Zobrazeno 1 - 10
of 19
pro vyhledávání: '"S. A. Plyasunova"'
Autor:
I. A. Demina, Т. Yu. Verzhbitskaya, S. A. Kashpor, L. V. Baidun, T. V. Koniuhova, S. A. Plyasunova, G. А. Tsaur, E. B. Rusanova, M. V. Gorchakova, E. E. Zueva, A. N. Kazakova, E. A. Zerkalenkova, Yu. V. Olshanskaya, Yu. G. Abugova, L. G. Fechina, N. V. Miakova, E. V. Samochatova, А. А. Maschan, А. M. Popov
Publikováno v:
Онкогематология, Vol 12, Iss 4, Pp 34-40 (2018)
Introduction. Surface immunoglobulin expression is a main immunophenotypic criteria of mature subtype of B-lineage acute lymphoblastic leukemia. Although the majority of such cases represents Burkitt leukemia/lymphoma, it was shown for several times
Externí odkaz:
https://doaj.org/article/f627e049edb64d5ea4bf26c1dff209da
Autor:
I. A. Demina, T. Yu. Verzhbitskaya, S. A. Kashpor, S. A. Plyasunova, M. E. Dubrovina, L. G. Fechina, N. V. Myakova, E. V. Samochatova, A. A. Maschan, A. M. Popov
Publikováno v:
Онкогематология, Vol 12, Iss 1, Pp 55-61 (2017)
Bone marrow tumor blasts immunophenotyping is an essential part of Burkitt lymphoma/leukemia (BL) and B-cell precursor acute lymphoblastic leukemia (BCP-ALL) differential diagnostics. Nevertheless immunoglobulin heavy and light chains detection on th
Externí odkaz:
https://doaj.org/article/b2d72b8b43424c72afdccbce18b588f7
Autor:
A. M. Popov, M. V. Belevtsev, E. V. Boyakova, T. Yu. Verzhbitskaya, L. V. Movchan, M. S. Fadeeva, А. B. Pashchenko, V. P. Savitskiy, А. A. Levadnyy, G. А. Tsaur, S. A. Kashpor, S. A. Plyasunova, L. G. Fechina, O. V. Aleynikova, A. I. Karachunskiy
Publikováno v:
Онкогематология, Vol 11, Iss 4, Pp 64-73 (2017)
We developed and implemented in multicenter setting the standardized approach for flow cytometric minimal residual disease (MRD) monitoring in childhood B-cell precursor acute lymphoblastic leukemia (BCP-ALL). Participation of multicenter group refer
Externí odkaz:
https://doaj.org/article/3c5cd98211d04789a620de530334df1a
Autor:
A. M. Popov, T. U. Verzhbitskaya, E. E. Zueva, O. V. Anan’eva, E. V. Babenko, L. V. Baydun, E. A. Belyakova, E. V. Boyakova, O. G. Bortnikova, M. V. Gorchakova, L. Yu. Grivtsova, E. N. Grinkevich, Yu. V. Davydova, E. I. Zakhar’ko, O. I. Illarionova, N. M. Kaprano, E. A. Koroleva, S. A. Kochengina, E. G. Kuz’mina, E. A. Kustova, T. A. Makarova, Yu. V. Mirolyubova, O. E. Murashkina, T. Yu. Mushkarina, E. S. Nisheva, I. A. Novikova, E. Yu. Osipova, G. E. Pluzhnikova, M. E. Pochtar, N. V. Pronkina, E. V. Rusanova, E. B. Rybkina, O. V. Seliverstova, N. N. Tupitsin, G. I. Uleyskaya, N. T. Urazalieva, L. G. Fechina, O. V. Khoroshikh, O. E. Tsareva, L. A. Shchekina, S. A. Plyasunova, S. A. Lugovskaya
Publikováno v:
Онкогематология, Vol 11, Iss 3, Pp 68-75 (2016)
Comparison of interpretation of acute lymphoblastic leukemia (ALL) flow cytometric diagnostics data was the aim of the study. Immunophenotyping data obtained from 10 patients with ALL were analysed separately in 26 laboratories from Russian Federatio
Externí odkaz:
https://doaj.org/article/bc25e5d62d554850b622e9652ee96523
Autor:
E. A. Zerkalenkova, O. I. Illarionova, A. N. Kazakova, N. I. Ponomareva, L. V. Baydun, E. Yu. Osipova, M. E. Dubrovina, A. M. Popov, T. V. Konyukhova, S. A. Plyasunova, N. V. Myakova, A. A. Maschan, Yu. V. Olshanskaya
Publikováno v:
Онкогематология, Vol 11, Iss 2, Pp 21-29 (2016)
