Publications
- Today's view of hereditary thrombophilia2022 | First Faculty of Medicine
- Multiple thrombophilia mutations as a possible cause of premature myocardial infarction2017 | First Faculty of Medicine
- The frequencies of thrombophilic alleles known from GWAS studies in healthy population and in group of patients with venous thromboembolism (VTE) in the Czech Republic2016 | Publication without faculty affiliation
- The frequencies of six important thrombophilic mutations in a population of the Czech Republic2014 | First Faculty of Medicine
- Frequencies of the new thrombophilic mutations of antithrombin (SERPINC1) (IVS +141G>A), glycoprotein GPVI (Ser219Pro) and cytochrome CYP4V2 (Lys259Gln) in healthy middle-aged people in Central Bohemia2012 | First Faculty of Medicine
- Prevalence of thrombophilic mutations of FV Leiden, prothrombin G20210A and PAI-1 4G/5G and their combinations in a group of 1,450 healthy middle-aged individuals in the Prague and Central Bohemian regions (results of FRET real-time PCR assay)2012 | First Faculty of Medicine
- Atherothrombosis and venous thromboembolism, common mechanisms2012 | First Faculty of Medicine
- The prevalence of CYP2C9 and VKORC1 polymorphisms in the Czech Republic and reflect on the views of anticoagulation therapy with warfarin2011 | First Faculty of Medicine
- Platelet gene polymorphisms and risk of bleeding in patients undergoing elective coronary angiography: A genetic substudy of the PRAGUE-8 trial2010 | First Faculty of Medicine, Third Faculty of Medicine
- Platelet glycoprotein GP VI 13254C allele is an independent risk factor of premature myocardial infarction2010 | First Faculty of Medicine, Third Faculty of Medicine
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