Comprehensive identification of dysregulated extracellular matrix molecules in the corneal endothelium of patients with Fuchs endothelial corneal dystrophy. [PDF]
Inagaki S +18 more
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Generation of a Mouse Model of Fuchs Endothelial Corneal Dystrophy by Knock-in of CTG Trinucleotide Repeat Expansion in the TCF4 Gene. [PDF]
Oyama Y +9 more
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Comparative Analysis of Descemet Membrane Endothelial Keratoplasty (DMEK) Versus Descemetorhexis Without Keratoplasty (DSO) in Patients with Fuchs Endothelial Corneal Dystrophy. [PDF]
Díaz-Mesa V +6 more
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Predicting corneal decompensation in Fuchs endothelial corneal dystrophy with Scheimpflug tomography and clinical parameters. [PDF]
Yesilirmak N +3 more
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Comparative Analysis of Tomographic Indicators Forecasting Decompensation in Fuchs Endothelial Corneal Dystrophy. [PDF]
Passaro ML +6 more
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Fuchs' Endothelial Corneal Dystrophy evaluation using a high-resolution wavefront sensor. [PDF]
Belda-Para C +6 more
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The genetic basis of fuchs endothelial corneal dystrophy.
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Related searches:
Fuchs endothelial corneal dystrophy
Vestnik oftal'mologii, 2017Fuchs endothelial dystrophy is a severe disease characterized by slowly progressing bilateral asymmetric corneal edema usually seen in elderly patients. The primary purpose of treatment is to minimize edema-related symptoms, such as ocular discomfort and visual acuity loss.
S V, Trufanov +3 more
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Corneal changes in Fuchs endothelial corneal dystrophy and bullous keratopathy
Russian Journal of Archive of Pathology, 2023Objective. Evaluation of structural and immunohistochemical features of cornea in Fuchs endothelial corneal dystrophy (FECD) and bullous keratopathy (BK). Material and methods. Group 1 — 44 patients (46 eyes) with FECD, group 2 — 42 patients (42 eyes) with BK. All patients underwent keratoplasty.
T.A. Demura +3 more
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