Disease: Corneal dystrophy- juvenile epithelial of Meesmann
- A novel mutation as the basis for asymptomatic meesmann dystrophy in a Danish family
- A novel mutation in the cornea-specific keratin 12 gene in Meesmann corneal dystrophy
- A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy
- Allele-specific siRNA silencing for the common keratin 12 founder mutation in Meesmann epithelial corneal dystrophy
- Autosomal-dominant Meesmann epithelial corneal dystrophy without an exon mutation in the keratin-3 or keratin-12 gene in a Chinese family
- Coexistence of Meesmann Corneal Dystrophy and a Pseudo-Unilateral Lattice Corneal Dystrophy in a Patient With a Novel Pathogenic Variant in the Keratin K3 Gene: A Case Report
- Corneal Dystrophy
- Corneal Dystrophy
- Development of allele-specific therapeutic siRNA in Meesmann epithelial corneal dystrophy
- Femtosecond laser-assisted laser in situ keratomileusis for the correction of high myopia in Meesmann corneal dystrophy: a case report
- Genetics of Meesmann corneal dystrophy: a novel mutation in the keratin 3 gene in an asymptomatic family suggests genotype-phenotype correlation
- Identification of presumed pathogenic KRT3 and KRT12 gene mutations associated with Meesmann corneal dystrophy
- Imaging the microstructural abnormalities of Meesmann corneal dystrophy by in vivo confocal microscopy
- In vivo histology and p.L132V mutation in KRT12 gene in Japanese patients with Meesmann corneal dystrophy
- Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy
- KRT12 mutations and in vivo confocal microscopy in two Japanese families with Meesmann corneal dystrophy
- Meesmann corneal dystrophy associated with epithelial basement membrane and posterior polymorphous corneal dystrophies
- Meesmann epithelial corneal dystrophy: recurrence following photorefractive keratectomy
- Meesmann's corneal dystrophy managed with an epithelial delaminator
- Phenotypic variability in Meesmann's dystrophy: clinical review of the literature and presentation of a family genetically identical to the original family
- Photorefractive Keratectomy With Mitomycin C in Meesmann's Epithelial Corneal Dystrophy
- Recurrent Meesmann's corneal dystrophy: treatment with keratectomy and mitomycin C
- Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12
- siRNA silencing of the mutant keratin 12 allele in corneal limbal epithelial cells grown from patients with Meesmann's epithelial corneal dystrophy
- The use of high modulus silicone hydrogel (SiHy) lens in the management of epithelial defects