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GENERALIZED SEBORRHOEIC DERMATITIS. CLINICAL AND THERAPEUTIC DATA OF 25 PATIENTS = DERMATITE SEBORRHEIQUE GENERALISEE. DONNEES CLINIQUES ET THERAPEUTIQUES SUR 25 MALADESMESSARITAKIS J; KATTAMIS C; KARABULA C et al.1975; ARCH. DIS. CHILDH.; G.B.; DA. 1975; VOL. 50; NO 11; PP. 871-874; BIBL. 28 REF.Article

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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 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

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

NEONATAL HEPATITIS ASSOCIATED WITH AUSTRALIA ANTIGEN (AU-1) = HEPATITE NEONATALE ASSOCIEE A L'ANTIGENE AUSTRALIA (AU-1)KATTAMIS C; DEMETRIOU D; KARAMBULA K et al.1973; ARCH. DIS. CHILDH.; G.B.; DA. 1973; VOL. 48; NO 2; PP. 133-136; BIBL. 11REF.Serial Issue

GENETIC AND MOLECULAR DIVERSITY IN NONDELETION HB H DISEASEHIGGS DR; PRESSLEY L; ALDRIDGE B et al.1981; PROC. NATL. ACAD. SCI. U.S.A., BIOL. SCI.; ISSN 0273-1134; USA; DA. 1981; VOL. 78; NO 9; PP. 5833-5837; BIBL. 22 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 DIRECT COOMBS TEST IN JUVENILE RHEUMATOID ARTHRITISMATSANIOTIS N; KATTAMIS C; PAIDOUSIS M et al.1974; HELV. PAEDIATR. ACTA; SUISSE; DA. 1974; VOL. 29; NO 6; PP. 609-613; ABS. ALLEM.; BIBL. 9REF.Article

Tissue oxygenation in patients with hemoglobinopathy HPAPASSOTIRIOU, I; KANAVAKIS, E; STAMOULAKATOU, A et al.Pediatric hematology and oncology. 1997, Vol 14, Num 4, pp 323-334, issn 0888-0018Article

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

Hepatitis in children hospitalized with measles : The experience acquired after a Greek epidemicPAPADOPOULOU, A. L; THEODORIDOU, M; SYRIOPOULOU, V et al.Journal of paediatrics and child health. 2000, Vol 37, Num 1, pp 55-57, issn 1034-4810Article

Prenatal diagnosis of the thalassaemia syndromes by rapid DNA analytical methodsKANAVAKIS, E; TRAEGER-SYNODINOS, J; VRETTOU, C et al.Molecular human reproduction. 1997, Vol 3, Num 6, pp 523-528, issn 1360-9947Article

Evaluation clinique de différentes méthodes préventives des réactions transfusionnelles non hémolytiques = Clinical evaluation of different prevention methods of non-hemolytic transfusion reactionsSPANOS, T; LADIS, V; KARAGEORGA, M et al.Transfusion clinique et biologique (Paris). 1995, Vol 2, Num 5, pp 373-380, issn 1246-7820Article

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

Cystic fibrosis mutation screening in CBAVD patients and men with obstructive azoospermia or severe oligozoospermiaKANAVAKIS, E; TZETIS, M; ANTONIADI, T et al.Molecular human reproduction. 1998, Vol 4, Num 4, pp 333-337, issn 1360-9947Article

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

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 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

Activity and function of hybrid ribonulease in cells of acute and chronic myelogenous leukemiaPAPAPHILIS, A. D; KAMPER, E. F; PANGALIS, G. A et al.Experimental cell biology. 1987, Vol 55, Num 3, pp 127-135, issn 0304-3568Article

Red cell alloantibodies in patients with thalassemiaSPANOS, T; KARAGEORGA, M; LADIS, V et al.Vox sanguinis (Basel. 1956). 1990, Vol 58, Num 1, pp 50-55, issn 0042-9007Article

Activity of ribonuclease H in cells of chronic B-lymphocytic leukaemia: correlation with clinical stagePAPAPHILIS, A. D; KAMPER, E. F; KATTAMIS, C et al.British journal of haematology. 1988, Vol 70, Num 3, pp 301-306, issn 0007-1048Article

Efficacy and tolerability of formoterol turbuhaler® in childrenVON BERG, A; SAXONI, F. Papageorgiou; WILLE, S et al.International journal of clinical practice (Esher). 2003, Vol 57, Num 10, pp 852-856, issn 1368-5031, 5 p.Article