- TRPM6 N-Terminal CaM- and S100A1-Binding Domains2019 | First Faculty of Medicine, Faculty of Physical Education and Sport, Faculty of Mathematics and Physics
- Novel mutations in TRPM6 gene associated with primary hypomagnesemia with secondary hypocalcemia. Case report2021 | First Faculty of Medicine
- Gitelman's syndrome as common cause of hypokalemia and hypomagnesemia2016 | First Faculty of Medicine
