Clinical monitoring and management of complications related to chelation therapy in patients with β-thalassemia.

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Analysis of protein profiling studies of β-thalassemia/Hb E disease.Deferasirox: Over a Decade of Experience in Thalassemia

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Clinical monitoring and management of complications related to chelation therapy in patients with β-thalassemia.

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2015 nî lūn-bûn

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Clinical monitoring and manage ...... n patients with β-thalassemia.

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Clinical monitoring and manage ...... n patients with β-thalassemia.

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Clinical monitoring and manage ...... n patients with β-thalassemia.

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Clinical monitoring and manage ...... n patients with β-thalassemia.

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Ali T Taher

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Antoine N Saliba

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Fuad El Rassi

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P2860

Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice

Lack of progressive hepatic fibrosis during long-term therapy with deferiprone in subjects with transfusion-dependent beta-thalassemia

Beta-thalassemia

Long-term safety and effectiveness of iron-chelation therapy with deferiprone for thalassemia major

A randomized, placebo-controlled, double-blind trial of the effect of combined therapy with deferoxamine and deferiprone on myocardial iron in thalassemia major using cardiovascular magnetic resonance

Acute renal insufficiency occurring during intravenous desferrioxamine therapy

Vision and hearing during deferoxamine therapy

Long-term assessment of efficacy and safety of L1, an oral iron chelator, in transfusion dependent thalassaemia: Indian trial.

Safety of oral iron chelator deferiprone in young thalassaemics.

Long-term response to deferiprone therapy in Asian Indians.

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151-168

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scholarly article

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10.1586/17474086.2016.1126176

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2015-11-27T00:00:00Z

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chelation therapy

Clinical monitoring and management of complications related to chelation therapy in patients with β-thalassemia.

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P2860

P2860

Clinical monitoring and management of complications related to chelation therapy in patients with β-thalassemia.

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