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Polyarteritis nodosa in patients with Familial Mediterranean fever (FMF): A concomitant disease or a feature of FMF?

dc.contributor.authorBen-Chetrit, E
dc.contributor.authorAkpolat, T
dc.contributor.authorBakkaloglu, A
dc.contributor.authorOzen, S
dc.contributor.authorBesbas, N
dc.contributor.authorDanaci, M
dc.contributor.authorAkpolat, I
dc.contributor.authorTurkmen, A
dc.contributor.authorTurgan, C
dc.contributor.authorCalguneri, M
dc.contributor.authorTinaztepe, K
dc.contributor.authorGur, H
dc.date.accessioned2021-03-06T09:07:21Z
dc.date.available2021-03-06T09:07:21Z
dc.date.issued2001
dc.identifier.citationOzen S., Ben-Chetrit E., Bakkaloglu A., Gur H., Tinaztepe K., Calguneri M., Turgan C., Turkmen A., Akpolat I., Danaci M., et al., "Polyarteritis nodosa in patients with Familial Mediterranean fever (FMF): A concomitant disease or a feature of FMF?", SEMINARS IN ARTHRITIS AND RHEUMATISM, cilt.30, ss.281-287, 2001
dc.identifier.issn0049-0172
dc.identifier.othervv_1032021
dc.identifier.otherav_e42c1b18-1f94-4da2-9667-0cd58d61771f
dc.identifier.urihttp://hdl.handle.net/20.500.12627/150146
dc.identifier.urihttps://doi.org/10.1053/sarh.2001.19958
dc.description.abstractBackground: Familial Mediterranean fever (FMF) is caused by mutations in the gene encoding pyrin and is characterized by self-limited, recurrent attacks of fever and serositis. Vasculitis has been increasingly reported in FMF, A study evaluating the prognosis in FMF and polyarteritis nodosa (PAN) patients has not been reported previously.
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectDahili Tıp Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectROMATOLOJİ
dc.subjectİmmünoloji ve Romatoloji
dc.titlePolyarteritis nodosa in patients with Familial Mediterranean fever (FMF): A concomitant disease or a feature of FMF?
dc.typeMakale
dc.relation.journalSEMINARS IN ARTHRITIS AND RHEUMATISM
dc.contributor.department, ,
dc.identifier.volume30
dc.identifier.issue4
dc.identifier.startpage281
dc.identifier.endpage287
dc.contributor.firstauthorID127822


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