Zobrazeno 1 - 10
of 99
pro vyhledávání: '"A M Galstyan"'
Publikováno v:
RUDN Journal of Agronomy and Animal Industries, Vol 12, Iss 1, Pp 47-57 (2017)
This article presents the results of field research of two total stations (the park of geodetic instruments of the experimentally-technological laboratory of remote sensing and land resources monitoring of the Agrarian Technological Institute of the
Externí odkaz:
https://doaj.org/article/d60cc37f68604acfb551eebb2ef7f78f
Publikováno v:
Вестник анестезиологии и реаниматологии, Vol 21, Iss 3, Pp 42-46 (2024)
Introduction. Approximately 21–27% of patients with blood system diseases receive opioid analgesics, with neuropathic pain being one of the most common reasons for prescription. Gabapentin is used as a first-line drug for neuropathic pain (NP), but
Externí odkaz:
https://doaj.org/article/f448282563b34d179009da09d00e8541
Autor:
Antonina E. Shchekina, Gennadii M. Galstyan, Olga A. Gavrilina, Natalia M. Arapova, Svetlana Iu. Bronyakina, Ekaterina S. Kotova, Vera V. Troitskaya, Elena N. Parovichnikova, Mikhail A. Maschan, Valerii G. Savchenko
Publikováno v:
Терапевтический архив, Vol 93, Iss 7, Pp 811-817 (2021)
Сytokine release syndrome is the common complication of CAR-T therapy. We report a case of patient with B-cell acute lymphoblastic leukemia developing сytokine release syndrome with shock and multiple organ failure and requiring cytokine removal an
Externí odkaz:
https://doaj.org/article/39d359839604411099cc88b3224f27db
Publikováno v:
Терапевтический архив, Vol 93, Iss 7, Pp 826-829 (2021)
The review discusses approaches to treatment of congenital thrombotic thrombocytopenic purpura (TTP) or Upshaw-Schulman syndrome. In congenital TTP, plasma transfusions are sufficient. Such treatment options as plasma exchange, administration of clot
Externí odkaz:
https://doaj.org/article/a9298776924844eb84312f7678190568
Autor:
G. M. Galstyan, E. E. Klebanova
Publikováno v:
Терапевтический архив, Vol 92, Iss 12, Pp 207-217 (2020)
Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening disease, disease, characterised by microangiopathic hemolytic anaemia, consumption thrombocytopenia, and organ dysfunction. The pathogenesis of TTP is attributed to the deficiency
Externí odkaz:
https://doaj.org/article/cee146f1863e4301bf6d387f607bc6ce
Autor:
T. Yu. Polyanskaya, I. S. Fevraleva, E. E. Karpov, N. V. Sadykova, M. S. Sampiev, A. V. Golobokov, G. V. Mishin, D. Yu. Petrovskiy, A. A. Koroleva, G. M. Galstyan, A. B. Sudarikov, V. Yu. Zorenko
Publikováno v:
Сибирский научный медицинский журнал, Vol 39, Iss 1, Pp 106-111 (2019)
Objective was to study genetic markers of thrombophilia in patients with hemophilia, which can affect the course of the disease and contribute to thrombotic complications. Material and methods. The study included 96 patients with severe hemophilia: 7
Externí odkaz:
https://doaj.org/article/a58242bb3c574a72918378882c15c458
Autor:
G. M. Galstyan, E. E. Klebanova, S. Yu. Mamleeva, S. Yu. Fedorova, M. Yu. Drokov, G. A. Yatsyk
Publikováno v:
Clinical Medicine (Russian Journal). 101:41-49
Aim: to analyze the first neurological manifestation in patient with thrombotic thrombocytopenic purpura (TTP). Material and methods. The appeals from physicians who suspected TTP were included in the study. The neurological symptoms in 40 patients w
Autor:
E. N. Parovichnikova, O. A. Aleshina, V. V. Troitskaya, Yu. A. Chabaeva, A. N. Sokolov, G. A. Isinova, E. S. Kotova, Z. H. Akhmerzaeva, G. A. Klyasova, I. V. Galtseva, Yu. O. Davydova, L. A. Kuzmina, S. N. Bondarenko, O. Yu. Baranova, A. S. Antipova, O. S. Samoilova, M. E. Grishunina, K. D. Kaplanov, T. S. Kaporskaya, T. S. Konstantinova, Yu. V. Sveshnikova, E. A. Borisenkova, E. S. Fokina, N. V. Minaeva, E. E. Zinina, V. A. Lapin, E. O. Gribanova, E. E. Zvonkov, V. N. Dvirnyk, G. M. Galstyan, T. N. Obukhova, A. B. Sudarikov, S. M. Kulikov
Publikováno v:
Russian journal of hematology and transfusiology. 67:460-477
Introduction. Over the past 5 years, signifi cant progress has been achieved in the treatment of patients with Ph-negative acute lymphoblastic leukemia (ALL). Treatment results were compared between two protocols of the Russian multicenter studies «
Autor:
E. E. Zvonkov, D. A. Koroleva, N. G. Gabeeva, A. E. Shchekina, M. A. Telyashov, O. A. Aleshina, B. V. Biderman, A. B. Sudarikov, T. N. Obukhova, I. V. Galtseva, V. N. Dvirnik, V. V. Troitskaya, G. M. Galstyan, M. A. Maschan, E. N. Parovichnikova
Publikováno v:
Russian journal of hematology and transfusiology. 67:441-452
Introduction. The tactics of therapy for elderly comorbid patients with mantle cell lymphoma with unfavorable prognosis factors (complex karyotype, 17p13 deletion, mutations in the TP53 gene) have not been developed. The use of intensive chemotherapy
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