Publications
- Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders2021 | First Faculty of Medicine
- Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 42018 | First Faculty of Medicine, Third Faculty of Medicine
- Active transforming growth factor-beta 2 in the aqueous humor of posterior polymorphous corneal dystrophy patients2017 | First Faculty of Medicine
- Clinical Tests Testing New Therapies for Stargardt Disease2016 | First Faculty of Medicine
- Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL22016 | First Faculty of Medicine
- The impairment of lysyl oxidase in keratoconus and in keratoconus-associated disorders2013 | First Faculty of Medicine
- Changes in lysyl oxidase (LOX) distribution and its decreased activity in keratoconus corneas2012 | First Faculty of Medicine
- Potentional role of copper and lysyl oxidase activity in keratoconus pathogenesisPublication without faculty affiliation
- Disruption of OVOL2 Distal Regulatory Elements as a Possible Mechanism Implicated in Corneal Endothelial Dystrophy2024 | First Faculty of Medicine, Second Faculty of Medicine
- Axenfeld-Rieger syndrome: more than meets the eye2023 | First Faculty of Medicine, Second Faculty of Medicine
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