Detalhe da pesquisa
1.
Immunophenotyping of the cerebrospinal fluid as a prognostic factor at diagnosis of acute lymphoblastic leukemia in children and adolescents.
Pediatr Hematol Oncol
; 34(2): 53-65, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28548878
2.
Detection of clonal immunoglobulin and T-cell receptor gene rearrangements in childhood acute lymphoblastic leukemia using a low-cost PCR strategy.
Pediatr Blood Cancer
; 55(7): 1278-86, 2010 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20730889
3.
The novel WT1 gene mutation p.H377N associated to Denys-Drash syndrome.
J Pediatr Hematol Oncol
; 32(6): 486-8, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20562648
4.
Current Strategies for the Detection of Minimal Residual Disease in Childhood Acute Lymphoblastic Leukemia.
Mediterr J Hematol Infect Dis
; 8(1): e2016024, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27158437
5.
Comparison between qualitative and real-time polymerase chain reaction to evaluate minimal residual disease in children with acute lymphoblastic leukemia.
Rev Bras Hematol Hemoter
; 37(6): 373-80, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26670399
6.
Correlation between FLT3-ITD status and clinical, cellular and molecular profiles in promyelocytic acute leukemias.
Leuk Res
; 39(2): 131-7, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25530565
7.
Identification of a neocentromere in a rearranged Y chromosome with no detectable DYZ3 centromeric sequence.
Am J Med Genet
; 113(3): 263-7, 2002 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-12439894
8.
Gene rearrangement study for minimal residual disease monitoring in children with acute lymphocytic leukemia.
Rev Bras Hematol Hemoter
; 35(5): 337-42, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24255617
9.
Characterization of NPM1, FLT3, and IDH1 mutations in adult patients with acute myeloid leukemia: a Brazilian cohort study.
Leuk Lymphoma
; 57(12): 2901-2904, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27071442
10.
Comparison between qualitative and real-time polymerase chain reaction to evaluate minimal residual disease in children with acute lymphoblastic leukemia
Rev. bras. hematol. hemoter
; 37(6): 373-380, Oct.-Dec. 2015. tab, graf
Artigo
em Inglês
| LILACS | ID: lil-769961
11.
Novel DMRT1 3'UTR+11insT mutation associated to XY partial gonadal dysgenesis.
Arq Bras Endocrinol Metabol
; 54(8): 749-53, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21340164
12.
Gene rearrangement study for minimal residual disease monitoring in children with acute lymphocytic leukemia
Rev. bras. hematol. hemoter
; 35(5): 337-342, 2013. tab, graf
Artigo
em Inglês
| LILACS | ID: lil-694084
13.
Novel DMRT1 3'UTR+11insT mutation associated to XY partial gonadal dysgenesis / Nova mutação 3'UTR+11insT no gene DMRT1 associada à disgenesia gonadal parcial XY
Arq. bras. endocrinol. metab
; 54(8): 749-753, Nov. 2010. ilus, tab
Artigo
em Inglês
| LILACS | ID: lil-578351
14.
TCRG gene rearrangement patterns in Brazilian children with ALL: an update.
Leuk Res
; 33(12): e228-9, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19615743