Results 31 to 40 of about 6,427 (219)
Fuchs endothelial corneal dystrophy and corneal endothelial diseases: East meets West [PDF]
Eye, 2019 Fuchs endothelial corneal dystrophy (FECD) is amongst one of the most common indications for endothelial keratoplasty worldwide. Despite being originally described among Caucasians, it is now known to be prevalent among a large number of populations, including Asians.
Y Q, Soh +3 more
openaire +2 more sources
Case Reports in Medicine, 2014 Four eyes of 2 patients with corneal edema due to Fuchs’ endothelial dystrophy were treated with CXL using the standard protocol. Since no improvement in visual acuity, corneal clarity, thickness, or pain sensation was evident in any eye at month 12, 2 ...
Omur O. Ucakhan, Ayhan Saglik
doaj +1 more source
Scientific Reports, 2022 The availability of corneal donor tissue is limited in most developing countries. This study evaluated whether patients with coexisting cataract and Fuchs’ dystrophy with corneal decompensation awaiting Descemet’s membrane endothelial keratoplasty (DMEK)
Wei-Yi Chou, Yih-Shiuan Kuo, Pei-Yu Lin
doaj +1 more source
Expression and Function of ZEB1 in the Cornea
Cells, 2021 ZEB1 is an important transcription factor for epithelial to mesenchymal transition (EMT) and in the regulation of cell differentiation and transformation.
Yingnan Zhang +5 more
doaj +1 more source
Primary graft failure associated with epithelial downgrowth: a case report [PDF]
, 2005 Background Epithelial downgrowth is a rare complication of ocular surgery. While the features of epithelial downgrowth following corneal transplantation are well described, its association with primary graft failure has only been reported once previously.
Anthony J Aldave +27 more
core +3 more sources
Data in Brief, 2019 Fuchs endothelial corneal dystrophy (FECD) is a bilateral inherited eye disease with advanced forms only treatable by corneal transplantation. The pathogenesis of FECD has not been worked out yet, however, trinucleotide repeat polymorphism CTG18.1 in the
Anastasia S. Nikitina +8 more
doaj +1 more source
Role of the TCF4 gene intronic variant in normal variation of corneal endothelium [PDF]
, 2012 PURPOSE: To identify early features of Fuchs endothelial dystrophy (FED) in carriers of the rs613872(G) transcription factor 4 gene (TCF4) aged 20 to 21 years.
Crawford, Geoffrey J. +8 more
core +1 more source
A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure. [PDF]
, 2017 Elevated intraocular pressure (IOP) is a major risk factor for glaucoma, a leading cause of blindness. IOP heritability has been estimated to up to 67%, and to date only 11 IOP loci have been reported, accounting for 1.5% of IOP variability.
Banda, Yambazi +10 more
core +3 more sources
Multimodal Highlighting of Structural Abnormalities in Diabetic Rat and Human Corneas. [PDF]
, 2013 PURPOSE: This study aimed to highlight structural corneal changes in a model of type 2 diabetes, using in vivo corneal confocal microscopy (CCM). The abnormalities were also characterized by transmission electron microscopy (TEM) and second harmonic ...
Behar-Cohen, F. +7 more
core +5 more sources
GMS Ophthalmology Cases, 2019 Objective: Descemet membrane endothelial keratoplasty (DMEK) is the gold standard procedure for treatment of primary corneal endothelial disorders. Graft detachment is a frequent complication of DMEK, which often requires re-operation or re-bubbling ...
Daravagka, Maria +3 more
doaj +1 more source