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Journal Abstract Search
884 related items for PubMed ID: 16102833
1. Phase III safety evaluation of cyclosporine 0.1% ophthalmic emulsion administered twice daily to dry eye disease patients for up to 3 years. Barber LD, Pflugfelder SC, Tauber J, Foulks GN. Ophthalmology; 2005 Oct; 112(10):1790-4. PubMed ID: 16102833 [Abstract] [Full Text] [Related]
5. Corneal and conjunctival sensitivity in patients with dry eye: the effect of topical cyclosporine therapy. Toker E, Asfuroğlu E. Cornea; 2010 Feb; 29(2):133-40. PubMed ID: 19966564 [Abstract] [Full Text] [Related]
6. Efficacy and safety of cyclosporin A ophthalmic emulsion in the treatment of moderate-to-severe dry eye disease: a dose-ranging, randomized trial. The Cyclosporin A Phase 2 Study Group. Stevenson D, Tauber J, Reis BL. Ophthalmology; 2000 May; 107(5):967-74. PubMed ID: 10811092 [Abstract] [Full Text] [Related]
9. Tofacitinib (CP-690,550), a Janus kinase inhibitor for dry eye disease: results from a phase 1/2 trial. Liew SH, Nichols KK, Klamerus KJ, Li JZ, Zhang M, Foulks GN. Ophthalmology; 2012 Jul; 119(7):1328-35. PubMed ID: 22525048 [Abstract] [Full Text] [Related]
10. The effect of decreasing the dosage of cyclosporine A 0.05% on dry eye disease after 1 year of twice-daily therapy. Su MY, Perry HD, Barsam A, Perry AR, Donnenfeld ED, Wittpenn JR, D'Aversa G. Cornea; 2011 Oct; 30(10):1098-104. PubMed ID: 21407074 [Abstract] [Full Text] [Related]
12. Long-term resolution of chronic dry eye symptoms and signs after topical cyclosporine treatment. Wilson SE, Perry HD. Ophthalmology; 2007 Jan; 114(1):76-9. PubMed ID: 17070588 [Abstract] [Full Text] [Related]