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IRON FORTIFIED MILKS AND IRON RESERVES IN INFANCY = LES LAITS ENRICHIS EN FER ET LES RESERVES EN FER DANS L'ENFANCEKATTAMIS C; METAXOTOU MAVROMATI A; PARASCHOPOULOU PREVEDOURAKI P et al.1972; HELV. PAEDIATR. ACTA; SUISSE; DA. 1972; VOL. 27; NO 5; PP. 513-517; ABS. ALLEM.; BIBL. 12REF.Serial Issue

THE CLINICAL PHENOTYPE OF BETA AND DELTA BETA THALASSEMIAS IN GREECEKATTAMIS C; METAXOTOU MAVROMATI A; LADIS V et al.1982; EUROPEAN JOURNAL OF PEDIATRICS; ISSN 0340-6199; DEU; DA. 1982; VOL. 139; NO 2; PP. 135-138; BIBL. 12 REF.Article

OBSERVATIONS CLINIQUES ET HEMATOLOGIQUES CHEZ DES ENFANTS HERITANT DE DEUX TYPES DE THALASSEMIE: BETA -THALASSEMIE DE TYPE A TAUX ELEVE DE A2 ET TYPE A TAUX ELEVE DE F OU DELTA-BETA -THALASSEMIEKATTAMIS C; METAXOTOU MAVROMATI A; KARAMBOULA K et al.1975; ; S.L.; DA. 1975; PP. 1-13; DE L'ANGL.: BRITISH JOURNAL OF HAEMATOLOGY, 1973; 25, NO 3, 375-384, 1 FIG., 5 TABLMiscellaneous

THE TRIPLICATED ALPHA GENE LOCUS AND BETA THALASSAEMIAKANAVAKIS E; METAXOTOU MAVROMATI A; KATTAMIS C et al.1983; BRITISH JOURNAL OF HAEMATOLOGY; ISSN 0007-1048; GBR; DA. 1983; VOL. 54; NO 2; PP. 201-207; BIBL. 17 REF.Article

The molecular basis of hbH disease in GreeceTZOTZOS, S; KANAVAKIS, E; METAXOTOU-MAVROMATI, A et al.British journal of haematology. 1986, Vol 63, Num 2, pp 263-271, issn 0007-1048Article

Hematologic phenotype of the mutations IVS1-n6 (T→C), IVS1-n110 (G→A), and CD39 (C→T) in carriers of β-thalassemia in GreeceSTEFANIS, L; KANABAKIS, E; TRAEGER-SYNODINOS, J et al.Pediatric hematology and oncology. 1994, Vol 11, Num 5, pp 509-517, issn 0888-0018Article

Molecular characterization of homozygous (high HbA2) β-thalassemia intermedia in GreeceKANAVAKIS, E; TRAEGER-SYNODINOS, J; TZETIS, M et al.Pediatric hematology and oncology. 1995, Vol 12, Num 1, pp 37-45, issn 0888-0018Article

HAEMOGLOBIN BART'S HYDROPS SYNDROME IN GREECEKATTAMIS C; METAXOTOU MAVROMATI A; TSIARTIA E et al.1980; BRIT. MED. J.; GBR; DA. 1980; VOL. 281; NO 6235; PP. 268-270; BIBL. 14 REF.Article

The Corfu δβ thallassaemia mutation in Greece : haematological phenotype and prevalenceTRAEGER-SYNODINOS, J; TZETIS, M; KANAVAKIS, E et al.British journal of haematology. 1991, Vol 79, Num 2, pp 302-305, issn 0007-1048Article

Clinical, haematological, and genetic studies of type 2 normal Hb A2 β thalassaemiaMETAXOTOU-MAVROMATI, a; KATTAMIS, C; MATATHIA, L et al.Journal of medical genetics. 1988, Vol 25, Num 3, pp 195-199, issn 0022-2593Article

The triplicated α-globin gene locus in β-thalassaemia heterozygotes : clinical, haematological, biosynthetic and molecular studiesTRAEGER-SYNODINOS, J; KANAVAKIS, E; VRETTOU, C et al.British journal of haematology. 1996, Vol 95, Num 3, pp 467-471, issn 0007-1048Article

A new δ chain variant hemoglobin A2-Corfu of α2δ2 116 Arg → Cys (G18), detected by δ-globin gene analysis in a Greek familyLOUDIANOS, G; MURRU, S; KANAVAKIS, E et al.Human genetics. 1991, Vol 87, Num 2, pp 237-238, issn 0340-6717Article

The interaction of α° thalassaemia with Hb Icaria : three unusual cases of haemoglobinopathy HKANAVAKIS, E; TRAEGER-SYNODINOS, J; PAPASOTIRIOU, I et al.British journal of haematology. 1996, Vol 92, Num 2, pp 332-335, issn 0007-1048Article

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