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Clinical and genetic ancestry profile of a large multi-centre sickle cell disease cohort in Brazil.

  • Read more about Clinical and genetic ancestry profile of a large multi-centre sickle cell disease cohort in Brazil.

Simvastatin reduces vaso-occlusive pain in sickle cell anaemia: a pilot efficacy trial.

  • Read more about Simvastatin reduces vaso-occlusive pain in sickle cell anaemia: a pilot efficacy trial.

Dysregulated arginine metabolism and cardiopulmonary dysfunction in patients with thalassaemia.

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A pilot randomized trial of red blood cell transfusion for acute treatment of vaso-occlusive pain episodes in sickle cell anaemia.

  • Read more about A pilot randomized trial of red blood cell transfusion for acute treatment of vaso-occlusive pain episodes in sickle cell anaemia.

Mechanisms of plasma non-transferrin bound iron generation: insights from comparing transfused diamond blackfan anaemia with sickle cell and thalassaemia patients.

  • Read more about Mechanisms of plasma non-transferrin bound iron generation: insights from comparing transfused diamond blackfan anaemia with sickle cell and thalassaemia patients.

Validation and reliability of a disease-specific quality of life measure (the TranQol) in adults and children with thalassaemia major.

  • Read more about Validation and reliability of a disease-specific quality of life measure (the TranQol) in adults and children with thalassaemia major.

Pain in thalassaemia: the effects of age on pain frequency and severity.

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Increased leucocyte apoptosis in transfused ß-thalassaemia patients.

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Pulmonary function in thalassaemia major and its correlation with body iron stores.

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Long-term safety and efficacy of deferasirox (Exjade) for up to 5 years in transfusional iron-overloaded patients with sickle cell disease.

  • Read more about Long-term safety and efficacy of deferasirox (Exjade) for up to 5 years in transfusional iron-overloaded patients with sickle cell disease.

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