Allogeneic Stem Cell Transplantation in Congenital Hemoglobinopathies Using a Tailored Busulfan-Based Conditioning Regimen: Single-Center Experience. [electronic resource]
Producer: 20180212Description: 1043-1048 p. digitalISSN:- 1523-6536
- Adolescent
- Adult
- Anemia, Sickle Cell -- mortality
- Busulfan -- pharmacokinetics
- Child
- Child, Preschool
- Chimerism
- Graft vs Host Disease -- etiology
- Hematopoietic Stem Cell Transplantation -- adverse effects
- Hemoglobinopathies -- genetics
- Humans
- Infant
- Survival Analysis
- Transplantation Conditioning -- methods
- Transplantation, Homologous
- Vascular Diseases -- etiology
- Young Adult
- beta-Thalassemia -- mortality
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Publication Type: Journal Article
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