Zobrazeno 1 - 10
of 16
pro vyhledávání: '"D. S. Badmazhapova"'
Autor:
D. S. Badmazhapova, I. V. Galtseva, E. E. Zvonkov, Yu. O. Davydova, M. M. Kapranov, T. N. Moiseeva, A. M. Kovrigina, U. L. Julhakyan, K. I. Danishyan, K. R. Sabirov, E. N. Parovichnikova, V. G. Savchenko
Publikováno v:
Онкогематология, Vol 15, Iss 4, Pp 18-28 (2020)
Background. Splenic marginal zone lymphoma (SMZL) is an indolent non-Hodgkin’s B-cell lymphoma. It presents morphologically by mature lymphoid B-cells. They conform to these immunological characteristics of marginal zone lymphocytes from secondary
Externí odkaz:
https://doaj.org/article/fc8dd7e701b246ce8459a6ee61591eb6
Autor:
N. G. Chernova, D. S. Badmazhapova, A. M. Kovrigina, A. E. Karamova, A. A. Vorontsova, M. N. Sinitcina, Yu. V. Sidorova, L. A. Grebenyuk, M. A. Nefedova, L. F. Znamenskaya, E. E. Zvonkov, V. G. Savchenko
Publikováno v:
Vestnik Dermatologii i Venerologii, Vol 94, Iss 4, Pp 30-42 (2018)
The aim of the study is to present a successful case in treating primary cutaneous anaplastic large cell lymphoma (PCALCL) occurring with common lesions of the skin and lung tissue.Materials and methods. For the verification of the diagnosis in a pat
Externí odkaz:
https://doaj.org/article/29d8f9e1f46e42ffafcb061a168918bd
Autor:
D. S. Badmazhapova, I. V. Galtseva, E. Е. Zvonkov, Yu. O. Davydova, N. M. Kapranov, N. G. Chernova, N. G. Gabeeva, T. N. Moiseeva, A. M. Kovrigina, V. N. Dvirnyk, U. L. Dzhulakyan, E. N. Parovichnikova, V. G. Savchenko
Publikováno v:
Онкогематология, Vol 13, Iss 1, Pp 103-114 (2018)
Background. Chronic lymphocytic leukemia (CLL) is a lymphoproliferative disease that manifests by the accumulation of tumor monoclonal B-lymphocytes in the bone marrow, peripheral blood and secondary lymphoid organs. Recently it was found that CLL ce
Externí odkaz:
https://doaj.org/article/230dc4bc0d5d46638cc2318f5a5b0f1f
Autor:
N. G. Gabeeva, D. A. Koroleva, S. A. Tatarnikova, A. K. Smolianinova, D. S. Badmazhapova, S. Yu. Smirnova, E. E. Nikulina, A. V. Belyaeva, E. G. Gemdzhian, V. A. Lapin, E. R. Moskalets, I. E. Kostina, Y. K. Mangasarova, S. A. Shutov, B. V. Biderman, A. B. Sudarikov, T. N. Obukhova, A. M. Kovrigina, G. M. Galstyan, E. E. Zvonkov
Publikováno v:
Russian journal of hematology and transfusiology. 67:328-350
Introduction. Primary mediastinal lymphoma (PML) is an aggressive lymphoid tumor treatment success of which is determined by induction therapy. To date, none of the standard chemotherapy regimens (CT) have demonstrated an advantage in efficacy. Inte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9e982c6740826df738fb2852f7b3049
https://doi.org/10.35754/0234-5730-2022-67-3-328-350
https://doi.org/10.35754/0234-5730-2022-67-3-328-350
Autor:
I. E. Kostina, Alla M. Kovrigina, E E Zvonkov, L A Grebenyuk, M N Sinitsyna, N G Chernova, D S Badmazhapova, T N Obukhova, Valery G. Savchenko, Yu. V. Sidorova, Andrey Sudarikov
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::8dd041134b13a9ca0219283df94470d2
https://doi.org/10.26442/terarkh201890777-81
https://doi.org/10.26442/terarkh201890777-81
Autor:
Yu E Vinogradova, N G Chernova, M N Sinitsyna, D S Badmazhapova, Valery G. Savchenko, E E Zvonkov, N P Soboleva, V N Dvirnyk, Yu. V. Sidorova, S A Mariina
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc51f2728945e6e75db87a8751bd629e
https://ter-arkhiv.ru/0040-3660/article/viewFile/32774/pdf
https://ter-arkhiv.ru/0040-3660/article/viewFile/32774/pdf
Autor:
V V Troitskaya, E N Parovichnikova, A N Sokolov, A V Kokhno, L A Kuzmina, D S Badmazhapova, Z T Fidarova, O A Gavrilina, A A Sidorova, G M Galstyan, S A Keselman, T V Gaponova, V S Galuzyak, S K Kravchenko, E O Gribanova, V G Savchenko
Publikováno v:
Терапевтический архив, Vol 87, Iss 7, Pp 33-40 (2015)
Aim. To evaluate the efficiency of the treatment policy for patients with acute myeloid leukemia (AML) and hyperleukocytosis (HL), which is aimed at preventing rapid hypercytolysis and massive tumor lysis (cytolysis) syndrome and/or at reducing the d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::26fc9c1dc695849c307b2bac2b95420f
https://ter-arkhiv.ru/0040-3660/article/view/31761
https://ter-arkhiv.ru/0040-3660/article/view/31761
[Breast implant-associated anaplastic large-cell lymphoma: A case report and a review of literature]
Autor:
Alla M. Kovrigina, T N Obukhova, E E Zvonkov, Andrey Sudarikov, D S Badmazhapova, N G Gabeeva, S R Karagyulyan, N G Chernova, Valeriy G. Savchenko
Publikováno v:
Терапевтический архив, Vol 89, Iss 7, Pp 93-98 (2017)
Breast implant-associated anaplastic large-cell lymphoma will be identified as a separate nosological entity in the 2017 adapted WHO classification due to differences in its clinical presentations, pathogenesis, and prognosis with those of nodal and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2b1cbaaa35a535b84b83f403c3f4a34
https://pubmed.ncbi.nlm.nih.gov/28766547
https://pubmed.ncbi.nlm.nih.gov/28766547
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