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See Latest ArticlesBeta-Thalassemia in the Korean population
International Journal of Hematology, 10/12/09
Park SS et al. – Beta–Thalassemia is uncommon in the Korean population, however it must be considered in the differential diagnosis of hypochromic anemia. The molecular characterization of beta–Thalassemia is absolutely necessary for molecular diagnosis as well as any genetic epidemiological study in this region. This mutation spectrum is characteristic of the low prevalent area of beta–thalassemia, however it is quite different even from the adjacent countries, Japan or China.
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Update on the use of deferasirox in the management of iron overload
Therapeutics and Clinical Risk Management, 11/05/09
Effect of combination therapy of hydroxyurea with l-carnitine and magnesium chloride on hematologic parameters and cardiac function of patients with beta-thalassemia intermedia
European Journal of Haematology, 11/04/09
Effect of Epoetin Alfa on Survival and Cancer Treatment-Related Anemia and Fatigue in Patients Receiving Radical Radiotherapy With Curative Intent for Head and Neck Cancer
Journal of Clinical Oncology, 11/09/09
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