Detalhe da pesquisa
1.
Identification of ZCCHC8 as fusion partner of ROS1 in a case of congenital glioblastoma multiforme with a t(6;12)(q21;q24.3).
Genes Chromosomes Cancer
; 55(9): 677-87, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27121553
2.
Lineage switch in childhood acute leukemia: an unusual event with poor outcome.
Am J Hematol
; 87(9): 890-7, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22685031
3.
A complex karyotype in an atypical teratoid/rhabdoid tumor: case report and review of the literature.
J Neurooncol
; 104(1): 375-80, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21127945
4.
Cytogenetic findings in a rare pediatric mixed glioneuronal tumor and review of the literature.
Childs Nerv Syst
; 25(11): 1485-90, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19387654
5.
Experience with four consecutive BFM-based protocols for treatment of childhood with non-promyelocytic acute myeloblastic leukemia in Argentina.
Leuk Lymphoma
; 57(9): 2090-9, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26734812
6.
B-cell acute lymphoblastic leukemia with mature phenotype and MLL rearrangement: report of five new cases and review of the literature.
Leuk Lymphoma
; 57(10): 2289-97, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-26857438
7.
Cytogenetic and Molecular Findings in Children with Acute Lymphoblastic Leukemia: Experience of a Single Institution in Argentina.
Mol Syndromol
; 6(4): 193-203, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26648836
8.
A case of pediatric ALL with t(16;21)(p11.2;q22) and FUS-ERG rearrangement.
Blood Res
; 50(1): 55-8, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25830133