PubMed

A late-onset unilateral variant of lattice corneal dystrophy not associated with a TGFBI mutation.

Yellore VS, Sonmez B, Rayner SA, Aldave AJ.

Br J Ophthalmol. 2008 Mar;92(3):426-7. No abstract available. PMID: 18303168 [PubMed - indexed for MEDLINE]Related articles

Unilateral lattice corneal dystrophy associated with the novel His572del mutation in the TGFBI gene.

Aldave AJ, Rayner SA, Kim BT, Prechanond A, Yellore VS.

Mol Vis. 2006 Feb 27;12:142-6.PMID: 16541014 [PubMed - indexed for MEDLINE]Related articlesFree article

Gene symbol: TGFBI. Disease: Corneal dystrophy, lattice type.

Livshits L, Pampukha VM, Tereshchenko FA, Drozhyna GI.

Hum Genet. 2008 Oct;124(3):296-7. No abstract available. PMID: 18846615 [PubMed - indexed for MEDLINE]Related articles

R124C and R555W TGFBI mutations in Spanish families with autosomal-dominant corneal dystrophies.

Blanco-Marchite C, Sánchez-Sánchez F, López-Sánchez E, Escribano J.

Mol Vis. 2007 Aug 10;13:1390-6.PMID: 17768377 [PubMed - indexed for MEDLINE]Related articlesFree article

[TGFBI gene mutations in the Ukrainian patients with inherited corneal stromal dystrophies]

Pampukha VN, Kravchenko SA, Tereshchenko F, Drozhzhina GI, Livshits LA.

Genetika. 2008 Oct;44(10):1392-6. Russian. PMID: 19062536 [PubMed - indexed for MEDLINE]Related articles

[Autosomal dominant inherited corneal dystrophies associated with TGFBI mutation]

Mashima Y, Yamada M, Oguchi Y.

Nippon Ganka Gakkai Zasshi. 2001 Oct;105(10):659-72. Review. Japanese. PMID: 11692612 [PubMed - indexed for MEDLINE]Related articles

H626R and R124C mutations of the TGFBI (BIGH3) gene caused lattice corneal dystrophy in Vietnamese people.

Chau HM, Ha NT, Cung LX, Thanh TK, Fujiki K, Murakami A, Kanai A.

Br J Ophthalmol. 2003 Jun;87(6):686-9.PMID: 12770961 [PubMed - indexed for MEDLINE]Related articlesFree article

[Six cases of late-onset lattice corneal dystrophy associated with gene mutations induced by the transforming growth factor-beta]

Kawashima M, Yamada M, Funayama T, Mashima Y.

Nippon Ganka Gakkai Zasshi. 2005 Feb;109(2):93-100. Japanese. PMID: 15770959 [PubMed - indexed for MEDLINE]Related articles

Corneal dystrophy-associated R124H mutation disrupts TGFBI interaction with Periostin and causes mislocalization to the lysosome.

Kim BY, Olzmann JA, Choi SI, Ahn SY, Kim TI, Cho HS, Suh H, Kim EK.

J Biol Chem. 2009 Jul 17;284(29):19580-91. Epub 2009 May 28.PMID: 19478074 [PubMed - indexed for MEDLINE]Related articles

Allelic homogeneity in Avellino corneal dystrophy due to a founder effect.

Tsujikawa K, Tsujikawa M, Watanabe H, Maeda N, Inoue Y, Fujikado T, Tano Y.

J Hum Genet. 2007;52(1):92-7. Epub 2006 Nov 10.PMID: 17096061 [PubMed - indexed for MEDLINE]Related articles

A unique corneal dystrophy of Bowman's layer and stroma associated with the Gly623Asp mutation in the transforming growth factor beta-induced (TGFBI) gene.

Aldave AJ, Rayner SA, King JA, Affeldt JA, Yellore VS.

Ophthalmology. 2005 Jun;112(6):1017-22.PMID: 15885785 [PubMed - indexed for MEDLINE]Related articles

A novel variant lattice corneal dystrophy caused by association of mutation (V625D) in TGFBI gene.

Tian X, Fujiki K, Zhang Y, Murakami A, Li Q, Kanai A, Wang W, Hao Y, Ma Z.

Am J Ophthalmol. 2007 Sep;144(3):473-5.PMID: 17765440 [PubMed - indexed for MEDLINE]Related articles

A clinical and molecular-genetic analysis of Chinese patients with lattice corneal dystrophy and novel Thr538Pro mutation in the TGFBI (BIGH3) gene.

Yu P, Gu Y, Yang Y, Yan X, Chen L, Ge Z, Qi M, Si J, Guo L.

J Genet. 2006 Apr;85(1):73-6. No abstract available. PMID: 16809844 [PubMed - indexed for MEDLINE]Related articlesFree article

Anterior basement membrane corneal dystrophy and pseudo-unilateral lattice corneal dystrophy in a patient with recurrent corneal erosions.

Aldave AJ, Lin DY, Principe AH, Yellore VS, Weissman BA.

Am J Ophthalmol. 2004 Jun;137(6):1124-7.PMID: 15183802 [PubMed - indexed for MEDLINE]Related articles

[Case of late onset and isolated lattice corneal dystrophy with Asn544Ser (N544S) mutation of transforming growth factor beta-induced (TGFBI, BIGH3) gene]

Nakagawa Asahina S, Fujiki K, Enomoto Y, Murakami A, Kanai A.

Nippon Ganka Gakkai Zasshi. 2004 Oct;108(10):618-20. Japanese. PMID: 15559315 [PubMed - indexed for MEDLINE]Related articles

A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI gene.

Aldave AJ, Yellore VS, Sonmez B, Bourla N, Salem AK, Khan MA, Rayner SA, Glasgow BJ.

Arch Ophthalmol. 2008 Mar;126(3):371-7.PMID: 18332318 [PubMed - indexed for MEDLINE]Related articlesFree article

A novel phenotype-genotype relationship with a TGFBI exon 14 mutation in a pedigree with a unique corneal dystrophy of Bowman's layer.

Wheeldon CE, de Karolyi BH, Patel DV, Sherwin T, McGhee CN, Vincent AL.

Mol Vis. 2008 Aug 18;14:1503-12.PMID: 18728790 [PubMed - indexed for MEDLINE]Related articlesFree article

[Molecular genetic and histopathological examinations for genotype-phenotype analysis in patients with TGFBI-linked corneal dystrophy]

Grünauer-Kloevekorn C, Braeutigam S, Weidle E, Wolter-Roessler M, Tost F, Auw-Haedrich C, Völcker HE, Heinritz W, Froster U, Duncker G.

Klin Monbl Augenheilkd. 2006 Oct;223(10):829-36. German. PMID: 17063427 [PubMed - indexed for MEDLINE]Related articles

Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.

Romero P, Vogel M, Diaz JM, Romero MP, Herrera L.

Mol Vis. 2008 May 7;14:829-35.PMID: 18470323 [PubMed - indexed for MEDLINE]Related articlesFree article

[Histopathological study of lattice corneal dystrophy with L 527 R mutation of transforming growth factor-beta induced gene]

Nakagawa E, Sakimoto T, Inada N, Shoji J, Sawa M, Kanno H, Nakagawa S.

Nippon Ganka Gakkai Zasshi. 2004 Feb;108(2):118-23. Japanese. PMID: 15022435 [PubMed - indexed for MEDLINE]Related articles