X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (26) 26
index medicus (25) 25
ophthalmology (25) 25
posterior polymorphous dystrophy (14) 14
corneal dystrophies, hereditary - genetics (12) 12
corneal dystrophy (11) 11
male (11) 11
posterior amorphous corneal dystrophy (11) 11
corneal dystrophies, hereditary - pathology (10) 10
adult (9) 9
female (9) 9
cornea (8) 8
middle aged (7) 7
mutation (7) 7
adolescent (6) 6
endothelium (6) 6
mutations (6) 6
congenital stromal corneal dystrophy (5) 5
cornea - pathology (5) 5
corneal endothelium (5) 5
epithelial basement membrane dystrophy (5) 5
fleck corneal dystrophy (5) 5
gelatinous drop-like corneal dystrophy (5) 5
gene (5) 5
genetics & heredity (5) 5
infant (5) 5
lattice corneal dystrophy (5) 5
linkage (5) 5
lisch epithelial corneal dystrophy (5) 5
macular corneal dystrophy (5) 5
posterior polymorphous corneal dystrophy (5) 5
pre-descemet corneal dystrophy (5) 5
schnyder corneal dystrophy (5) 5
subepithelial mucinous corneal dystrophy (5) 5
thiel-behnke corneal dystrophy (5) 5
aged (4) 4
avellino corneal dystrophy (4) 4
child, preschool (4) 4
collagen (4) 4
congenital hereditary endothelial dystrophy 1 (4) 4
corneal diseases - pathology (4) 4
corneal dystrophies, hereditary - diagnosis (4) 4
corneal histopathology (4) 4
dystrophy (4) 4
epithelial recurrent erosion dystrophy (4) 4
eponym (4) 4
family (4) 4
fuchs endothelial corneal dystrophy (4) 4
genetic corneal disease (4) 4
glaucoma (4) 4
granular corneal dystrophy 1 (4) 4
granular corneal dystrophy 2 (4) 4
grayson-wilbrandt corneal dystrophy (4) 4
hereditary endothelial dystrophy (4) 4
infant, newborn (4) 4
inherited corneal disease (4) 4
key reference (4) 4
lattice gelsolin type dystrophy (4) 4
meesmann corneal dystrophy (4) 4
pathology (4) 4
reis-bucklers corneal dystrophy (4) 4
schnyder crystalline corneal dystrophy (4) 4
vivo confocal microscopy (4) 4
article (3) 3
carbohydrate sulfotransferase gene (3) 3
central cloudy dystrophy (3) 3
child (3) 3
compound heterozygous mutations (3) 3
congenital hereditary endothelial dystrophy (3) 3
congenital hereditary endothelial dystrophy 2 (3) 3
cornea - ultrastructure (3) 3
corneal dystrophies, hereditary - classification (3) 3
corneal topography (3) 3
descemet membrane - ultrastructure (3) 3
descemets-membrane (3) 3
electron microscopy (3) 3
fibroblast growth-factor (3) 3
fuchs' endothelial dystrophy - pathology (3) 3
gelsolin-related amyloidosis (3) 3
genetics (3) 3
keratoconus (3) 3
locus (3) 3
small leucine-rich proteoglycans - genetics (3) 3
syndrome (3) 3
terminology as topic (3) 3
tgfbi bigh3 gene (3) 3
whorled microcystic dystrophy (3) 3
x-linked endothelial corneal dystrophy (3) 3
aging (2) 2
analysis (2) 2
basement membrane - pathology (2) 2
basement-membrane (2) 2
central cloudy dystrophy of francois (2) 2
central cloudy dystrophy of francxois (2) 2
children (2) 2
choroid diseases (2) 2
chromosome deletion (2) 2
chromosomes, human, pair 12 (2) 2
col8a2 gene (2) 2
collagen - ultrastructure (2) 2
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Cornea, ISSN 0277-3740, 12/2017, Volume 36, Issue 12, pp. 1562 - 1566
PURPOSE:Posterior amorphous corneal dystrophy (PACD) is a rare disorder characterized by sheet-like opacification of the posterior corneal stroma, corneal... 
Corneal dystrophy | Corneal ectasia | Posterior amorphous corneal dystrophy | Keratoglobus | keratoglobus | OPHTHALMOLOGY | corneal dystrophy | corneal ectasia | posterior amorphous corneal dystrophy | Female | Corneal Dystrophies, Hereditary - pathology | Corneal Diseases - pathology | Dilatation, Pathologic | Humans | Infant, Newborn | Index Medicus
Journal Article
Cornea, ISSN 0277-3740, 02/2015, Volume 34, Issue 2, pp. 117 - 159
PURPOSE:To update the 2008 International Classification of Corneal Dystrophies (IC3D) incorporating new clinical, histopathologic, and genetic information.... 
