Zobrazeno 1 - 10
of 315
pro vyhledávání: '"A M KOVRIGINA"'
Autor:
E S Nesterova, S K Kravchenko, A M Kovrigina, E G Gemdzhian, L V Plastinina, F E Babaeva, T N Obukhova, A U Magomedova, T V Gaponova, A M Kremenetskaya, A I Vorobyev
Publikováno v:
Терапевтический архив, Vol 91, Iss 8, Pp 75-83 (2019)
Follicular lymphoma (FL) is a tumor that develops from the B cells of the germinal center; characterized by recurrent and remitting course of the disease, the transformation of a tumor into diffuse large B-cell lymphoma (DLBCL) is possible. In genera
Externí odkaz:
https://doaj.org/article/3da6121a47664f0d8efeea23446a0aa2
Autor:
A E Misyurina, S K Kravchenko, A M Kovrigina, A U Magomedova, L V Plastinina, T N Obukhova, A V Misyurin, V A Misyurin, L A Grebenuk, F E Babaeva, E A Baryakh, A I Vorobiev
Publikováno v:
Терапевтический архив, Vol 91, Iss 7, Pp 52-62 (2019)
Aim of the issue was to compare clinical characteristics and treatment results of patients with follicular lymphoma (FL) with translocations involving loci of c-MYC/8q24, BCL2/18q21 and/or BCL6/3q27 genes and patients with high - grade B-cell lymphom
Externí odkaz:
https://doaj.org/article/57c54f39fbf94c129a713cef4676acaa
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:
E V Sokol, V I Vasilyev, S G Palshina, N V Kokosadze, N A Probatova, A M Kovrigina, T N Safonova, E B Rodionova, I V Gaiduk, E I Selifanova
Publikováno v:
Терапевтический архив, Vol 91, Iss 5, Pp 40-48 (2019)
Aim: to propose diagnostic algorithm of IgG4-related disease (IgG4-RD). Materials and methods. One center retrospective research. 52 pts with IgG4-RD were included. The diagnosis was proved histologically and immunohistochemically. 48 out of 52 pts r
Externí odkaz:
https://doaj.org/article/aea07e5fadd747bcbfd55d7249309150
Autor:
A E Misyurina, S K Kravchenko, Ya K Mangasarova, A U Magomedova, A M Kovrigina, L T Shimanovskaya, E A Fastova, V A Misyurin, S V Model, D I Chebotarev, I E Kostina, V G Savchenko
Publikováno v:
Терапевтический архив, Vol 91, Iss 4, Pp 107-113 (2019)
Mediastinal gray-zone lymphoma (MGZL, lymphoma with features intermediate between classical Hodgkin lymphoma and diffuse large B-cell lymphoma) was declared as a separate entity in WHO classification of Tumors of Haematopoetic and Lymphoid Tissues in
Externí odkaz:
https://doaj.org/article/7cbcda28488c4a5181098ce8cb8dfb7b
Autor:
A L MELIKYAN, I N SUBORTSEVA, E A GILYAZITDINOVA, T I KOLOSHEJNOVA, E I PUSTOVAYA, E K EGOROVA, A M KOVRIGINA, A B SUDARIKOV, A O ABDULLAEV, E G LOMAIA, N T SIORDIYA, A Yu ZARITSKEY, V G SAVCHENKO
Publikováno v:
Терапевтический архив, Vol 90, Iss 7, Pp 23-29 (2018)
Purpose of the study. A comparative evaluation of the effectiveness of different therapeutic strategies in patients with polycythemia vera (PV) and essential thrombocythemia (ET). Materials and methods. Patients with PV or ET, diagnosed according to
Externí odkaz:
https://doaj.org/article/24b0a0e7af394e34811b114da05d6bfc
Publikováno v:
Терапевтический архив, Vol 90, Iss 7, Pp 96-101 (2018)
Diffuse large B-cell lymphoma is categorized by gene expression profiling into germinal center (GCB) and activated B-cell (ABC) subtype, also referred to as non-germinal center B-cell (non-GCB) by immunohistochemistry. ABC DLBCL is characterized by N
Externí odkaz:
https://doaj.org/article/b9f56c72312e4c719fc8eab9c36cae52
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:
V I Vasilyev, T N Safonova, E V Socol, N A Probatova, N V Kokosadze, A I Pavlovskaya, A M Kovrigina, S G Radenska-Lopovok, V R Gorodetsky, E B Rodionova, S G Palshina, E N Aleksandrova, N S Shornikova, I V Gaiduk
Publikováno v:
Терапевтический архив, Vol 90, Iss 5, Pp 61-71 (2018)
Purpose of the study. To provide demographic, clinical, laboratory, ultrasound, radiological, morphological/ immunomorphological phenotype of IgG4-related ophthalmic diseases, which allowsmaking a differential diagnosis with granulomatous, autoimmune
Externí odkaz:
https://doaj.org/article/5f4d5a2178b24246b17eff4b48fb8113
Autor:
O A Gavrilina, V V Troitskaya, E E Zvonkov, E N Parovichnikova, G M Galstyan, L S Biryukova, I V Nesterenko, A M Kovrigina, A V Bazhenov, V G Savchenko
Publikováno v:
Терапевтический архив, Vol 89, Iss 7, Pp 69-75 (2017)
Primary central nervous system (CNS) lymphomas account for 13-20% of the posttransplant lymphoproliferative disorders (PTLD) and rank among the most aggressive conditions. Reduction of immunosuppressive therapy should be mandatory to treat PTLD, but
Externí odkaz:
https://doaj.org/article/42f6c3caa4f847508d481d69f8149fae