Von Hippel - Lindau sendromu (olgu sunumu)

dc.contributor.buuauthorSadıkoğlu, M. Yurtkuran
dc.contributor.buuauthorÖzkan, Ragıp
dc.contributor.buuauthorAdapınar, Baki
dc.contributor.buuauthorSavcı, Gürsel
dc.contributor.buuauthorTuncel, Ercan
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Radyoloji Anabilim Dalı.tr_TR
dc.date.accessioned2022-03-16T05:46:06Z
dc.date.available2022-03-16T05:46:06Z
dc.date.issued1990
dc.description.abstractVon Hippel-Lindau (VHL) sendromu nadir görülen heredofamilyal bir hastalıktır. Klasik bulgulan retinatla anjiomlar ve serebellumda hemanjioblastomlardır. Bu çalışmada iki VHL sendromu olgusu sunularak ilgili literatür gözden geçirilmiştir.tr_TR
dc.description.abstractVon Hippel-Lindau syndrome is a heredofamilial disease. lt is rarely seen. Classical findings are retinal angiomas and cerebellar hemangioblastomas. In this study two cases of Von Hippel-Lindau syndrome are presented and related literature is reviewed.en_US
dc.identifier.citationSadıkoğlu, M. Y. vd. (1990). ''Von Hippel - Lindau sendromu (olgu sunumu)''. Uludağ Üniversitesi Tıp Fakültesi Dergisi, 17(1), 181-186.tr_TR
dc.identifier.endpage186tr_TR
dc.identifier.issue1tr_TR
dc.identifier.startpage181tr_TR
dc.identifier.urihttp://hdl.handle.net/11452/25058
dc.identifier.volume17tr_TR
dc.language.isotrtr_TR
dc.publisherUludağ Üniversitesitr_TR
dc.relation.journalUludağ Üniversitesi Tıp Fakültesi Dergisitr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectVon Hippel Lindau sendromutr_TR
dc.subjectOlgu sunumutr_TR
dc.subjectCase reporten_US
dc.subjectVon Hippel Lindau syndromeen_US
dc.titleVon Hippel - Lindau sendromu (olgu sunumu)tr_TR
dc.title.alternativeVon Hippel- Lindau syndrome (case report)en_US
dc.typeArticleen_US

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