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dc.contributor.authorOZYAZGAN, Y
dc.contributor.authorPAZARLI, H
dc.contributor.authorHAMURYUDAN, V
dc.contributor.authorMUFTUOGLU, A
dc.contributor.authorYURDAKUL, S
dc.contributor.authorYAZICI, H
dc.contributor.authorTUZUN, B
dc.contributor.authorISCIMEN, A
dc.contributor.authorTUZUN, Y
dc.contributor.authorAKTUNC, T
dc.date.accessioned2021-03-03T11:56:10Z
dc.date.available2021-03-03T11:56:10Z
dc.date.issued1992
dc.identifier.citationOZYAZGAN Y., YURDAKUL S., YAZICI H., TUZUN B., ISCIMEN A., TUZUN Y., AKTUNC T., PAZARLI H., HAMURYUDAN V., MUFTUOGLU A., "LOW-DOSE CYCLOSPORINE-A VERSUS PULSED CYCLOPHOSPHAMIDE IN BEHCETS-SYNDROME - A SINGLE MASKED TRIAL", BRITISH JOURNAL OF OPHTHALMOLOGY, cilt.76, sa.4, ss.241-243, 1992
dc.identifier.issn0007-1161
dc.identifier.othervv_1032021
dc.identifier.otherav_2ae8d7e9-5e66-4dc3-b3a9-a937d75fad8a
dc.identifier.urihttp://hdl.handle.net/20.500.12627/33592
dc.identifier.urihttps://doi.org/10.1136/bjo.76.4.241
dc.description.abstractA single masked trial of cyclosporin A 5 mg/kg/day versus monthly 1 g intravenous boluses of cyclophosphamide was conducted among 23 patients with Behcet's syndrome and active, potentially reversible uveitis. The trial was unmasked after a mean of 12 (SD 2) months for the cyclosporin A group (n = 12) and a mean of 10 (SD 3) months for the cyclophosphamide group (n = 11). During the initial 6 months the visual acuity significantly improved (p < 0.001) in the cyclosporin A group whereas this was not observed in the cyclophosphamide group. The subsequent follow-up of patients up to 24 months suggested that the initial improvement in visual acuity with cyclosporin A was not sustained. More extensive and especially long-term studies of cyclosporin A in the uveitis of Behcet's syndrome are warranted.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.subjectCerrahi Tıp Bilimleri
dc.subjectGöz Hastalıkları ve Cerrahisi
dc.subjectKlinik Tıp
dc.subjectOFTALMOLOJİ
dc.subjectTıp
dc.titleLOW-DOSE CYCLOSPORINE-A VERSUS PULSED CYCLOPHOSPHAMIDE IN BEHCETS-SYNDROME - A SINGLE MASKED TRIAL
dc.typeMakale
dc.relation.journalBRITISH JOURNAL OF OPHTHALMOLOGY
dc.contributor.department, ,
dc.identifier.volume76
dc.identifier.issue4
dc.identifier.startpage241
dc.identifier.endpage243
dc.contributor.firstauthorID3166


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