Publications
- DNA Analysis of Renal Electrolyte Transporter Genes Among Patients Suffering from Bartter and Gitelman Syndromes - Summary of Mutation Screening2011 | First Faculty of Medicine
- Hypokalemia in renal tubulopathy2008 | First Faculty of Medicine
- Bartter syndrome or renal tubular acidosis?2003 | First Faculty of Medicine
- The most common founder pathogenic variant c.868G > A (p.Val290Met) in the NPHS2 gene in a representative adult Czech cohort with focal segmental glomerulosclerosis is associated with a milder disease and its underdiagnosis in childhood2023 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Faculty of Medicine in Pilsen, Second Faculty of Medicine, Third Faculty of Medicine
- Current and Future Therapeutical Options in Alport Syndrome2023 | First Faculty of Medicine
- Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome2023 | First Faculty of Medicine
- Současné možnosti léčby autozomálně dominantní polycystické choroby ledvin2023 | First Faculty of Medicine
- Novinky v léčbě Alportova syndromu2023 | First Faculty of Medicine
- Těžký průběh ADPKD u rodičů asociuje s hypertenzí u dětí2023 | First Faculty of Medicine
- Dlouhodobý efekt migalastatu na kardiální, cerebrovaskulární a renální ukazatele pacientů s Fabryho chorobou2023 | First Faculty of Medicine
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