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dc.contributor.authorKuskonmaz, Baris
dc.contributor.authorGocer, Safak
dc.contributor.authorErsoy-Ewans, Sibel
dc.contributor.authorCetin Ozman, Fatma
dc.contributor.authorCetin, Mualla
dc.date.accessioned2020-10-21T08:47:20Z
dc.date.available2020-10-21T08:47:20Z
dc.date.issued2007
dc.identifier.issn1399-3046
dc.identifier.urihttp://hdl.handle.net/11655/22990
dc.description.abstracthaGVHD has been described following bone marrow and peripheral blood stem cell transplantation and in a single case who received unrelated HLA mismatched CB. An unusual case of haGVHD following HLA 6/6-matched sibling CBT in a child with AML is presented. The development of haGVHD in a fully matched CBT and without precipitating factors may suggest the role of still undefined and perhaps individual contributory factors.tr_TR
dc.language.isoentr_TR
dc.publisherWileytr_TR
dc.relation.isversionof10.1111/j.1399-3046.2007.00786.x
dc.rightsinfo:eu-repo/semantics/openAccesstr_TR
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectHyperacute graft-vs.-host diseasetr_TR
dc.titleHyperacute Graft-vs.-Host Disease After Related HLA-Identical Umbilical Cord Blood Transplantationtr_TR
dc.typeinfo:eu-repo/semantics/articletr_TR
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalPediatric Transplantationtr_TR
dc.contributor.departmentÇocuk Sağlığı ve Hastalıklarıtr_TR
dc.identifier.volume11tr_TR
dc.identifier.issue7tr_TR
dc.description.indexWoStr_TR
dc.fundingYoktr_TR


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