Phenotypic and molecular diversity of haemoglobin H disease: a Greek experienceEmmanuel Kanavakis, Joanne Traeger‐Synodinos, Christos Kattamis 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
Distinct Phenotypic Expression Associated with a New Hyperunstable Alpha Globin Variant (Hb Heraklion, α1cd37(C2)Pro>0): Comparison to Other α-Thalassemic HemoglobinopathiesJoanne Traeger‐Synodinos, Emmanuel Kanavakis, Ioannis Papassotiriou et al.|Blood Cells Molecules and Diseases|2000Cited by 34
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, Joanne Traeger‐Synodinos et al.|Blood Cells Molecules and Diseases|2004Cited by 34
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 25