Results 61 to 70 of about 200,407 (146)

Corneal dystrophies and degenerations Part 2: The stroma

Part 2 in our continuing review of corneal dystrophies deals with stromal dystrophies. An earlier paper (Part 1) discussed dystrophies of the anterior layers of the cornea and a subsequent paper (Part 3) will do the same for dystrophies involving the ...
Monika Braun, William M. Lyle
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Corneal dystrophies and degenerations in dogs [PDF]

, 2006
The aim of the paper is the presentation of a not very well known group of corneal diseases in dogs: dystrophies and degenerations. The course of these diseases involves changes in the metabolism of corneal cells, which leads to the loss of ...
Madany, Jacek
core  

Molecular genetics and genotype-phenotype correlation of inherited corneal dystrophies [PDF]

, 2017
Corneal dystrophies are a group of inherited, primarily monogenic, disorders that compromise the transparency of the cornea and cause visual impairment. A large cohort, consisting of 191 corneal dystrophy probands, was recruited to the study with the aim
Evans, CJ
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N-Acetylcarnosine sustained drug delivery eye drops to control the signs of ageless vision: Glare sensitivity, cataract amelioration and quality of vision currently available treatment for the challenging 50,000-patient population

Clinical Interventions in Aging, 2008
Mark A Babizhayev1, Leslie Burke2, Philip Micans3, Stuart P Richer4,51Innovative Vision Products, Inc., County of New Castle, Delaware, USA; 2Wise Choice Products LLC, London, England, United Kingdom; 3IAS Group, Sark, United Kingdom; 4Eye Clinic DVA ...
Mark A Babizhayev, Leslie Burke, Philip Micans, Stuart P Richer   +3 more
doaj  

A new corneal disease with recurrent erosive episodes and autosomal-dominant inheritance

, 2008
Purpose: The aim of this study was to characterize the phenotype in a large family with autosomal-dominant recurrent corneal erosions, and also to exclude genetic linkage to known autosomal-dominant inherited corneal dystrophies with clinical resemblance.
Hammar, B, Lagerstedt, Kristina,, Hammar, Björn, Erik Björck, Anette Dellby, Bjorck, Erik, Dellby, Anette,, Fagerholm, Per,, Lagerstedt, Kristina, Kristina Lagerstedt, Björk, Erik,, Fagerholm, Per, Per Fagerholm, Lagerstedt, K,, Dellby, Anette, Dellby, A, Fagerholm, P, Hammar, Björn,, Björn Hammar, Bjorck, E   +19 more
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Surgical do's and don'ts of corneal dystrophies

, 2003
PURPOSE OF REVIEW: Characteristics of corneal dystrophies have been described with regards to such as location in the cornea, morphology, material composition, and recurrence after penetrating keratoplasty. The main goal of this review is to describe the
김응권
core  

Avellino corneal dystrophy: corneal stars [PDF]

Revista Brasileira de Oftalmologia
Laaribi Nisrine, Abdellaoui Taoufik, Oubaaz Abdelbarre   +2 more
doaj   +1 more source

Deep Anterior Lamellar Keratoplasty for the Treatment of Stromal Corneal Dystrophies

, 2013
Purpose: To report the perioperative complications and clinical outcomes after deep anterior lamellar keratoplasty (DALK) using the big bubble technique in eyes with stromal corneal ...
Mangan, Mehmet S., BİLGİN, AHMET BURAK, Atalay, Eray, ÜNAL, MUSTAFA, Arslan, Osman S., Arslan, Osman Şevki   +5 more
core   +1 more source

Antivascular Endothelial Growth Factor in Hereditary Dystrophies

, 2010
Choroidal neovascularization can rarely complicate the course of a number of chorioretinal hereditary dystrophies leading to an even further impaired vision function.
Iacono P, Maurizio Battaglia Parodi, Bandello F., Francesco Bandello, Pierluigi Iacono, Battaglia Parodi M   +5 more
core   +1 more source

On the role of kerato-epithelin in the pathogenesis of 5q31-linked corneal dystrophies.

, 1999
PURPOSE: Recently, the authors identified a gene, BIGH3, in which different mutations cause a group of hereditary corneal dystrophies: lattice type I and IIIA (CDLI and CDLIIIA), granular Groenouw type I (CDGGI), Avellino (CDA), and Reis-Bücklers' (CDRB).
Uffer, S., Mashima, Y., Munier, F.L., Chaubert, P., Korvatska, E., Zografos, L., Wang, M.X., Yamada, M., Schorderet, D.F.   +8 more
core   +1 more source