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dc.contributor.authorKarakuş, Volkan
dc.contributor.authorKaya, Egemen
dc.contributor.authorDere, Yelda
dc.contributor.authorKurtoğlu, Erdal
dc.date.accessioned2020-11-20T14:41:25Z
dc.date.available2020-11-20T14:41:25Z
dc.date.issued2019
dc.identifier.issn1473-0502
dc.identifier.urihttps://doi.org/10.1016/j.transci.2019.04.030
dc.identifier.urihttps://hdl.handle.net/20.500.12809/923
dc.description0000-0003-0238-2236; 0000-0001-9178-2850en_US
dc.descriptionWOS: 000484872100020en_US
dc.descriptionPubMed ID: 31320278en_US
dc.description.abstractAcquired hemophilia A, due to spontaneous autoantibody against FVIII, is a rare hemorrhagic disorder with an incidence of about 1 per million population per year. If unrecognized and untreated, it is associated with a high morbidly and mortality rate of 8-12%. Autoantibody against coagulation factor VIII neutralizes procoagulant activity. We report herein is such a rare case of acquired hemophilia in a patient with CLL.en_US
dc.item-language.isoengen_US
dc.publisherPergamon-Elsevier Science Ltden_US
dc.item-rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChronic Lymphocytic Leukemiaen_US
dc.subjectAcquired Hemophilia Aen_US
dc.subjectMalignanten_US
dc.titleAcquired hemophilia A in chronic lymphocytic leukemia: A case reporten_US
dc.item-typearticleen_US
dc.contributor.departmentMÜ, Tıp Fakültesi, Temel Tıp Bilimleri Bölümüen_US
dc.contributor.institutionauthorKarakuş, Volkan
dc.contributor.institutionauthorKaya, Egemen
dc.contributor.institutionauthorDere, Yelda
dc.identifier.doi10.1016/j.transci.2019.04.030
dc.identifier.volume58en_US
dc.identifier.issue4en_US
dc.identifier.startpage447en_US
dc.identifier.endpage448en_US
dc.relation.journalTransfusion and Apheresis Scienceen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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