Fleck corneal dystrophy | Cornea | Epithelial and subepithelial dystrophies | Descemetmembrane | Posterior amorphous corneal dystrophy | Confocal microscopy | Cornea pathology | Thiel-Behnke corneal dystrophy | Lattice corneal dystrophy | Macular corneal dystrophy | Stromal dystrophies | Hereditary disease | Epithelial basement membranedystrophy | Pre-Descemet corneal dystrophy | Histopathology | Keratoconus | Congenital corneal endothelial dystrophy and X-linked endothelialdystrophy | Bowman membrane | Subepithelialmucinous corneal dystrophy | Endothelial dystrophies | Genetics | Schnyder corneal dystrophy | Gelatinousdrop-like corneal dystrophy | Fuchsendothelial corneal dystrophy | Epithelial-stromal TGFBI dystrophies | Lisch epithelial corneal dystrophy | Stroma | Histology | Meesmann dystrophy | Epithelium | Endothelium | Genetic disease | Epithelial recurrent erosion dystrophies | Posteror polymorphous corneal dystrophy | Centralcloudy dystrophy of François | Granular corneal dystrophy type 1 | Granular corneal dystrophy type 2 | TGFBI | Reis-Bücklers corneal dystrophy | Congenital stromal corneal dystrophy | Cornea dystrophy | cornea | endothelial dystrophies | histology | epithelial basement membrane dystrophy | genetic disease | epithelial and subepithelial dystrophies | central cloudy dystrophy of Francois | macular corneal dystrophy | subepithelial mucinous corneal dystrophy | cornea pathology | stroma | FRANCOIS | congenital corneal endothelial dystrophy and X-linked endothelial dystrophy | posteror polymorphous corneal dystrophy | DISEASE | epithelium | Fuchs endothelial corneal dystrophy | lattice corneal dystrophy | Reis-Bucklers corneal dystrophy | pre-Descemet corneal dystrophy | histopathology | INDIVIDUAL PHENOTYPIC VARIANCES | FAMILY | epithelial recurrent erosion dystrophies | granular corneal dystrophy type 1 | granular corneal dystrophy type 2 | genetics | cornea dystrophy | UBIAD1 GENE | MUTATIONS | Descemet membrane | endothelium | hereditary disease | epithelial-stromal TGFBI dystrophies | keratoconus | posterior amorphous corneal dystrophy | congenital stromal corneal dystrophy | stromal dystrophies | fleck corneal dystrophy | confocal microscopy | gelatinous drop-like corneal dystrophy | EDEMA | OPHTHALMOLOGY | LINKAGE | Corneal Dystrophies, Hereditary - genetics | Terminology as Topic | International Classification of Diseases | Corneal Dystrophies, Hereditary - classification | Corneal Dystrophies, Hereditary - pathology | Humans | Index Medicus
Journal Article
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
Clinical & Experimental Ophthalmology, ISSN 1442-6404, 01/2007, Volume 35, Issue 1, pp. 99 - 102
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
Journal Article
Clinical Genetics, ISSN 0009-9163, 08/2013, Volume 84, Issue 2, pp. 109 - 119
The aim of this review was to provide an evidenced‐based review of the genetic basis of the corneal endothelial dystrophies. A review of the English language... 
corneal dystrophy, Fuchs endothelial, 2 | corneal dystrophy, Fuchs endothelial, early onset | corneal dystrophy, Fuchs endothelial, 1 | corneal endothelial dystrophy 1 | corneal endothelial dystrophy 2 | corneal dystrophy, Fuchs endothelial, late onset | corneal dystrophy, posterior polymorphous, 2 | corneal dystrophy, posterior polymorphous, 3 | corneal dystrophy, posterior polymorphous, 1 | Corneal dystrophy, Fuchs endothelial, early onset | Corneal dystrophy, posterior polymorphous, 1 | Corneal dystrophy, posterior polymorphous, 3 | Corneal dystrophy, posterior polymorphous, 2 | Corneal dystrophy, Fuchs endothelial, 1 | Corneal dystrophy, Fuchs endothelial, 2 | Corneal dystrophy, Fuchs endothelial, late onset | Corneal endothelial dystrophy 2 | Corneal endothelial dystrophy 1 | SLC4A11 GENE | posterior polymorphous | early onset | PENETRATING KERATOPLASTY | CANDIDATE GENES | corneal dystrophy | LOCUS | MISSENSE MUTATIONS | COL8A2 GENE | Fuchs endothelial | VIII COLLAGEN | POSTERIOR POLYMORPHOUS DYSTROPHY | GENETICS & HEREDITY | late onset | LINKAGE | SAUDI-ARABIA | Corneal Dystrophies, Hereditary - genetics | Corneal Dystrophies, Hereditary - diagnosis | Evidence-Based Medicine | Humans | Genetic aspects | Genetic disorders | Gene mutations | Endothelium | Eye diseases | Ophthalmology | Evidence-based medicine | Index Medicus | Corneal Dystrophy, Posterior Polymorphous, 3 | Corneal Dystrophy, Posterior Polymorphous, 2 | Corneal Dystrophy, Fuchs Endothelial, 2 | Corneal Dystrophy, Fuchs Endothelial, Late-Onset | Corneal Endothelial Dystrophy 1 | Corneal Endothelial Dystrophy 2 | Corneal Dystrophy, Fuchs Endothelial, 1 | Corneal Dystrophy, Posterior Polymorphous,1 | Corneal Dystrophy, Fuchs Endothelial, Early-Onset
Journal Article
Experimental Eye Research, ISSN 0014-4835, 1995, Volume 61, Issue 3, pp. 323 - 333
Journal Article