Výsledky vyhledávání - "E. Maragoudaki"

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Molecular, haematological and clinical studies of the −101 C → T substitution of the β-globin gene promoter in 25 β-thalassaemia intermedia patients and 45 heterozygotes

Autor: Emmanouel Kanavakis, Maria Tzetis, Christina Vrettou, Christos Kattamis, Anna Metaxotou-Mavrommati, E. Maragoudaki, J. Traeger-Synodinos

Publikováno v: British Journal of Haematology. 107:699-706

We report the clinical, haematological, biosynthetic and molecular data of 25 double heterozygote β-thalassaemia intermedia patients and 45 β-thalassaemia heterozygotes with the C T substitution at nucleotide position −101 from the Cap site, in t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8caa6ace5e8d319341fa47a648b81b12
https://doi.org/10.1046/j.1365-2141.1999.01788.x

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The triplicated α-globin gene locus in β-thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies

Autor: Christina Vrettou, A. Metaxotou-Mavromati, J. Traeger-Synodinos, Christos Kattamis, Th. Michael, E. Maragoudaki, Emmanuel Kanavakis

Publikováno v: Scopus-Elsevier

Excess alpha-globin chains play a major role in the pathophysiology of homozygous beta-thalassaemia. In beta-thalassaemia carriers a minor effect of alpha-globin chain excess is reflected in a minimal or mild anaemia without clinical symptoms. Factor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba80cac17237bf82ecd8db132537c23d
https://doi.org/10.1046/j.1365-2141.1996.d01-1939.x

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Star-burst regions in the LMC* (Research Note)

Autor: Livanou, E. Kontizas, M. Gonidakis, I. Kontizas, E. Maragoudaki, F. Oliver, S. Efstathiou, A. Klein, U.

Aims. Filamentary structures of early type stars are found to be a common feature of the Magellanic Clouds formed at an age of about 0.9-2 × 10 8 yr. As we go to younger ages these large structures appear fragmented and sooner or later form young cl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::378d48ed92756e4469573cc5d8113036
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3017625

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Gilbert syndrome associated with beta-thalassemia

Autor: Maria Tzetis, E. Kavazarakis, Vasilis Ladis, T. Georgakopoulou, Themistocles Karpathios, S. Kitsiou-Tzeli, Aspasia Tsezou, Emmanouel Kanavakis, E. Maragoudaki, E. Pateraki

Publikováno v: Pediatric hematology and oncology. 18(8)

The authors investigated whether the considerable variability in serum bilirubin levels (STB) found in transfusion-dependent beta-thalassemia, beta-thal intermedia, and heterozygous beta-thalassemia individuals could be related to the coexistence of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e8087f5c6806ef171c5de0ed75828b9
https://pubmed.ncbi.nlm.nih.gov/11764096

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Gilbert syndrome associated with beta-thalassemia

Autor: Tzetis, M Kanavakis, E Tsezou, A Ladis, V Pateraki, E and Georgakopoulou, T Kavazarakis, E Maragoudaki, E and Karpathios, T Kitsiou-Tzeli, S

The authors investigated whether the considerable variability in serum bilirubin levels (STB) found in transfusion-dependent beta -thalassemia, beta -thal intermedia, and heterozygous beta -thalassemia individuals could be related to the coexistence

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::7d8f684134169d43344d900722a8f02c
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3081049

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Akademický článek

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Molecular studies of beta-thalassemia heterozygotes with raised Hb F levels

Autor: Christina Vrettou, E. Kanavakis, Anna Metaxotou-Mavrommati, Ioannis Papassotiriou, J. Traeger-Synodinos, A. Stamoulakatou, Christos Kattamis, I. Basiakos, E. Maragoudaki

Publikováno v: Scopus-Elsevier

Hb F levels in beta-thalassemia heterozygotes are usually less than 2%, but amongst 1,059 patients studied, 73 (7%) had Hb F levels above 2.5% (2.6-14.0%). To investigate factors that may influence the increase of Hb F levels in these heterozygotes,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd18c965d4bf27cf363390a26fdb1574
https://pubmed.ncbi.nlm.nih.gov/10975440

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Molecular, haematological and clinical studies of the -101 C --T substitution of the beta-globin gene promoter in 25 beta-thalassaemia intermedia patients and 45 heterozygotes

Autor: E, Maragoudaki, E, Kanavakis, J, Traeger-Synodinos, C, Vrettou, M, Tzetis, A, Metaxotou-Mavrommati, C, Kattamis

Publikováno v: British journal of haematology. 107(4)

We report the clinical, haematological, biosynthetic and molecular data of 25 double heterozygote beta-thalassaemia intermedia patients and 45 beta-thalassaemia heterozygotes with the C --T substitution at nucleotide position -101 from the Cap site,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e83b16c94f2431a35b684f697c7164f1
https://pubmed.ncbi.nlm.nih.gov/10606872

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