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Items: 6

1.

A rare form of hereditary epithelial dystrophy of the cornea: a genetic, clinical, and pathologic study.

STOCKER FW, HOLT LB.

Trans Am Ophthalmol Soc. 1954-1955;52:133-44. No abstract available.

2.

The molecular genetics of the corneal dystrophies--current status.

Klintworth GK.

Front Biosci. 2003 May 1;8:d687-713. Review.

PMID:
12700042
3.

[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
4.

Differential diagnosis of Schnyder corneal dystrophy.

Weiss JS, Khemichian AJ.

Dev Ophthalmol. 2011;48:67-96. doi: 10.1159/000324078. Epub 2011 Apr 26. Review.

PMID:
21540632
5.

Fuchs' dystrophy.

Wilson SE, Bourne WM.

Cornea. 1988;7(1):2-18. Review.

PMID:
3280235
6.

[Corneal dystrophy (CD)-induced pain and visual impairment in childhood].

Lisch W.

Klin Monbl Augenheilkd. 2013 Jun;230(6):582-6. doi: 10.1055/s-0032-1328312. Epub 2013 Jun 21. Review. German.

PMID:
23794427
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