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dc.contributor.authorFisgin, Nuriye Tasdelen
dc.contributor.authorFisgin, Tunc
dc.contributor.authorTanyel, Esra
dc.contributor.authorDoganci, Levent
dc.contributor.authorTulek, Necla
dc.contributor.authorGuler, Nil
dc.contributor.authorDuru, Feride
dc.date.accessioned2020-06-21T15:17:57Z
dc.date.available2020-06-21T15:17:57Z
dc.date.issued2008
dc.identifier.issn0361-8609
dc.identifier.issn1096-8652
dc.identifier.urihttps://doi.org/10.1002/ajh.20969
dc.identifier.urihttps://hdl.handle.net/20.500.12712/19511
dc.descriptionWOS: 000252259200015en_US
dc.descriptionPubMed: 17597475en_US
dc.description.abstractThree pediatric and two adult Turkish patients with Crimean Congo Hemorrhagic Fever (CCHF) induced hemophagocytic syndrome (HPS) were admitted to Ondokuz Mayis University Hospital, which is in the Middle Black Sea Region of Turkey. All of them had remarkable hemophagocytosis in the bone marrow with severe bleeding symptoms along with the other known clinical and laboratory findings of CCHF. We would like to present these patients and to discuss the pathophysiology and the effect of acquired HPS on the severity of the disease.en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.relation.isversionof10.1002/ajh.20969en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleCrimean-Congo hemorrhagic fever: Five patients with hemophagocytic syndromeen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume83en_US
dc.identifier.issue1en_US
dc.identifier.startpage73en_US
dc.identifier.endpage76en_US
dc.relation.journalAmerican Journal of Hematologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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