A. Metaxotou-Mavrommati

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Molecular Studies of β-Thalassemia Heterozygotes with Raised Hb F Levels

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2000 .

Molecular, haematological and clinical studies of the −101 C → T substitution of the β‐globin gene promoter in 25 β‐thalassaemia intermedia patients and 45 heterozygotes

J. Traeger-Synodinos, M. Tzetis, E. Kanavakis, 1999, British journal of haematology.

Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2000, British journal of haematology.

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 syndromes

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2004 .

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.

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2003, Haematologica.

Clinical Response and Adverse Events in Young Patients with Sickle Cell Disease Treated with Hydroxyurea

E. Kanavakis, A. Kattamis, C. Kattamis, 2004, Pediatric hematology and oncology.

A Rare Thalassemic Syndrome Caused by Interaction of Hb Adana [α59(E8)Gly→Asp] with an α+-Thalassemia Deletion: Clinical Aspects in Two Cases

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2008, Hemoglobin.

CORRELATION OF CLINICAL PHENOTYPE TO GENOTYPE IN HAEMOGLOBIN H DISEASE

E. Kanavakis, S. Tzotzos, C. Kattamis, 1988, The Lancet.

Molecular studies of beta-thalassemia heterozygotes with raised Hb F levels.

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2000, Hemoglobin.

Interaction of an α+-Thalassemia Deletion with Either a Highly Unstable α-Globin Variant (α2, Codon 59, GGC→GAC) or a Nondeletional α-Thalassemia Mutation (AATAA→AATAAG): Comparison of Phenotypes Illustrating “Dominant” α-Thalassemia

I. Papassotiriou, J. Traeger-Synodinos, E. Kanavakis, 1999 .

Distinct Phenotypic Expression Associated with a New Hyperunstable Alpha Globin Variant (Hb Heraklion, α1cd37(C2)Pro>0): Comparison to Other α-Thalassemic Hemoglobinopathies

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2000 .

Interaction of an alpha(+)-thalassemia deletion with either a highly unstable alpha-globin variant (alpha2, codon 59, GGC-->GAC) or a nondeletional alpha-thalassemia mutation (AATAAA-->AATAAG): comparison of phenotypes illustrating "dominant" alpha-thalassemia.

I. Papassotiriou, J. Traeger-Synodinos, E. Kanavakis, 1999, Hemoglobin.

A rare example that coinheritance of a severe form of beta-thalassemia and alpha-thalassemia interact in a "synergistic" manner to balance the phenotype of classic thalassemic syndromes.

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2004, Blood Cells, Molecules & Diseases.

Further Identification of The Hyperunstable α-Globin Chain Variant Hb Heraklion [codons 36/37 (–CCC); Pro→0 (α1)] in Greek Cases With Co-Inherited α+-Thalassemia Mutations

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2008, Hemoglobin.

Association of Mild and Severely Unstable α Chain Variants: The First Observation of a Compound Heterozygote with Hb Setif [α94(G1)Asp→Tyr (α2)] and Hb Agrinio [α29(B10)Leu→Pro (α2)] in a Greek Family

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2008, Hemoglobin.

ASSOCIATION OF MILD AND SEVERELY UNSTABLE a CHAIN VARIANTS : THE FIRST OBSERVATION OF A COMPOUND

I. Papassotiriou, E. Kanavakis, J. Traeger-Synodinos, 2008 .