Progression of liver fibrosis can be controlled by adequate chelation in transfusion-dependent thalassemia (TDT)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
http://link.springer.com/article/10.1007/s00277-017-3120-9/fulltext.html
Reference31 articles.
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2. Coates TD, Carson S, Wood JC et al (2016) Management of iron overload in hemoglobinopathies: what is the appropriate target iron level? Ann N Y Acad Sci 1368:95–106
3. Kwiatkowski JL (2016) Current recommendations for chelation for transfusion-dependent thalassemia. Ann N Y Acad Sci 1368:107–114
4. Oikonomidou PR, Casu C, Rivella S (2016) New strategies to target iron metabolism for the treatment of beta thalassemia. Ann N Y Acad Sci 1368:162–168
5. Ghavamzadeh A, Mirzania M, Kamalian N et al (2015) Hepatic iron overload and fibrosis in patients with beta thalassemia major after hematopoietic stem cell transplantation: a pilot study. Int J Hematol Oncol Stem Cell Res 9:55–59
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