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dc.contributor.authorTascilar, Koray
dc.contributor.authorMelikoglu, Melike
dc.contributor.authorYazici, Hasan
dc.contributor.authorKural-Seyahi, Emire
dc.date.accessioned2021-03-03T08:16:39Z
dc.date.available2021-03-03T08:16:39Z
dc.identifier.citationMelikoglu M., Kural-Seyahi E., Tascilar K., Yazici H., "The unique features of vasculitis in Behcet's syndrome", CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY, cilt.35, ss.40-46, 2008
dc.identifier.issn1080-0549
dc.identifier.othervv_1032021
dc.identifier.otherav_16aa3ac5-1a2c-478f-bc36-2dbfe6241a3e
dc.identifier.urihttp://hdl.handle.net/20.500.12627/20568
dc.identifier.urihttps://doi.org/10.1007/s12016-007-8064-8
dc.description.abstractThe presence of a true vasculitis is difficult to discern in some of the more common manifestations of Behcet's syndrome, like the papulopustular lesions of the skin. On the other hand, a true vasculitis is seen in all vessel sizes in the majority of the patients. The pathogenesis is not yet known. A Th1-type inflammatory reaction is seen like in some other primary vasculitides. However, in contrast to other vasculitides, granuloma formation is absent. Behcet's syndrome is unique among the vasculitides with its differing geographic distribution in disease expression, the distinctly more severe disease among the male, the predominance of venous disease, and the generally abating disease course with lack of associated increased atherosclerosis.
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectİmmünoloji
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectALERJİ
dc.titleThe unique features of vasculitis in Behcet's syndrome
dc.typeMakale
dc.relation.journalCLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume35
dc.identifier.startpage40
dc.identifier.endpage46
dc.contributor.firstauthorID189691


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