dc.contributor.author | Sayarlioglu, M | |
dc.contributor.author | Inanc, Murat | |
dc.contributor.author | Cefle, A | |
dc.contributor.author | Aral, O | |
dc.contributor.author | Konice, M | |
dc.contributor.author | Kamali, S | |
dc.contributor.author | Gul, A | |
dc.contributor.author | Poyanli, A | |
dc.date.accessioned | 2021-03-04T10:45:01Z | |
dc.date.available | 2021-03-04T10:45:01Z | |
dc.date.issued | 2003 | |
dc.identifier.citation | Kamali S., Gul A., Poyanli A., Cefle A., Sayarlioglu M., Inanc M., Aral O., Konice M., "A patient with classical polyarteritis nodosa evolving into end stage renal failure", RENAL FAILURE, cilt.25, sa.6, ss.1037-1041, 2003 | |
dc.identifier.issn | 0886-022X | |
dc.identifier.other | av_6ebec493-1db1-411b-bc7e-c2e00334a370 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/76459 | |
dc.identifier.uri | https://doi.org/10.1081/jdi-120026039 | |
dc.description.abstract | Classical polyarteritis nodosa (c-PAN) is a form of systemic necrotizing vasculitis mainly affecting medium-size arteries, is not associated with renal glomerular disease and acute renal failure. Perirenal hematoma can be seen in up to fifty percent of c-PAN patients and minority of them develop mild renal impairment. Herein, we describe a 34-year-old male with c-PAN who presented with rapidly progressive renal failure and evolved into end stage renal disease. | |
dc.language.iso | eng | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Nefroloji | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | İç Hastalıkları | |
dc.subject | Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Klinik Tıp | |
dc.subject | ÜROLOJİ VE NEFROLOJİ | |
dc.title | A patient with classical polyarteritis nodosa evolving into end stage renal failure | |
dc.type | Makale | |
dc.relation.journal | RENAL FAILURE | |
dc.contributor.department | , , | |
dc.identifier.volume | 25 | |
dc.identifier.issue | 6 | |
dc.identifier.startpage | 1037 | |
dc.identifier.endpage | 1041 | |
dc.contributor.firstauthorID | 166920 | |