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grayson-wilbrandt corneal dystrophy (5) 5
ophthalmology (5) 5
reis-bucklers corneal dystrophy (5) 5
thiel-behnke corneal dystrophy (5) 5
avellino corneal dystrophy (4) 4
congenital hereditary endothelial dystrophy 1 (4) 4
congenital stromal corneal dystrophy (4) 4
corneal dystrophy (4) 4
corneal histopathology (4) 4
epithelial basement membrane dystrophy (4) 4
epithelial recurrent erosion dystrophy (4) 4
eponym (4) 4
fleck corneal dystrophy (4) 4
gelatinous drop-like corneal dystrophy (4) 4
gene (4) 4
genetic corneal disease (4) 4
granular corneal dystrophy 1 (4) 4
granular corneal dystrophy 2 (4) 4
inherited corneal disease (4) 4
key reference (4) 4
lattice corneal dystrophy (4) 4
lattice gelsolin type dystrophy (4) 4
lisch epithelial corneal dystrophy (4) 4
macular corneal dystrophy (4) 4
meesmann corneal dystrophy (4) 4
mutation (4) 4
posterior amorphous corneal dystrophy (4) 4
pre-descemet corneal dystrophy (4) 4
schnyder corneal dystrophy (4) 4
schnyder crystalline corneal dystrophy (4) 4
subepithelial mucinous corneal dystrophy (4) 4
carbohydrate sulfotransferase gene (3) 3
central cloudy dystrophy (3) 3
compound heterozygous mutations (3) 3
congenital hereditary endothelial dystrophy 2 (3) 3
corneal dystrophies, hereditary - pathology (3) 3
fuchs endothelial corneal dystrophy (3) 3
gelsolin-related amyloidosis (3) 3
hereditary endothelial dystrophy (3) 3
humans (3) 3
index medicus (3) 3
posterior polymorphous corneal dystrophy (3) 3
posterior polymorphous dystrophy (3) 3
tgfbi bigh3 gene (3) 3
vivo confocal microscopy (3) 3
whorled microcystic dystrophy (3) 3
x-linked endothelial corneal dystrophy (3) 3
central cloudy dystrophy of francxois (2) 2
corneal dystrophies, hereditary - genetics (2) 2
female (2) 2
helix termination motif (2) 2
male (2) 2
middle aged (2) 2
pedigree (2) 2
2. x-linked endothelial corneal dystrophy (1) 1
adolescent (1) 1
aged (1) 1
article (1) 1
central cloudy dystrophy of francois (1) 1
central cloudy dystrophy of françois (1) 1
collagen - ultrastructure (1) 1
collagen diseases - genetics (1) 1
collagen diseases - pathology (1) 1
collagen type-i, type-iii, and type-iv fibers (1) 1
congenital hereditary endothelial dystrophy (1) 1
corneal dystrophies, hereditary - classification (1) 1
corneal dystrophies, hereditary - history (1) 1
corneal dystrophies, hereditary/classification; corneal dystrophies, hereditary/genetics; history, 19th century; humans; international cooperation; ophthalmology/trends; phenotype; terminology as topic (1) 1
corneal opacity - diagnosis (1) 1
corneal stroma - ultrastructure (1) 1
epithelium - ultrastructure (1) 1
fuchs endothelial corneal dystrophy posterior (1) 1
grayson-wilbrandt variant (1) 1
grayston-wilbrandt variant (1) 1
groenouw type-i (1) 1
history, 19th century (1) 1
honeycomb corneal dystrophy (1) 1
international cooperation (1) 1
japan (1) 1
microscopy, fluorescence (1) 1
ophthalmology - trends (1) 1
phenotype (1) 1
polymorphous corneal dystrophy (1) 1
reis-bücklers corneal dystrophy (1) 1
terminology as topic (1) 1
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CORNEA, ISSN 0277-3740, 12/2008, Volume 27, Issue 10, pp. S1 - S42
Background: The recent availability of genetic analyses has demonstrated the shortcomings of the current phenotypic method of corneal dystrophy classification.... 
