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Association d'une dystrophie grillagée et d'un keratocone: étude anatomo-clinique à propos d'un cas = Association of lattice dystrophy and Keratoconns: clinicopathological study about one caseHOANG-XUAN, T; ELMALEH, C; DHERMY, P et al.Bulletin des sociétés d'ophtalmologie de France. 1989, Vol 89, Num 1, pp 35-38, issn 0081-1270, 3 p.Article

Transmission génétique et lattice corneal dystrophy : à propos d'un arbre généalogique intéressant = Lattice corneal dystrophy and geneticsDURAND, L; MUTTI, P.Bulletin des sociétés d'ophtalmologie de France. 1992, Vol 92, Num 8-9, pp 843-846, issn 0081-1270Article

Lectin binding sites in normal, scarred, and lattice dystrophy corneasBISHOP, P. N; BONSHEK, R. E; JONES, C. J. P et al.British journal of ophthalmology. 1991, Vol 75, Num 1, pp 22-27, issn 0007-1161, 6 p.Article

Superficial involvement in lattice corneal dystrophyZECHNER, E. M; CROXATTO, J. O; MALBRAN, E. S et al.Ophthalmologica (Basel). 1986, Vol 193, Num 4, pp 193-199, issn 0030-3755Article

Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI geneALDAVE, Anthony J; GUTMARK, Julie G; YELLORE, Vivek S et al.American journal of ophthalmology. 2004, Vol 138, Num 5, pp 772-781, issn 0002-9394, 10 p.Article

Amyloid and Pro501Thr-mutated βig-h3 gene product colocalize in lattice corneal dystrophy type IIIaKAWASAKI, S; NISHIDA, K; QUANTOCK, A. J et al.American journal of ophthalmology. 1999, Vol 127, Num 4, pp 456-458, issn 0002-9394Article

Ultrastructural localization of gelsolin in lattice corneal dystrophy type ILONGANESI, L; CAVALLINI, G. M; IAMMARINO, A et al.Ophthalmologica (Basel). 1998, Vol 212, Num 6, pp 415-421, issn 0030-3755Article

Corneal elastosis within lattice dystrophy lesionsPE'ER, J; FINE, B. S; DIXON, A et al.British journal of ophthalmology. 1988, Vol 72, Num 3, pp 183-188, issn 0007-1161Article

Lattice dystrophy of the cornea: a clinicopathological case reportSKRYPUCH, O. W; WILLIS, N. R.Canadian journal of ophthalmology. 1987, Vol 22, Num 3, pp 181-185, issn 0008-4182Conference Paper

Lattice corneal dystrophy type IIIA : clinical and histopathologic correlationsLEE STOCK, E; FEDER, R. S; O'GRADY, R. B et al.Archives of ophthalmology (1960). 1991, Vol 109, Num 3, pp 354-358, issn 0003-9950, 5 p.Article

Lattice dystrophy type 1: a report of 8 familiesTSUBOTA, K; HIDA, T; MURATA, H et al.Ophthalmologica (Basel). 1987, Vol 194, Num 2-3, pp 71-76, issn 0030-3755Article

Mise au point sur une entité anatomoclinique: la dystrophie grillagée de Biber-Haab-Dimmer = Restatement of an anatomical and clinical entity: the Biber-Haab-Dimmer's lattice dystrophyDURAND, L; RESAL, R; BURILLON, C et al.Journal français d'ophtalmologie. 1985, Vol 8, Num 11, pp 729-734, issn 0181-5512Article

Excimer laser phototherapeutic keratectomy for granular and lattice corneal dystrophy : A comparative studyDAS, Sujata; LANGENBUCHER, Achim; SEITZ, Berthold et al.Journal of refractive surgery (1995). 2005, Vol 21, Num 6, pp 727-731, issn 1081-597X, 5 p.Article

Lattice corneal dystrophy type I without typical lattice lines: Role of mutational analysisYOSHIDA, Shigeo; YOSHIDA, Ayako; NAKAO, Shintaro et al.American journal of ophthalmology. 2004, Vol 137, Num 3, pp 586-588, issn 0002-9394, 3 p.Article

Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English familySTEWART, H. S; PARVEEN, R; RIDGWAY, A. E et al.British journal of ophthalmology. 2000, Vol 84, Num 4, pp 390-394, issn 0007-1161Article

A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophySTEWART, H; BLACK, G. C. M; DONNAI, D et al.Ophthalmology (Rochester, MN). 1999, Vol 106, Num 5, pp 964-970, issn 0161-6420Article

Lattice corneal dystrophy type 1 in a Canadian kindred is associated with the Arg¹²⁴ → Cys mutation in the kerato-epithelin geneGUPTA, S. K; HODGE, W. G; DAMJI, K. F et al.American journal of ophthalmology. 1998, Vol 125, Num 4, pp 547-549, issn 0002-9394Article

Hereditary lattice corneal dystrophy is associated with corneal amyloid deposits enclosing C-terminal fragments of keratoepithelinSTIX, Barbara; LEBER, Martina; RÖCKEN, Christoph et al.Investigative ophthalmology & visual science. 2005, Vol 46, Num 4, pp 1133-1139, issn 0146-0404, 7 p.Article

Corneal lattice dystrophy, a concealed ophthalmic problem in ThailandPRABHASAWAT, Pinnita; TESAVIBUL, Nattaporn; ATCHANEEYASAKUL, La-Ongsri et al.Chot Mai Het Thang Phaet. 2003, Vol 86, Num 8, pp 727-736, issn 0125-2208, 10 p.Article

BIGH3 exon 14 mutations lead to intermediate type I/IIIa of lattice corneal dystrophiesSCHMITT-BERNARD, C.-F; GUITTARD, C; ARNAUD, B et al.Investigative ophthalmology & visual science. 2000, Vol 41, Num 6, pp 1302-1308, issn 0146-0404Article

Arg124Cys mutation of the ssig-h3 gene in a Japanese family with lattice corneal dystrophy type IHOTTA, Y; FUJIKI, K; ONO, K et al.Japanese journal of ophthalmology. 1998, Vol 42, Num 6, pp 450-455, issn 0021-5155Article

Unesterified cholesterol in granular, lattice, and macular dystrophiesRODRIGUES, M. M; KRUTH, H. S; RAJAGOPALAN, S et al.American journal of ophthalmology. 1993, Vol 115, Num 1, pp 112-114, issn 0002-9394Article

A novel mutation in transforming growth factor-beta induced protein (TGFβIp) reveals secondary structure perturbation in lattice corneal dystrophyLAKSHMINARAYANAN, Rajamani; VITHANA, Eranga N; BEUERMAN, Roger W et al.British journal of ophthalmology. 2011, Vol 95, Num 10, pp 1457-1462, issn 0007-1161, 6 p.Article

A Novel Variant of Combined Granular-Lattice Corneal Dystrophy Associated With the Met619Lys Mutation in the TGFBI GeneALDAVE, Anthony J; YELLORE, Vivek S; SONMEZ, Baris et al.Archives of ophthalmology (1960). 2008, Vol 126, Num 3, pp 371-377, issn 0003-9950, 7 p.Article