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A Severe [alpha] Thalassemia Case Compound Heterozygous for Hb Adana in [alpha]1 Gene and 20.5 kb Double Gene Deletion
Journal of Pediatric Hematology/Oncology, 09/10/09

Durmaz AA et al. – This case represents another example of the nondeletional mutation underlying Hb Adana, which is rarely seen in alpha 1 gene, and illustrates the distinctive phenotypes of both the deletional and nondeletional forms of hemoglobin H disease within the same family.

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Interaction of malaria with a common form of severe thalassemia in an Asian population
Proceedings of the National Academy of Sciences of the United States of America, 11/04/09 Relevance Score: 90%

Beta-Thalassemia in the Korean population
International Journal of Hematology, 10/12/09 Relevance Score: 90%

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 Relevance Score: 89%

Thalassemia Incidence and Treatment in China with Special Reference to Shenzhen City and Guangdong Province
Hemoglobin, 10/23/09 Relevance Score: 89%

Iron chelation therapy in the management of thalassemia: the Asian perspectives
International Journal of Hematology, 11/04/09 Relevance Score: 88%