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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
PLoS ONE, ISSN 1932-6203, 09/2017, Volume 12, Issue 9, pp. e0184906 - e0184906
Vps35 (vacuolar protein sorting 35) is a major component of retromer that selectively promotes endosome-to-Golgi retrieval of transmembrane proteins.... 
PROTEIN | ION-TRANSPORT | ENDOTHELIAL DYSTROPHY | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | RETROMER COMPLEX | VPS35 | ALPHA-SYNUCLEIN | MUTATIONS | GOLGI RETRIEVAL | PARKINSONS-DISEASE | Retina - metabolism | Epithelial Cells - metabolism | Humans | Vesicular Transport Proteins - genetics | Cell Proliferation - physiology | Epithelial Cells - pathology | Mice, Transgenic | Corneal Dystrophies, Hereditary - metabolism | Anion Transport Proteins - metabolism | Blotting, Western | Symporters - metabolism | Cornea - metabolism | Microscopy, Confocal | Animals | Transfection | Vesicular Transport Proteins - deficiency | Corneal Dystrophies, Hereditary - pathology | Biological Transport, Active - physiology | Fluorescent Antibody Technique | HEK293 Cells | Cornea - pathology | Retina - pathology | Disease Models, Animal | Physiological aspects | Corneal diseases | Development and progression | Genetic aspects | Research | Membrane proteins | Cell proliferation | Neurosciences | Cornea | Parkinson's disease | Neuropathology | Pathogenesis | Epithelial cells | Trafficking | Heterozygotes | Retina | Cell surface | Risk factors | Eye | Proteins | Surgery | Genetics | Physiology | Protein transport | Alzheimer's disease | Movement disorders | Edema | Congenital diseases | Neurodegenerative diseases | Stroma | Endothelium | Golgi apparatus | Medicine | Studies | Neurology | Hospitals | Corneal dystrophy | Mutation | Dystrophy | Index Medicus
Journal Article
Clinical and Experimental Optometry, ISSN 0816-4622, 07/2018, Volume 101, Issue 4, pp. 596 - 598
We wish to demonstrate the variety of imaging techniques available to help the clinician in the assessment of microcystic corneal opacities, through clinical... 
recurrence | OCT | anterior segment imaging | Lisch corneal epithelial dystrophy | histology | topography | OPHTHALMOLOGY | WHORLED MICROCYSTIC DYSTROPHY | Eye diseases | Optometry | Cornea | Medical imaging | Dystrophy | Index Medicus
Journal Article
Journal Article
Cornea, ISSN 0277-3740, 02/2019, Volume 38, Issue 2, pp. 243 - 245
PURPOSE:To present a new technique for treating Lisch epithelial corneal dystrophy (LECD) in cases of recurrence of the disease. METHODS:We present a single... 
OPHTHALMOLOGY | epithelial keratectomy | Lisch corneal dystrophy | limbal cauterization | epithelial debridement | WHORLED MICROCYSTIC DYSTROPHY | Case studies | Cautery | Corneal diseases | Photorefractive keratectomy | Index Medicus
Journal Article
KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, ISSN 0023-2165, 06/2018, Volume 235, Issue 6, pp. 697 - 701
The corneal epithelium is the most important structure of the ocular optical system. Recurrent corneal erosions can result from inflammation, trauma,... 
PHOTOTHERAPEUTIC-KERATECTOMY | pathogenesis | ALCOHOL DELAMINATION | OPHTHALMOLOGY | recurrent corneal erosion | epithelial basement membrane brandystrophy | epithelial recurrent erosion dystrophy (Franceschetti) | Meesmanns dystrophy | MUTATIONS | Cogans dystrophy | IC3D CLASSIFICATION
Journal Article
Journal Article