Publications
- High Prevalence of Posterior Polymorphous Corneal Dystrophy in the Czech Republic; Linkage Disequilibrium Mapping and Dating an Ancestral Mutation2012 | First Faculty of Medicine
- Minimal Ocular Findings in a Patient with Best Disease Caused by the c.653G>A Mutation in BEST12011 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Recurrence of posterior polymorphous corneal dystrophy is caused by the overgrowth of the original diseased host endothelium2011 | First Faculty of Medicine
- Large Proteoglycan Complexes and Disturbed Collagen Architecture in the Corneal Extracellular Matrix of Mucopolysaccharidosis Type VII (Sly Syndrome)2011 | First Faculty of Medicine
- Minimal ocular findings in a patient with Best disease caused by the c.653>A mutation in Best 12011 | First Faculty of Medicine
- Variable ocular phenotypes of posterior polymorphous corneal dystrophy caused by mutations in the ZEB1 gene2010 | First Faculty of Medicine
- Phenotype Associated with the H626P Mutation and Other Changes in the TGFBI Gene in Czech Families2008 | First Faculty of Medicine
- Sequencing of the CHST6 gene in Czech macular corneal dystrophy patients supports the evidence of a founder mutation2008 | First Faculty of Medicine
- British family with early-onset Fuchs ´ endothelial corneal dystrophy associated with p.L450W mutation in the COL8A2 gene2007 | First Faculty of Medicine
- Novel mutations in the ZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy2007 | First Faculty of Medicine
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