Publications
- Novel Mutations in the Tyrosine Hydroxylase Gene in the First Czech Patient with Tyrosine Hydroxylase Deficiency2012 | First Faculty of Medicine
- Buccal epithelial cells as potential non-invasive materials for the monitoring of mitochondrial disturbances to track Huntington's disease progression : a pilot study2015 | First Faculty of Medicine
- Non-invasive screening of cytochrome c Oxidase Deficiency in Children Using a Dipstick Immunocapture Assay2014 | First Faculty of Medicine
- High-resolution melting analysis of 15 genes in 60 patients with cytochrome-c oxidase deficiency2012 | First Faculty of Medicine
- Rare cause of blindness in patient with nasal polyposis: Lebers hereditary neuropathy of the optic nerve2011 | First Faculty of Medicine
- MtDNA haplogroups in Czech populationPublication without faculty affiliation
- Nová mutace v genu CHRNE u romského pacienta s kongenitální myasteniíPublication without faculty affiliation
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