Magnetic resonance imaging in the evaluation of iron overload in patients with beta thalassaemia and sickle cell diseaseErsi Voskaridou, Dimitris Loukopoulos, Maroussa Douskou et al.|British Journal of Haematology|2004Cited by 148
Phenotypic and molecular diversity of haemoglobin H disease: a Greek experienceEmmanuel Kanavakis, Joanne Traeger‐Synodinos, Ioannis Papassotiriou et al.|British Journal of Haematology|2000Cited by 102
Erythroid bone marrow activity and red cell hemoglobinization in iron sufficient beta-thalassemia heterozygotes as reflected by soluble transferrin receptor and reticulocyte hemoglobin in content. Correlation with genotypes and Hb A(2) levels.Christophille Skarmoutsou, Emmanuel Kanavakis, Ioannis Papassotiriou et al.|PubMed|2003Cited by 40
Deferiprone as an oral iron chelator in sickle cell diseaseErsi Voskaridou, Dimitris Loukopoulos, Maroussa Douskou et al.|Annals of Hematology|2005Cited by 36
A rare example that coinheritance of a severe form of β-thalassemia and α-thalassemia interact in a “synergistic” manner to balance the phenotype of classic thalassemic syndromesEmmanuel Kanavakis, Ioannis Papassotiriou, Theodora Liakopoulou et al.|Blood Cells Molecules and Diseases|2004Cited by 34