Martin Filipec
Prague, PR 12808, Czech Republic
Last Updated: 09/26/2026
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Found 8 publications
Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4.
Journal: American journal of human genetics
Published: December 15, 2017
Familial Limbal Stem Cell Deficiency: Clinical, Cytological and Genetic Characterization.
Journal: Stem cell reviews and reports
Published: November 15, 2017
Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2.
Journal: American journal of human genetics
Published: September 17, 2015
Identification of six novel mutations in ZEB1 and description of the associated phenotypes in patients with posterior polymorphous corneal dystrophy 3.
Journal: Annals of human genetics
Published: July 09, 2014
The application of autologous serum eye drops in severe dry eye patients; subjective and objective parameters before and after treatment.
Journal: Current eye research
Published: October 01, 2013
High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutation.
Journal: PloS one
Published: May 30, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026