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Allogeneic bone marrow transplantation for children with histiocytic disorders: use of TBI and omission of etoposide in the conditioning regimen

✍ Scribed by Hale, G A; Bowman, L C; Woodard, J P; Cunningham, J M; Benaim, E; Horwitz, E M; Heslop, H E; Krance, R A; Leung, W; Shearer, P D


Book ID
110013741
Publisher
Nature Publishing Group
Year
2003
Tongue
English
Weight
120 KB
Volume
31
Category
Article
ISSN
0007-1188

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## Abstract Myelodisplastic syndromes (MDS) in childhood deserve a negative prognosis even though disease‐free survival has been obtained in 20% of cases by using aggressive chemotherapy. We describe three children with refractory anemia with excess of blasts in transformation (RAEB‐T) who underwen