Long-term survival of beta thalassemia major patients treated with hematopoietic stem cell transplantation compared with survival with conventional treatment-Reference-Cited by-同舟云学术

Long-term survival of beta thalassemia major patients treated with hematopoietic stem cell transplantation compared with survival with conventional treatment

Published:2017-09-25 Issue:12 Volume:92 Page:1303-1310
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am J Hematol

Author:

Caocci Giovanni¹²^ORCID,Orofino Maria Grazia¹,Vacca Adriana¹,Piroddi Antonio¹,Piras Eugenia¹,Addari Maria Carmen¹,Caria Rossella¹,Pilia Maria Paola³,Origa Raffaella³,Moi Paolo²³,La Nasa Giorgio¹²

Affiliation:

1. Bone Marrow Transplant Center, Hospital Binaghi and Microcitemico; Cagliari Italy

2. Department of Medical Sciences and Public Health; University of Cagliari; Cagliari Italy

3. Pediatric Clinic, Thalassemias and Rare Diseases; Pediatric Hospital “Microcitemico A. Cao”; Cagliari Italy

Publisher

Wiley

Subject

Hematology

Reference31 articles.

1. Marrow transplantation in patients with thalassemia responsive to iron chelation therapy;Lucarelli;N Engl J Med.,1993

2. Allogeneic hematopoietic stem cell transplantation in thalassemia major: results of a reduced-toxicity conditioning regimen based on the use of treosulfan;Bernardo;Blood.,2012

3. Improved clinical outcomes of high risk beta thalassemia major patients undergoing a HLA matched related allogeneic stem cell transplant with a treosulfan based conditioning regimen and peripheral blood stem cell grafts;Mathews;PLoS One.,2013

4. Long-term health-related quality of life evaluated more than 20 years after hematopoietic stem cell transplantation for thalassemia;La Nasa;Blood.,2013

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