X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (28) 28
humans (27) 27
female (18) 18
ophthalmology (18) 18
mutation (17) 17
male (14) 14
adult (12) 12
genetics & heredity (9) 9
middle aged (9) 9
child (8) 8
genetic aspects (8) 8
phenotype (8) 8
adolescent (7) 7
corneal dystrophies, hereditary - genetics (7) 7
pedigree (7) 7
research (7) 7
congenital stromal corneal dystrophy (6) 6
corneal dystrophies, hereditary - pathology (6) 6
family (6) 6
young adult (6) 6
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
gene mutations (5) 5
infant, newborn (5) 5
lattice corneal dystrophy (5) 5
lisch epithelial corneal dystrophy (5) 5
macular corneal dystrophy (5) 5
mutations (5) 5
posterior amorphous corneal dystrophy (5) 5
pre-descemet corneal dystrophy (5) 5
report (5) 5
risk factors (5) 5
schnyder corneal dystrophy (5) 5
subepithelial mucinous corneal dystrophy (5) 5
thiel-behnke corneal dystrophy (5) 5
abridged index medicus (4) 4
aged (4) 4
avellino corneal dystrophy (4) 4
congenital hereditary endothelial dystrophy 1 (4) 4
corneal dystrophies, hereditary - metabolism (4) 4
corneal histopathology (4) 4
decorin (4) 4
dna mutational analysis (4) 4
electroretinography (4) 4
epithelial recurrent erosion dystrophy (4) 4
eponym (4) 4
fuchs endothelial corneal dystrophy (4) 4
genetic corneal disease (4) 4
genetic disorders (4) 4
genetics (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
norway - epidemiology (4) 4
patients (4) 4
proteins (4) 4
reis-bucklers corneal dystrophy (4) 4
schnyder crystalline corneal dystrophy (4) 4
tomography, optical coherence (4) 4
animals (3) 3
carbohydrate sulfotransferase gene (3) 3
cells, cultured (3) 3
central cloudy dystrophy (3) 3
children (3) 3
collagen (3) 3
compound heterozygous mutations (3) 3
congenital hereditary endothelial dystrophy 2 (3) 3
cornea (3) 3
corneal dystrophies, hereditary - classification (3) 3
decorin - metabolism (3) 3
fibroblasts (3) 3
fibroblasts - metabolism (3) 3
gelsolin-related amyloidosis (3) 3
gene expression (3) 3
genotype (3) 3
glaucoma (3) 3
hereditary endothelial dystrophy (3) 3
infants (3) 3
low-birth-weight (3) 3
medical research (3) 3
mutation, missense (3) 3
neovascularization (3) 3
obstetrics & gynecology (3) 3
posterior polymorphous corneal dystrophy (3) 3
posterior polymorphous dystrophy (3) 3
pregnancy (3) 3
prematurity (3) 3
preterm infants (3) 3
psychology, developmental (3) 3
retinitis pigmentosa (3) 3
retrospective studies (3) 3
terminology as topic (3) 3
tgfbi bigh3 gene (3) 3
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


Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 11/2011, Volume 89, Issue 5, pp. 634 - 643
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2017, Volume 100, Issue 2, pp. 323 - 333
Journal Article
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
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 09/2010, Volume 87, Issue 3, pp. 410 - 417
Journal Article
Journal Article
American journal of medical genetics. Part A, ISSN 1552-4825, 2014, Volume 164AA, Issue 11, pp. 2901 - 2907
Journal Article
Orphanet journal of rare diseases, ISSN 1750-1172, 2013, Volume 8, Issue 1, pp. 1 - 1
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