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dc.contributor.authorYAZICI, H
dc.contributor.authorHAMURYUDAN, V
dc.contributor.authorYURDAKUL, S
dc.date.accessioned2021-03-05T16:53:55Z
dc.date.available2021-03-05T16:53:55Z
dc.date.issued1995
dc.identifier.citationYAZICI H., YURDAKUL S., HAMURYUDAN V., "BEHCETS-SYNDROME - HOW SHOULD WE TREAT IT", CLINICAL IMMUNOTHERAPEUTICS, cilt.3, ss.102-107, 1995
dc.identifier.issn1172-7039
dc.identifier.otherav_c2d4d241-ae8a-4c53-b71c-8fa423b02e79
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/129305
dc.identifier.urihttps://doi.org/10.1007/bf03259272
dc.description.abstractBehcet's syndrome is a multisystem vasculitis of unknown aetiology. Eye involvement, the main cause of morbidity, can lead to blindness in 20% of those affected. Other lesions, ranging from aphthous and genital ulceration to sometimes fatal central nervous system involvement, also cause considerable morbidity and, we have become more recently aware, mortality.
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectEczacılık
dc.subjectTemel Eczacılık Bilimleri
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectİmmünoloji
dc.titleBEHCETS-SYNDROME - HOW SHOULD WE TREAT IT
dc.typeMakale
dc.relation.journalCLINICAL IMMUNOTHERAPEUTICS
dc.contributor.department, ,
dc.identifier.volume3
dc.identifier.issue2
dc.identifier.startpage102
dc.identifier.endpage107
dc.contributor.firstauthorID116013


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