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childhood AML
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Standardization of WT1 mRNA quantitation for minimal residual disease monitoring in childhood AML and implications of WT1 gene mutations: a European multicenter study
2009 |
Second Faculty of Medicine
publication
Prenatal origin of childhood AML occurs less frequently than in childhood ALL
2006 |
Second Faculty of Medicine, Third Faculty of Medicine
publication
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 cytometry
2002 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Development of treatment and clinical results in childhood acute myeloid leukemia in the Czech Republic
2013 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia
2009 |
Second Faculty of Medicine
publication
Genomic DNA-based measurable residual disease monitoring in pediatric acute myeloid leukemia: unselected consecutive cohort study
2024 |
Second Faculty of Medicine
publication
Diagnosis and management of acute myeloid leukemia in children and adolescents: recommendations from an international expert panel
2012 |
Second Faculty of Medicine