- Hereditary xanthinuria is not so rare disorder of purine metabolism2018 | First Faculty of Medicine
- Modern diagnostic approach to hereditary xanthinuria2015 | First Faculty of Medicine
- Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: Biochemical and molecular genetic analysis in two Czech families with xanthinuria type I2012 | First Faculty of Medicine
- Thiopurine-induced toxicity is associated with dysfunction variant of the human molybdenum cofactor sulfurase gene (xanthinuria type II)2018 | First Faculty of Medicine
- Urinary pterins in classical xanthinuriaPublication without faculty affiliation
- Analysis of Purine Metabolism to Elucidate the Pathogenesis of Acute Kidney Injury in Renal Hypouricemia2022 | First Faculty of Medicine
- Modified forearm ischemic test in hypouricemic patients2020 | First Faculty of Medicine
- Purine disorders with hypouricemia2014 | First Faculty of Medicine