- De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy2021 | First Faculty of Medicine, Third Faculty of Medicine
- A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Ca(v)3.2 T-type channel activity2020 | Central Library of Charles University
- Electrophysiological characterization of a Ca(v)3.2 calcium channel missense variant associated with epilepsy and hearing loss2023 | First Faculty of Medicine, Third Faculty of Medicine
- Electrophysiological and computational analysis of Ca(v)3.2 channel variants associated with familial trigeminal neuralgia2022 | Third Faculty of Medicine