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Iron chelating in thalassaemia with left ventricular dysfunction
  1. G Cagirci,
  2. O Tufekcioglu,
  3. M Yetim

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β thalassaemia major is the most common form of hereditary anaemia in the Mediterranean region; the affected individual develops severe anaemia requiring multiple blood transfusions. The clinical course is modified significantly by transfusion therapy; however, the main complication of …

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