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17 - Therapeutic decision making in BMT/SCT for hemoglobinopathies

Published online by Cambridge University Press:  31 July 2009

Reinhold Munker ,
Hillard M. Lazarus  and
Kerry Atkinson
By
Shalini Shenoy
Reinhold Munker
Affiliation:
Louisiana State University
Hillard M. Lazarus
Affiliation:
University Hospitals Case Medical Center
Kerry Atkinson
Affiliation:
University of Queensland
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Chapter
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The BMT Data Book , pp. 215 - 226
Publisher: Cambridge University Press
Print publication year: 2009

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References

Gaziev, J, Lucarelli, G. 2003. Stem cell transplantation for hemoglobinopathies. Curr Op Pediatr 15: 24–31.CrossRefGoogle ScholarPubMed
Jacobsohn, DA, Duerst, R, Tse, W, et al. 2004. Reduced intensity haematopoietic stem-cell transplantation for treatment of non-malignant diseases in childrenLancet 364: 156–62.CrossRefGoogle ScholarPubMed
Nasa, G, Caocci, G, Argiolu, F, et al. 2005 Unrelated donor stem cell transplantation in adult patients with thalassemia. Bone Marr Transpl 36: 971–75.CrossRefGoogle ScholarPubMed
Locatelli, F, Rocha, V, Reed, W, et al. 2003. Related umbilical cord transplantation in patients with thalassemia. Blood 101: 2137–43.CrossRefGoogle ScholarPubMed
Olivieri, NF, Nathan, DG, MacMillan, JH, et al. 1994. Survival in medically treated people with homozygous beta-thalassemia. N Engl J Med 331: 574–78.CrossRefGoogle ScholarPubMed
Panepinto, JA, Walters, MC, Carreras, J, et al. 2007. Matched-related donor transplantation for sickle cell disease: report from the Center for International Blood and Marrow Transplant Research. Br J Haematol 137: 479–85.CrossRefGoogle Scholar
Powars, DR, Chan, LS, Hiti, A, et al. 2005 Outcome of sickle cell anemia. A 4 decade observational study of 1056 patients. Medicine 84: 363–76.CrossRefGoogle ScholarPubMed
Shenoy, S, Grossman, WJ, di Persio, J, et al. 2005. A novel reduced-intensity stem cell transplant regimen for non-malignant disordersBone Marr Transpl 35: 345–52.CrossRefGoogle Scholar
Sodani, P, Gaziev, D, Polchi, P, et al. 2004. New approach for bone marrow transplantation in patients with class 3 thalassemia aged younger than 17 years. Blood 104: 1201–03.CrossRefGoogle ScholarPubMed
Walters, MC. Stem cell therapy for sickle cell disease: transplantation and gene therapy. 2005Hematology (Educational Book of American Society of Hematology) p. 66–73.

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