We report on 2 cases of granular dystrophy (Groenouw type I). We studied the nature and the ultrastructure of the typical stromal deposits by means of histochemical methods and of electron-microscopic examination. These deposits did not stain with Alcian blue, periodic acid-Schiff, Mallory, van Gieson, von Kossa or Congo red so that they are not constituted of proteoglycans, collagen, calcium or amyloid. They probably contain a proteic material. At the electron-microscopic level we observed electron-dense material which was made up of filaments immersed into an amorphous matrix
In the light of recent studies into lattice corneal dystrophies, with particular reference to gelsol...
Purpose: To elucidate changes of clinical manifestation of granular corneal deposits after recurrent...
This thesis describes results and observations from an ultrastructural study of the stroma of variou...
Objective: To investigate the origin and distribution of granular deposits in the corneas of 3 pati...
We examined seven corneas from five patients with a new form of lattice corneal dystrophy (designate...
Purpose Granular corneal dystrophy (GCD) is a hereditary disease involving the formation of opaque g...
Purpose: To determine the frequency and describe the histopathologic features of stromal corneal dys...
Corneal changes are frequently associated with X-linked ichthyosis. We present the first ultrastruct...
Keratan sulfate (KS) proteoglycans are of importance for the maintenance of corneal transparency as ...
We investigated an individual macular corneal dystrophy (MCD) type II cornea from a 42-year-old woma...
Keratan sulfate (KS) proteoglycans are of importance for the maintenance of corneal transparency as ...
PURPOSE: To evaluate the ultrastructure of the cornea of Avellino corneal dystrophy (ACD) exacerbate...
Two case reports of recurrent granular dystrophy in corneal grafts after penetrating keratoplasty ar...
Abstract The human cornea was studied by using transmission and scanning electron microscopic techni...
Corneal stromal dystrophies are a group of inherited disorders of the cornea that are caused by prog...
In the light of recent studies into lattice corneal dystrophies, with particular reference to gelsol...
Purpose: To elucidate changes of clinical manifestation of granular corneal deposits after recurrent...
This thesis describes results and observations from an ultrastructural study of the stroma of variou...
Objective: To investigate the origin and distribution of granular deposits in the corneas of 3 pati...
We examined seven corneas from five patients with a new form of lattice corneal dystrophy (designate...
Purpose Granular corneal dystrophy (GCD) is a hereditary disease involving the formation of opaque g...
Purpose: To determine the frequency and describe the histopathologic features of stromal corneal dys...
Corneal changes are frequently associated with X-linked ichthyosis. We present the first ultrastruct...
Keratan sulfate (KS) proteoglycans are of importance for the maintenance of corneal transparency as ...
We investigated an individual macular corneal dystrophy (MCD) type II cornea from a 42-year-old woma...
Keratan sulfate (KS) proteoglycans are of importance for the maintenance of corneal transparency as ...
PURPOSE: To evaluate the ultrastructure of the cornea of Avellino corneal dystrophy (ACD) exacerbate...
Two case reports of recurrent granular dystrophy in corneal grafts after penetrating keratoplasty ar...
Abstract The human cornea was studied by using transmission and scanning electron microscopic techni...
Corneal stromal dystrophies are a group of inherited disorders of the cornea that are caused by prog...
In the light of recent studies into lattice corneal dystrophies, with particular reference to gelsol...
Purpose: To elucidate changes of clinical manifestation of granular corneal deposits after recurrent...
This thesis describes results and observations from an ultrastructural study of the stroma of variou...