Zobrazeno 1 - 5
of 5
pro vyhledávání: '"O. S. Pankratova"'
Autor:
E. V. Semenova, Natalia B. Mikhailova, Boris V. Afanasyev, Andrey Yu. Zaritskey, L. S. Zoubarovskaya, Naoto T. Ueno, Gabriela Rondon, Richard E. Champlin, Susan O'Brien, Michael Andreeff, Athanasios Anagnostopoulos, O. S. Pankratova
Publikováno v:
British Journal of Haematology. 119:131-134
In this report, we describe two patients with idiopathic hypereosinophilic syndrome (HES) who received a non-myeloablative allogeneic transplantation following a reduced-intensity preparative regimen of melphalan and fludarabine. In both cases, compl
Autor:
Ludmila S. Zubarovskaya, A.B. Chukhlovin, Y A Eismont, O. S. Pankratova, V N Vavilov, Boris V. Afanasyev, S N Shiryaev
Publikováno v:
Bone marrow transplantation. 48(10)
We have read with great interest an article by van der Beek et al.1 published in Bone Marrow Transplantation. The authors reported that HSV-1 shedding in oral fluid after hematopoietic SCT (HSCT) is a significant predictor for oral mucosal ulceration
Publikováno v:
Genetika. 47(6)
Analysis of sperm aneupoidy in 11 healthy men using two- or three-color FISH permitted to determine the average frequency of disomy in chromosomes 13 and 21 (0.11% and 0.2%, respectively), disomy in chromosome 18 (0.05%) and reveal gonosomal aneuploi
Autor:
Naoto T, Ueno, Athanasios, Anagnostopoulos, Gabriela, Rondón, Richard E, Champlin, N, Mikhailova, O S, Pankratova, L S, Zoubarovskaya, E V, Semenova, B V, Afanasyev, Susan, O'Brien, Michael, Andreeff, Andrey Y, Zaritskey
Publikováno v:
British journal of haematology. 119(1)
In this report, we describe two patients with idiopathic hypereosinophilic syndrome (HES) who received a non-myeloablative allogeneic transplantation following a reduced-intensity preparative regimen of melphalan and fludarabine. In both cases, compl
Publikováno v:
Scopus-Elsevier
Analysis of sperm aneuploidy in 11 healthy men using two-or three-color FISH permitted to determine the average frequency of disomy for chromosomes 13 and 21 (0.11% and 0.2%, respectively), disomy for chromosome 18 (0.05%) and to reveal gonosomal ane
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