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Journal of Pediatric Endocrinology & Metabolism : JPEM|March 26, 1999
Growth and management of short stature in thalassaemia majorC Theodoridis, V Ladis, A Papatheodorou, et al.Human Genetics|April 17, 1998
Analysis of low density lipoprotein receptor gene mutations and microsatellite haplotypes in Greek FH heterozygous children: six independent ancestors account for 60% of probandsJ Traeger-Synodinos, N Mavroidis, E Kanavakis, et al.Hemoglobin|September 7, 2000
Molecular studies of beta-thalassemia heterozygotes with raised Hb F levelsC Vrettou, E Kanavakis, J Traeger-Synodinos, et al.British Journal of Haematology|March 1, 1990
Molecular characterization of beta-thalassaemia in 174 Greek patients with thalassaemia majorC Kattamis, H Hu, G Cheng, et al.British Journal of Haematology|May 1, 1990
Two novel polyadenylation mutations leading to beta(+)-thalassemiaL Jankovic, G D Efremov, G Petkov, et al.Pediatric Radiology|June 13, 2003
Abdominal ultrasonographic findings in patients with sickle-cell anaemia and thalassaemia intermediaMarina G Papadaki, Antonios C Kattamis, Irene G Papadaki, et al.Haematologica|January 9, 2001
Different geographic origins of Hb Constant Spring [alpha(2) codon 142 TAA-->CAA]C L Harteveld, J Traeger-Synodinos, A Ragusa, et al.British Journal of Haematology|November 1, 1993
A base substitution (T-->C) in codon 29 of the alpha 2-globin gene causes alpha thalassaemiaG W Hall, S L Thein, A C Newland, et al.Hemoglobin|March 1, 1997
Hb Osler [beta 145(HC2)Tyr-->Asp] results from posttranslational modificationA C Kattamis, K M Kelly, K Ohene-Frempong, et al.European Journal of Human Genetics : EJHG|November 5, 1998
Haplotype and mutation analysis in Greek patients with Wilson diseaseG Loudianos, V Dessì, M Lovicu, et al.Pageof 9