- Phenotype Associated with the H626P Mutation and Other Changes in the TGFBI Gene in Czech Families2008 | First Faculty of Medicine
- Spectrum of Mutations in the TGFBI Gene in Patiens with Corneal Stromal DystrophiesPublication without faculty affiliation
- Novel TGFBI mutation p.(Leu558Arg) in a lattice corneal dystrophy patient2016 | First Faculty of Medicine
- Phenotype Associated with the H626P Mutation and Other Changes in the TGFBI Gene in Czech Families2008 | Publication without faculty affiliation
- Paraproteinemic keratopathy associated with monoclonal gammopathy of undetermined significance (MGUS): clinical findings in twelve patients including recurrence after keratoplasty2019 | First Faculty of Medicine