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    Results: 1 to 20 of 247

    1.

    A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophy.

    Irvine AD, Coleman CM, Moore JE, Swensson O, Morgan SJ, McCarthy JH, Smith FJ, Black GC, McLean WH.

    Br J Ophthalmol. 2002 Jul;86(7):729-32.PMID: 12084738 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy.

    Sullivan LS, Baylin EB, Font R, Daiger SP, Pepose JS, Clinch TE, Nakamura H, Zhao XC, Yee RW.

    Mol Vis. 2007 Jun 21;13:975-80.PMID: 17653038 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Meesmann corneal dystrophy (MECD): report of 2 families and a novel mutation in the cornea specific keratin 12 (KRT12) gene.

    Nichini O, Manzi V, Munier FL, Schorderet DF.

    Ophthalmic Genet. 2005 Dec;26(4):169-73.PMID: 16352477 [PubMed - indexed for MEDLINE]Related articles

    4.

    Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy.

    Irvine AD, Corden LD, Swensson O, Swensson B, Moore JE, Frazer DG, Smith FJ, Knowlton RG, Christophers E, Rochels R, Uitto J, McLean WH.

    Nat Genet. 1997 Jun;16(2):184-7.PMID: 9171831 [PubMed - indexed for MEDLINE]Related articles

    5.

    A novel arginine substitution mutation in 1A domain and a novel 27 bp insertion mutation in 2B domain of keratin 12 gene associated with Meesmann's corneal dystrophy.

    Yoon MK, Warren JF, Holsclaw DS, Gritz DC, Margolis TP.

    Br J Ophthalmol. 2004 Jun;88(6):752-6.PMID: 15148206 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy.

    Corden LD, Swensson O, Swensson B, Rochels R, Wannke B, Thiel HJ, McLean WH.

    Br J Ophthalmol. 2000 May;84(5):527-30.PMID: 10781519 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene.

    Corden LD, Swensson O, Swensson B, Smith FJ, Rochels R, Uitto J, McLEAN WH.

    Exp Eye Res. 2000 Jan;70(1):41-9.PMID: 10644419 [PubMed - indexed for MEDLINE]Related articles

    8.

    [Mutations in the keratin gene as a cause of Meesman-Wilke corneal dystrophy and autosomal dominant skin cornification disorders]

    Swensson O, Swensson B, Nölle B, Rochels R, Wannke B, Thiel HJ.

    Klin Monbl Augenheilkd. 2000 Jul;217(1):43-51. Review. German. PMID: 10949816 [PubMed - indexed for MEDLINE]Related articles

    9.

    Genetics of Meesmann corneal dystrophy: a novel mutation in the keratin 3 gene in an asymptomatic family suggests genotype-phenotype correlation.

    Szaflik JP, Ołdak M, Maksym RB, Kamińska A, Pollak A, Udziela M, Płoski R, Szaflik J.

    Mol Vis. 2008 Sep 15;14:1713-8.PMID: 18806880 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    [Analysis of mutation in KRT12 gene in a Chinese family with Meesmann's corneal dystrophy]

    Wang LJ, Tian X, Zhang QS, Liu L.

    Zhonghua Yan Ke Za Zhi. 2007 Oct;43(10):885-9. Chinese. PMID: 18201524 [PubMed - in process]Related articles

    11.

    Novel mutations in the helix termination motif of keratin 3 and keratin 12 in 2 Taiwanese families with Meesmann corneal dystrophy.

    Chen YT, Tseng SH, Chao SC.

    Cornea. 2005 Nov;24(8):928-32.PMID: 16227835 [PubMed - indexed for MEDLINE]Related articles

    12.

    A novel mutation in the helix termination motif of keratin K12 in a US family with Meesmann corneal dystrophy.

    Coleman CM, Hannush S, Covello SP, Smith FJ, Uitto J, McLean WH.

    Am J Ophthalmol. 1999 Dec;128(6):687-91.PMID: 10612503 [PubMed - indexed for MEDLINE]Related articles

    13.

    Recurrent Meesmann's corneal epithelial dystrophy after penetrating keratoplasty.

    Chiou AG, Florakis GJ, Copeland RL, Williams VA, McCormick SA, Chiesa R.

    Cornea. 1998 Sep;17(5):566-70.PMID: 9756454 [PubMed - indexed for MEDLINE]Related articles

    14.

    Heterozygous Ala137Pro mutation in keratin 12 gene found in Japanese with Meesmann's corneal dystrophy.

    Takahashi K, Takahashi K, Murakami A, Okisaka S, Kimura T, Kanai A.

    Jpn J Ophthalmol. 2002 Nov-Dec;46(6):673-4.PMID: 12543196 [PubMed - indexed for MEDLINE]Related articles

    15.

    Meesmann's corneal dystrophy: ultrastructural features.

    Tremblay M, Dubé I.

    Can J Ophthalmol. 1982 Feb;17(1):24-8.PMID: 6979375 [PubMed - indexed for MEDLINE]Related articles

    16.

    Isolation and chromosomal localization of a cornea-specific human keratin 12 gene and detection of four mutations in Meesmann corneal epithelial dystrophy.

    Nishida K, Honma Y, Dota A, Kawasaki S, Adachi W, Nakamura T, Quantock AJ, Hosotani H, Yamamoto S, Okada M, Shimomura Y, Kinoshita S.

    Am J Hum Genet. 1997 Dec;61(6):1268-75.PMID: 9399908 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    A novel mutation in the cornea-specific keratin 12 gene in Meesmann corneal dystrophy.

    Seto T, Fujiki K, Kishishita H, Fujimaki T, Murakami A, Kanai A.

    Jpn J Ophthalmol. 2008 May-Jun;52(3):224-6. Epub 2008 Jul 27.PMID: 18661274 [PubMed - indexed for MEDLINE]Related articles

    18.

    Meesmann's epithelial dystrophy of the cornea.

    Fine BS, Yanoff M, Pitts E, Slaughter FD.

    Am J Ophthalmol. 1977 May;83(5):633-42.PMID: 301357 [PubMed - indexed for MEDLINE]Related articles

    19.

    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

    20.

    Unilateral Meesmann's dystrophy.

    Goldberg A, Schlötzer-Schrehardt U, Seiler T.

    Int Ophthalmol. 1997;21(3):117-20. Review.PMID: 9587826 [PubMed - indexed for MEDLINE]Related articles

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