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dc.contributor.authorTavil, Betül
dc.contributor.authorKazık, Mediha
dc.contributor.authorKuskonmaz, Baris
dc.contributor.authorCetin, Mualla
dc.contributor.authorUckan, Duygu
dc.date.accessioned2020-10-21T07:15:58Z
dc.date.available2020-10-21T07:15:58Z
dc.date.issued2006
dc.identifier.issn1476-5365
dc.identifier.urihttp://hdl.handle.net/11655/22983
dc.description.abstractStable mixed chimerism is a common event in children with thalassemia major who have undergone bone marrow transplantation (BMT). However, persistence of unstable mixed chimerism in these children is associated with a greater risk of rejection and/or relapse of the disease. Andreani et al.1 has reported that rejection and/or disease recurrence occurs in approximately one third of patients with early mixed chimerism in thalassemia major.
dc.publisherNature
dc.relation.isversionof10.1038/sj.bmt.1705432
dc.rightsinfo:eu-repo/semantics/openAccesstr_TR
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectGrart versus thalassemiatr_TR
dc.titleA Prompt Graft-Versus-Thalassemia Effect upon Withdrawal of CyclosporineA in A Child Who Received Allogeneic Peripheral Blood Stem Cell Transplantationtr_TR
dc.typeinfo:eu-repo/semantics/articletr_TR
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.contributor.departmentÇocuk Sağlığı ve Hastalıklarıtr_TR
dc.description.indexWoStr_TR
dc.fundingYoktr_TR


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