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British Journal of Haematology|October 29, 1998
Molecular, haematological and clinical studies of a silent beta-gene C-->G mutation at 6 bp 3' to the termination codon (+1480 C-->G) in twelve Greek familiesE Maragoudaki, C Vrettou, E Kanavakis, et al.
Vox Sanguinis|January 1, 1996
The impact of neocyte transfusion in the management of thalassaemiaT Spanos, V Ladis, F Palamidou, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|January 1, 1995
[Clinical evaluation of various preventive methods for non-hemolytic transfusion reactions]T Spanos, V Ladis, M Karageorga, et al.
Pediatric Hematology and Oncology|January 1, 1995
Molecular characterization of homozygous (high HbA2) beta-thalassemia intermedia in GreeceE Kanavakis, J Traeger-Synodinos, M Tzetis, et al.
Human Genetics|November 1, 1994
Preliminary mutation analysis in the phenylalanine hydroxylase gene in Greek PKU and HPA patientsJ Traeger-Synodinos, E Kanavakis, M Kalogerakou, et al.
International Journal of Clinical Practice|January 10, 2004
Efficacy and tolerability of formoterol Turbuhaler in childrenA Von Berg, F Papageorgiou Saxoni, S Wille, et al.
Hepato-Gastroenterology|October 16, 1999
Tissue immunodetection of c100 hepatitis C virus antigen in major thalassemic patientsL Nakopoulou, N Manolaki, A C Lazaris, et al.
Molecular and Cellular Probes|August 1, 1995
Identification of two novel mutations (296 + 1G-C and A46D) in exon 2 of the CFTR gene in Greek cystic fibrosis patientsM Tzetis, E Kanavakis, T Antoniadi, et al.
British Journal of Haematology|May 1, 1982
Globin gene mapping in normal Hb A2 types of beta-thalassaemiaE Kanavakis, A Metaxotou-Mavromati, C Kattamis, et al.
AIDS Care|January 1, 1990
A multi-level intervention approach for care of HIV-positive haemophiliac and thalassaemic patients and their familiesJ Tsiantis, D Anastasopoulos, M Meyer, et al.
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