Publications
- Clinical Findings in Members of a Czech Family with Retinitis Pigmentosa Caused by the c.2426_2427delAG Mutation in RPGR2013 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Faculty of Physical Education and Sport
- 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
- Molecular genetic cause of X-linked retinitis pigmentosa in a Czech family2011 | First Faculty of Medicine
- 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
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