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Correlation of liver iron concentration determined by R2 magnetic resonance imaging with serum ferritin in patients with thalassemia intermedia
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Elevated liver iron concentration is a marker of increased morbidity in patients with beta thalassemia intermedia
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Musallam K.M., Cappellini M.D., Wood J.C., et al. Elevated liver iron concentration is a marker of increased morbidity in patients with beta thalassemia intermedia. Haematologica 2011, 96:1605-1612.
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Deferasirox reduces iron overload significantly in nontransfusion-dependent thalassemia: 1-year results from a prospective, randomized, double-blind, placebo-controlled study
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Taher A.T., Porter J., Viprakasit V., et al. Deferasirox reduces iron overload significantly in nontransfusion-dependent thalassemia: 1-year results from a prospective, randomized, double-blind, placebo-controlled study. Blood 2012, 120:970-977.
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Noninvasive measurement and imaging of liver iron concentrations using proton magnetic resonance
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MRI R2 and R2* mapping accurately estimates hepatic iron concentration in transfusion-dependent thalassemia and sickle cell disease patients
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Wood J.C., Enriquez C., Ghugre N., et al. MRI R2 and R2* mapping accurately estimates hepatic iron concentration in transfusion-dependent thalassemia and sickle cell disease patients. Blood 2005, 106:1460-1465.
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Overview on practices in thalassemia intermedia management aiming for lowering complication rates across a region of endemicity: the OPTIMAL CARE study
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Taher A.T., Musallam K.M., Karimi M., et al. Overview on practices in thalassemia intermedia management aiming for lowering complication rates across a region of endemicity: the OPTIMAL CARE study. Blood 2010, 115:1886-1892.
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Taher, A.T.1
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Iron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseases
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Kell D.B. Iron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseases. BMC Med. Genomics 2009, 2:2.
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Cerebral infarction in beta-thalassemia intermedia: breaking the silence
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Musallam K.M., Taher A.T., Karimi M., Rachmilewitz E.A. Cerebral infarction in beta-thalassemia intermedia: breaking the silence. Thromb. Res. 2012, 130:695-702.
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Thrombosis in thalassemia: why are we so concerned?
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Musallam K.M., Taher A.T. Thrombosis in thalassemia: why are we so concerned?. Hemoglobin 2011, 35:503-510.
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Longitudinal changes in serum ferritin levels correlate with measures of hepatic stiffness in transfusion-independent patients with beta-thalassemia intermedia
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Musallam K.M., Motta I., Salvatori M., et al. Longitudinal changes in serum ferritin levels correlate with measures of hepatic stiffness in transfusion-independent patients with beta-thalassemia intermedia. Blood Cells Mol. Dis. 2012, 49:136-139.
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Serum ferritin levels and endocrinopathy in medically treated patients with beta thalassemia major
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Bone disease and skeletal complications in patients with beta thalassemia major
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Haidar R., Musallam K.M., Taher A.T. Bone disease and skeletal complications in patients with beta thalassemia major. Bone 2011, 48:425-432.
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The role of ineffective erythropoiesis in non-transfusion-dependent thalassemia
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