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Darbepoetin alfa for the treatment of anaemia in alpha- or beta- thalassaemia intermedia syndromes.

  • Read more about Darbepoetin alfa for the treatment of anaemia in alpha- or beta- thalassaemia intermedia syndromes.

A pilot study of the short-term use of simvastatin in sickle cell disease: effects on markers of vascular dysfunction.

  • Read more about A pilot study of the short-term use of simvastatin in sickle cell disease: effects on markers of vascular dysfunction.

Renal dysfunction in patients with thalassaemia.

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Red cell alloimmunization in a diverse population of transfused patients with thalassaemia.

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The effects of hydroxycarbamide and magnesium on haemoglobin SC disease: results of the multi-centre CHAMPS trial

  • Read more about The effects of hydroxycarbamide and magnesium on haemoglobin SC disease: results of the multi-centre CHAMPS trial

Efficacy and safety of deferasirox doses of >30 mg/kg per d in patients with transfusion-dependent anaemia and iron overload.

  • Read more about Efficacy and safety of deferasirox doses of >30 mg/kg per d in patients with transfusion-dependent anaemia and iron overload.

Differences in the prevalence of growth, endocrine and vitamin D abnormalities among the various thalassaemia syndromes in North America.

  • Read more about Differences in the prevalence of growth, endocrine and vitamin D abnormalities among the various thalassaemia syndromes in North America.

Advances in clinical research in sickle cell disease.

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Mixed haematopoietic chimerism for sickle cell disease prevents intravascular haemolysis.

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Phase Ib clinical trial of starch-conjugated deferoxamine (40SD02): a novel long-acting iron chelator.

  • Read more about Phase Ib clinical trial of starch-conjugated deferoxamine (40SD02): a novel long-acting iron chelator.

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