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Journal of the Korean Ophthalmological Society, ISSN 0378-6471, 04/2013, Volume 54, Issue 4, pp. 667 - 670
To report the first case of lattice corneal dystrophy, gelsolin type in Korea. A 61-year-old man visited our clinic with severe dry eye symptom in both eyes.... 
Amyloidosis | Gelsolin | Lattice corneal dystrophy | Meretoja syndrome
Journal Article
Clinica Terapeutica, ISSN 0009-9074, 2014, Volume 165, Issue 1, pp. e73 - e75
Phenotypic characteristics associated with mutations in the transforming growth factor beta-induced (TGFBI) gene in two twin sisters suffering from lattice... 
Lattice corneal dystrophies | Corneal dystrophy | TGFBI gene | Transforming Growth Factor beta - genetics | Exons | Extracellular Matrix Proteins - genetics | Humans | Middle Aged | Corneal Dystrophies, Hereditary - genetics | Female | Mutation | Siblings
Journal Article
国际眼科杂志:英文版, ISSN 2222-3959, 2011, Volume 4, Issue 3, pp. 275 - 279
AIM: To analyze phenotype and genotype of a Chinese pedigree with Avellino corneal dystrophy (ACD).METHODS: Complete ophthalmic examinations were performed on... 
keratomileusis | genetics | corneal | dystrophy | opacity | LASIK | Genetics | Keratomileusis | Corneal opacity | Corneal dystrophy | MOLECULAR-GENETICS | IN-SITU KERATOMILEUSIS | PHOTOTHERAPEUTIC KERATECTOMY | corneal dystrophy | EXACERBATION | corneal opacity | BIGH3 GENE | OPHTHALMOLOGY | RECURRENCE | R124H MUTATION | LATTICE
Journal Article
Human Mutation, ISSN 1059-7794, 07/2006, Volume 27, Issue 7, pp. 615 - 625
Journal Article
Cornea, ISSN 0277-3740, 07/2018, Volume 37, Issue 7, pp. 824 - 828
PURPOSE:To describe inadvertent persistent staining of stromal amyloid deposits by trypan blue (TB) after penetrating keratoplasty (PK) and Descemet membrane... 
keratoplasty | SURGERY | LATTICE CORNEAL-DYSTROPHY | CELLS | amyloid | ENDOTHELIUM | OPHTHALMOLOGY | trypan blue | lattice corneal dystrophy | Glycoproteins | Amyloidosis | Research | Index Medicus
Journal Article
国际眼科杂志:英文版, ISSN 2222-3959, 2011, Volume 4, Issue 3, pp. 235 - 238
AIM: To analyze mutations in transforming growth factor beta-induced (TGFBI) gene in a Chinese pedigree with Reis-Bücklers corneal dystrophy (RBCD,also known... 
mutation | genetics | corneal | R124C | molecular | Reis-Bücklers | TGFBI | dystrophy | Mutation | Molecular genetics | Reis-Bücklers corneal dystrophy | molecular genetics | BIGH3 GENE | OPHTHALMOLOGY | R124C MUTATION | LATTICE | Reis-Bucklers corneal dystrophy
Journal Article
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