Zobrazeno 1 - 10
of 155
pro vyhledávání: '"A. Metaxotou-Mavromati"'
Autor:
Chakalova, Lyubomira, Osborne, Cameron S., Dai, Yan-Feng, Goyenechea, Beatriz, Metaxotou-Mavromati, Anna, Kattamis, Antonios, Kattamis, Christos, Fraser, Peter *
Publikováno v:
In Blood 1 March 2005 105(5):2154-2160
Autor:
Kattamis, C., Metaxotou-Mavromati, A., Tsiarta, E., Metaxatou, C., Wasi, P., Wood, W. G., Pressley, L., Higgs, D. R., Clegg, J. B., Weatherall, D. J.
Publikováno v:
The British Medical Journal, 1980 Jul . 281(6235), 268-270.
Externí odkaz:
https://www.jstor.org/stable/25440684
Publikováno v:
The British Medical Journal, 1972 Aug . 3(5824), 470-471.
Externí odkaz:
https://www.jstor.org/stable/25419814
Publikováno v:
British Journal of Haematology. 63:263-271
Globin gene mapping in 16 Greek individuals with HbH disease and their parents has demonstrated the occurrence of several HbH genotypes brought about by the interaction of two alpha zero-thalassaemia and two alpha+-thalassaemia haplotypes. Eight of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::988247f577ee5196e241d000904e93a7
https://doi.org/10.1111/j.1365-2141.1986.tb05549.x
https://doi.org/10.1111/j.1365-2141.1986.tb05549.x
Autor:
Cameron S. Osborne, A. Metaxotou-Mavromati, Peter Fraser, Yan-Feng Dai, Lyubomira Chakalova, Christos Kattamis, Antonios Kattamis, Beatriz Goyenechea
Publikováno v:
Blood. 105:2154-2160
The 7.2 kilobase (kb) Corfu δβ thalassemia mutation is the smallest known deletion encompassing a region upstream of the human δ gene that has been suggested to account for the vastly different phenotypes in hereditary persistence of fetal hemoglo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9baa66ce8336e07a60412355f12d2d5
https://doi.org/10.1182/blood-2003-11-4069
https://doi.org/10.1182/blood-2003-11-4069
Autor:
Th. Michael, E. Kanavakis, I. Papassotiriou, J. Traeger-Synodinos, Christina Vrettou, A. Metaxotou-Mavromati, Christos Kattamis
Publikováno v:
Scopus-Elsevier
This report describes the first case of homozygosity for the Hb Agrinio [alpha 29(B10)Leu--Pro] alpha 2-globin gene variant (codon 29, CTG--CCG) in a Greek patient. At 12 months of age, the proband presented with a marked hypochromic, microcytic anem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97c098716dc45546357215096ba4772f
https://doi.org/10.3109/03630269809113135
https://doi.org/10.3109/03630269809113135
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
https://doi.org/10.1046/j.1365-2141.1996.d01-1939.x
Autor:
Vasilis Ladis, Emmanuel Kanavakis, Joanne Traeger-Synodinos, Maria Tzetis, Christos Kattamis, A. Metaxotou-Mavromati
Publikováno v:
Pediatric Hematology and Oncology. 12:37-45
Homozygous beta-thalassemia is usually characterized by severe anemia requiring regular blood transfusion for survival. For homozygous patients with milder clinical manifestations and no dependence on transfusion therapy, the term thalassemia interme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d10dc716a00590770ac6010f37bbdf51
https://doi.org/10.3109/08880019509029526
https://doi.org/10.3109/08880019509029526
Autor:
J. Traeger-Synodinos, Emmanouel Kanavakis, Christos Kattamis, Maria Tzetis, L Stefanis, A. Metaxotou-Mavromati
Publikováno v:
Pediatric Hematology and Oncology. 11:509-517
The hematologic phenotype was characterized in heterozygotes for three of the most common beta-thalassemia mutations in the Greek population. The study included 17 carriers of beta++ IVS1-n6 (T-->C), 21 carriers of beta+ IVS1-n110 (G-->A), and 17 car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76d3170a593139425f57cb8059a27ba6
https://doi.org/10.3109/08880019409141689
https://doi.org/10.3109/08880019409141689
The 7.2 kilobase (kb) Corfu deltabeta thalassemia mutation is the smallest known deletion encompassing a region upstream of the human delta gene that has been suggested to account for the vastly different phenotypes in hereditary persistence of fetal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::f7529b53ecd322dfca3c17e7edfe2b15
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3093458
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3093458
