Detalhe da pesquisa
1.
Epigenetic regulator genes direct lineage switching in MLL/AF4 leukemia.
Blood
; 140(17): 1875-1890, 2022 10 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35839448
2.
Genomic breakpoint-specific monitoring of measurable residual disease in pediatric non-standard-risk acute myeloid leukemia.
Haematologica
; 109(3): 740-750, 2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37345487
3.
Perception and management of cancer predisposition in pediatric cancer centers: A European-wide questionnaire-based survey.
Pediatr Blood Cancer
; 70(5): e30229, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36860090
4.
Lmo2 expression defines tumor cell identity during T-cell leukemogenesis.
EMBO J
; 37(14)2018 07 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-29880602
5.
Single nucleotide polymorphism array-based signature of low hypodiploidy in acute lymphoblastic leukemia.
Genes Chromosomes Cancer
; 60(9): 604-615, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33938069
6.
Novel phenotypes observed in patients with ETV6-linked leukaemia/familial thrombocytopenia syndrome and a biallelic ARID5B risk allele as leukaemogenic cofactor.
J Med Genet
; 57(6): 427-433, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31704777
7.
Relapses and treatment-related events contributed equally to poor prognosis in children with ABL-class fusion positive B-cell acute lymphoblastic leukemia treated according to AIEOP-BFM protocols.
Haematologica
; 105(7): 1887-1894, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31601692
8.
Transfer and loss of allergen-specific responses via stem cell transplantation: A prospective observational study.
Allergy
; 75(9): 2243-2253, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32181893
9.
Aneuploidy in children with relapsed B-cell precursor acute lymphoblastic leukaemia: clinical importance of detecting a hypodiploid origin of relapse.
Br J Haematol
; 185(2): 266-283, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30714092
10.
Somatic mosaicisms of chromosome 1 at two different stages of ontogenetic development detected by Rh blood group discrepancies.
Haematologica
; 104(3): 632-638, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30237270
11.
Somatic mosaic monosomy 7 and UPD7q in a child with MIRAGE syndrome caused by a novel SAMD9 mutation.
Pediatr Blood Cancer
; 66(4): e27589, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30565860
12.
Targeted mutation screening of 292 candidate genes in 38 children with inborn haematological cytopenias efficiently identifies novel disease-causing mutations.
Br J Haematol
; 182(2): 251-258, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29797310
13.
Dominant inherited ß-thalassemia intermedia in a Polish family due to a novel frameshift mutation in HBB.
Pediatr Blood Cancer
; 70(10): e30511, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37353956
14.
Concurrent Acute Myelofibrosis and Acute Lymphoblastic Leukemia in Childhood: Case Report and Review of the Literature.
J Pediatr Hematol Oncol
; 40(3): 235-237, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29557917
15.
Use of HuH6 and other human-derived hepatoma lines for the detection of genotoxins: a new hope for laboratory animals?
Arch Toxicol
; 92(2): 921-934, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-29218508
16.
Band 3 nullVIENNA , a novel homozygous SLC4A1 p.Ser477X variant causing severe hemolytic anemia, dyserythropoiesis and complete distal renal tubular acidosis.
Pediatr Blood Cancer
; 64(3)2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27718309
17.
High hyperdiploid acute lymphoblastic leukemia (ALL)-A 25-year population-based survey of the Austrian ALL-BFM (Berlin-Frankfurt-Münster) Study Group.
Pediatr Blood Cancer
; 64(6)2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27804199
18.
Peripheral blood late mixed chimerism in leucocyte subpopulations following allogeneic stem cell transplantation for childhood malignancies: does it matter?
Br J Haematol
; 173(6): 905-17, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26996395
19.
Characterization of leukemias with ETV6-ABL1 fusion.
Haematologica
; 101(9): 1082-93, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27229714
20.
Two Novel Missense Mutations and a 5bp Deletion in the Erythroid-Specific Promoter of the PKLR Gene in Two Unrelated Patients With Pyruvate Kinase Deficient Transfusion-Dependent Chronic Nonspherocytic Hemolytic Anemia.
Pediatr Blood Cancer
; 63(5): 914-6, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26728349