL) is associated with the Epstein-Barr virus (EBV) in most cases. It is believed polyclonal hypergammaglobulinaemia observed in 53-80% of AITL patients has anti-herpes viral antibodies as its subst
Externí odkaz:
https://doaj.org/article/8193967fc3f34011900a1ac1854bbf5c
Publikováno v:
Medical Visualization. 26:130-138
Autor:
N. G. Chernova, M. N. Sinitsyna, A. M. Kovrigina, Y. V. Sidorova, I. V. Galtseva, S. A. Mar’ina, V. N. Dvirnyk, E. E. Zvonkov
Publikováno v:
Onkogematologiâ, Vol 12, Iss 4, Pp 28-33 (2018)
Angioimmunoblastic T-cell lymphoma is a rare T-cell lymphoproliferative disease with generalized lymphadenopathy, hepatosplenomegaly, intoxication and polyclonal hypergammaglobulinemia. The persistence of plasma cells in peripheral blood can be a man