Grayson-Wilbrandt corneal dystrophy | Meesmann corneal dystrophy | TGFBI BIGH3 GENE | pre-Descemet corneal dystrophy | GROENOUW TYPE-I | corneal histopathology | GELSOLIN-RELATED AMYLOIDOSIS | Thiel-Behnke corneal dystrophy | posterior polymorphous corneal dystrophy | epithelial basement membrane dystrophy | POSTERIOR POLYMORPHOUS DYSTROPHY | granular corneal dystrophy 2 | COMPOUND HETEROZYGOUS MUTATIONS | granular corneal dystrophy 1 | genetic corneal disease | Schnyder corneal dystrophy | inherited corneal disease | WHORLED MICROCYSTIC DYSTROPHY | congenital hereditary endothelial dystrophy 1 | congenital hereditary endothelial dystrophy 2 | posterior amorphous corneal dystrophy | central cloudy dystrophy of Francois | macular corneal dystrophy | Schnyder crystalline corneal dystrophy | congenital stromal corneal dystrophy | gene | subepithelial mucinous corneal dystrophy | VIVO CONFOCAL MICROSCOPY | CENTRAL CLOUDY DYSTROPHY | Lisch epithelial corneal dystrophy | corneal dystrophy | eponym | X-linked endothelial corneal dystrophy | mutation | key reference | CARBOHYDRATE SULFOTRANSFERASE GENE | fleck corneal dystrophy | HEREDITARY ENDOTHELIAL DYSTROPHY | epithelial recurrent erosion dystrophy | gelatinous drop-like corneal dystrophy | OPHTHALMOLOGY | Avellino corneal dystrophy | lattice gelsolin type dystrophy | Fuchs endothelial corneal dystrophy | lattice corneal dystrophy | Reis-Bucklers corneal dystrophy
Journal Article
KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, ISSN 0023-2165, 01/2011, Volume 228, pp. S1 - S39
Background: The recent availability of genetic analyses has demonstrated the shortcomings of the current phenotypic method of corneal dystrophy classification.... 
Grayson-Wilbrandt corneal dystrophy | Meesmann corneal dystrophy | TGFBI BIGH3 GENE | pre-Descemet corneal dystrophy | central cloudy dystrophy of Francxois | corneal histopathology | GELSOLIN-RELATED AMYLOIDOSIS | Thiel-Behnke corneal dystrophy | epithelial basement membrane dystrophy | POSTERIOR POLYMORPHOUS DYSTROPHY | granular corneal dystrophy 2 | COMPOUND HETEROZYGOUS MUTATIONS | granular corneal dystrophy 1 | genetic corneal disease | Schnyder corneal dystrophy | inherited corneal disease | WHORLED MICROCYSTIC DYSTROPHY | congenital hereditary endothelial dystrophy 1 | congenital hereditary endothelial dystrophy 2 | posterior amorphous corneal dystrophy | HELIX TERMINATION MOTIF | macular corneal dystrophy | Schnyder crystalline corneal dystrophy | congenital stromal corneal dystrophy | gene | subepithelial mucinous corneal dystrophy | VIVO CONFOCAL MICROSCOPY | CENTRAL CLOUDY DYSTROPHY | Lisch epithelial corneal dystrophy | corneal dystrophy | eponym | Fuchs endothelial corneal dystrophy posterior | X-linked endothelial corneal dystrophy | mutation | key reference | CARBOHYDRATE SULFOTRANSFERASE GENE | fleck corneal dystrophy | HEREDITARY ENDOTHELIAL DYSTROPHY | epithelial recurrent erosion dystrophy | gelatinous drop-like corneal dystrophy | polymorphous corneal dystrophy | OPHTHALMOLOGY | Avellino corneal dystrophy | lattice gelsolin type dystrophy | lattice corneal dystrophy | Reis-Bucklers corneal dystrophy
Journal Article
Cornea, ISSN 0277-3740, 12/2008, Volume 27 Suppl 2, Issue Suppl 2, pp. S1 - S42
The recent availability of genetic analyses has demonstrated the shortcomings of the current phenotypic method of corneal dystrophy classification.... 
