- Hereditary xanthinuria is not so rare disorder of purine metabolism2018 | 1. lékařská fakulta
- Modern diagnostic approach to hereditary xanthinuria2015 | 1. lékařská fakulta
- Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: Biochemical and molecular genetic analysis in two Czech families with xanthinuria type I2012 | 1. lékařská fakulta
- Thiopurine-induced toxicity is associated with dysfunction variant of the human molybdenum cofactor sulfurase gene (xanthinuria type II)2018 | 1. lékařská fakulta
- Urinary pterins in classical xanthinuriaPublikace bez příslušnosti k fakultě
- Analysis of Purine Metabolism to Elucidate the Pathogenesis of Acute Kidney Injury in Renal Hypouricemia2022 | 1. lékařská fakulta
- Modified forearm ischemic test in hypouricemic patients2020 | 1. lékařská fakulta
- Purine disorders with hypouricemia2014 | 1. lékařská fakulta