- The role of whiskers in compensation of visual deficit in a mouse model of retinal degeneration2014 | Faculty of Medicine in Pilsen, First Faculty of Medicine
- Current Management of Patients with RPE65 Mutation Associated Inherited Retinal Degenerations in Europe: Results of a 2-Year Follow-Up Multinational SurveyPublication without faculty affiliation
- Motor and visuospatial abilities in a model of olivocerebellar and retinal degeneration-Lurcher mutant mice of C3H strain2007 | Faculty of Medicine in Pilsen
- Motor and visuospatial abilities in a model of olivocerebellar and retinal degeneration-Lurcher mutant mice of C3H strain2007 | Faculty of Medicine in Pilsen, First Faculty of Medicine
- Neural functional and morphological consequences of retinal degeneration in C3H Lurcher mutant and wild type mice2006 | Faculty of Medicine in Pilsen
- Functional consequences of retinal degeneration in spatial orientation in C3H wild type and Lurcher mutant mice2005 | Faculty of Medicine in Pilsen, Central Library of Charles University
- Severe retinal degeneration in women with a c .2543del mutation in ORF15 of the RPGR gene2014 | First Faculty of Medicine
- Motor manifestation of olivocerebellar and retinal degeneration in Lurcher mutant mice of the C3H strain2008 | Faculty of Medicine in Pilsen
- Does the retinal degeneration influence tests of motor functions in normal and neurodefective Lurcher mutant mice?2006 | Faculty of Medicine in Pilsen
- Spinocerebellar Ataxia 7 - a Case Report2013 | First Faculty of Medicine, Second Faculty of Medicine
- Current Management of Inherited Retinal Degeneration Patients in Europe: Results of a 2-Year Follow-Up Multinational Survey by the European Vision Institute Clinical Research Network – EVICR.netPublication without faculty affiliation
- Cerebellar degeneration averts blindness-induced despaired behavior during spatial task in mice2020 | Faculty of Medicine in Pilsen
- Navigation to the visible object in wild type and Lurcher mutant mice of the strain C3H2006 | Faculty of Medicine in Pilsen
- Navigation to the visible object in wild type and Lurcher mutant mice of the strain C3H +12006 | Faculty of Medicine in Pilsen, First Faculty of Medicine
- Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness2015 | First Faculty of Medicine
- VEGF: A key player not only in macular generation. A review2020 | Third Faculty of Medicine
- First cases in the Czech Republic of the Hallervorden-Spatz Disease resulting from mutation in the Pantothenate Kinase 2 Gene2005 | Second Faculty of Medicine
- Spinocerebellar ataxias. Part II. Problematics of autosomal dominant spinocerebellar ataxias2001 | Second Faculty of Medicine
- SD-OCT imaging as a valuable tool to support molecular genetic diagnostics of Usher syndrome type 12018 | First Faculty of Medicine, Second Faculty of Medicine
- Absence of MMACHC in peripheral retinal cells does not lead to an ocular phenotype in mice2021 | First Faculty of Medicine
- Advantages of nanofibrous membranes for culturing of primary RPE cells compared to commercial scaffolds2022 | Third Faculty of Medicine, Faculty of Science