Zobrazeno 1 - 10
of 56
pro vyhledávání: '"G M Galstyan"'
Autor:
A V Bazhenov, G M Galstyan, E N Parovichnikova, V V Troitskaya, L A Kuzmina, Z T Fidarova, E O Gribanova, S A Makhinya, O A Latyshkevich, U A Chabaeva, S M Kulikov, V G Savchenko
Publikováno v:
Терапевтический архив, Vol 91, Iss 7, Pp 14-24 (2019)
Aim. Remission induction can be associate, with the life threatening complications and transfer to ICU of de novo acute myeloid leukemia (AML) patients (pts). We evaluate influence of transfer to ICU and life threatening complication on early mortali
Externí odkaz:
https://doaj.org/article/0f9fa6f9da044e4fb6fbb3950117b512
Autor:
G M Galstyan, M V Pashkova, O Y Popova, P M Makarova, D S Dubnyak, L A Kuzmina, E N Parovichnikova
Publikováno v:
Терапевтический архив, Vol 90, Iss 1, Pp 60-64 (2018)
The case report of botulinum toxin treatment of gastroparesis in a patient following allogenic bone marrow transplantation is described. The causes of gastroparesis and methods of prevention and treatment are discussed. It was noted that pyloric inje
Externí odkaz:
https://doaj.org/article/94bdf149d7b94c038cae1f02550c0123
Publikováno v:
Терапевтический архив, Vol 89, Iss 10, Pp 71-74 (2017)
Gaucher disease is the most common form of hereditary enzymopathies combined into a group of lysosomal storage diseases. The basis for the disease is a hereditary deficiency of the activity of acid β-glucosidase, a lysosomal enzyme involved in the c
Externí odkaz:
https://doaj.org/article/b9231b1af7c64d6180a57c17d8dfa532
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
Autor:
G M Galstyan, O A Polevodova, A Yu Gavrish, T Yu Polyanskaya, V Yu Zorenko, M S Sampiev, L S Biryukova, S V Model, L A Gorgidze, V G Savchenko
Publikováno v:
Терапевтический архив, Vol 89, Iss 7, Pp 76-84 (2017)
The paper describes 4 clinical cases of thrombotic events (pulmonary embolism, deep vein thrombophlebitis, acute myocardial infarction, ischemic stroke) that have occurred in patients with hemophilia. It discusses the possible causes of their develop
Externí odkaz:
https://doaj.org/article/949a7dffa14449d19f08c89ce4b630f1
Publikováno v:
Терапевтический архив, Vol 88, Iss 7, Pp 109-113 (2016)
The paper describes 4 cases of laparoscopic splenectomy in pregnant women with immune thrombocytopenic purpura. No complications of surgery were noted in all the patients. The postoperative period was marked by sustained clinical and hematological re
Externí odkaz:
https://doaj.org/article/0317944356934ccebf9d84b2fe237020
Autor:
E N Parovichnikova, A N Sokolov, V V Troitskaya, G A Klyasova, M A Rusinov, Z Kh Akhmerzaeva, L A Kuzmina, S N Bondarenko, O Yu Baranova, T S Kaporskaya, E N Zotina, E E Zinina, O S Samoilova, L V Gavrilova, K D Kaplanov, T S Konstantinova, V A Lapin, S K Kravchenko, E O Gribanova, E E Zvonkov, O A Gavrilina, G A Baskhaeva, G M Galstyan, T N Obukhova, I V Galtseva, S M Kulikov, V G Savchenko
Publikováno v:
Терапевтический архив, Vol 88, Iss 7, Pp 15-24 (2016)
Aim. To analyze well-known risk factors (RFs), such as age, immunophenotype, baseline leukocytosis, enhanced lactate dehydrogenase (LDH) activity, time to achieve complete remission, a risk group, and cytogenetic abnormalities) in patients with acute
Externí odkaz:
https://doaj.org/article/b71326aeda7841e4b4714c86f887ce4f
Publikováno v:
Терапевтический архив, Vol 88, Iss 7, Pp 84-88 (2016)
Aim. To study the nature of pain in hemophilic arthropathy and its prevention ways used by patients with hemophilia. Subjects and methods. A prospective, multicenter, cross-sectional study was conducted to interview 136 patients with hemophilia A or
Externí odkaz:
https://doaj.org/article/549f39bf6ce84cd08fac8fed059788d5
Autor:
I S Nemchenko, A G Turkina, E Yu Chelysheva, G M Galstyan, A M Kovrigina, N K Khuazheva, V G Savchenko
Publikováno v:
Терапевтический архив, Vol 87, Iss 12, Pp 89-95 (2015)
The described case of FIP1L1-PDGFRА-positive myeloproliferative disease is characterized by an atypical aggressive course to develop severe specific complications as injuries to the brain, heart, lung, and intestine. Pathogenetic therapy with imatin
Externí odkaz:
https://doaj.org/article/0e14bdbcc0964fee84f3d820fdd9b587
Autor:
E A Baryakh, N G Tyurina, V I Vorobyev, E G Gemdzhyan, Ya K Mangasarova, G A Klyasova, A M Kovrigina, T N Obukhova, E E Zvonkov, M A Vernyuk, A M Chervontseva, Yu Yu Polyakov, А Е Misyurina, T T Valiev, V A Zherebtsova, A U Magomedova, G M Galstyan, K V Yatskov, E S Nesterova, A I Vorobyev, S K Kravchenko
Publikováno v:
Терапевтический архив, Vol 87, Iss 7, Pp 4-14 (2015)
Aim. To evaluate the efficiency and toxicity of the intensive Burkitt’s lymphoma (BL) therapy protocol BL-M-04. Subjects and methods. A total of 70 patients diagnosed with BL, including 45 men and 25 women whose age was 15 to 62 years (median age 3
Externí odkaz:
https://doaj.org/article/298e63f168c2470392a0b2cc5db43d82