Detalhe da pesquisa
1.
Frequent and sex-biased deletion of SLX4IP by illegitimate V(D)J-mediated recombination in childhood acute lymphoblastic leukemia.
Hum Mol Genet
; 23(3): 590-601, 2014 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24045615
2.
Hematopoietic stem cell transplantation in children and young adults with secondary myelodysplastic syndrome and acute myelogenous leukemia after aplastic anemia.
Biol Blood Marrow Transplant
; 20(3): 425-9, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24316460
3.
Protocol II vs protocol III given twice during reinduction therapy in children with medium-risk ALL.
Blood
; 130(19): 2146-2149, 2017 11 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28939722
4.
Next-generation-sequencing-based risk stratification and identification of new genes involved in structural and sequence variations in near haploid lymphoblastic leukemia.
Genes Chromosomes Cancer
; 52(6): 564-79, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23508829
5.
Second induction with high-dose cytarabine and mitoxantrone: different impact on pediatric AML patients with t(8;21) and with inv(16).
Blood
; 118(20): 5409-15, 2011 Nov 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-21948298
6.
IKZF1 deletion is an independent predictor of outcome in pediatric acute lymphoblastic leukemia treated according to the ALL-BFM 2000 protocol.
Haematologica
; 98(3): 428-32, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22875627
7.
Low platelet counts after induction therapy for childhood acute lymphoblastic leukemia are strongly associated with poor early response to treatment as measured by minimal residual disease and are prognostic for treatment outcome.
Haematologica
; 97(3): 402-9, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22058224
8.
Constitutional trisomy 8p11.21-q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemia.
Br J Haematol
; 155(2): 209-17, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21848520
9.
Parallel evaluation of cellbased phage display panning strategies: Optimized selection and depletion steps result in AML blastbinding consensus antibodies.
Mol Med Rep
; 24(5)2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34490477
10.
Prognostic relevance of dic(9;20)(p11;q13) in childhood B-cell precursor acute lymphoblastic leukaemia treated with Berlin-Frankfurt-Münster (BFM) protocols containing an intensive induction and post-induction consolidation therapy.
Br J Haematol
; 149(1): 93-100, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20067563
11.
Immunophenotypic differences between diagnosis and relapse in childhood AML: Implications for MRD monitoring.
Cytometry B Clin Cytom
; 63(1): 1-9, 2005 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-15624201
12.
Next-generation-sequencing of recurrent childhood high hyperdiploid acute lymphoblastic leukemia reveals mutations typically associated with high risk patients.
Leuk Res
; 39(9): 990-1001, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26189108
13.
MicroRNAs distinguish cytogenetic subgroups in pediatric AML and contribute to complex regulatory networks in AML-relevant pathways.
PLoS One
; 8(2): e56334, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23418555
14.
Quantification of minimal residual disease (MRD) in acute lymphoblastic leukemia (ALL) using amplicon-fusion-site polymerase chain reaction (AFS-PCR).
Exp Hematol Oncol
; 1(1): 33, 2012 Nov 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-23210797
15.
Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotype.
PLoS One
; 6(6): e20607, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21694761
16.
Cytogenetic features of acute lymphoblastic and myeloid leukemias in pediatric patients with Down syndrome: an iBFM-SG study.
Blood
; 111(3): 1575-83, 2008 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17971484
17.
Characterization of 6q abnormalities in childhood acute myeloid leukemia and identification of a novel t(6;11)(q24.1;p15.5) resulting in a NUP98-C6orf80 fusion in a case of acute megakaryoblastic leukemia.
Genes Chromosomes Cancer
; 44(3): 225-32, 2005 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-16028218
18.
Cryptic chromosomal aberrations leading to an AML1/ETO rearrangement are frequently caused by small insertions.
Genes Chromosomes Cancer
; 36(3): 261-72, 2003 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-12557226
19.
Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21.
Blood
; 102(3): 981-6, 2003 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-12649131
20.
Occurrence of an MLL/LAF4 fusion gene caused by the insertion ins(11;2)(q23;q11.2q11.2) in an infant with acute lymphoblastic leukemia.
Genes Chromosomes Cancer
; 37(1): 106-9, 2003 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-12661012