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index medicus (121) 121
humans (119) 119
ophthalmology (107) 107
posterior polymorphous dystrophy (83) 83
female (70) 70
male (61) 61
middle aged (49) 49
adult (47) 47
aged (43) 43
posterior polymorphous corneal dystrophy (41) 41
endothelium (38) 38
cornea (37) 37
corneal dystrophies, hereditary - pathology (36) 36
endothelium, corneal - pathology (36) 36
corneal dystrophies, hereditary - genetics (35) 35
keratoconus (32) 32
adolescent (29) 29
corneal dystrophy (27) 27
eye diseases (27) 27
mutation (25) 25
corneal endothelium (24) 24
gene (19) 19
mutations (19) 19
child (18) 18
homeodomain proteins - genetics (18) 18
linkage (18) 18
penetrating keratoplasty (18) 18
sense organs (18) 18
genetic structures (17) 17
pedigree (17) 17
posterior lamellar keratoplasty (17) 17
syndrome (17) 17
visual acuity (17) 17
cornea - pathology (16) 16
genetics & heredity (16) 16
corneal diseases - pathology (15) 15
corneal dystrophies, hereditary - diagnosis (15) 15
microscopy, confocal (15) 15
transcription factors - genetics (15) 15
dna mutational analysis (14) 14
genetic aspects (14) 14
genetics (14) 14
glaucoma (14) 14
specular microscopy (14) 14
child, preschool (13) 13
confocal microscopy (13) 13
corneal topography (13) 13
eye proteins - genetics (13) 13
infant (13) 13
young adult (13) 13
zeb1 (13) 13
cell count (12) 12
corneal diseases (12) 12
endothelial dystrophy (12) 12
hereditary endothelial dystrophy (12) 12
phenotype (12) 12
research (12) 12
abridged index medicus (11) 11
aged, 80 and over (11) 11
care and treatment (11) 11
expression (11) 11
health aspects (11) 11
microscopy (11) 11
vivo confocal microscopy (11) 11
zinc finger e-box-binding homeobox 1 (11) 11
congenital hereditary endothelial dystrophy (10) 10
corneal dystrophies, hereditary - metabolism (10) 10
corneal dystrophies, hereditary - surgery (10) 10
diagnosis (10) 10
dystrophy (10) 10
immunohistochemistry (10) 10
retrospective studies (10) 10
surgery (10) 10
article (9) 9
biochemistry & molecular biology (9) 9
chromosome-20 (9) 9
descemet membrane - pathology (9) 9
diabetic retinopathy (9) 9
diagnosis, differential (9) 9
endothelial keratoplasty (9) 9
endothelium, corneal - metabolism (9) 9
eye (9) 9
keratoconus - genetics (9) 9
keratoplasty, penetrating (9) 9
pathology (9) 9
autosomal-dominant keratoconus (8) 8
classification (8) 8
collagen (8) 8
features (8) 8
follow-up studies (8) 8
genetic disorders (8) 8
in vivo confocal microscopy (8) 8
iridocorneal endothelial syndrome (8) 8
myopia (8) 8
brief communications (7) 7
corneal stroma - pathology (7) 7
corneal transplantation (7) 7
descemet membrane endothelial keratoplasty with a stromal rim (7) 7
essential iris atrophy (7) 7
fuchs' endothelial dystrophy - pathology (7) 7
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Cornea, ISSN 0277-3740, 07/2005, Volume 24, Issue 5, pp. 599 - 602
Journal Article
Optometry - Journal of the American Optometric Association, ISSN 1529-1839, 2009, Volume 80, Issue 8, pp. 431 - 436
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 1986, Volume 7, Issue 2, pp. 101 - 107
Corneal endothelial conditions in two children with posterior polymorphous endothelial dystrophy were studied by specular microscopy. The localized vesicular... 
epithelial-like cell | specular microscopy | posterior polymorphous endothelial dystrophy | coalescence | Posterior polymorphous endothelial dystrophy | Epithelial-like cell | Coalescence | Specular microscopy | Endothelium - pathology | Male | Corneal Dystrophies, Hereditary - pathology | Child | Humans | Index Medicus
Journal Article
American Journal of Ophthalmology Case Reports, ISSN 2451-9936, 2017, Volume 7, Issue C, pp. 23 - 26
Abstract Purpose To report a case of endothelial keratoplasties (EKs) performed in a 4 month old with a posterior polymorphous corneal dystrophy. Observations... 
