Is the Benefit–Risk Ratio for Patients with Transfusion-Dependent Thalassemia Treated by Unrelated Cord Blood Transplantation Favorable?

Transfusion-dependent thalassemia (TDT) is an inherited disorder characterized by absent or defective production of α- or β-hemoglobin chains. If untreated, the disease invariably culminates in death in early infancy due to cardiac failure or overwhelming infection. Although there is clear evidence...

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Detalles Bibliográficos
Autor principal: Jaing, Tang-Her
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713438/
https://www.ncbi.nlm.nih.gov/pubmed/29156642
http://dx.doi.org/10.3390/ijms18112472

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713438/
https://www.ncbi.nlm.nih.gov/pubmed/29156642
http://dx.doi.org/10.3390/ijms18112472

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