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Items: 1 to 20 of 390

1.

Lattice corneal dystrophy type I without typical lattice lines: role of mutational analysis.

Yoshida S, Yoshida A, Nakao S, Emori A, Nakamura T, Fujisawa K, Kumano Y, Ishibashi T.

Am J Ophthalmol. 2004 Mar;137(3):586-8.

PMID:
15013897
2.
3.

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.

4.

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
5.

Late-onset form of lattice corneal dystrophy caused by leu527Arg mutation of the TGFBI gene.

Hirano K, Hotta Y, Nakamura M, Fujiki K, Kanai A, Yamamoto N.

Cornea. 2001 Jul;20(5):525-9.

PMID:
11413411
6.

A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophy.

Stewart H, Black GC, Donnai D, Bonshek RE, McCarthy J, Morgan S, Dixon MJ, Ridgway AA.

Ophthalmology. 1999 May;106(5):964-70.

PMID:
10328397
7.
8.
9.

The TGFBI A546D mutation causes an atypical type of lattice corneal dystrophy.

Correa-Gomez V, Villalvazo-Cordero L, Zenteno JC.

Mol Vis. 2007 Sep 17;13:1695-700.

PMID:
17893671
10.

Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene.

Aldave AJ, Gutmark JG, Yellore VS, Affeldt JA, Meallet MA, Udar N, Rao NA, Small KW, Klintworth GK.

Am J Ophthalmol. 2004 Nov;138(5):772-81.

PMID:
15531312
11.

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.

12.

A new mutation (Leu569Arg) within exon 13 of the TGFBI (BIGH3) gene causes lattice corneal dystrophy type I.

Warren JF, Abbott RL, Yoon MK, Crawford JB, Spencer WH, Margolis TP.

Am J Ophthalmol. 2003 Nov;136(5):872-8.

PMID:
14597039
13.

[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
14.

A novel H572R mutation in the transforming growth factor-beta-induced gene in a Thai family with lattice corneal dystrophy type I.

Atchaneeyasakul LO, Appukuttan B, Pingsuthiwong S, Yenchitsomanus PT, Trinavarat A, Srisawat C; Study Group..

Jpn J Ophthalmol. 2006 Sep-Oct;50(5):403-8.

PMID:
17013691
15.

A clinical and histopathologic examination of accelerated TGFBIp deposition after LASIK in combined granular-lattice corneal dystrophy.

Aldave AJ, Sonmez B, Forstot SL, Rayner SA, Yellore VS, Glasgow BJ.

Am J Ophthalmol. 2007 Mar;143(3):416-9. Epub 2006 Dec 29.

PMID:
17317389
16.

Novel mutation (V505D) of the TGFBI gene found in a Chinese family with lattice corneal dystrophy, type I.

Tian X, Fujiki K, Wang W, Murakami A, Xie P, Kanai A, Liu Z.

Jpn J Ophthalmol. 2005 Mar-Apr;49(2):84-8.

PMID:
15838722
17.

TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis.

Takács L, Losonczy G, Matesz K, Balogh I, Sohajda Z, Tóth K, Fazakas F, Vereb G, Berta A.

Mol Vis. 2007 Oct 18;13:1976-83.

PMID:
17982422
18.

Late-onset lattice corneal dystrophy without typical lattice lines caused by a novel mutation in the TGFBI gene.

Ołdak M, Szaflik JP, Ścieżyńska A, Udziela M, Maksym RB, Rymgayłło-Jankowska B, Hofmann-Rummelt C, Menzel-Severing J, Płoski R, Żarnowski T, Kruse FE, Szaflik J.

Cornea. 2014 Mar;33(3):294-9. doi: 10.1097/ICO.0000000000000062.

PMID:
24473223
19.

Two mutations in the TGFBI (BIGH3) gene associated with lattice corneal dystrophy in an extensively studied family.

Klintworth GK, Bao W, Afshari NA.

Invest Ophthalmol Vis Sci. 2004 May;45(5):1382-8.

PMID:
15111592

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