Results 181 to 190 of about 8,757 (220)
Some of the next articles are maybe not open access.

Fuchs Endothelial Corneal Dystrophy and Mitochondria

Cornea, 2018
Abstract: Fuchs endothelial corneal dystrophy (FECD) is a bilateral progressive corneal endothelial disease characterized by guttae, which present as partial Descemet membrane thickening, inducing corneal edema at the final stage. Oxidative stress has been reported to play an important role in the pathogenesis of FECD.
openaire   +2 more sources

Cytochrome oxidase activity of Fuchs' endothelial dystrophy

Current Eye Research, 1986
The normal human corneal endothelial monolayer maintains stromal water equilibrium and thus, transparency, by means of a pump-leak mechanism. Water leaks into the stroma through non-tight lateral cell junctional complexes and is drawn out by an energy dependent cell membrane ion pump. We investigated the histochemical localization of cytochrome oxidase
A W, Tuberville   +2 more
openaire   +2 more sources

Regenerative Therapy for Fuchs Endothelial Corneal Dystrophy

Cornea, 2018
Purpose: Fuchs endothelial corneal dystrophy (FECD) is an acquired corneal endotheliopathy and is one of the most common indications for corneal transplantation surgery worldwide. Endothelial keratoplasty (EK) is the most popular form of corneal transplantation for FECD. In standard EK surgery, the patient's corneal endothelium
Yu Qiang, Soh, Jodhbir S, Mehta
openaire   +2 more sources

Fuchs’ Endothelial Dystrophy and Glaucoma

2010
Fuchs’ Endothelial Dystrophy (FED) is a common disorder of the cornea that causes slow progressive endothelial degeneration with subsequent corneal edema and loss of vision in late stages. It is characterized by a thickened Descemet’s membrane (DM) from the aberrant deposition of wide-spaced collagen and the development of guttae, or posterior ...
Blair Boehmer, Clark Springs
openaire   +1 more source

Genotyping methods for Fuchs corneal endothelial dystrophy

Journal Français d'Ophtalmologie
Fuchs endothelial corneal dystrophy (FECD) is a genetic degenerative disease characterized by the progressive degradation of the corneal endothelium, often leading to vision loss. It is the leading cause of corneal transplantation in the Western world. FECD is more common in Europe and the United States, particularly among women.
D. Onitiu   +9 more
openaire   +2 more sources

Fuchs endothelial corneal dystrophy: an updated review

International Ophthalmology
The present review will summarize FECD-associated genes and pathophysiology, diagnosis, current  therapeutic approaches, and future treatment perspectives.Literature review.Fuchs' endothelial corneal dystrophy (FECD) is the most common bilateral corneal dystrophy and accounts for one-third of all corneal transplants performed in the US.
Francisco Altamirano   +5 more
openaire   +2 more sources

Endothelial keratoplasty versus penetrating keratoplasty for Fuchs endothelial dystrophy

2011
Fuchs endothelial dystrophy (FED), first described by Ernst Fuchsis in 1910, is a condition in which there is premature degeneration of corneal endothelial cells. When the number of endothelial cells is reduced to a significant degree fluid begins to accumulate within the cornea.
Mayank A, Nanavaty, Alex J, Shortt
openaire   +2 more sources

Fuch's Endothelial Dystrophy

2004
Prema Padmanabhan, SS Badrinath
openaire   +2 more sources

Vision With Fuchs Endothelial Dystrophy

JAMA Ophthalmology, 2015
Lucas M M, Vianna   +2 more
openaire   +2 more sources

TCF4-mediated Fuchs endothelial corneal dystrophy: Insights into a common trinucleotide repeat-associated disease

Progress in Retinal and Eye Research, 2021
Michael P Fautsch   +2 more
exaly  

Home - About - Disclaimer - Privacy