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dc.contributor.authorSÜT, NECDET
dc.contributor.authorHatemi, Gulen
dc.contributor.authorYazici, Hasan
dc.contributor.authorKaraca, Mehmet
dc.date.accessioned2021-03-03T19:56:50Z
dc.date.available2021-03-03T19:56:50Z
dc.date.issued2012
dc.identifier.citationKaraca M., Hatemi G., SÜT N., Yazici H., "The papulopustular lesion/arthritis cluster of Behcet's syndrome also clusters in families", RHEUMATOLOGY, cilt.51, sa.6, ss.1053-1060, 2012
dc.identifier.issn1462-0324
dc.identifier.otherav_573fea48-4d0d-48e0-b3be-0dc4caa75a2b
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/61552
dc.identifier.urihttps://doi.org/10.1093/rheumatology/ker423
dc.description.abstractObjective. We have previously reported distinct symptom clusters among our patients with Behcet's syndrome (BS). The presence of such clusters suggests that more than one pathogenetic mechanism might be operative in BS. Increases in the frequency of certain clusters in familial BS cases, if present, would further support this notion. To test this hypothesis, we compared the frequency of symptom clusters between familial (Group F) and non-familial (Group NF) cases of BS.
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.titleThe papulopustular lesion/arthritis cluster of Behcet's syndrome also clusters in families
dc.typeMakale
dc.relation.journalRHEUMATOLOGY
dc.contributor.departmentİstanbul Teknik Üniversitesi , Avrasya Yer Bilimleri Enstitüsü ,
dc.identifier.volume51
dc.identifier.issue6
dc.identifier.startpage1053
dc.identifier.endpage1060
dc.contributor.firstauthorID204445


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