Disease: Corneal endothelial dystrophy type 2
- Association Between Fuchs Endothelial Corneal Dystrophy, Diabetes Mellitus, and Multimorbidity
- Bilateral cloudy cornea: is the usual suspect congenital hereditary endothelial dystrophy or stromal dystrophy?
- Congenital hereditary endothelial dystrophy, not glaucoma, in a child with iris colobomas
- Corneal dystrophies
- Corneal dystrophy mutations R125H and R804H disable SLC4A11 by altering the extracellular pH dependence of the intracellular pK that governs H<sup>+</sup>(OH<sup>-</sup>) transport
- Corneal dystrophy-causing SLC4A11 mutants: suitability for folding-correction therapy
- Delayed onset of congenital hereditary endothelial dystrophy due to compound heterozygous SLC4A11 mutations
- Descemet's membrane endothelial keratoplasty tissue type and endothelial cell loss over time
- Descemetorhexis Without Endothelial Keratoplasty in Fuchs Endothelial Corneal Dystrophy: A Systematic Review and Meta-Analysis
- Energy Shortage in Human and Mouse Models of SLC4A11-Associated Corneal Endothelial Dystrophies
- Experimental Oxidative Stress Breaks Down the Barrier Function of the Corneal Endothelium
- Fuchs Endothelial Corneal Dystrophy in a Heterozygous Carrier of Congenital Hereditary Endothelial Dystrophy Type 2 with a Novel Mutation in SLC4A11
- High Throughput Assay Identifies Glafenine as a Corrector for the Folding Defect in Corneal Dystrophy-Causing Mutants of SLC4A11
- Homozygous SLC4A11 mutation in a large Irish CHED2 pedigree
- Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy
- Imaging features of posterior polymorphous corneal dystrophy observed by <em>in vivo</em> confocal microscopy
- Mini-Review: Clinical Features and Management of Granular Corneal Dystrophy Type 2
- Mutations in the Corneal Endothelial Dystrophy-Associated Gene SLC4A11 Render the Cells More Vulnerable to Oxidative Insults
- North Carolina Macular Dystrophy: Long-term Follow-up of the Original Family
- Observation of nine previously reported and 10 non-reported <em>SLC4A11</em> mutations among 20 Iranian CHED probands and identification of an <em>MPDZ</em> mutation as possible cause of CHED and FECD in one family
- Ocular Features and Clinical Approach to Cataract and Corneal Refractive Surgery in Patients with Myotonic Dystrophy
- Oxidative Stress Induces a Breakdown of the Cytoskeleton and Tight Junctions of the Corneal Endothelial Cells
- Penetrating Keratoplasty Versus Descemet Stripping Automated Endothelial Keratoplasty in Children With Congenital Hereditary Endothelial Dystrophy: Long-Term Results
- Rescue of the Congenital Hereditary Endothelial Dystrophy Mouse Model by Adeno-Associated Viruse-Mediated <em>Slc4a11</em> Replacement
- Scheimpflug Corneal Densitometry Values and Severity of Guttae in Relation to Visual Acuity in Fuchs Endothelial Corneal Dystrophy
- SLC4A11 depletion impairs NRF2 mediated antioxidant signaling and increases reactive oxygen species in human corneal endothelial cells during oxidative stress
- Transcriptomic Analysis of Cultured Corneal Endothelial Cells as a Validation for Their Use in Cell Replacement Therapy
- Two novel mutations including a large deletion of the SLC4A11 gene causing autosomal recessive hereditary endothelial dystrophy
- Update on the genetics of corneal endothelial dystrophies