AAAAAA
Results:
1-11
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Results: 11
Authors:
Tsomi, K
Karagiorga-Lagana, M
Karabatsos, F
Fragodimitri, C
van Vliet-Konstantinidou, C
Premetis, E
Stamoulakatou, A
Citation: K. Tsomi et al., Arterial elastorrhexis in beta-thalassaemia intermedia, sickle cell thalassaemia and hereditary spherocytosis, EUR J HAEMA, 67(3), 2001, pp. 135-141
Authors:
Politou, M
Kollia, P
Akel, S
Papassotiriou, Y
Stamoulakatou, A
Loukopoulos, D
Citation: M. Politou et al., Valproic acid, trichostatin and their combination with hemin preferentially enhance gamma-globin gene expression in human erythroid liquid cultures, HAEMATOLOG, 86(7), 2001, pp. 700-705
Authors:
Traeger-Synodinos, J
Papassotiriou, I
Vrettou, C
Skarmoutsou, C
Stamoulakatou, A
Kanavakis, E
Citation: J. Traeger-synodinos et al., Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional alpha-globin and beta-globin gene, HAEMATOLOG, 86(4), 2001, pp. 363-367
Authors:
Papassotiriou, I
Traeger-Synodinos, J
Prome, D
Kister, J
Vrettou, C
Xaidara, A
Marden, M
Stamoulakatou, A
Wajcman, H
Kanavakis, E
Citation: I. Papassotiriou et al., Hb Sitia [beta 128(H6)Ala -> Val]: An unstable variant with a substitutionin the alpha 1 beta 1 interface, HEMOGLOBIN, 25(1), 2001, pp. 45-56
Authors:
Traeger-Synodinos, J
Papassotiriou, I
Metaxotou-Mavrommati, A
Vrettou, C
Stamoulakatou, A
Kanavakis, E
Citation: J. Traeger-synodinos et al., Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb Heraklion, alpha 1cd37(C2)Pro > 0): Comparison to other alpha-thalassemic hemoglobinopathies, BL CELL M D, 26(4), 2000, pp. 276-284
Authors:
Vrettou, C
Kanavakis, E
Traeger-Synodinos, J
Metaxotou-Mavrommati, A
Basiakos, I
Maragoudaki, E
Stamoulakatou, A
Papassotiriou, I
Kattamis, C
Citation: C. Vrettou et al., Molecular studies of beta-thalassemia heterozygotes with raised Hb F levels, HEMOGLOBIN, 24(3), 2000, pp. 203-220
Authors:
Kanavakis, E
Papassotiriou, I
Karagiorga, M
Vrettou, C
Metaxotou-Mavrommati, A
Stamoulakatou, A
Kattamis, C
Traeger-Synodinos, J
Citation: E. Kanavakis et al., Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience, BR J HAEM, 111(3), 2000, pp. 915-923
Authors:
Traeger-Synodinos, J
Metaxotou-Mavrommati, A
Karagiorga, M
Vrettou, C
Papassotiriou, I
Stamoulakatou, A
Kanavakis, E
Citation: J. Traeger-synodinos et al., Interaction of an alpha(+)-thalassemia deletion with either a highly unstable alpha-globin variant (alpha 2, codon 59, G(G)under-barC -> G(A)under-barC) or a nondeletional alpha-thalassemia mutation (AATAA(A)under-bar -> AATAA(G)under-bar): Comparison of phenotypes illustrating "dominant" alpha-thalassemia, HEMOGLOBIN, 23(4), 1999, pp. 325-337
Authors:
Papassotiriou, I
Traeger-Synodinos, J
Vlachou, C
Karagiorga, M
Metaxotou, A
Kanavakis, E
Stamoulakatou, A
Citation: I. Papassotiriou et al., Rapid and accurate quantitation of Hb Bart's and Hb H using weak cation exchange high performance liquid chromatography: Correlation with the alpha-thalassemia genotype, HEMOGLOBIN, 23(3), 1999, pp. 203-211
Authors:
Papassotiriou, I
Traeger-Synodinos, J
Prome, D
Kister, J
Stamou, E
Liakopoulou, T
Stamoulakatou, A
Kanavakis, E
Wajcman, H
Citation: I. Papassotiriou et al., Association of unstable hemoglobin variants and heterozygous beta-thalassemia: Example of a new variant Hb Acharnes or [beta 53(D4) Ala -> Thr], AM J HEMAT, 62(3), 1999, pp. 186-192
Authors:
Papassotiriou, I
Traeger-Synodinos, J
Kanavakis, E
Karagiorga, M
Stamoulakatou, A
Kattamis, C
Citation: I. Papassotiriou et al., Erythroid marrow activity and hemoglobin H levels in hemoglobin H disease, J PED H ONC, 20(6), 1998, pp. 539-544
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