- The screening of congenital cataract in the Czech republic was introduced2005 | Second Faculty of Medicine
- Congenital cataracts2016 | Second Faculty of Medicine
- Congenital cataracts2016 | Second Faculty of Medicine, Central Library of Charles University
- Introduction of congenital cataract screening in the Czech Republic and our first functional results in operated children2003 | Second Faculty of Medicine
- A novel missense mutation in LIM2 causing isolated autosomal dominant congenital cataract2020 | First Faculty of Medicine
- Central corneal thickness in microphthalmic eyes with or without history of congenital cataract surgery2011 | Second Faculty of Medicine
- Segregation of a novel p.(Ser270Tyr) MAF mutation and p.(Tyr56*) CRYGD variant in a family with dominantly inherited congenital cataracts2017 | First Faculty of Medicine
- Results of congenital cataract operationsPublication without faculty affiliation
- Our experience of the primary implantation of IOL in children with congenital cataract up to the age of three2005 | Second Faculty of Medicine
- Risk of visual axis opacification in infants with and without primary IOL implantation after congenital cataract surgery performed during the first 4 months of age2023 | Second Faculty of Medicine
- Congenital cataract, facial dysmorphism and demyelinating neuropathy (CCFDN) in 10 Czech gypsy children - frequent and underestimated cause of disability among Czech gypsies2014 | Second Faculty of Medicine, Faculty of Physical Education and Sport, First Faculty of Medicine
- Two novel variants of the MBTPS1 gene in Czech family with Kondo-Fu type spondyloepiphyseal dysplasia and cataract2023 | Second Faculty of Medicine, First Faculty of Medicine
- Phenotype Variability in Czech Patients Carrying PAX6 Disease-Causing Variants2020 | First Faculty of Medicine
- Autosomal recessive ethnical diseases of Czech Roma2006 | Second Faculty of Medicine
- Link between a novel human gammaD-crystallin allele and a unique cataract phenotype explained by protein crystallography2000 | Faculty of Science
- X-linked Microcephaly, Microphthalmia, Microcornea, Congenital Catarct, Hypogenitalism, Mental Deficiency Growth Retardation, Spasticity: Possible New Syndrome1996 | Second Faculty of Medicine
- Pseudodominant Nanophthalmos in a Roma Family Caused by a Novel PRSS56 Variant2020 | Second Faculty of Medicine, First Faculty of Medicine
- Link between a novel human gammaD-crystallin allele and a unique cataract phenotype explained by protein crystallography2000 | Faculty of Physical Education and Sport, First Faculty of Medicine
- Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies2011 | Second Faculty of Medicine