Ophthalmology | Descemet stripping automated endothelial keratoplasty | Infant | Descemet membrane endothelial keratoplasty | Posterior polymorphous corneal dystrophy
Journal Article
Indian Journal of Ophthalmology, ISSN 0301-4738, 01/2012, Volume 60, Issue 1, pp. 59 - 60
A 20-year-old patient, diagnosed with posterior polymorphous corneal dystrophy, developed corneal edema for which he underwent Descemet membrane endothelial... 
endothelial keratoplasty | Descemet membrane endothelial keratoplasty with a stromal rim | posterior polymorphous corneal dystrophy | posterior lamellar keratoplasty | OPHTHALMOLOGY | DMEK | Descemet Membrane - surgery | Follow-Up Studies | Fuchs' Endothelial Dystrophy - surgery | Humans | Male | Endothelium, Corneal - pathology | Visual Acuity | Descemet Membrane - pathology | Descemet Stripping Endothelial Keratoplasty - methods | Fuchs' Endothelial Dystrophy - pathology | Endothelium, Corneal - surgery | Time Factors | Adolescent | Corneal Stroma - pathology | Corneal Stroma - surgery | Case studies | Care and treatment | Cornea | Patient outcomes | Corneal diseases | Transplantation | Diagnosis | Health aspects | Risk factors | Surgical techniques | Surgery | Endothelium | Index Medicus | Brief Communications | refractive surgery | optical coherence tomography | photodynamic therapy | Myopia | and Salzmann nodular degeneration | Anterior chamber contamination | Cardiovascular disease | sutureless vitrectomy | microperimetry | cataract surgery | multivariate Cox Proportional Hazard Regression analysis | Macular microhole | Band-shaped keratopathy | Deep anterior lamellar keratoplasty | conjunctival flora | 23-Gauge vitrectomy | endothelial cell density | penetrating keratoplasty | optical penetrating keratoplasties | Kaplan Meier survival analysis | keratoconus | vitreous traction | normative database | choroidal neovascularization | phototherapeutic keratectomy | framingham risk score | corneal dystrophy | phakic refractive intraocular lens | diabetic retinopathy | scar | rhegmatogenous retinal detachment | Central macular thickness | multifocal electroretinogram | spectral domain optical coherence tomography | Age-related macular degeneration | diabetics | phototherapeutic keratectomy with amniotic membrane grafts | diabetes
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 2013, Volume 54, Issue 5, pp. 3215 - 3223
Journal Article
HUMAN MOLECULAR GENETICS, ISSN 0964-6906, 10/2001, Volume 10, Issue 21, pp. 2415 - 2423
Journal Article
Journal of the Korean Ophthalmological Society, ISSN 0378-6471, 03/2014, Volume 55, Issue 3, pp. 368 - 373
To analyze the clinical features and the relationship between endothelial cell changes and progression of posterior polymorphous corneal dystrophy (PPCD)... 
Progression | Gender | Endothelial Cells | Bilaterality | Posterior Polymorphous Dystrophy
Journal Article
Journal of the Korean Ophthalmological Society, ISSN 0378-6471, 08/2014, Volume 55, Issue 8, pp. 1238 - 1241
To present a case of a 72-year-old woman with posterior polymorphous corneal dystrophy (PPCD) combined with traumatic Descemet's membrane fold due to forceps... 
Progression | Descemet\'s membrane | Endothelial Cells | Posterior polymorphous corneal dystrophy | Forceps injury
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
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