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Results: 1 to 20 of 114

Similar articles for PubMed (Select 19741557)

1.

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
2.

[Therapeutic strategies in recurrent erosion. Mechanical trauma, epithelial basal membrane dystrophy and idiopathic genesis].

Reinhard T, Sundmacher R.

Ophthalmologe. 2000 Feb;97(2):157-72. Review. German. No abstract available.

PMID:
10734744
3.

Differentiation of corneal complications observed in contact lens wearers.

Josephson JE, Zantos S, Caffery B, Herman JP.

J Am Optom Assoc. 1988 Sep;59(9):679-85.

PMID:
3263406
4.

Association of keratoconus with granular corneal dystrophy.

Vajpayee RB, Snibson GR, Taylor HR.

Aust N Z J Ophthalmol. 1996 Nov;24(4):369-71.

PMID:
8985551
5.

Contact lens intolerance in association with epithelial dystrophy.

McMonnies CW.

Am J Optom Physiol Opt. 1981 May;58(5):414-8.

PMID:
6973279
6.

Recurrent corneal erosions and epithelial basement membrane dystrophy.

Laibson PR.

Eye Contact Lens. 2010 Sep;36(5):315-7. doi: 10.1097/ICL.0b013e3181f18ff7. Review.

PMID:
20724847
7.

Corneal dystrophies.

Bass SJ.

Optom Clin. 1991;1(4):31-44. Review.

PMID:
1799834
8.

Nonfamilial anterior corneal dystrophy.

Kielar RA, Wallace GR.

Ann Ophthalmol. 1979 Mar;11(3):341-6.

PMID:
378081
9.

Granular corneal dystrophy: treatment with soft contact lenses.

Severin M, Konen W, Kirchhof B.

Graefes Arch Clin Exp Ophthalmol. 1998 Apr;236(4):291-4.

PMID:
9561363
10.

[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
11.
12.

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

Patel DV, Grupcheva CN, McGhee CN.

Cornea. 2005 Aug;24(6):669-73.

PMID:
16015084
13.
14.

Meesmann corneal epithelial dystrophy in a Saudi Arabian family.

Badr IA, Basaffar S, Jabak M, Wagoner MD.

Am J Ophthalmol. 1998 Feb;125(2):182-6.

PMID:
9467444
15.

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
16.

Phototherapeutic keratectomy for macular corneal dystrophy.

Wagoner MD, Badr IA.

J Refract Surg. 1999 Jul-Aug;15(4):481-4.

PMID:
10445722
17.
18.

Excimer laser phototherapeutic keratectomy for granular and lattice corneal dystrophy: a comparative study.

Das S, Langenbucher A, Seitz B.

J Refract Surg. 2005 Nov-Dec;21(6):727-31.

PMID:
16329366
19.

New contact lens challenges: the epithelial basement membrane dystrophy.

Siegel D.

J Am Optom Assoc. 1986 Oct;57(10):746-50. Erratum in: J Am Optom Assoc 1986 Dec;57(12):883.

PMID:
3490503
20.

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.

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