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dc.contributor.authorElli, M
dc.contributor.authorPinarli, FG
dc.contributor.authorDagdemir, A
dc.contributor.authorDabak, N
dc.contributor.authorFisgin, T
dc.contributor.authorSelcuk, MB
dc.contributor.authorAcar, S
dc.date.accessioned2020-06-21T15:29:08Z
dc.date.available2020-06-21T15:29:08Z
dc.date.issued2006
dc.identifier.issn0888-0018
dc.identifier.urihttps://doi.org/10.1080/08880010500457749
dc.identifier.urihttps://hdl.handle.net/20.500.12712/20711
dc.descriptionPinarli, Faruk Guclu/0000-0002-3241-2478en_US
dc.descriptionWOS: 000236144100004en_US
dc.descriptionPubMed: 16651239en_US
dc.description.abstractAcquired von Willebrand syndronze is a rare bleeding disorder with clinical and laboratory features closely resembling to hereditary von Willebrand disease. The syndrome may accompany various conditions, including malignant disorders, most often with Wilms tumor and adrenal cell carcinoma. In this report, the authors present a patient with AvWS in association with Ewing sarcoma for the first time in the literature. The abnormal bleeding tendency was successfully treated with fresh frozen plasma and did not recur after the first two courses of chemotherapy with clinical improvement.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francis Incen_US
dc.relation.isversionof10.1080/08880010500457749en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectacquired von Willebrand syndromeen_US
dc.subjectEwing sarcomaen_US
dc.titleAcquired von Willebrand syndrome in a patient with Ewing sarcomaen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume23en_US
dc.identifier.issue2en_US
dc.identifier.startpage111en_US
dc.identifier.endpage114en_US
dc.relation.journalPediatric Hematology and Oncologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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