Detalhe da pesquisa
1.
Hematopoietic stem cell transplantation for Wiskott-Aldrich syndrome: an EBMT Inborn Errors Working Party analysis.
Blood
; 139(13): 2066-2079, 2022 03 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-35100336
2.
Nijmegen breakage syndrome in two half sibs with peripheral T-cell lymphoma and cortical T-cell acute lymphoid leukemia.
Cent Eur J Immunol
; 45(4): 507-510, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33658897
3.
Heterozygous activating mutation in RAC2 causes infantile-onset combined immunodeficiency with susceptibility to viral infections.
Clin Immunol
; 205: 1-5, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31071452
4.
Novel biallelic ATM mutations coexist with a mosaic form of triple X syndrome in an 11-year-old girl at remission after T cell acute leukemia.
Immunogenetics
; 70(9): 613-617, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29492593
5.
Novel Mutations in SH2D1A Gene in X-linked Lymphoproliferative Syndrome, Diagnosed After B-Cell Non-Hodgkin Lymphoma.
J Pediatr Hematol Oncol
; 39(4): e203-e206, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28267077
6.
Next generation sequencing revealed DNA ligase IV deficiency in a "developmentally normal" patient with massive brain Epstein-Barr virus-positive diffuse large B-cell lymphoma.
Clin Immunol
; 163: 108-10, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26774591
7.
Molecular Characteristics, Clinical and Immunologic Manifestations of 11 Children with Omenn Syndrome in East Slavs (Russia, Belarus, Ukraine).
J Clin Immunol
; 36(1): 46-55, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26596586
8.
Novel LRBA Mutation and Possible Germinal Mosaicism in a Slavic Family.
J Clin Immunol
; 38(4): 471-474, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29804237
9.
Phenotypic and functional characterisation of locally produced natural killer cells ex vivo expanded with the K562-41BBL-mbIL21 cell line.
Clin Exp Med
; 23(6): 2551-2560, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36527513
10.
Variable CD18 expression in a 22-year-old female with leukocyte adhesion deficiency I: Clinical case and literature review.
Clin Case Rep
; 11(8): e7791, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37601427
11.
AML1/RUNX1 gene point mutations in childhood myeloid malignancies.
Pediatr Blood Cancer
; 57(4): 583-7, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21294243
12.
Geographical Distribution, Incidence, Malignancies, and Outcome of 136 Eastern Slavic Patients With Nijmegen Breakage Syndrome and NBN Founder Variant c.657_661del5.
Front Immunol
; 11: 602482, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33488600
13.
Decoding of exon splicing patterns in the human RUNX1-RUNX1T1 fusion gene.
Int J Biochem Cell Biol
; 68: 48-58, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26320575
14.
RUNX1T1/MTG8/ETO gene expression status in human t(8;21)(q22;q22)-positive acute myeloid leukemia cells.
Leuk Res
; 38(9): 1102-10, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24976338
15.
Epidemiology of venous thromboembolism in children with malignant diseases: a single-center study of the Belarusian Center for Pediatric Oncology and Hematology.
Thromb Res
; 128(2): 130-4, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21492908
16.
Prognostic value of MRD-dynamics in childhood acute lymphoblastic leukemia treated according to the MB-2002/2008 protocols.
Leuk Res
; 35(10): 1312-20, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21596436
17.
Frequencies of immature CD34 + CD38 - and CD34 + CD38-CD19 + blasts correlate with minimal residual disease level in pediatric B-cell precursor acute lymphoblastic leukemia.
Leuk Lymphoma
; 54(11): 2560-2, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23432723
18.
CD34+ leukemic subpopulation predominantly displays lower spontaneous apoptosis and has higher expression levels of Bcl-2 and MDR1 genes than CD34- cells in childhood AML.
Ann Hematol
; 87(5): 353-60, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18228020
19.
Apoptosis and proliferation differences between CD34+ and CD34- leukemic subpopulations in childhood acute leukemia.
Hematology
; 12(5): 403-7, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17852445
20.
Immunophenotypically heterogeneous acute T-lymphoblastic leukemia has invariable immunogenotype: analysis of two cases.
J Pediatr Hematol Oncol
; 28(1): 50-2, 2006 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-16394895