Disease: Macular dystrophy- corneal type 1
- <em>TCF4</em> and <em>COL8A2</em> Gene Polymorphism Screening in a Greek Population of Late-onset Fuchs Endothelial Corneal Dystrophy
- "Descemet Membrane Detachment": A Novel Concept in Diagnosis and Classification
- A letter to the editor regarding "A novel tandem duplication of PRDM13 in a Chinese family with North Carolina macular dystrophy"
- A novel duplication involving <em>PRDM13</em> in a Turkish family supports its role in North Carolina macular dystrophy (NCMD/MCDR1)
- A novel tandem duplication of PRDM13 in a Chinese family with North Carolina macular dystrophy
- A Small Molecule that Binds an RNA Repeat Expansion Stimulates Its Decay via the Exosome Complex
- A unique <em>PRDM13</em>-associated variant in a Georgian Jewish family with probable North Carolina macular dystrophy and the possible contribution of a unique <em>CFH</em> variant
- AAV2-mediated gene therapy for Bietti crystalline dystrophy provides functional CYP4V2 in multiple relevant cell models
- Alterations in GRHL2-OVOL2-ZEB1 axis and aberrant activation of Wnt signaling lead to altered gene transcription in posterior polymorphous corneal dystrophy
- An Arg124Cys mutation in transforming growth factor β-induced gene associated with lattice corneal dystrophy type I in a Chinese pedigree
- APP processing and metabolism in corneal fibroblasts and epithelium as a potential biomarker for Alzheimer's disease
- Association Between Fuchs Endothelial Corneal Dystrophy, Diabetes Mellitus, and Multimorbidity
- Band keratopathy in children previously treated with diode laser for type 1 retinopathy of prematurity
- Case report: North Carolina macular dystrophy misdiagnosed as congenital ocular toxoplasmosis
- CHOROIDAL NEOVASCULARIZATION IN NORTH CAROLINA MACULAR DYSTROPHY RESPONSIVE TO ANTI-VASCULAR ENDOTHELIAL GROWTH FACTOR THERAPY
- Clinical and genetic update of corneal dystrophies
- Clinical and Histopathologic Characteristics and Template of the TGFBI p.(His626Arg) Missense Variant Lattice Corneal Dystrophy
- Clinical Evaluation of Electrolysis for Reis-Bücklers Corneal Dystrophies and In Vivo Histological Analysis Using Anterior Segment Optical Coherence Tomography
- Coexistence of bilateral macular edema and pale optic disc in the patient with Cohen syndrome
- Coincidental Occurrence of Schnyder Corneal Dystrophy and Posterior Polymorphous Corneal Dystrophy Type 3
- Collagen Fibrils and Proteoglycans of Macular Dystrophy Cornea: Ultrastructure and 3D Transmission Electron Tomography
- Compound heterozygous mutations in TGFBI cause a severe phenotype of granular corneal dystrophy type 2
- Cornea guttata associated with special phenotypic variants of granular corneal dystrophy type 2 in a Chinese family
- Corneal dystrophies in optical coherence tomography
- 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 Electrolysis for Granular Corneal Dystrophy Type 2 (Avellino Corneal Dystrophy) Exacerbation After LASIK
- Corneal irregularity and visual function using anterior segment optical coherence tomography in TGFBI corneal dystrophy
- Correlation of extracellular matrix-related gene expression with objective Fuchs endothelial corneal dystrophy severity
- Crystals deposits in the anterior and posterior lens cortex in Bietti corneo-retinal dystrophy
- Culture of corneal endothelial cells obtained by descemetorhexis of corneas with Fuchs endothelial corneal dystrophy
- 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
- Detailed phenotypic description of stromal corneal dystrophy in a large pedigree carrying the uncommon TGFBI p.Ala546Asp pathogenic variant
- Detection of Salmonella Typhi nucleic acid by RT-PCR and anti-HlyE, -CdtB, -PilL, and -Vi IgM by ELISA at sites in Ghana, Madagascar and Ethiopia
- Drug-induced corneal deposits: an up-to-date review
- Dual corneal involvement by endothelial and epithelial corneal dystrophies in Steinert's disease: A case of triple dystrophy
- EFFECT OF SODIUM COBALTINITRITE ON THE MINIMAL CARCINOGENIC DOSE-50 (MCD-50) OF METHYLCHOLANTHRENE IN ALBINO MICE
- Endothelial cell density in children with posterior polymorphous corneal dystrophy: a longitudinal case-control study
- Epithelial Ingrowth After Descemet Membrane Endothelial Keratoplasty
- Factors Affecting Formation of Type-1 and Type-2 Big Bubble during Deep Anterior Lamellar Keratoplasty
- Generation of iPSC line (GLNNFi001-A) from peripheral blood mononuclear cells of a patient with macular corneal dystrophy
- Generation of mouse model of TGFBI-R124C corneal dystrophy using CRISPR/Cas9-mediated homology-directed repair
- Generation of TGFBI knockout ABCG2+/ABCB5+ double-positive limbal epithelial stem cells by CRISPR/Cas9-mediated genome editing
- Genotypic Homogeneity in Distinctive Transforming Growth Factor-Beta Induced (TGFBI) Protein Phenotypes
- Granular dystrophy: Not always easy to classify
- Groenouw type II macular corneal dystrophy: case report
- 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
