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dc.contributor.authorDalkilic, Ediz
dc.contributor.authorKamali, Sevil
dc.contributor.authorAlkis, Nihan
dc.date.accessioned2021-03-03T15:06:40Z
dc.date.available2021-03-03T15:06:40Z
dc.date.issued2012
dc.identifier.citationDalkilic E., Alkis N., Kamali S., "Rituximab as a new therapeutic option in granulomatosis with polyangiitis: a report of two cases", MODERN RHEUMATOLOGY, cilt.22, sa.3, ss.463-466, 2012
dc.identifier.issn1439-7595
dc.identifier.otherav_3d3bdc33-0ccb-4296-a762-e1feb7a42047
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/45070
dc.identifier.urihttps://doi.org/10.1007/s10165-011-0507-7
dc.description.abstractFindings of several reports suggest that rituximab, a chimeric monoclonal anti-CD20 antibody causing B-lymphocyte depletion, might represent a treatment option for people with granulomatosis with polyangiitis (GPA) (former Wegener's granulomatosis). This study presents the results of rituximab treatment in two patients with treatment-refractory GPA. First patient received rituximab for a granulomatous posterior orbital mass lesion, and eye symptoms were resolved after three courses of treatment. The second patient had eye and paranasal sinus involvement and benefited from two courses of rituximab treatment, with significant clinical improvement. Rituximab may represent an effective novel treatment for remission induction in GPA.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectİmmünoloji ve Romatoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectROMATOLOJİ
dc.titleRituximab as a new therapeutic option in granulomatosis with polyangiitis: a report of two cases
dc.typeMakale
dc.relation.journalMODERN RHEUMATOLOGY
dc.contributor.departmentBursa Uludağ Üniversitesi , ,
dc.identifier.volume22
dc.identifier.issue3
dc.identifier.startpage463
dc.identifier.endpage466
dc.contributor.firstauthorID204383


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