Hemoglobin disorders in the developing world: A perspective from Sri Lanka†
	Hepcidin is suppressed by erythropoiesis in hemoglobin E b-thalassemia and b-thalassemia trait
	Alpha Thalassaemia and extended alpha globin genes in Sri Lanka
	Methemoglobinemia and ascorbate deficiency in hemoglobin E β thalassemia:metabolic and clinical implications
	The Thal-index with the BTT prediction.exe to discriminate β-thalassaemia traits from other microcytic anaemias
	A Functional Element Necessary for Fetal Hemoglobin Silencing
	Adaptation to anemia in hemoglobin E-β thalassemia
	Emerging insights in the management
	Interaction of malaria with a common form of severe thalassemia.pdf
	Research articles to be collected.pdf

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