Corneal Dystrophies, Hereditary - history | Ophthalmology - trends | Phenotype | Corneal Dystrophies, Hereditary - pathology | Humans | Corneal Dystrophies, Hereditary - genetics | Terminology as Topic | History, 19th Century | International Cooperation | Corneal Dystrophies, Hereditary - classification | Grayson-Wilbrandt corneal dystrophy | Meesmann corneal dystrophy | pre-Descemet corneal dystrophy | corneal histopathology | Thiel-Behnke corneal dystrophy | posterior polymorphous corneal dystrophy | epithelial basement membrane dystrophy | granular corneal dystrophy 2 | granular corneal dystrophy 1 | genetic corneal disease | Schnyder corneal dystrophy | inherited corneal disease | congenital hereditary endothelial dystrophy 1 | congenital hereditary endothelial dystrophy 2 | posterior amorphous corneal dystrophy | central cloudy dystrophy of François | macular corneal dystrophy | Schnyder crystalline corneal dystrophy | congenital stromal corneal dystrophy | gene | subepithelial mucinous corneal dystrophy | Lisch epithelial corneal dystrophy | corneal dystrophy | eponym | X-linked endothelial corneal dystrophy | mutation | key reference | fleck corneal dystrophy | epithelial recurrent erosion dystrophy | gelatinous drop-like corneal dystrophy | Avellino corneal dystrophy | lattice gelsolin type dystrophy | Fuchs endothelial corneal dystrophy | lattice corneal dystrophy | Reis-Bücklers corneal dystrophy
Journal Article
KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, ISSN 0023-2165, 02/2011, Volume 228, pp. S1 - S39
Background: The recent availability of genetic analyses has demonstrated the shortcomings of the current phenotypic method of corneal dystrophy classification.... 
Grayson-Wilbrandt corneal dystrophy | Meesmann corneal dystrophy | TGFBI BIGH3 GENE | pre-Descemet corneal dystrophy | 2. X-linked endothelial corneal dystrophy | central cloudy dystrophy of Francxois | corneal histopathology | GELSOLIN-RELATED AMYLOIDOSIS | Thiel-Behnke corneal dystrophy | posterior polymorphous corneal dystrophy | epithelial basement membrane dystrophy | POSTERIOR POLYMORPHOUS DYSTROPHY | granular corneal dystrophy 2 | COMPOUND HETEROZYGOUS MUTATIONS | granular corneal dystrophy 1 | genetic corneal disease | Schnyder corneal dystrophy | inherited corneal disease | WHORLED MICROCYSTIC DYSTROPHY | congenital hereditary endothelial dystrophy 1 | posterior amorphous corneal dystrophy | HELIX TERMINATION MOTIF | macular corneal dystrophy | Schnyder crystalline corneal dystrophy | congenital stromal corneal dystrophy | gene | subepithelial mucinous corneal dystrophy | VIVO CONFOCAL MICROSCOPY | CENTRAL CLOUDY DYSTROPHY | Lisch epithelial corneal dystrophy | corneal dystrophy | eponym | congenital hereditary endothelial dystrophy | mutation | key reference | CARBOHYDRATE SULFOTRANSFERASE GENE | fleck corneal dystrophy | HEREDITARY ENDOTHELIAL DYSTROPHY | epithelial recurrent erosion dystrophy | gelatinous drop-like corneal dystrophy | OPHTHALMOLOGY | Avellino corneal dystrophy | lattice gelsolin type dystrophy | Fuchs endothelial corneal dystrophy | lattice corneal dystrophy | Reis-Bucklers corneal dystrophy
Journal Article
Japanese Journal of Ophthalmology, ISSN 0021-5155, 1993, Volume 37, Issue 2, pp. 143 - 147
A 50-year-old man (the proband) experienced recurring attacks of ocular irritation and had had bilateral ring-shaped anterior corneal opacity since... 
Grayston-Wilbrandt variant | Reis-Bucklers corneal dystrophy | OPHTHALMOLOGY | GRAYSON-WILBRANDT VARIANT | REIS-BUCKLERS CORNEAL DYSTROPHY | Corneal Dystrophies, Hereditary - pathology | Pedigree | Corneal Opacity - diagnosis | Humans | Japan | Middle Aged | Adolescent | Female | Male
Journal Article
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