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Results: 1 to 20 of 49

1.

KRT12 mutations and in vivo confocal microscopy in two Japanese families with Meesmann corneal dystrophy.

Ogasawara M, Matsumoto Y, Hayashi T, Ohno K, Yamada H, Kawakita T, Dogru M, Shimazaki J, Tsubota K, Tsuneoka H.

Am J Ophthalmol. 2014 Jan;157(1):93-102.e1. doi: 10.1016/j.ajo.2013.08.008. Epub 2013 Oct 5.

PMID:
24099278
[PubMed - indexed for MEDLINE]
2.

Autosomal-dominant Meesmann epithelial corneal dystrophy without an exon mutation in the keratin-3 or keratin-12 gene in a Chinese family.

Cao W, Yan M, Hao Q, Wang S, Wu L, Liu Q, Li M, Biddle FG, Wu W.

J Int Med Res. 2013 Apr;41(2):511-8. doi: 10.1177/0300060513477306. Epub 2013 Mar 12.

PMID:
23569037
[PubMed - indexed for MEDLINE]
3.

Allele-specific siRNA silencing for the common keratin 12 founder mutation in Meesmann epithelial corneal dystrophy.

Allen EH, Atkinson SD, Liao H, Moore JE, Leslie Pedrioli DM, Smith FJ, McLean WH, Moore CB.

Invest Ophthalmol Vis Sci. 2013 Jan 17;54(1):494-502. doi: 10.1167/iovs.12-10528.

PMID:
23233254
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12.

Hassan H, Thaung C, Ebenezer ND, Larkin G, Hardcastle AJ, Tuft SJ.

Eye (Lond). 2013 Mar;27(3):367-73. doi: 10.1038/eye.2012.261. Epub 2012 Dec 7.

PMID:
23222558
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Development of allele-specific therapeutic siRNA in Meesmann epithelial corneal dystrophy.

Liao H, Irvine AD, Macewen CJ, Weed KH, Porter L, Corden LD, Gibson AB, Moore JE, Smith FJ, McLean WH, Moore CB.

PLoS One. 2011;6(12):e28582. doi: 10.1371/journal.pone.0028582. Epub 2011 Dec 12.

PMID:
22174841
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Stage-related therapy of corneal dystrophies.

Seitz B, Lisch W.

Dev Ophthalmol. 2011;48:116-53. doi: 10.1159/000324081. Epub 2011 Apr 26. Review.

PMID:
21540634
[PubMed - indexed for MEDLINE]
7.

Morphological evaluation of normal human corneal epithelium.

Ehlers N, Heegaard S, Hjortdal J, Ivarsen A, Nielsen K, Prause JU.

Acta Ophthalmol. 2010 Dec;88(8):858-61. doi: 10.1111/j.1755-3768.2009.01610.x.

PMID:
21114634
[PubMed - indexed for MEDLINE]
8.

Identification of a novel mutation in the cornea specific keratin 12 gene causing Meesmann's corneal dystrophy in a German family.

Clausen I, Duncker GI, Grünauer-Kloevekorn C.

Mol Vis. 2010 May 29;16:954-60.

PMID:
20577595
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Management of symptomatic Meesmann dystrophy.

Jalbert I, Stapleton F.

Optom Vis Sci. 2009 Oct;86(10):E1202-6. doi: 10.1097/OPX.0b013e3181baad27.

PMID:
19741557
[PubMed - indexed for MEDLINE]
10.

Recurrent Meesmann's corneal dystrophy: treatment with keratectomy and mitomycin C.

Yeung JY, Hodge WG.

Can J Ophthalmol. 2009 Feb;44(1):103-4. doi: 10.3129/i08-179. No abstract available.

PMID:
19169328
[PubMed - indexed for MEDLINE]
11.

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]
Free PMC Article
12.

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. doi: 10.1007/s10384-007-0518-2. Epub 2008 Jul 27.

PMID:
18661274
[PubMed - indexed for MEDLINE]
13.

Meesmann corneal dystrophy associated with epithelial basement membrane and posterior polymorphous corneal dystrophies.

Cremona FA, Ghosheh FR, Laibson PR, Rapuano CJ, Cohen EJ.

Cornea. 2008 Apr;27(3):374-7. doi: 10.1097/ICO.0b013e31815c18fa.

PMID:
18362674
[PubMed - indexed for MEDLINE]
14.

A novel mutation as the basis for asymptomatic meesmann dystrophy in a Danish family.

Nielsen K, Orntoft T, Hjortdal J, Rasmussen T, Ehlers N.

Cornea. 2008 Jan;27(1):100-2. doi: 10.1097/ICO.0b013e31815652fd.

PMID:
18245975
[PubMed - indexed for MEDLINE]
15.

Meesmann's corneal dystrophy managed with an epithelial delaminator.

Gooi P, Brownstein S, Jackson WB, Mintsioulis G.

Can J Ophthalmol. 2007 Dec;42(6):878-9. No abstract available.

PMID:
18059516
[PubMed - indexed for MEDLINE]
16.

Phenotypic variability in Meesmann's dystrophy: clinical review of the literature and presentation of a family genetically identical to the original family.

Ehlers N, Hjortdal J, Nielsen K, Thiel HJ, Ørntoft T.

Acta Ophthalmol. 2008 Feb;86(1):40-4. Epub 2007 Nov 6. Review.

PMID:
17986293
[PubMed - indexed for MEDLINE]
17.

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]
Free PMC Article
18.

Imaging the microstructural abnormalities of Meesmann corneal dystrophy by in vivo confocal microscopy.

Tuft S, Bron AJ.

Cornea. 2006 Aug;25(7):868; author reply 868-70. No abstract available.

PMID:
17068472
[PubMed - indexed for MEDLINE]
19.

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

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

Ophthalmic Genet. 2005 Dec;26(4):169-73.

PMID:
16352477
[PubMed - indexed for MEDLINE]
20.

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]

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