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index medicus (12) 12
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ophthalmology (9) 9
corneal dystrophy (6) 6
animals (5) 5
congenital stromal corneal dystrophy (5) 5
epithelial basement membrane dystrophy (5) 5
fleck corneal dystrophy (5) 5
gelatinous drop-like corneal dystrophy (5) 5
gene (5) 5
lattice corneal dystrophy (5) 5
lisch epithelial corneal dystrophy (5) 5
macular corneal dystrophy (5) 5
mutation (5) 5
phenotype (5) 5
posterior amorphous 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
avellino corneal dystrophy (4) 4
congenital hereditary endothelial dystrophy 1 (4) 4
corneal dystrophies, hereditary - genetics (4) 4
corneal histopathology (4) 4
epithelial recurrent erosion dystrophy (4) 4
eponym (4) 4
fuchs endothelial corneal dystrophy (4) 4
genetic corneal disease (4) 4
granular corneal dystrophy 1 (4) 4
granular corneal dystrophy 2 (4) 4
grayson-wilbrandt corneal dystrophy (4) 4
inherited corneal disease (4) 4
key reference (4) 4
lattice gelsolin type dystrophy (4) 4
meesmann corneal dystrophy (4) 4
posterior polymorphous dystrophy (4) 4
reis-bucklers corneal dystrophy (4) 4
schnyder crystalline corneal dystrophy (4) 4
article (3) 3
carbohydrate sulfotransferase gene (3) 3
central cloudy dystrophy (3) 3
child, preschool (3) 3
compound heterozygous mutations (3) 3
congenital hereditary endothelial dystrophy 2 (3) 3
corneal dystrophies, hereditary - pathology (3) 3
diseases (3) 3
gelsolin-related amyloidosis (3) 3
genetics (3) 3
hereditary endothelial dystrophy (3) 3
infant, newborn (3) 3
physiology (3) 3
posterior polymorphous corneal 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
adolescent (2) 2
biochemistry & molecular biology (2) 2
cell line (2) 2
cells (2) 2
central cloudy dystrophy of francois (2) 2
central cloudy dystrophy of francxois (2) 2
child (2) 2
collagen (2) 2
corneal dystrophies, hereditary - classification (2) 2
diagnosis (2) 2
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endothelium (2) 2
eye (2) 2
gene expression (2) 2
genetic aspects (2) 2
genetic predisposition to disease (2) 2
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glaucoma (2) 2
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helix termination motif (2) 2
infant (2) 2
linkage (2) 2
mental-retardation (2) 2
mice (2) 2
missense mutations (2) 2
mutations (2) 2
neurosciences (2) 2
reis-bücklers corneal dystrophy (2) 2
retina (2) 2
signal transduction - genetics (2) 2
terminology as topic (2) 2
1. microbiology.,2. medical microbiology (1) 1
1st 2 years (1) 1
2 small proteoglycans (1) 1
2. cytology (1) 1
2. x-linked endothelial corneal dystrophy (1) 1
3. developmental biology (1) 1
abnormalities, multiple (1) 1
acids (1) 1
adult (1) 1
aged (1) 1
agenesis (1) 1
agenesis of corpus callosum - genetics (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
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
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
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
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
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
Journal Article
Seminars in Ophthalmology, ISSN 0882-0538, 5/2013, Volume 28, Issue 3, pp. 131 - 143
Journal Article
1984, ISBN 9780444007995, xvi, 473
Book
2004, ISBN 9780721681542, xxi, 1168 p., [12] p. of plates
Book
1993, ISBN 9780697005304, xvii, 806
Book
1988, ISBN 0815135610, xvi, 455
Book
Annals of Neurology, ISSN 0364-5134, 09/2017, Volume 82, Issue 3, pp. 466 - 478
Journal Article
Journal Article