Hematopoietic stem cell transplantation for Shwachman-Diamond syndrome: experience of the French neutropenia registry
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thalassemia is an autosomal recessive disorder associated with defective synthesis of the α- or β-chain of hemoglobin. for β-thalassemia major patients, therapeutic options are either monthly red cell transfusions and chelation therapy or allogeneic stem cell transplant. stem cell transplant is the only curative approach and success is inversely correlated with the degree of iron overload and h...
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ژورنال
عنوان ژورنال: Bone Marrow Transplantation
سال: 2005
ISSN: 0268-3369,1476-5365
DOI: 10.1038/sj.bmt.1705141