Publications
- Next generation sequencing - a science tool or routine pathology?2021 | Second Faculty of Medicine, Central Library of Charles University
- Gastrointestinal stromal tumors - Summary of mutational status of the primary/secondary KIT/PDGFRA mutations, BRAF mutations and SDH defects2019 | Second Faculty of Medicine, Central Library of Charles University
- Potential loss of prognostic significance of minimal residual disease assessment after R-CHOP-based induction in elderly patients with mantle cell lymphoma in the era of rituximab maintenance2018 | Second Faculty of Medicine, First Faculty of Medicine, Third Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Detection of EGFR Mutations in Circulating Tumor DNA (ctDNA) Retrieved from Plasma - Interlaboratory Quality Assessment in the Czech Republic2018 | Second Faculty of Medicine, First Faculty of Medicine, Central Library of Charles University, Faculty of Medicine in Hradec Králové
- Malignant Melanoma - from Classical Histology towards Molecular Genetic Testing2017 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Gastrointestinal stromal tumors - quantitative detection of the Ki-67, TPX2, TOP2A, and hTERT telomerase subunit mRNA levels to determine proliferation activity and a potential for aggressive biological behavior2016 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- The use of formalin-fixed, paraffin-embedded lymph node samples for the detection of minimal residual disease in mantle cell lymphoma2015 | Second Faculty of Medicine, First Faculty of Medicine, Third Faculty of Medicine
- Minimal residual disease – detection possibilities in haematological and non-haematological malignancies2013 | Second Faculty of Medicine
- The presence of clonal cells in nonmalignant lymphadenopathy with follicular hyperplasia2011 | Second Faculty of Medicine
- Standardization of WT1 mRNA quantitation for minimal residual disease monitoring in childhood AML and implications of WT1 gene mutations: a European multicenter study2009 | Second Faculty of Medicine
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