Publications
- NUP98/JARID1A is a novel recurrent abnormality in pediatric acute megakaryoblastic leukemia with a distinct HOX gene expression pattern2013 | Second Faculty of Medicine
- Telomere length and telomerase complex mutations in pediatric acute myeloid leukemia2013 | Second Faculty of Medicine
- Evaluation of WT1 expression in bone marrow vs peripheral blood samples of children with acute myeloid leukemia-impact on minimal residual disease detection2013 | Second Faculty of Medicine
- HOX Gene Expression in Phenotypic and Genotypic Subgroups and Low HOXA Gene Expression as an Adverse Prognostic Factor in Pediatric ALL2010 | Faculty of Science, Second Faculty of Medicine
- Real-time quantitative PCR detection of WT1 gene expression in children with AML: prognostic significance, correlation with disease status and residual disease detection by flow cytometry2002 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Acute lymphoblastic leukemia incidence during socioeconomic transition: selective increase in children from 1 to 4 years2002 | Second Faculty of Medicine
- Acute lymphoblastic leukemia in infants2002 | Second Faculty of Medicine
- Monitoring minimal residual disease in pediatric patients with acute lymphoblastic leukemia2000 | Second Faculty of Medicine
- Detection of BCR/ABL, MLL/AF4 and TEL/AML1 hybrid genes and monitoring of minimal residual disease in pediatric patients with acute lymphoblastic leukemia1999 | Second Faculty of Medicine
- Genomic DNA-based measurable residual disease monitoring in pediatric acute myeloid leukemia: unselected consecutive cohort study2024 | Second Faculty of Medicine
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