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Items: 13

1.

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
2.

Decorin accumulation contributes to the stromal opacities found in congenital stromal corneal dystrophy.

Bredrup C, Stang E, Bruland O, Palka BP, Young RD, Haavik J, Knappskog PM, Rødahl E.

Invest Ophthalmol Vis Sci. 2010 Nov;51(11):5578-82. doi: 10.1167/iovs.09-4933. Epub 2010 May 19.

PMID:
20484579
3.

The IC3D classification of the corneal dystrophies.

Weiss JS, Møller HU, Lisch W, Kinoshita S, Aldave AJ, Belin MW, Kivelä T, Busin M, Munier FL, Seitz B, Sutphin J, Bredrup C, Mannis MJ, Rapuano CJ, Van Rij G, Kim EK, Klintworth GK.

Cornea. 2008 Dec;27 Suppl 2:S1-83. doi: 10.1097/ICO.0b013e31817780fb. Review. English, Spanish.

4.

Genetic evidence for the coordinated regulation of collagen fibrillogenesis in the cornea by decorin and biglycan.

Zhang G, Chen S, Goldoni S, Calder BW, Simpson HC, Owens RT, McQuillan DJ, Young MF, Iozzo RV, Birk DE.

J Biol Chem. 2009 Mar 27;284(13):8888-97. doi: 10.1074/jbc.M806590200. Epub 2009 Jan 9.

5.

Biological functions of the small leucine-rich proteoglycans: from genetics to signal transduction.

Schaefer L, Iozzo RV.

J Biol Chem. 2008 Aug 1;283(31):21305-9. doi: 10.1074/jbc.R800020200. Epub 2008 May 6. Review.

6.

Congenital corneal opacities: a review with a focus on genetics.

Ciralsky J, Colby K.

Semin Ophthalmol. 2007 Oct-Dec;22(4):241-6. Review.

PMID:
18097987
7.

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
8.

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.

PMID:
15671264
9.

The Decorin gene 179 allelic variant is associated with a slower progression of renal disease in patients with type 1 diabetes.

De Cosmo S, Tassi V, Thomas S, Piras GP, Trevisan R, Cavallo Perin P, Bacci S, Zucaro L, Cisternino C, Trischitta V, Viberti GC.

Nephron. 2002 Sep;92(1):72-6.

PMID:
12187087
10.

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
11.

Dystrophia corneae parenchymatosa congenita. A clinical, morphological and histochemical examination.

Odland M.

Acta Ophthalmol (Copenh). 1968;46(3):477-85. No abstract available.

PMID:
5304426
12.

Congenital hereditary stromal dystrophy of the cornea.

Witschel H, Fine BS, Grützner P, McTigue JW.

Arch Ophthalmol. 1978 Jun;96(6):1043-51.

PMID:
350201
13.

[Familial congenital dystrophy of the corneal stroma: Turpin's syndrome (author's transl)].

Pouliquen Y, Lacombe E, Schreinzer C, Giraud JP, Savoldelli M.

J Fr Ophtalmol. 1979 Feb;2(2):115-25. French.

PMID:
312637
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