- The study ODYSSEY FH I and II with alirokumabem: other pieces in the mosaic of influences inhibition of PCSK92015 | First Faculty of Medicine
- Laboratory information systeme in FH Motol2008 | Publication without faculty affiliation
- ScreenPro FH - Screening project for familial hypercholesterolemia in central, Southern and Eastern Europe: Basic epidemiology2017 | First Faculty of Medicine
- ScreenPro FH - Screening project for familial hypercholesterolemia in central, southern and eastern Europe: Rationale and design2017 | First Faculty of Medicine
- ScreenPro FH: From the Czech MedPed to International Collaboration. ScreenPro FH Is a Participating Project of the EAS-FHCS2017 | First Faculty of Medicine
- The Impact of the International Cooperation On Familial Hypercholesterolemia Screening and Treatment: Results from the ScreenPro FH Project2019 | First Faculty of Medicine
- Comparison of the characteristics at diagnosis and treatment of children with heterozygous familial hypercholesterolaemia (FH) from eight European countries2020 | First Faculty of Medicine
- ODYSSEY FH I and FH II: 78 week results with alirocumab treatment in 735 patients with heterozygous familial hypercholesterolaemia2015 | First Faculty of Medicine
- Genetics of hypercholesterolemia: Lesson from FH and FDBPublication without faculty affiliation
- Project MedPed - spotlight on patients with familial hypercholesterolaemia2016 | First Faculty of Medicine
- Poslední výsledky z výzkumného programu ODYSSEY: od léčby dětí po nemocné s homozygotní FH2020 | First Faculty of Medicine
- Effect of torcetrapib on carotid atherosclerosis in FH2007 | First Faculty of Medicine
- Effect of torcetrapib on carotid atherosclerosis in FH2007 | Faculty of Physical Education and Sport
- CERGE and FHS UK Workshop on Non-profit organizationsPublication without faculty affiliation
- Lecture How to get into the media? for Longevity Studies PhD students FHS UK2022 | Publication without faculty affiliation
- Academic walks through Prague as part of lifelong learning 112 at FHS UK2022 | Faculty of Humanities
- Fumarate hydratase gene mutation in two young patients with sporadic uterine fibroids2013 | First Faculty of Medicine
- Comparison of the mutation spectrum and association with pre and post treatment lipid measures of children with heterozygous familial hypercholesterolaemia (FH) from eight European countries2021 | First Faculty of Medicine
- Genetics of Familial Hypercholesterolemia: New Insights2020 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- A summary of the consensus panel of experts International Atherosclerosis Society on the issue of the definition, diagnosis and treatment of severe forms of familial hypercholesterolemia2016 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Period changes in six contact binaries: WZ And, V803 Aql, DF Hya, PY Lyr, FZ Ori, and AH Tau2009 | Faculty of Mathematics and Physics
- Genetic testing of leiomyoma tissue in women younger than 30 years old might provide an effective screening approach for the hereditary leiomyomatosis and renal cell cancer syndrome (HLRCC)2015 | Faculty of Medicine in Pilsen
- MedPed project in Czech Republic2017 | First Faculty of Medicine
- Familial hypercholesterolemia in the Czech Republic in 20162016 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Inherited HLP2007 | First Faculty of Medicine
- Inherited HLP2007 | Faculty of Physical Education and Sport
- Komentář k "Praktickému doporučení pro použití PCSK9-inhibitorů" aneb Proč renomovaní autoři píší dokumenty, které si samy odporují2018 | First Faculty of Medicine
- Fumarate Hydratase-deficient Renal Cell Carcinoma Is Strongly Correlated With Fumarate Hydratase Mutation and Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome2016 | Faculty of Medicine in Pilsen
- MedPed - the reality of familial hypercholesterolemia care at the biggest center2018 | First Faculty of Medicine
- Fumarate hydratase deficient renal cell carcinoma and fumarate hydratase deficient-like renal cell carcinoma: Morphologic comparative study of 23 genetically tested cases2019 | Faculty of Medicine in Pilsen
