dc.contributor.author | Nadir, I | |
dc.contributor.author | Gultekin, F | |
dc.contributor.author | Yonem, O | |
dc.contributor.author | Yildiz, E | |
dc.date.accessioned | 2019-07-27T12:10:23Z | |
dc.date.accessioned | 2019-07-28T10:23:55Z | |
dc.date.available | 2019-07-27T12:10:23Z | |
dc.date.available | 2019-07-28T10:23:55Z | |
dc.date.issued | 2003 | |
dc.identifier.issn | 0886-022X | |
dc.identifier.uri | https://dx.doi.org/10.1081/JDI-120018734 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12418/11460 | |
dc.description | WOS: 000182676600019 | en_US |
dc.description | PubMed ID: 12739840 | en_US |
dc.description.abstract | Behcets 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.iso | eng | en_US |
dc.publisher | MARCEL DEKKER INC | en_US |
dc.relation.isversionof | 10.1081/JDI-120018734 | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Behcet's disease | en_US |
dc.subject | amyloidosis | en_US |
dc.subject | nephrotic syndrome | en_US |
dc.title | A Behcet case with renal amyloidosis | en_US |
dc.type | article | en_US |
dc.relation.journal | RENAL FAILURE | en_US |
dc.contributor.department | Cumhuriyet Univ, Fac Med, Dept Pathol, Sivas, Turkey -- Cumhuriyet Univ, Fac Med, Dept Internal Med, Sivas, Turkey | en_US |
dc.identifier.volume | 25 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.endpage | 326 | en_US |
dc.identifier.startpage | 323 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |