dc.contributor.author | Kuskonmaz, Baris | |
dc.contributor.author | Gocer, Safak | |
dc.contributor.author | Ersoy-Ewans, Sibel | |
dc.contributor.author | Cetin Ozman, Fatma | |
dc.contributor.author | Cetin, Mualla | |
dc.date.accessioned | 2020-10-21T08:47:20Z | |
dc.date.available | 2020-10-21T08:47:20Z | |
dc.date.issued | 2007 | |
dc.identifier.issn | 1399-3046 | |
dc.identifier.uri | http://hdl.handle.net/11655/22990 | |
dc.description.abstract | haGVHD 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.iso | en | tr_TR |
dc.publisher | Wiley | tr_TR |
dc.relation.isversionof | 10.1111/j.1399-3046.2007.00786.x | |
dc.rights | info:eu-repo/semantics/openAccess | tr_TR |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
dc.subject | Hyperacute graft-vs.-host disease | tr_TR |
dc.title | Hyperacute Graft-vs.-Host Disease After Related HLA-Identical Umbilical Cord Blood Transplantation | tr_TR |
dc.type | info:eu-repo/semantics/article | tr_TR |
dc.type | info:eu-repo/semantics/publishedVersion | |
dc.relation.journal | Pediatric Transplantation | tr_TR |
dc.contributor.department | Çocuk Sağlığı ve Hastalıkları | tr_TR |
dc.identifier.volume | 11 | tr_TR |
dc.identifier.issue | 7 | tr_TR |
dc.description.index | WoS | tr_TR |
dc.funding | Yok | tr_TR |