X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (24) 24
humans (22) 22
ophthalmology (17) 17
male (12) 12
female (8) 8
corneal dystrophies, hereditary - genetics (7) 7
gene (7) 7
mutation (7) 7
posterior polymorphous dystrophy (7) 7
genetics (6) 6
genetics & heredity (6) 6
pre-descemet corneal dystrophy (6) 6
adult (5) 5
congenital stromal corneal dystrophy (5) 5
cornea (5) 5
corneal dystrophy (5) 5
epithelial basement membrane dystrophy (5) 5
fleck corneal dystrophy (5) 5
gelatinous drop-like corneal dystrophy (5) 5
hereditary endothelial dystrophy (5) 5
lattice corneal dystrophy (5) 5
lisch epithelial corneal dystrophy (5) 5
macular corneal dystrophy (5) 5
posterior amorphous corneal dystrophy (5) 5
schnyder corneal dystrophy (5) 5
subepithelial mucinous corneal dystrophy (5) 5
thiel-behnke corneal dystrophy (5) 5
article (4) 4
avellino corneal dystrophy (4) 4
congenital hereditary endothelial dystrophy 1 (4) 4
corneal dystrophies, hereditary - pathology (4) 4
corneal histopathology (4) 4
epithelial recurrent erosion dystrophy (4) 4
eponym (4) 4
expression (4) 4
fuchs endothelial corneal dystrophy (4) 4
genetic aspects (4) 4
genetic corneal disease (4) 4
genetic disorders (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
middle aged (4) 4
phenotype (4) 4
reis-bucklers corneal dystrophy (4) 4
schnyder crystalline corneal dystrophy (4) 4
tgfbi bigh3 gene (4) 4
whorled microcystic dystrophy (4) 4
x-linked ichthyosis (4) 4
x-linked megalocornea (4) 4
abridged index medicus (3) 3
animals (3) 3
anterior eye segment - abnormalities (3) 3
carbohydrate sulfotransferase gene (3) 3
cataract (3) 3
central cloudy dystrophy (3) 3
compound heterozygous mutations (3) 3
congenital hereditary endothelial dystrophy 2 (3) 3
dystrophy (3) 3
eye (3) 3
eye diseases (3) 3
gelsolin-related amyloidosis (3) 3
glaucoma (3) 3
linkage (3) 3
mutations (3) 3
pediatrics (3) 3
pedigree (3) 3
posterior polymorphous corneal dystrophy (3) 3
sense organs (3) 3
vivo confocal microscopy (3) 3
x-linked endothelial corneal dystrophy (3) 3
aged (2) 2
blindness (2) 2
case report (2) 2
central cloudy dystrophy of francois (2) 2
central cloudy dystrophy of francxois (2) 2
child (2) 2
child, preschool (2) 2
children (2) 2
chromosome mapping (2) 2
chromosomes, human, x - genetics (2) 2
confocal microscopy (2) 2
congenital hereditary endothelial dystrophy (2) 2
corneal diseases (2) 2
corneal dystrophies, hereditary - classification (2) 2
corneal dystrophies, hereditary - etiology (2) 2
corneal dystrophies, hereditary - metabolism (2) 2
developmental glaucoma (2) 2
diagnosis (2) 2
diagnosis, differential (2) 2
disease progression (2) 2
dna copy number variations - genetics (2) 2
dogs (2) 2
endothelium (2) 2
eye diseases - therapy (2) 2
eye proteins - genetics (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


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
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
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
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2012, Volume 90, Issue 2, pp. 247 - 259
X-linked megalocornea (MGC1) is an ocular anterior segment disorder characterized by an increased cornea diameter and deep anterior chamber evident at birth... 
EYE | WATER DIFFUSION | BONE MORPHOGENETIC PROTEIN | ACQUISITION | GENETICS & HEREDITY | BIOMETRY | UPDATE | ISCEV STANDARD | CHORDIN | LINKAGE | BRAIN | Anterior Eye Segment - embryology | Cerebral Palsy - metabolism | Humans | Middle Aged | Eye Abnormalities - embryology | Genetic Diseases, X-Linked - complications | Molecular Sequence Data | Corneal Diseases - metabolism | Male | Retina - embryology | Anterior Eye Segment - abnormalities | Intellectual Disability - genetics | Intellectual Disability - metabolism | Young Adult | Corneal Diseases - genetics | Genes, X-Linked | Base Sequence | Nerve Tissue Proteins - biosynthesis | Adult | Female | Genetic Diseases, X-Linked - genetics | Eye Proteins - genetics | Megalencephaly - genetics | DNA Copy Number Variations - genetics | Megalencephaly - metabolism | Genetic Diseases, X-Linked - metabolism | Eye Abnormalities - genetics | Nerve Tissue Proteins - genetics | Genetic Diseases, X-Linked - embryology | Phenotype | Pedigree | Retina - abnormalities | Brain - pathology | Cornea - abnormalities | Mutation | Quantitative Trait Loci | Cerebral Palsy - genetics | Eye Abnormalities - complications | Eye Proteins - biosynthesis | Brain | Gene mutations | Genetic variation | Physiological aspects | Causes of | Corneal diseases | Retina | Genetic aspects | Research | Ophthalmology | Proteins | Cornea | Genetic disorders | Morphology | Cognitive ability | Genetic research | Gene expression | Index Medicus
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 1999, Volume 128, Issue 6, pp. 747 - 754
Journal Article