- C3 glomerulopathy - a new clinical entity2018 | Faculty of Medicine in Pilsen
- Genetics of hemolytic uremic syndromes2012 | Second Faculty of Medicine
- Molecular basis and outcomes of atypical haemolytic uraemic syndrome in Czech children2020 | Second Faculty of Medicine
- Complement Inhibition in ANCA-Associated Vasculitis2022 | First Faculty of Medicine
- Avacopan in the treatment of ANCA-associated vasculitis2018 | First Faculty of Medicine
- Manifestation of atypical hemolytic uremic syndrome caused by novel mutations in MCP2012 | Second Faculty of Medicine
- Macrovascular involvement in a child with atypical hemolytic uremic syndrome2014 | Second Faculty of Medicine
- Atypical hemolytic uremic syndrome and current view on the treatment2017 | First Faculty of Medicine
- Complement System Deficiencies in Elite Athletes2024 | First Faculty of Medicine
- Complement activation is associated with more severe course of diarrhea-associated hemolytic uremic syndrome, a preliminary study2018 | Second Faculty of Medicine
- Defective gene expression of the membrane complement inhibitor CD46 in patients with progressive immunoglobulin A nephropathy2019 | First Faculty of Medicine
- The Czech Experience with Eculizumab in Severe Paediatric Shiga Toxin-Producing Escherichia coli-Associated Haemolytic Uremic Syndrome Patients2022 | Second Faculty of Medicine