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    Results: 1 to 20 of 181

    1.

    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

    2.

    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 [PubMed - indexed for MEDLINE]Related articles

    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.PMID: 18470323 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Mutation analysis of the TGFBI gene in Vietnamese with granular and Avellino corneal dystrophy.

    Cung le X, Ha NT, Chau HM, Thanh TK, Fujiki K, Murakami A, Hiratsuka Y, Kanai A.

    Jpn J Ophthalmol. 2004 Jan-Feb;48(1):12-6.PMID: 14767644 [PubMed - indexed for MEDLINE]Related articles

    5.

    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

    6.

    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 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    [Molecular genetic study on patients with lattice corneal dystrophy in China.]

    Dong WL, Zou LH, Pan ZQ, Jin T, Yu J.

    Zhonghua Yan Ke Za Zhi. 2005 Jun;41(6):523-6. Chinese. PMID: 16008913 [PubMed - indexed for MEDLINE]Related articles

    8.

    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 [PubMed - indexed for MEDLINE]Related articles

    9.

    An R124C mutation in TGFBI caused lattice corneal dystrophy type I with a variable phenotype in three Chinese families.

    Liu Z, Wang YQ, Gong QH, Xie LX.

    Mol Vis. 2008 Jun 30;14:1234-9.PMID: 18615206 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    BIGH3 exon 14 mutations lead to intermediate type I/IIIA of lattice corneal dystrophies.

    Schmitt-Bernard CF, Guittard C, Arnaud B, Demaille J, Argiles A, Claustres M, Tuffery-Giraud S.

    Invest Ophthalmol Vis Sci. 2000 May;41(6):1302-8.PMID: 10798644 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Six different mutations of TGFBI (betaig-h3, keratoepithelin) gene found in Japanese corneal dystrophies.

    Fujiki K, Hotta Y, Nakayasu K, Yamaguchi T, Kato T, Uesugi Y, Ha NT, Endo S, Ishida N, Lu WN, Kanai A.

    Cornea. 2000 Nov;19(6):842-5.PMID: 11095060 [PubMed - indexed for MEDLINE]Related articles

    12.

    Clinical outcome of eight BIGH3-linked corneal dystrophies.

    Ellies P, Renard G, Valleix S, Boelle PY, Dighiero P.

    Ophthalmology. 2002 Apr;109(4):793-7.PMID: 11927442 [PubMed - indexed for MEDLINE]Related articles

    13.

    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 [PubMed - indexed for MEDLINE]Related articles

    14.

    Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech families.

    Liskova P, Klintworth GK, Bowling BL, Filipec M, Jirsova K, Tuft SJ, Bhattacharya SS, Hardcastle AJ, Ebenezer ND.

    Ophthalmic Res. 2008;40(2):105-8. Epub 2008 Feb 6.PMID: 18259096 [PubMed - indexed for MEDLINE]Related articles

    15.

    TGFBI gene mutation analysis in families with hereditary corneal dystrophies from Ukraine.

    Pampukha VM, Drozhyna GI, Livshits LA.

    Ophthalmologica. 2004 Nov-Dec;218(6):411-4.PMID: 15564760 [PubMed - indexed for MEDLINE]Related articles

    16.

    A novel mutation of the TGFBI gene found in a Vietnamese family with atypical granular corneal dystrophy.

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

    Jpn J Ophthalmol. 2003 May-Jun;47(3):246-8.PMID: 12782158 [PubMed - indexed for MEDLINE]Related articles

    17.

    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 [PubMed - indexed for MEDLINE]Related articles

    18.

    [TGFBI gene mutations in three Chinese families with autosomal dominant corneal dystrophy]

    Wang LM, Wang YC, Qiu DL, Ying M, Li ND.

    Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Apr;26(2):179-82. Chinese. PMID: 19350511 [PubMed - indexed for MEDLINE]Related articles

    19.

    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 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients.

    Chakravarthi SV, Kannabiran C, Sridhar MS, Vemuganti GK.

    Invest Ophthalmol Vis Sci. 2005 Jan;46(1):121-5.PMID: 15623763 [PubMed - indexed for MEDLINE]Related articlesFree article

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