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dc.contributor.authorOzyazgan, Yılmaz
dc.date.accessioned2021-03-06T12:26:40Z
dc.date.available2021-03-06T12:26:40Z
dc.identifier.citationOzyazgan Y., "Ocular Involvement in Behcet's Disease", TURKDERM-ARCHIVES OF THE TURKISH DERMATOLOGY AND VENEROLOGY, cilt.43, ss.48-53, 2009
dc.identifier.issn1019-214X
dc.identifier.othervv_1032021
dc.identifier.otherav_f3da8fd9-b8fd-4cc0-9a81-0a4ad2c0d0b8
dc.identifier.urihttp://hdl.handle.net/20.500.12627/159898
dc.identifier.urihttps://doi.org/10.1007/s00417-008-0983-4
dc.description.abstractUveitis secondary to systemic diseases and in particular to Behcet's disease is frequent in Turkey. Eye involvement is not confined to the uvea; it also involves the optic nerve and the retina due to the participation of the retinal vascular system. The clinical course is characterized by activations and remissions. Severity of eye involvement is heterogeneous among patients. The analysis of the frequency and severity of activations along with detection of sequel formation has prognostic significance. There is no specific medication for treatment of Behcet's disease. Local and systemic corticosteroids, immunosuppressives and immunomodulators are used and their side effects are monitored. Treatment end points are to decrease the frequency and severity of attacks and the prevention of sequelae. (Turkderm 2009; 43 Suppl 2: 48-53)
dc.language.isoeng
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectDERMATOLOJİ
dc.subjectDahili Tıp Bilimleri
dc.subjectDermatoloji
dc.subjectSağlık Bilimleri
dc.titleOcular Involvement in Behcet's Disease
dc.typeMakale
dc.relation.journalTURKDERM-ARCHIVES OF THE TURKISH DERMATOLOGY AND VENEROLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume43
dc.identifier.startpage48
dc.identifier.endpage53
dc.contributor.firstauthorID6613


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