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
Inglês
| MEDLINE | ID: mdl-35100336
2.
Matched unrelated donor transplantation versus haploidentical transplantation with post-transplant cyclophosphamide in children with acute myeloid leukemia: a PDWP-EBMT study.
Haematologica
; 2024 Jan 04.
Artigo
Inglês
| MEDLINE | ID: mdl-38186346
3.
Genetic characteristics and treatment outcome in infants with KMT2A germline B-cell precursor acute lymphoblastic leukemia: Results of MLL-Baby protocol.
Pediatr Blood Cancer
; 70(4): e30204, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-36715125
4.
A simple procedure to identify children with B-lineage acute lymphoblastic leukemia who can be successfully treated with low or moderate intensity: Sequential versus single-point minimal residual disease measurement.
Pediatr Blood Cancer
; 70(6): e30295, 2023 06.
Artigo
Inglês
| MEDLINE | ID: mdl-36975157
5.
Incidence and prognostic value of central nervous system involvement in infants with B-cell precursor acute lymphoblastic leukemia treated according to the MLL-Baby protocol.
Pediatr Blood Cancer
; 69(9): e29860, 2022 09.
Artigo
Inglês
| MEDLINE | ID: mdl-35713168
6.
Prognostic value of minimal residual disease measured by fusion-gene transcript in infants with KMT2A-rearranged acute lymphoblastic leukaemia treated according to the MLL-Baby protocol.
Br J Haematol
; 193(6): 1151-1156, 2021 06.
Artigo
Inglês
| MEDLINE | ID: mdl-33583020
7.
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
Inglês
| MEDLINE | ID: mdl-33658897
8.
Heterozygous activating mutation in RAC2 causes infantile-onset combined immunodeficiency with susceptibility to viral infections.
Clin Immunol
; 205: 1-5, 2019 08.
Artigo
Inglês
| MEDLINE | ID: mdl-31071452
9.
Rituximab and reduced-intensity chemotherapy in children and adolescents with mature B-cell lymphoma: interim results for 231 patients enrolled in the second Russian-Belorussian multicentre study B-NHL-2010M.
Br J Haematol
; 186(3): 477-483, 2019 08.
Artigo
Inglês
| MEDLINE | ID: mdl-31069789
10.
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
Inglês
| MEDLINE | ID: mdl-29492593
11.
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
Inglês
| MEDLINE | ID: mdl-28267077
12.
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
Inglês
| MEDLINE | ID: mdl-26774591
13.
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
Inglês
| MEDLINE | ID: mdl-26596586
14.
Flow cytometric minimal residual disease measurement accounting for cytogenetics in children with non-high-risk acute lymphoblastic leukemia treated according to the ALL-MB 2008 protocol.
Cancer Med
; 13(8): e7172, 2024 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-38651186
15.
Novel LRBA Mutation and Possible Germinal Mosaicism in a Slavic Family.
J Clin Immunol
; 38(4): 471-474, 2018 05.
Artigo
Inglês
| MEDLINE | ID: mdl-29804237
16.
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
Inglês
| MEDLINE | ID: mdl-36527513
17.
One-point flow cytometric MRD measurement to identify children with excellent outcome after intermediate-risk BCP-ALL: results of the ALL-MB 2008 study.
J Cancer Res Clin Oncol
; 149(8): 4629-4637, 2023 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-36169717
18.
A Single Dose of PEG-Asparaginase at the Beginning of Induction Not Only Accelerates MRD Clearance but Also Improves Long-Term Outcome in Children with B-Lineage ALL.
Cancers (Basel)
; 15(23)2023 Nov 23.
Artigo
Inglês
| MEDLINE | ID: mdl-38067249
19.
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
Inglês
| MEDLINE | ID: mdl-37601427
20.
AML1/RUNX1 gene point mutations in childhood myeloid malignancies.
Pediatr Blood Cancer
; 57(4): 583-7, 2011 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-21294243