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dc.contributor.authorNadir, I
dc.contributor.authorGultekin, F
dc.contributor.authorYonem, O
dc.contributor.authorYildiz, E
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:23:55Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:23:55Z
dc.date.issued2003
dc.identifier.issn0886-022X
dc.identifier.urihttps://dx.doi.org/10.1081/JDI-120018734
dc.identifier.urihttps://hdl.handle.net/20.500.12418/11460
dc.descriptionWOS: 000182676600019en_US
dc.descriptionPubMed ID: 12739840en_US
dc.description.abstractBehcets disease is a chronic systemic vasculitis with unknown etiology characterized by recurrent oral and genital ulcerations, ocular inflammation, having manifestations related to the skin and joints. Neurologic, pulmonary and gastrointestinal findings can also be observed during the course of the disease. In this report a case of Behcet's disease that had amyloidosis due to renal parenchymal involvement of the disease showing itself by nephrotic syndrome is presented.en_US
dc.language.isoengen_US
dc.publisherMARCEL DEKKER INCen_US
dc.relation.isversionof10.1081/JDI-120018734en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBehcet's diseaseen_US
dc.subjectamyloidosisen_US
dc.subjectnephrotic syndromeen_US
dc.titleA Behcet case with renal amyloidosisen_US
dc.typearticleen_US
dc.relation.journalRENAL FAILUREen_US
dc.contributor.departmentCumhuriyet Univ, Fac Med, Dept Pathol, Sivas, Turkey -- Cumhuriyet Univ, Fac Med, Dept Internal Med, Sivas, Turkeyen_US
dc.identifier.volume25en_US
dc.identifier.issue2en_US
dc.identifier.endpage326en_US
dc.identifier.startpage323en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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