Show simple item record

dc.contributor.authorSayarlioglu, M
dc.contributor.authorInanc, Murat
dc.contributor.authorCefle, A
dc.contributor.authorAral, O
dc.contributor.authorKonice, M
dc.contributor.authorKamali, S
dc.contributor.authorGul, A
dc.contributor.authorPoyanli, A
dc.date.accessioned2021-03-04T10:45:01Z
dc.date.available2021-03-04T10:45:01Z
dc.date.issued2003
dc.identifier.citationKamali 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.issn0886-022X
dc.identifier.otherav_6ebec493-1db1-411b-bc7e-c2e00334a370
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/76459
dc.identifier.urihttps://doi.org/10.1081/jdi-120026039
dc.description.abstractClassical 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.isoeng
dc.subjectSağlık Bilimleri
dc.subjectNefroloji
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectÜROLOJİ VE NEFROLOJİ
dc.titleA patient with classical polyarteritis nodosa evolving into end stage renal failure
dc.typeMakale
dc.relation.journalRENAL FAILURE
dc.contributor.department, ,
dc.identifier.volume25
dc.identifier.issue6
dc.identifier.startpage1037
dc.identifier.endpage1041
dc.contributor.firstauthorID166920


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record