Publications
- 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
- Leber hereditary optic neuropathy2017 | First Faculty of Medicine
- OPA1 analysis in an international series of probands with bilateral optic atrophy2017 | First Faculty of Medicine
- Gene therapy for inherited retinal and optic nerve disorders : current knowledge2016 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Unique presentation of LHON/MELAS overlap syndrome caused by m.13046T > C in MTND52016 | First Faculty of Medicine, Second Faculty of Medicine
- Children's Ophthalmology2022 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University, Faculty of Medicine in Pilsen, Faculty of Education, Faculty of Medicine in Hradec Králové
- Transient Hyperphosphatasemia in a Child with Autism Spectrum Disorder2022 | First Faculty of Medicine, Central Library of Charles University, Faculty of Medicine in Pilsen
- Metabolic myopathies2022 | First Faculty of Medicine
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