Detalhe da pesquisa
1.
KMT2A-MLLT1 and the Novel SEC16A-KMT2A in a Cryptic 3-Way Translocation t(9;11;19) Present in an Infant With Acute Lymphoblastic Leukemia.
J Pediatr Hematol Oncol
; 44(3): e719-e722, 2022 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34966090
2.
Ammonia level as a proxy of asparaginase inactivation in children: A strategy for classification of infusion reactions.
J Oncol Pharm Pract
; 28(3): 551-559, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33645327
3.
An Original Complex Rearrangement Involving Chromosomes 9, 11, and 14, Harboring a Complex KMT2A Gene Rearrangement in an Infant With Mixed-phenotype Acute Leukemia.
J Pediatr Hematol Oncol
; 43(3): e371-e374, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32134839
4.
A New Complex Karyotype Involving a KMT2A-r Variant Three-Way Translocation in a Rare Clinical Presentation of a Pediatric Patient with Acute Myeloid Leukemia.
Cytogenet Genome Res
; 157(4): 213-219, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30974445
5.
Maturation-associated gene expression profiles along normal human bone marrow monopoiesis.
Br J Haematol
; 176(3): 464-474, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28079251
6.
Molecular characterization of KMT2A fusion partner genes in 13 cases of pediatric leukemia with complex or cryptic karyotypes.
Hematol Oncol
; 35(4): 760-768, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27282883
7.
Comment on: Limited sensitivity and specificity of the ACR/EULAR-2019 classification criteria for SLE in JSLE?-observations from the UK JSLE Cohort Study.
Rheumatology (Oxford)
; 61(1): e25-e26, 2021 12 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-34459897
8.
Response to comment on Ammonia level as a proxy of asparaginase inactivation in children: A strategy for classification of infusion reactions.
J Oncol Pharm Pract
; 27(4): 1053-1054, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33847194
9.
Clinical and biological correlates of the expression of select Polycomb complex genes in Brazilian children with acute promyelocytic leukaemia.
Br J Haematol
; 189(6): e245-e248, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32314797
10.
Comparison between three systems of classification criteria in juvenile systemic lupus erythematous.
Rheumatology (Oxford)
; 54(2): 241-7, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25125590
11.
EOMES/TBET and soluble CTLA4/full length CTLA4 expression ratios impact on the therapeutic response in patients with classical Hodgkin lymphoma.
Br J Haematol
; 184(6): 1061-1064, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29741770
12.
Pediatric chronic kidney disease mortality in Brazil-A time trend analysis.
PLOS Glob Public Health
; 4(1): e0002304, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38266023
13.
Outcome of childhood acute lymphoblastic leukemia treatment in a single center in Brazil: A survival analysis study.
Cancer Rep (Hoboken)
; 5(1): e1452, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34114751
14.
Novel Decision Tool for More Severe α-Thalassemia Genotypes Screening with Functional Loss of Two or More α-Globin Genes: A Diagnostic Test Study.
Diagnostics (Basel)
; 12(12)2022 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36553015
15.
Immunophenotypic shifts during minimal residual evaluation in a case of leukemic form of anaplastic large cell lymphoma ALK.
Cancer Rep (Hoboken)
; 5(7): e1526, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34382381
16.
Bone Marrow Stromal Cell Regeneration Profile in Treated B-Cell Precursor Acute Lymphoblastic Leukemia Patients: Association with MRD Status and Patient Outcome.
Cancers (Basel)
; 14(13)2022 Jun 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-35804860
17.
Maturation-associated gene expression profiles during normal human bone marrow erythropoiesis.
Cell Death Discov
; 5: 69, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30854228
18.
Survival predictors in children on chronic dialysis in Rio de Janeiro, Brazil: a single center survival analysis study.
J Nephrol
; 36(6): 1711-1713, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37294403
19.
Molecular approaches identify a cryptic MECOM rearrangement in a child with a rapidly progressive myeloid neoplasm.
Cancer Genet
; 221: 25-30, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29405993
20.
A rare case of myelodysplastic syndrome with i(9q) in a child associated to osteochondromatosis.
Pediatr Blood Cancer
; 58(2): 308-9, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22009523