Zobrazeno 1 - 4
of 4
pro vyhledávání: '"V Iu Aksenova"'
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:
I S, Martynkevich, S V, Gritsaev, M V, Moskalenko, M P, Ivanova, V Iu, Aksenova, S A, Tiranova, K M, Abdulkadyrov
Publikováno v:
Terapevticheskii arkhiv. 82(12)
To estimate the extent of FLT3 and NPM1 gene mutations and the impact of mutations of FLT3-ITD on the survival of patients with acute myeloid leukemias (AML).The nucleus-containing cells of bone marrow and blood were studied in 43 patients with AML.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b9c3817b309ec1bd847bbb0d6c412446
https://pubmed.ncbi.nlm.nih.gov/21516736
https://pubmed.ncbi.nlm.nih.gov/21516736
Autor:
S V, Gritsaev, I S, Martynkevich, L S, Martynenko, M P, Ivanova, V Iu, Aksenova, M V, Moskalenko, I M, Zapreeva, K M, Abdulkadyrov
Publikováno v:
Terapevticheskii arkhiv. 83(1)
To study distribution of some karyotype variants among patients of different age with acute myeloid leukemia (AML).Distribution of balanced, normal, unbalanced, complex and monosomic karyotype among 244 patients with de novo AML in age groups 16-20,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9c9ab5bfb74f610f9989c88ec08be7e1
https://pubmed.ncbi.nlm.nih.gov/21446203
https://pubmed.ncbi.nlm.nih.gov/21446203
Autor:
S V, Gritsaev, I S, Martynkevich, M P, Ivanova, M V, Moskalenko, V Iu, Aksenova, S A, Tiranova, K M, Abdulkadyrov
Publikováno v:
Voprosy onkologii. 56(6)
Two FLT3-ITD mutations, one FLT3-TKD) and five NPM1 mutations were detected in 7 patients with de novo myelodysplastic syndrome (MDS) out of 44 cases of MDS and MDS/mixed myeloid diseases. Expression of one of the three investigated mutations was ide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b94e59ab929e85808e88f9093cf70be8
https://pubmed.ncbi.nlm.nih.gov/21395122
https://pubmed.ncbi.nlm.nih.gov/21395122