Abstract
Sickle cell disease (SCD) is a group of inherited hemoglobinopathies, associated with chronic hemolytic anemia, recurrent vaso-occlusive pain episodes, and progressive organ damage. To date, allogeneic hematopoietic stem cell transplantation (HSCT) is the only established curative treatment for patients with SCD. Historically, HSCT was used in children with severe SCD and
| Original language | English |
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| Qualification | Doctor of Philosophy |
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| Award date | 9 Oct 2025 |
| Print ISBNs | 9789465224978 |
| Publication status | Published - 2025 |
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