Zobrazeno 1 - 10
of 174
pro vyhledávání: '"E. A. Lukina"'
Autor:
N. G. Mokrysheva, M. V. Shestakova, A. S. Ametov, M. B. Antsiferov, I. G. Bakulin, T. V. Vavilova, G. R. Galstyan, T. Y. Demidova, F. K. Dzgoeva, T. L. Karonova, E. A. Lukina, A. M. Mkrtumyan, N. A. Petunina, R. V. Ponomaryov, N. A. Suponeva, O. Y. Sukhareva, M. S. Shamkhalova
Publikováno v:
Сахарный диабет, Vol 27, Iss 3, Pp 314-320 (2024)
On March 20, 2024, an interdisciplinary meeting of the Expert Council on the current problem of B12 insufficiency/deficiency and the prevalence of this condition among endocrine patients was held at the Endocrinology Research Centre (Moscow). The pur
Externí odkaz:
https://doaj.org/article/8829d05cc33f43caab1c815842313903
Autor:
V. D. Latyshev, Z. T. Fidarova, R. V. Ponomarev, N. V. Tsvetaeva, E. A. Mikhaylova, E. A. Lukina, E. N. Parovichnikova
Publikováno v:
Онкогематология, Vol 19, Iss 1, Pp 83-91 (2024)
Background. Paroxysmal nocturnal hemoglobinuria is a rare clonal disease of the hematopoietic system, with the key manifestations of hemolytic anemia, a high thrombosis rate, and bone marrow failure. Despite the high efficacy of C5‑inhibitors in in
Externí odkaz:
https://doaj.org/article/719811036e4c4f839846b9282e0ac275
Autor:
A. D. Kulagin, E. A. Lukina, V. V. Ptushkin, M. P. Kostinov, E. G. Arshanskaya, T. N. Babaeva, T. I. Ksenzova, Z. T. Fidarova, M. V. Marchenko
Publikováno v:
Онкогематология, Vol 18, Iss 3, Pp 140-144 (2023)
On June 24, 2023, an Expert Council was held in St. Petersburg, during which leading experts in the field of hematology discussed current achievements and answered a number of unresolved issues of targeted therapy of paroxysmal nocturnal hemoglobinur
Externí odkaz:
https://doaj.org/article/7a0ccf75cd9245f48e4ac2e80b45a701
Publikováno v:
Онкогематология, Vol 0, Iss 1, Pp 65-70 (2022)
Externí odkaz:
https://doaj.org/article/1610c574053e4dc89e3f4d54c4925d31
Publikováno v:
Онкогематология, Vol 18, Iss 2 (2023)
Autoimmune hemolytic anemia is a rare disease characterized by the appearance of anti-erythrocyte autoantibodies and subsequent destruction of red blood cells by cells of the immune system. The destruction mechanisms of erythrocytes loaded with autoa
Externí odkaz:
https://doaj.org/article/5598b022203845c49fc24422493fc490
Publikováno v:
Онкогематология, Vol 0, Iss 1 (2022)
Externí odkaz:
https://doaj.org/article/bf28c14decdf49cb91ef9084e4cbe7ef
Autor:
V. V. Ptushkin, A. D. Kulagin, E. A. Lukina, I. L. Davydkin, T. S. Konstantinova, V. S. Shamrai, N. V. Minaeva, D. A. Kudlay, E. V. Gapchenko, O. A. Markova, A. Yu. Borozinets
Publikováno v:
Терапевтический архив, Vol 92, Iss 7, Pp 77-84 (2020)
Currently, the main pathogenetic method for the treatment of paroxysmal nocturnal hemoglobinuria (PNH) is the treatment with recombinant monoclonal antibodies that block the C5 component of the complement system. Eculizumab is the first biotechnologi
Externí odkaz:
https://doaj.org/article/c8727c8295774e18b3a446395b05b823
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
Autor:
E. A. Mershina, O. V. Kulikova, R. P. Myasnikov, E. A. Lukina, A. N. Meshkov, A. V. Kiseleva, P. S. Pilyus, S. N. Koretsky, M. S. Kharlap, R. V. Ponomarev, N. V. Tsvetaeva, O. F. Nikulina, S. A. Boytsov, V. E. Sinitsyn, O. M. Drapkina
Publikováno v:
Российский кардиологический журнал, Vol 25, Iss 4 (2020)
This article presents the results of studies on high prevalence of left ventricular noncompaction (LVNC) in patients with secondary hemochromatosis (SH). We also included case reports of patients with SH and LVNC and compared imaging data using modif
Externí odkaz:
https://doaj.org/article/2d5656491b0f4b6297ffe0e3125a8453
Publikováno v:
Онкогематология, Vol 13, Iss 2, Pp 100-104 (2018)
Storage diseases (thesaurismosis, storage reticuloses) are the complex and extensive group of diseases in which differential diagnosis of pathological changes from the internal organs is difficult. For diagnosis and dynamic observation of liver and s
Externí odkaz:
https://doaj.org/article/a99cc30d1bec4936aa144c4591f52b17