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dc.contributor.authorUnal, Sule
dc.contributor.authorRusso, R
dc.contributor.authorKuskonmaz, Baris
dc.contributor.authorCetin, Mualla
dc.contributor.authorSayli, T
dc.contributor.authorTavil, Betül
dc.contributor.authorLangella, C
dc.contributor.authorIolascon, A
dc.contributor.authorUckan Cetinkaya, Duygu
dc.date.accessioned2020-10-21T10:25:45Z
dc.date.available2020-10-21T10:25:45Z
dc.date.issued2014
dc.identifier.issn1399-3046
dc.identifier.urihttp://hdl.handle.net/11655/22992
dc.identifier.urihttps://doi.org/10.1111/petr.12254
dc.description.abstractAbstract CDA are a group of inherited, rare diseases that are characterized by dyserythropoiesis and ineffective erythropoiesis associated with transfusion dependency in approximately 10% of cases. For these latter patients, the only curative treatment is HSCT. There are very limited data on HSCT experience in this rare disease. Herein, we report a five-yr six-month-old girl with compound heterozygous mutations in SEC23B gene, who was diagnosed to have CDA type II and underwent successful HSCT from her matched sibling donor.tr_TR
dc.language.isoentr_TR
dc.publisherWILEYtr_TR
dc.relation.isversionof10.1111/petr.12254tr_TR
dc.rightsinfo:eu-repo/semantics/openAccesstr_TR
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.rights.urihttps://doi.org/10.1111/petr.12254
dc.subjectWith congenital dyserythropoietic anemiatr_TR
dc.subjectTransplantationtr_TR
dc.titleSuccessful Hematopoietic Stem Cell Transplantation in a Patient with Congenital Dyserythropoietic Anemia Type II.tr_TR
dc.typeinfo:eu-repo/semantics/articletr_TR
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalPediatric Transplantationtr_TR
dc.contributor.departmentAcil Tıptr_TR
dc.identifier.volume18tr_TR
dc.identifier.issue4tr_TR
dc.identifier.startpageE130tr_TR
dc.identifier.endpageE133tr_TR
dc.description.indexWoStr_TR
dc.fundingYoktr_TR


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