X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
ophthalmology (57) 57
humans (54) 54
index medicus (52) 52
corneal dystrophies, hereditary - genetics (41) 41
reis-bucklers (37) 37
female (32) 32
male (29) 29
adult (27) 27
corneal dystrophies, hereditary - pathology (27) 27
corneal dystrophy (25) 25
middle aged (23) 23
mutation (23) 23
pedigree (21) 21
transforming growth factor beta - genetics (19) 19
reis-bucklers corneal dystrophy (16) 16
aged (14) 14
extracellular matrix proteins - genetics (14) 14
child (13) 13
kerato-epithelin mutations (13) 13
lattice (12) 12
bowmans layer (11) 11
corneal dystrophies, hereditary - surgery (11) 11
dna mutational analysis (11) 11
growth-factor-beta (11) 11
polymerase chain reaction (11) 11
bigh3 gene (10) 10
cornea - pathology (10) 10
granular dystrophy (10) 10
lattice corneal dystrophy (10) 10
phenotype (10) 10
thiel-behnke corneal dystrophy (10) 10
adolescent (9) 9
corneal dystrophies, hereditary - diagnosis (9) 9
phototherapeutic keratectomy (9) 9
recurrence (9) 9
reis-bücklers corneal dystrophy (9) 9
beta-ig-h3 (8) 8
child, preschool (8) 8
cornea (8) 8
cornea - ultrastructure (8) 8
extracellular matrix proteins (8) 8
mutations (8) 8
neoplasm proteins - genetics (8) 8
posterior polymorphous dystrophy (8) 8
reis-bucklers dystrophy (8) 8
corneal dystrophies, hereditary - metabolism (7) 7
gene (7) 7
genetics (7) 7
granular corneal dystrophy (7) 7
keratoplasty, penetrating (7) 7
microscopy, confocal (7) 7
tgfbi (7) 7
avellino corneal dystrophy (6) 6
bigh3 (6) 6
corneal dystrophies, hereditary - classification (6) 6
epithelial basement membrane dystrophy (6) 6
epithelium (6) 6
exons (6) 6
follow-up studies (6) 6
hereditary endothelial dystrophy (6) 6
macular corneal dystrophy (6) 6
penetrating keratoplasty (6) 6
photorefractive keratectomy (6) 6
tgfbi gene (6) 6
visual acuity (6) 6
abridged index medicus (5) 5
base sequence (5) 5
biochemistry & molecular biology (5) 5
chromosome mapping (5) 5
congenital stromal corneal dystrophy (5) 5
cornea - metabolism (5) 5
corneal dystrophies (5) 5
eye diseases (5) 5
fleck corneal dystrophy (5) 5
gelatinous drop-like corneal dystrophy (5) 5
grayson-wilbrandt corneal dystrophy (5) 5
lisch epithelial corneal dystrophy (5) 5
point mutation (5) 5
posterior amorphous corneal dystrophy (5) 5
pre-descemet corneal dystrophy (5) 5
protein (5) 5
schnyder corneal dystrophy (5) 5
subepithelial mucinous corneal dystrophy (5) 5
young adult (5) 5
aged, 80 and over (4) 4
basement membrane - pathology (4) 4
congenital hereditary endothelial dystrophy 1 (4) 4
corneal histopathology (4) 4
corneal stroma - pathology (4) 4
corneal stroma - ultrastructure (4) 4
corneal transplantation (4) 4
electron microscopy (4) 4
epithelial recurrent erosion dystrophy (4) 4
eponym (4) 4
excimer laser (4) 4
fuchs endothelial corneal dystrophy (4) 4
genetic aspects (4) 4
genetic corneal disease (4) 4
genetic linkage (4) 4
genetics & heredity (4) 4
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, 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
Journal Article
KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, ISSN 0023-2165, 03/2012, Volume 229, Issue 3, pp. 257 - 258
Journal Article
Molecular Vision, ISSN 1090-0535, 2003, Volume 9, Issue 56, pp. 440 - 448
Purpose: A progressive alteration of the cornea resulting in loss of transparency occurs in a set of hereditary diseases known as corneal dystrophies. A number... 
SEQUENCE-ANALYSIS | GROWTH-FACTOR-BETA | CELL-ADHESION MOLECULE | FASCICLIN-I | STROMAL DYSTROPHY | GENE | REIS-BUCKLERS | BIOCHEMISTRY & MOLECULAR BIOLOGY | OPHTHALMOLOGY | EXTRACELLULAR-MATRIX | MUTATIONS | JAPANESE PATIENTS
Journal Article
Journal Article
Ophthalmology, ISSN 0161-6420, 2000, Volume 107, Issue 3, pp. 565 - 573
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 1998, Volume 62, Issue 2, pp. 320 - 324
Journal Article
CORNEA, ISSN 0277-3740, 08/2002, Volume 21, Issue 6, pp. 570 - 573
Purpose. The purpose of the study was to investigate the recurrence-free interval after phototherapeutic keratectomy (PTK) in patients with corneal dystrophies... 
recurrence | R124H mutation PTK | GENE | GROENOUW TYPE-I | REIS-BUCKLERS | FORM | Big-h3 gene | OPHTHALMOLOGY | corneal dystrophy | CHROMOSOME 5Q | JAPANESE PATIENTS
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
Eye, ISSN 0950-222X, 2007, Volume 21, Issue 5, pp. 587 - 590
Journal Article
Ophthalmology, ISSN 0161-6420, 1999, Volume 106, Issue 9, pp. 1697 - 1704
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.