Zobrazeno 1 - 10
of 63
pro vyhledávání: '"T. N. MOISEEVA"'
Autor:
S. A. Vasiliev, L. A. Gorgidze, E. E. Efremov, G. Yu. Belinin, T. N. Moiseeva, L. S. Al-Radi, M. A. Sokolova, G. T. Guria, N. I. Zozulya, A. V. Kokhno
Publikováno v:
Атеротромбоз, Vol 12, Iss 1, Pp 138-158 (2022)
Plasma fibronectin is a high molecular weight adhesive glycoprotein. There are two types of fibronectin: plasma (soluble) and cellular derived (insoluble). Electron microscopy revealed two types of structural organization of fibronectin: compact and
Externí odkaz:
https://doaj.org/article/1ec369a36e0f44a49c62b4461251aeec
Publikováno v:
Онкогематология, Vol 16, Iss 2, Pp 40-47 (2021)
Cytopenia commonly occurs in case of chronic lymphocytic leukemia. It can either precede the diagnosis of chronic lymphocytic leukemia or appear at any time during the disease. Autoimmune hemolytic anemia, immune thrombocytopenia, and partial red cel
Externí odkaz:
https://doaj.org/article/c88e409eec3f41dba15511e2019d5e0a
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:
G. Ju. Belinin, V. I. Vasiliev, E. E. Efremov, L. A. Gorgidze, N. I. Zozulya, T. N. Moiseeva, L. S. Al-Radi, S. A. Vasiliev
Publikováno v:
Медицинский совет, Vol 0, Iss 11, Pp 210-218 (2020)
Introduction. The term “cryoglobulinemia” is currently used to identify immunoglobulins in vitro in the blood serum that precipitate at temperatures below 37 °C; in vivo they form immune complexes that can be deposited in small vessels and activ
Externí odkaz:
https://doaj.org/article/101dc13d4f934001b26269721b804c66
Autor:
E. A. Demina, G. S. Tumyan, T. N. Moiseeva, N. B. Mikhailova, N. V. Myakova, A. G. Rumyantsev, A. A. Maschan, K. D. Kaplanov, R. G. Shmakov, N. A. Falaleeva, V. V. Ptushkin, E. A. Osmanov, I. V. Poddubnaya, V. V. Baikov, A. M. Kovrigina, D. M. Konovalov, O. P. Trofimova, V. M. Sotnikov, N. V. Ilin, Yu. N. Vinogradova, A. V. Nechesnyuk, R. A. Parkhomenko, D. N. Stefanov, A. A. Nevolsky, S. A. Ivanov, Zh. V. Khaylova
Publikováno v:
Современная онкология, Vol 22, Iss 2, Pp 6-33 (2020)
Clinical recommendations.
Externí odkaz:
https://doaj.org/article/4d378856a70144d1a32656a6393cad38
Autor:
S. A. Vasiliev, L. A. Gorgidze, T. N. Moiseeva, L. S. Al’-Radi, N. I. Zozulya, M. A. Sokolova, A. V. Mazurov
Publikováno v:
Атеротромбоз, Vol 0, Iss 1, Pp 99-114 (2019)
Heparin-induced thrombocytopenia (HIT) is a serious and potentially life-threatening side effect of heparinotherapy. It is an antibody-mediated process that causes platelet activation, increases the procoagulant characteristics of the blood and, as a
Externí odkaz:
https://doaj.org/article/78308fb7c6a0437cb1ecd1c2d026f9f3
Publikováno v:
Сибирский научный медицинский журнал, Vol 39, Iss 1, Pp 27-33 (2019)
The aim of the study is to compare the tumour growth pattern with immunohystoarchitectural patterns in patients with nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) in the debut of the disease. Material and methods. The diagnosis of NLPHL in
Externí odkaz:
https://doaj.org/article/75b0593dc6a34bd09084667f3a4e6eac
Autor:
O. Yu. Davydova, I. V. Galtseva, E. N. Parovichnikova, A. V. Kokhno, N. M. Kapranov, V. V. Troitskaya, E. A. Mikhailova, Z. T. Fidarova, T. N. Moiseeva, L. A. Kuzmina, E. A. Lukina, T. N. Obukhova, L. A. Grebenyuk, A. M. Kovrigina, V. N. Dvirnyk, V. G. Savchenko
Publikováno v:
Онкогематология, Vol 13, Iss 4, Pp 75-88 (2019)
Background . Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal diseases of the hematopoiesis system characterized by dismyelopoiesis and cytopenia, the presence of cytogenetic aberrations and a high risk of transformation into acute
Externí odkaz:
https://doaj.org/article/592c04ba19584ab391e530dd088ab289
Publikováno v:
Медицинский совет, Vol 0, Iss 10, Pp 92-96 (2018)
The description of the clinical observation of the successful therapy with ibrutinib recurrent B-cell chronic lymphocytic leukemia associated with autoimmune complications is given. The reasons for occurrence the autoimmune complications of CLL, thei
Externí odkaz:
https://doaj.org/article/5fb08417d9ef4d26ad4c19ee5a6d9a71
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