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Paul Harmatz

Children's Hospital Los Angeles

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Deferasirox (Exjade ® ) Monotherapy Significantly Reduces Cardiac Iron Burden in Chronically Transfused β-Thalassemia Patients: An MRI T2* Study

2008 Blood
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Prolonged QTc in Sickle Cell Disease: A Potential Risk Factor for Early Death?

2008 Blood
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Comparison of LIC Obtained from Biopsy, BLS and R 2 -MRI in Iron Overloaded Patients with β-Thalassemia, Treated with Deferasirox (Exjade®, ICL670).

2005 Blood
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