- Peripapillary microcirculation in Leber hereditary optic neuropathy2019 | 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
- Leber hereditary optic neuropathy2017 | First Faculty of Medicine
- Case report: A rare variant m.4135T>C in the MT-ND1 gene leads to Leber hereditary optic neuropathy and altered respiratory chain supercomplexes +12023 | First Faculty of Medicine, Faculty of Science
- Lebers Hereditary Optic Neuropathy: functional impact of mtDNA mutation G3460A in activities of respiratory chain complexesPublication without faculty affiliation
- DNAJC30 defect: a frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndrome2022 | First Faculty of Medicine
- Vitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort study2022 | First Faculty of Medicine
- Subjective and polysomnographic evaluation of sleep in mitochondrial optic neuropathies2021 | First Faculty of Medicine
- Dominant (Kjer's) optic atrophy associated with mutations in OPA1 gene2020 | First Faculty of Medicine
- Unique presentation of LHON/MELAS overlap syndrome caused by m.13046T > C in MTND52016 | First Faculty of Medicine, Second Faculty of Medicine