Lineage switch is a rare phenomenon in which a transition from lymphoid to myeloid was observed in relapse of acute leukemia, or vice versa. This paper presents the four clinical case reports of acute lymphoblastic leukemia with MLL gene rearrangemen
Externí odkaz:
https://doaj.org/article/1cb2879f77984511ab1e04d6a383de28
Autor:
S. G. Mann, M. V. Krasilnikova, N. A. Karamjan, M. E. Lokhmatova, A. O. Koposova, E. A. Litvin, S. A. Plyasunova
Publikováno v:
Pediatric Hematology/Oncology and Immunopathology. 21:77-83
Here we report the first case of unstable hemoglobin Hakkari identified in Russia to our knowledge. It was diagnosed in a two-year-old Russian boy with severe transfusion-dependent anemia caused by a de novo mutation in the b-globin gene [b31(B13) Le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b1f81f4abf4e08fdc70498b4a94b886
https://doi.org/10.24287/1726-1708-2022-21-3-77-83
https://doi.org/10.24287/1726-1708-2022-21-3-77-83
Autor:
M. E. Lokhmatova, N. E. Sokolova, M. V. Krasilnikova, E. A. Litvin, N. A. Karamjan, S. G. Mann, S. A. Plyasunova, N. S. Smetanina
Publikováno v:
Pediatric Hematology/Oncology and Immunopathology. 21:13-21
From 2010 to 2020, we investigated 197 children with hemolytic anemia of unknown etiology at the Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology of Ministry of Healthcare of the Russian Federation. Fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d97eac2f37cc9a9fcf2d15a078134c8
https://doi.org/10.24287/1726-1708-2022-21-3-13-21
https://doi.org/10.24287/1726-1708-2022-21-3-13-21
Autor:
E. V. Mikhailova, N. S. Mochalova, S. A. Kashpor, E. A. Zerkalenkova, T. V. Konyukhova, S. A. Plyasunova, Yu. V. Olshanskaya, I. I. Kalinina, M. A. Maschan, A. A. Maschan, G. A. Novichkova, A. M. Popov
Publikováno v:
Pediatric Hematology/Oncology and Immunopathology. 21:42-48
Contemporary therapy of acute promyelocytic leukemia (APL) is based on the use of all-trans retinoic acid, which is effective against tumor cells harboring RARa gene rearrangements (most common – t(15;17)(q24;q21)/PML::RARa). In several studies, it
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2159f4679bd1c2da934c353ac65c3a80
https://doi.org/10.24287/1726-1708-2022-21-1-42-48
https://doi.org/10.24287/1726-1708-2022-21-1-42-48
Autor:
S. G. Mann, A. V. Poletaev, E.A. Seregina, S. A. Plyasunova, M. A. Kurnikova, D. V. Fedorova, D. M. Polokhov, A.V. Pshonkin, E. V. Raykina, P. A. Zharkov, A. O. Koposova
Publikováno v:
Pediatric Hematology/Oncology and Immunopathology. 20:126-131
Hemorrhagic thrombocytopathy with defective signal transduction CalDAG-GEFI is a rare disease associated with a mutation in the RASGRP2 gene. At the moment, this disease is described in 10 person in the world. We present clinical case report of this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a93bc603c9927c432aedf69721c5b14
https://doi.org/10.24287/1726-1708-2021-20-3-126-131
https://doi.org/10.24287/1726-1708-2021-20-3-126-131
Autor:
N.V. Miakova, Olga Illarionova, Alexander Popov, E.V. Gluhanyuk, S. A. Plyasunova, S. A. Kashpor, A.A. Maschan
Publikováno v:
Voprosy gematologii/onkologii i immunopatologii v pediatrii. 16:21-26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4b7701431c9c05141ac505ae43135e1
https://doi.org/10.24287/1726-1708-2017-16-4-21-26
https://doi.org/10.24287/1726-1708-2017-16-4-21-26