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dc.contributor.authorBasoglu, T
dc.contributor.authorAkpolat, T
dc.contributor.authorCanbaz, F
dc.contributor.authorBernay, I
dc.contributor.authorAlbayrak, S
dc.contributor.authorKilic, M
dc.contributor.authorDanaci, M
dc.date.accessioned2020-06-21T15:50:44Z
dc.date.available2020-06-21T15:50:44Z
dc.date.issued1999
dc.identifier.issn0363-9762
dc.identifier.urihttps://doi.org/10.1097/00003072-199903000-00020
dc.identifier.urihttps://hdl.handle.net/20.500.12712/22448
dc.descriptionWOS: 000078684400020en_US
dc.descriptionPubMed: 10069740en_US
dc.description.abstractPolyarteritis nodosa is a multisystemic disorder that results in various signs and symptoms depending on the specific site of the blood vessel involved. The disease affects the kidneys in 70% of cases, sometimes with aneurysm formation, which can result in perirenal and intrarenal bleeding. The authors describe a patient with polyarteritis nodosa with multiple bilateral aneurysmal dilatations confirmed by angiography. The Tc-99m DMSA renal scan revealed bilateral intraparenchymal photopenic areas mimicking polycystic renal disease.en_US
dc.language.isoengen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.isversionof10.1097/00003072-199903000-00020en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectpolyarteritis nodosaen_US
dc.subjectrenal artery aneurysmen_US
dc.subjectTc-99m DMSAen_US
dc.titleTc-99m DMSA renal scan in polyarteritis nodosa with bilateral intraparenchymal renal artery aneurysmsen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume24en_US
dc.identifier.issue3en_US
dc.identifier.startpage201en_US
dc.identifier.endpage202en_US
dc.relation.journalClinical Nuclear Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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