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Results: 1 to 20 of 582

Related Citations for PubMed (Select 15671264)

1.

Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene.

Bredrup C, Knappskog PM, Majewski J, Rødahl E, Boman H.

Invest Ophthalmol Vis Sci. 2005 Feb;46(2):420-6.

2.

A novel mutation of the decorin gene identified in a Korean family with congenital hereditary stromal dystrophy.

Kim JH, Ko JM, Lee I, Kim JY, Kim MJ, Tchah H.

Cornea. 2011 Dec;30(12):1473-7. doi: 10.1097/ICO.0b013e3182137788.

PMID:
21993463
3.

A second decorin frame shift mutation in a family with congenital stromal corneal dystrophy.

Rødahl E, Van Ginderdeuren R, Knappskog PM, Bredrup C, Boman H.

Am J Ophthalmol. 2006 Sep;142(3):520-1.

PMID:
16935612
4.

Report of a new family with dominant congenital heredity stromal dystrophy of the cornea.

Van Ginderdeuren R, De Vos R, Casteels I, Foets B.

Cornea. 2002 Jan;21(1):118-20.

PMID:
11805522
5.

Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to xp22.3.

Lisch W, Büttner A, Oeffner F, Böddeker I, Engel H, Lisch C, Ziegler A, Grzeschik K.

Am J Ophthalmol. 2000 Oct;130(4):461-8.

PMID:
11024418
6.

Exclusion of known corneal dystrophy genes in an autosomal dominant pedigree of a unique anterior membrane corneal dystrophy.

Vincent AL, Markie DM, De Karolyi B, Wheeldon CE, Patel DV, Grupcheva CN, McGhee CN.

Mol Vis. 2009 Aug 26;15:1700-8.

7.

Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2.

Aldave AJ, Sonmez B, Bourla N, Schultz G, Papp JC, Salem AK, Rayner SA, Yellore VS.

Ophthalmic Genet. 2007 Jun;28(2):57-67.

PMID:
17558846
8.

A new, X-linked endothelial corneal dystrophy.

Schmid E, Lisch W, Philipp W, Lechner S, Göttinger W, Schlötzer-Schrehardt U, Müller T, Utermann G, Janecke AR.

Am J Ophthalmol. 2006 Mar;141(3):478-487.

PMID:
16490493
9.
10.

Novel decorin mutation in a Chinese family with congenital stromal corneal dystrophy.

Jing Y, Kumar PR, Zhu L, Edward DP, Tao S, Wang L, Chuck R, Zhang C.

Cornea. 2014 Mar;33(3):288-93. doi: 10.1097/ICO.0000000000000055.

PMID:
24413633
11.

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.

12.

Polymorphic corneal amyloidosis: a disorder due to a novel mutation in the transforming growth factor beta-induced (BIGH3) gene.

Eifrig DE Jr, Afshari NA, Buchanan HW 4th, Bowling BL, Klintworth GK.

Ophthalmology. 2004 Jun;111(6):1108-14.

PMID:
15177960
13.

Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC.

Aldave AJ, Rosenwasser GO, Yellore VS, Papp JC, Sobel EM, Pham MN, Chen MC, Dandekar S, Sripracha R, Rayner SA, Sassani JW, Gorin MB.

Invest Ophthalmol Vis Sci. 2010 Aug;51(8):4006-12. doi: 10.1167/iovs.09-4067. Epub 2010 Mar 31.

14.

[Type I lattice corneal dystrophy. Clinical and molecular genetic study of a large family].

Meins M, Kohlhaas M, Richard G, Gal A.

Klin Monbl Augenheilkd. 1998 Mar;212(3):154-8. German.

PMID:
9592740
15.

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.

16.
17.

A new locus for congenital cataract, microcornea, microphthalmia, and atypical iris coloboma maps to chromosome 2.

Abouzeid H, Meire FM, Osman I, ElShakankiri N, Bolay S, Munier FL, Schorderet DF.

Ophthalmology. 2009 Jan;116(1):154-162.e1. doi: 10.1016/j.ophtha.2008.08.044. Epub 2008 Nov 12.

PMID:
19004499
18.

The benign concentric annular macular dystrophy locus maps to 6p12.3-q16.

van Lith-Verhoeven JJ, Hoyng CB, van den Helm B, Deutman AF, Brink HM, Kemperman MH, de Jong WH, Kremer H, Cremers FP.

Invest Ophthalmol Vis Sci. 2004 Jan;45(1):30-5.

19.

The phenotype of arg555trp mutation in a large Turkish family with corneal granular dystrophy.

Kiratli H, Irkeç M, Ozgül K, Ogüş A.

Eur J Ophthalmol. 2001 Oct-Dec;11(4):333-7.

PMID:
11820303
20.

Granular corneal dystrophy with early stromal manifestation. A clinical and electron microscopical study.

Ruusuvaara P, Setälä K, Tarkkanen A.

Acta Ophthalmol (Copenh). 1990 Oct;68(5):525-31.

PMID:
2275345
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