Zobrazeno 1 - 10
of 31
pro vyhledávání: '"N A Potikhonova"'
Autor:
S V Gritsaev, I I Kostroma, G M Ryadnova, S A Tiranova, Zh V Chubukina, V A Balashova, M N Zenina, I S Martynkevich, N A Potikhonova, K M Abdulkadyrov
Publikováno v:
Терапевтический архив, Vol 87, Iss 7, Pp 97-100 (2015)
This rare type of acute leukemia, blast cells of which express myeloid and/or lymphoid markers, is mainly diagnosed using flow cytometric findings. The paper describes a clinical case of mixed-phenotype acute leukemia, in which B-cell lymphoid antige
Externí odkaz:
https://doaj.org/article/0c420ee9fa5f44e8b8fb4a4f38fab805
Autor:
S V Gritsaev, I S Martynkevich, I S Ziuzgin, E V Kariagina, L S Martynenko, E V Petrova, N Iu Tsybakova, M P Ivanova, I I Kostroma, S A Tiranova, N A Potikhonova, K M Abdulkadyrov
Publikováno v:
Терапевтический архив, Vol 86, Iss 7, Pp 45-52 (2014)
AIM. To characterize the clinical and hematological variability of acute myeloid leukemia (AML) with t(8;21) and to identify the signs associated with the likelihood of its relapse. MATERIALS AND METHODS. The results of examining 44 patients aged 11
Externí odkaz:
https://doaj.org/article/c9705188e8214ff487de5afa236d89e1
Autor:
S V Gritsaev, I S Martynkevich, Zh V Chubukina, E V Petrova, I I Kostroma, M P Ivanova, L S Martynenko, N A Potikhonova, L N Bubnova, K M Abdulkadyrov
Publikováno v:
Терапевтический архив, Vol 86, Iss 3, Pp 71-77 (2014)
AIM: To study the specific features of de novo acute myeloid leukemia (AML) with FLT3-ITD mutation/MATERIAL AND METHODS: The results of examination were analyzed in 101 patients. Bone marrow morphological specimens were stained with Pappenheim stain.
Externí odkaz:
https://doaj.org/article/cf33ba5b52b148e7af8ab32039d08460
Autor:
S V Gritsaev, I S Martynkevich, E V Petrova, L S Martynenko, M P Ivanova, V Iu Aksenova, N Iu Tsybakova, N A Potikhonova, K M Abdulkadyrov
Publikováno v:
Терапевтический архив, Vol 85, Iss 7, Pp 43-49 (2013)
AIM: To analyze the prevalence of chromosome aberrations presented in the revised International Prognostic Scoring System (R-IPSS) in patients with de novo myelodysplastic syndrome (MDS)/MATERIAL AND METHODS: Chromosome aberrations were analyzed in 1
Externí odkaz:
https://doaj.org/article/645d8dec936f417189f66ee8d0997aba
Autor:
S V Gritsaev, I S Martynkevich, K M Abdulkadyrov, M P Ivanova, E V Petrova, I M Zapreeva, S A Tiranova, N A Potikhonova
Publikováno v:
Терапевтический архив, Vol 84, Iss 7, Pp 16-21 (2012)
Aim. To identify a category of persons with very low overall survival (OS) rates, whose intensive chemotherapy is unreasonable, amongst the patients with acute myeloid leukemia (AML) with extended forms of myelodysplastic syndrome (MDS) and complex k
Externí odkaz:
https://doaj.org/article/ffdef64d13b6447eb4c57b32d9376ff7
Publikováno v:
Современная онкология, Vol 14, Iss 2, Pp 45-50 (2012)
Externí odkaz:
https://doaj.org/article/17b0adf5edc0482ebd7fad8825f45b5a
Publikováno v:
Онкогематология, Vol 17, Iss 4, Pp 16-32 (2022)
Langerhans cells histiocytosis is a variant of malignant histiocytosis. The course and symptoms vary. patients with localized forms have a better prognosis, because local therapy is effective. patients with multifocal forms of histiocytosis receive s
Externí odkaz:
https://doaj.org/article/c30e51672d9c4aec8fcd97e69127b38c
Autor:
V. G. Potapenko, M. M. Antonov, N. V. Vinogradova, E. V. Doguzhieva, V. E. Karev, E. S. Karamurzin, G. V. Kachenya, A. V. Klimovich, S. S. Kozlov, Yu. A. Krivolapov, S. V. Lapin, M. Yu. Pervakova, N. A. Potikhonova, I. P. Fedunyak, N. V. Medvedeva
Publikováno v:
Oncohematology. 17:89-97
Secondary hemophagocytic syndrome (sHLH) is a hyperinflammatory reaction which manifests with fever, cytopenia and organ damage. possible causes of sHLH include leishmaniasis. The article describes a clinical case of sHLH in patient with visceral lei
Autor:
S. V. Voloshin, A. D. Garifullin, A. A. Kuzyaeva, N. N. Sinitsina, N. N. Alekseeva, A. V. Schmidt, S. Y. Linnikov, V. A. Shuvaev, A. Y. Kuvshinov, N. A. Potikhonova, A. V. Seltser, V. A. Balashova, Z. V. Chubukina, A. N. Bogdanov, S. V. Sidorkevich
Publikováno v:
Oncohematology. 17:82-94
Autor:
V. G. Potapenko, A. V. Klimovich, M. Yu. Pervakova, S. V. Lapin, O. V. Goloshchapov, A. K. Titov, E. A. Surkova, E. S. Pavluchenko, N. A. Potikhonova, N. V. Vinogradova, E. V. Doguzhieva, G. V. Kachenya, D. D. Avdoshina, I. P. Fedunyak, V. V. Ryabchikova, T. G. Kulibaba, A. V. Rysev, E. V. Karyagina, N. V. Мedvedeva
Publikováno v:
Onkogematologiâ, Vol 15, Iss 4, Pp 52-64 (2020)
Background. Secondary hemophagocytic lymphohystiocytosis (sHLH) is a hyperinflammatory reaction provoked by some trigger (cancer, autoimmune or infection). The majority of affected patients are at high risk of fatal multiple organ failure without get