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dc.contributor.authorElmali, Muzaffer
dc.contributor.authorAkan, Huseyin
dc.contributor.authorFindik, Serhat
dc.contributor.authorKale, Melike
dc.contributor.authorCelenk, Cetin
dc.date.accessioned2020-06-21T15:12:55Z
dc.date.available2020-06-21T15:12:55Z
dc.date.issued2008
dc.identifier.issn0883-5993
dc.identifier.urihttps://doi.org/10.1097/RTI.0b013e3181820867
dc.identifier.urihttps://hdl.handle.net/20.500.12712/19134
dc.descriptionWOS: 000261436600014en_US
dc.descriptionPubMed: 19204479en_US
dc.description.abstractA 51-year-old woman was admitted to emergency unit complaining of sudden onset chest pain. The patient had a family history of hereditary hemorrhagic telangiectasia. Thorax computed tomographic angiography demonstrated high-density left pleural effusion, and 3 giant arteriovenous malformations. Thoracentesis revealed hemorrhagic fluid. We present successful coil embolization of pulmonary arteriovenous malformations associated with hereditary hemorrhagic telangiectasia.en_US
dc.language.isoengen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.isversionof10.1097/RTI.0b013e3181820867en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectarteriovenous malformationen_US
dc.subjecthereditary hemorrhagic telangiectasiaen_US
dc.subjectRendu-Osler-Weberen_US
dc.subjectembolizationen_US
dc.subjecthemothoraxen_US
dc.titleHereditary Hemorrhagic Telangiectasia Associated With Pulmonary Arteriovenous Malformations Presenting as Hemothoraxen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume23en_US
dc.identifier.issue4en_US
dc.identifier.startpage295en_US
dc.identifier.endpage297en_US
dc.relation.journalJournal of Thoracic Imagingen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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