- Imaging of Reis-Bückler corneal dystrophy
- Impaired Autophagic Degradation of Transforming Growth Factor-β-Induced Protein by Macrophages in Lattice Corneal Dystrophy
- Investigation of TGFBI (transforming growth factor beta-induced) Gene Mutations in Families with Granular Corneal Dystrophy Type 1 in the Konya Region
- Letter to the editor regarding "A novel tandem duplication of PRDM13 in a Chinese family with North Carolina macular dystrophy"
- Letter to the Editor Regarding: "Modern diagnostic and therapeutic approaches in familial maculopathy with reference to North Carolina macular dystrophy" by Jana Nekolova et al
- Long-term restoration of corneal sensitivity in neurotrophic keratopathy after rhNGF treatment
- Macular Corneal Dystrophy in an Adolescent Managed with Deep Anterior Lamellar Keratoplasty
- Macular corneal dystrophy with isolated peripheral Descemet membrane deposits
- Macular Corneal Dystrophy: An Updated Review
- Matrix metalloproteinases and their inhibitors in Fuchs endothelial corneal dystrophy
- Modern diagnostic and therapeutic approaches in familial maculopathy with reference to North Carolina macular dystrophy
- Molecular genetic analysis of macular corneal dystrophy patients from North India
- Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy
- Multimodal Imaging and Functional Testing in a North Carolina Macular Disease Family: Toxoplasmosis, Fovea Plana, and Torpedo Maculopathy Are Phenocopies
- Multimodal ocular imaging of known and novel corneal stromal disorders in dogs
- Mutation effects on FAS1 domain 4 based on structure and solubility
- Mutation update: TGFBI pathogenic and likely pathogenic variants in corneal dystrophies
- Neurotrophic keratitis in autoimmune polyglandular syndrome type 1: a case report
- Non-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function <em>ZEB1</em> Alleles
- North Carolina Macular Dystrophy
- North Carolina macular dystrophy shows a particular drusen phenotype and atrophy progression
- North Carolina macular dystrophy: A case report
- North Carolina Macular Dystrophy: Long-term Follow-up of the Original Family
- North Carolina Macular Dystrophy: Phenotypic Variability and Computational Analysis of Disease-Associated Noncoding Variants
- Novel mutation in the CHST6 gene causes macular corneal dystrophy in a black South African family
- Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report
- Observation of the characteristics of the natural course of Bietti crystalline dystrophy by fundus fluorescein angiography
- Ocular alterations in patients with Alport syndrome-An update
- Ocular findings in a Spanish cohort of myotonic dystrophy type 1
- Optimizing pre-Descemet endothelial keratoplasty technique
- Oxidative Stress Induces a Breakdown of the Cytoskeleton and Tight Junctions of the Corneal Endothelial Cells
- Pathogenic mutations of TGFBI and CHST6 genes in Chinese patients with Avellino, lattice, and macular corneal dystrophies
- Penetrating Keratoplasty Versus Descemet Stripping Automated Endothelial Keratoplasty in Children With Congenital Hereditary Endothelial Dystrophy: Long-Term Results
- Phenotype and genotype analysis in patients with macular corneal dystrophy
- Reduced Corneal Sensitivity With Neuronal Degeneration is a Novel Clinical Feature in Wolfram Syndrome
- Repeated phototherapeutic keratectomy (PTK) followed by PTK with photorefractive keratectomy for anterior granular corneal dystrophy
- Retinal and Corneal Neurodegeneration and Their Association with Systemic Signs of Peripheral Neuropathy in Type 2 Diabetes
- Risk factors for endothelial cell loss after Descemet membrane endothelial keratoplasty (DMEK)
- Risk factors for failure of pre-cut eye bank UT-DSAEK grafts
- Schnyder corneal dystrophy-associated UBIAD1 mutations cause corneal cholesterol accumulation by stabilizing HMG-CoA reductase
- Sequential Custom Therapeutic Keratectomy for the Treatment of Granular Corneal Dystrophy Type 1: A Long-term Study
- Sequential Customized Therapeutic Keratectomy for Reis-Bücklers' Corneal Dystrophy: Long-term Follow-up
- Sorsby Pseudoinflammatory Fundus Dystrophy
- Surgical outcomes of re-excimer laser phototherapeutic keratectomy (re-PTK)
- TGFBI-associated corneal dystrophy and nephropathy: a novel syndrome?
- The alterations of corneal biomechanics in adult patients with corneal dystrophy
- The possible pathogenesis of macular caldera in patients with North Carolina macular dystrophy
- The role of corneal endothelium in macular corneal dystrophy development and recurrence
- The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosis
- Topical Losartan: Practical Guidance for Clinical Trials in the Prevention and Treatment of Corneal Scarring Fibrosis and Other Eye Diseases and Disorders
- Torin 1 alleviates impairment of TFEB-mediated lysosomal biogenesis and autophagy in <em>TGFBI</em> (p.G623_H626del)-linked Thiel-Behnke corneal dystrophy
- Update on the genetics of corneal endothelial dystrophies