Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Markissia Karagiorga"'
Autor:
Athanassios Aessopos, Christina Fragodimitri, Fotios Karabatsos, Antonia Hatziliami, Jacqueline Yousef, Anastasios Giakoumis, Aikaterini Dokou, Efstathios D. Gotsis, Vasilis Berdoukas, Markissia Karagiorga
Publikováno v:
Haematologica, Vol 92, Iss 1 (2007)
Recent advances in magnetic resonance imaging (MRI) techniques allow the assessment of iron overload in tissues1 especially the heart,2 in transfusion- dependent thalassemia patients. The R2* value (1/T2*) recorded in the intraventricular septum of t
Externí odkaz:
https://doaj.org/article/3edabd3429d946128099dffa14937905
Autor:
Athanasios Lagiandreou, Efthimios Dalagiorgos, John Koskinas, Helen Berdoussi, Nikolaos J. Tsagarakis, Evanthia Diamanti-Kandarakis, Niki Vgontza, Ersi Voskaridou, Konstantinos Kaligeros, Dimitrios Kountouras, Paraskevi Roussou, Evangelia Fatourou, Nikolaos Chrysanthos, Markissia Karagiorga
Publikováno v:
Liver International. 33:420-427
Background Iron overload and hepatitis-C virus (HCV) infection, have been implicated in the evolution of liver disease, in patients with transfusion-dependent beta-thalassaemia major (BTM). However, the impact of these factors in late stages of liver
Autor:
Martijn van der Kraan, Mariska Geerts, Alexandra Stamoulakatou, Greet Bakker, J. Traeger-Synodinos, Emmanuel Kanavakis, Piero C. Giordano, Cornelis L. Harteveld, Markissia Karagiorga, Marion Phylipsen, Peter van Delft
Publikováno v:
European Journal of Haematology. 88:356-362
Objectives: To determine the molecular basis in a Greek child suspected of having HbH disease and β-thalassemia trait. Methods: Standard hematology, Hb electrophoresis, and HPLC. Multiplex ligation-dependent probe amplification (MLPA), direct sequen
Autor:
Christodoulos Stefanadis, Yannis Barbetseas, Demosthenes B. Panagiotakos, Christina Chrysohoou, Stella Brilli, Markissia Karagiorga, Spyros Lambrou, Vassilis A. Ladis, Christos Pitsavos
Publikováno v:
International Journal of Hematology. 80:336-340
Despite intense iron-chelation therapy, the life expectancy of patients with s-thalassemia major (s-TM) is still limited by the occurrence of heart failure. In the present study, we sought to evaluate the prognostic significance of several clinical f
Autor:
Christina Vrettou, Joanne Traeger-Synodinos, Anna Metaxotou-Mavrommati, Markissia Karagiorga, Emmanuel Kanavakis, Ioannis Papassotiriou, Alexandra Stamoulakatou, Christos Kattamis
Publikováno v:
British Journal of Haematology. 111:915-923
Haemoglobin H (Hb H) disease is the severest form of alpha-thalassaemia compatible with post-natal life and occurs when alpha-thalassaemia mutations interact to reduce alpha-globin synthesis to levels approximately equivalent to the output of a singl
Autor:
Markissia Karagiorga, E. Kavouklis, Athanasios Aessopos, Christina Fragodimitri, Dimitris Loukopoulos, Ersi Voskaridou, Michael Samarkos, Vassiliki Kalotychou
Publikováno v:
American Journal of Hematology. 63:63-67
In this study we investigated the possible role of neutrophil (PMN) elastase and its natural inhibitor, alpha1-proteinase inhibitor (alpha1-PI) in the pathogenesis of the pseudoxanthoma elasticum (PXE)-like syndrome which is found in patients with ho
Autor:
E. Kanavakis, Christina Vrettou, Ioannis Papassotiriou, Markissia Karagiorga, Alexandra Stamoulakatou, Anna Metaxotou-Mavrommati, J. Traeger-Synodinos
Publikováno v:
Scopus-Elsevier
Thalassemia syndromes and unstable hemoglobins traditionally represent two phenotypically separate disorders of hemoglobin synthesis. Highly unstable hemoglobin variants, however, often have phenotypic characteristics associated with both ineffective
Autor:
Marion, Phylipsen, Jan, Traeger-Synodinos, Martijn, van der Kraan, Peter, van Delft, Greet, Bakker, Mariska, Geerts, Emmanuel, Kanavakis, Alexandra, Stamoulakatou, Markissia, Karagiorga, Piero C, Giordano, Cornelis L, Harteveld
Publikováno v:
European journal of haematology. 88(4)
To determine the molecular basis in a Greek child suspected of having HbH disease and β-thalassemia trait. Standard hematology, Hb electrophoresis, and HPLC. Multiplex ligation-dependent probe amplification (MLPA), direct sequencing, and breakpoint
Autor:
Ioannis Papassotiriou, Emmanuel Kanavakis, Joanne Traeger-Synodinos, Markissia Karagiorga, Alexandra Stamoulakatou, Evangelos Premetis
Publikováno v:
British Journal of Haematology. 119:265-267
Summary. A single patient with a rare Haemoglobin H (HbH) disease genotype (- -Med/αTSaudiα) was observed to have exceptionally high levels of HbH (> 60%) and paradoxically high total haemoglobin levels. Studies of haematological parameters, blood
Autor:
Vassilis, Ladis, Giorgos, Chouliaras, Vasilios, Berdoukas, Antonia, Chatziliami, Christina, Fragodimitri, Fotis, Karabatsos, Jacqueline, Youssef, Antonis, Kattamis, Markissia, Karagiorga-Lagana
Publikováno v:
European journal of haematology. 86(4)
With transfusions and chelation therapy, the prognosis for transfusion-dependent beta thalassaemia has changed from being fatal in early childhood to a chronic disorder with prolonged survival. In this historical prospective study, we present surviva