Detalhe da pesquisa
1.
Hemophagocytic syndrome in a patient with Fanconi anemia and VACTERL association / Síndrome hemofagocítica em paciente com anemia de Fanconi e associação VACTERL
ABCS health sci
; 48: e023401, 14 fev. 2023. tab, ilus
Artigo
em Inglês
| LILACS | ID: biblio-1414643
2.
Acute lymphoblastic leukemia complicating with adrenal insufficiency due cytomegalovirus infection.
Hematol Transfus Cell Ther
; 44(3): 447-449, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-33716022
3.
Association between the MTHFR A1298C polymorphism and increased risk of acute myeloid leukemia in Brazilian children.
Leuk Lymphoma
; 47(10): 2070-5, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17071478
4.
Minimally differentiated acute myeloid leukemia with ring/marker derived from chromosome 7 in a child with Down syndrome.
Hematol Transfus Cell Ther
; 41(1): 84-87, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30793109
5.
Polymorphisms involved in folate metabolism pathways and the risk of the development of childhood acute leukemia.
Genet Test Mol Biomarkers
; 17(2): 147-52, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23336575
6.
Extra Copies of der(21)t(12;21) plus Deletion of ETV6 Gene due to dic(12;18) in B-Cell Precursor ALL with Poor Outcome.
Case Rep Genet
; 2012: 186532, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23074685
7.
Molecular cytogenetic studies characterize a near-triploid complex karyotype in a child with acute lymphoblastic leukemia.
Cancer Genet Cytogenet
; 197(1): 71-4, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20113840
8.
Complex karyotype defined by molecular cytogenetic FISH and M-FISH in an infant with acute megakaryoblastic leukemia and neurofibromatosis.
Cancer Genet Cytogenet
; 200(2): 167-9, 2010 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20620601
9.
Minimally differentiated acute myeloid leukemia with ring/marker derived from chromosome 7 in a child with Down syndrome
Hematol., Transfus. Cell Ther. (Impr.)
; 41(1): 84-87, Jan.-Mar. 2019. ilus
Artigo
em Inglês
| LILACS | ID: biblio-1002035
10.
A rare cryptic and complex rearrangement leading to MLL-MLLT10 gene fusion masked by del(10)(p12) in a child with acute monoblastic leukemia (AML-M5).
Leuk Res
; 36(4): e74-7, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22261229
11.
Unusual childhood biphenotypic acute leukemia with a yet unreported t(3;13)(p25.1;q13).
Leuk Res
; 34(8): e206-7, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20338638
12.
Myeloproliferative syndrome of monosomy 7: a brief report
Genet. mol. biol
; 31(1): 36-38, 2008.
Artigo
em Inglês
| LILACS | ID: lil-476147