- Mitochondrial DNA mutations in patients with encephalopathy and hypertrophic cardiomyopathy +1Publication without faculty affiliation
- Hypertrophic cardiomyopathy due to the mitochondrial DNA mutation m.3303C>T diagnosed in an adult male2012 | First Faculty of Medicine
- Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB92012 | First Faculty of Medicine
- High-resolution melting analysis of 15 genes in 60 patients with cytochrome-c oxidase deficiency2012 | First Faculty of Medicine
- Alternative assembly of respiratory complex II connects energy stress to metabolic checkpoints2018 | Central Library of Charles University
- Mitochondrial diabetes in common clinical practice2020 | Third Faculty of Medicine
- A rear cause of blindness in a patient with nasal polyposis. Leber's hereditary optic atrophy of visual nerve2011 | Publication without faculty affiliation
- Multiple Roles of Mitochondria in Aging Processes2016 | Faculty of Medicine in Pilsen
- Rare cause of blindness in patient with nasal polyposis: Lebers hereditary neuropathy of the optic nerve2011 | First Faculty of Medicine
- Mitochondrial Dysfunctions in Bipolar Disorder: Effect of the Disease and Pharmacotherapy2017 | First Faculty of Medicine
- Leber's Hereditary Optic Neuropathy with Oligoclonal Bands in the Serum Regarded as Multiple Sclerosis - a Case Report2009 | Central Library of Charles University, Third Faculty of Medicine
- Revisiting mitochondrial diagnostic criteria in the new era of genomics2018 | First Faculty of Medicine