Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Athanassios Aessopos"'
Publikováno v:
Advances in Hematology, Vol 2009 (2009)
Transfusion and iron chelation therapy revolutionised survival and reduced morbidity in patients with transfusion-dependent beta thalassaemia major. Despite these improvements, cardiac disease remained the most common cause of death in those patients
Externí odkaz:
https://doaj.org/article/55c8934a9177450e97740f318c5ec503
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:
Katerina Polonofi, Maria Tsironi, George Assimakopoulos, Athanassios Aessopos, Kalliopi Rigaki
Publikováno v:
Hemoglobin. 32:29-34
The benefits of combined deferoxamine (DFO) and deferiprone (L1) chelation therapy, focusing on reducing myocardial iron loading, have been widely reported. Herein, we present the efficacy of combined chelation and its effects on iron load indices. F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47b37303ef52019ec810fea28c615ce5
https://doi.org/10.1080/03630260701680474
https://doi.org/10.1080/03630260701680474
Intensive chelation therapy in β-thalassemia and possible adverse cardiac effects of desferrioxamine
Autor:
Athanassios Aessopos, Maria Kati, Dimitrios Farmakis, Ekaterini Polonifi, Spyros Deftereos, Maria Tsironi
Publikováno v:
International Journal of Hematology. 86:212-215
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4cfba531c937e43eeffc95663b8bb1e
https://doi.org/10.1007/bf03006922
https://doi.org/10.1007/bf03006922
Publikováno v:
Transfusion. 47:792-800
BACKGROUND: b-Thalassemia is an inherited hemoglobin disorder characterized by reduced synthesis of b-globin chain. The severity of clinical course distinguishes this heterogeneous disease in two main subtypes: thalassemia major (TM) and thalassemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d66fe7467bc67e2162289ff775b05d5
https://doi.org/10.1111/j.1537-2995.2007.01192.x
https://doi.org/10.1111/j.1537-2995.2007.01192.x
Autor:
Maria Tsironi, Athanassios Aessopos, Ioannis Moyssakis, Stergios Tassiopoulos, Dimitrios Farmakis, Katerina Polonifi, Maria Kati
Publikováno v:
The Annals of Thoracic Surgery. 81:2037-2043
Background Thalassemia intermedia has a later clinical onset and a milder anemia than thalassemia major, characterized by high output state, left ventricle remodeling, and age-related pulmonary hypertension. Bone deformities, extramedullary hematopoi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::117b97ceba4d20745d6634a4b0c1fe89
https://doi.org/10.1016/j.athoracsur.2006.01.026
https://doi.org/10.1016/j.athoracsur.2006.01.026
Autor:
Spyros Deftereos, Kostas Konstantopoulos, D. Farmakis, Maria Tsironi, Stergios Tassiopoulos, Athanassios Aessopos, Michalis Kyriakidis
Publikováno v:
Annals of the New York Academy of Sciences. 1054:467-470
Six hundred and thirty-eight patients who presented with clinical symptoms and/or electrocardiographic findings suggestive of stable angina pectoris were studied; they were also investigated by coronary arteriography. Hemoglobin electrophoresis was p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89d2ce87b2b776fb3621117a6e88d3a1
https://doi.org/10.1196/annals.1345.068
https://doi.org/10.1196/annals.1345.068
Autor:
Athanassios Aessopos, Robert Lindeman, Keshani de Silva, Vivienne Tobias, Ian S. Fraser, Vasili Berdoukas, Timothy D Bohane
Publikováno v:
The Hematology Journal. 5:572-578
Secondary iron overload is associated with significant mortality and morbidity. Although new, less invasive techniques are becoming available, the most acceptable and readily accessible way to assess iron overload is to measure hepatic iron by liver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::429578115fc4497e30f453f3ab412831
https://doi.org/10.1038/sj.thj.6200569
https://doi.org/10.1038/sj.thj.6200569
Autor:
Athanassios Aessopos, Konstantinos Korovesis, Aikaterini Ismailou-Parassi, Stergios Tassiopoulos, Georgios Lefakis, Kyriaki Alatzoglou
Publikováno v:
American Journal of Nephrology. 20:217-221
Adamantiades-Behçet’s disease is a multisystem recurrent syndrome with vasculitis being the underlying histopathological lesion. We report on a patient with Behçet’s disease who developed a renal mass raising the suspicion of a malignant neopla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c23e0ed8e9aaf586246baee5e87f0616
https://doi.org/10.1159/000013591
https://doi.org/10.1159/000013591
Autor:
Athanassios Aessopos, M. Karagiorga-Lagana, Michael B. Petersen, Christina Fragodimitri, Athina Kladi, Dimitrios Th. Kremastinos, Fotis Karabatsos, Effrosini Economou-Petersen, Panagiota Flevari, Dimitris Vassilopoulos, Peter Nicolaidis, Helen Vrettou
Publikováno v:
Blood. 92:3455-3459
In homozygous β-thalassemia, the organ damage is mainly attributed to excessive iron deposition through the formation of oxygen free radicals. Despite appropriate transfusion and chelation therapy and low ferritin levels, patients still develop orga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ec606aae3b665069ac5509350af971c
https://doi.org/10.1182/blood.v92.9.3455.421k03_3455_3459
https://doi.org/10.1182/blood.v92.9.3455.421k03_3455_3459