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dc.contributor.authorBuechner, S
dc.contributor.authorCerundolo, V
dc.contributor.authorJones, M
dc.contributor.authorColonna, M
dc.contributor.authorGross, WL
dc.contributor.authorBaykal, Can
dc.contributor.authorMoins-Teisserenc, HT
dc.contributor.authorGadola, SD
dc.contributor.authorCella, M
dc.contributor.authorDunbar, PR
dc.contributor.authorExley, A
dc.contributor.authorBlake, N
dc.contributor.authorLambert, J
dc.contributor.authorBigliardi, P
dc.contributor.authorWillemsen, M
dc.date.accessioned2021-03-03T18:33:33Z
dc.date.available2021-03-03T18:33:33Z
dc.date.issued1999
dc.identifier.citationMoins-Teisserenc H., Gadola S., Cella M., Dunbar P., Exley A., Blake N., Baykal C., Lambert J., Bigliardi P., Willemsen M., et al., "Association of a syndrome resembling Wegener's granulomatosis with low surface expression of HLA class-I molecules", LANCET, cilt.354, sa.9190, ss.1598-1603, 1999
dc.identifier.issn0140-6736
dc.identifier.othervv_1032021
dc.identifier.otherav_4fb71963-7210-40ec-b59e-3c954564a5c2
dc.identifier.urihttp://hdl.handle.net/20.500.12627/56830
dc.identifier.urihttps://doi.org/10.1016/s0140-6736(99)04206-3
dc.description.abstractBackground Granulomatous syndromes, such as Wegener's granulomatosis, are defined according to complex criteria, but the underlying cause is rarely identified. We present evidence for a new aetiology for chronic granulomatous lesions associated with a recessive genetic defect, which is linked to the human leucocyte antigen (HLA) locus.
dc.language.isoeng
dc.subjectTemel Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectTIP, GENEL & İÇECEK
dc.titleAssociation of a syndrome resembling Wegener's granulomatosis with low surface expression of HLA class-I molecules
dc.typeMakale
dc.relation.journalLANCET
dc.contributor.departmentİstanbul Üniversitesi , İstanbul Tıp Fakültesi , Dahili Tıp Bilimleri Bölümü
dc.identifier.volume354
dc.identifier.issue9190
dc.identifier.startpage1598
dc.identifier.endpage1603
dc.contributor.firstauthorID124291


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