Zobrazeno 1 - 10
of 140
pro vyhledávání: '"M. Karagiorga"'
Autor:
Giorgos Chouliaras, Vasilios Berdoukas, Vassilis Ladis, Antonis Kattamis, Christina Fragodimitri, Antonia Chatziliami, M. Karagiorga-Lagana, Fotis Karabatsos, Jacqueline Youssef
Publikováno v:
European Journal of Haematology. 86:332-338
Background: 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. Design and methods: In this historical prosp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d901822adfd21bb6cfd14c25d50d0a10
https://doi.org/10.1111/j.1600-0609.2011.01582.x
https://doi.org/10.1111/j.1600-0609.2011.01582.x
Publikováno v:
European Journal of Haematology. 63:287-294
Pseudoxanthoma elasticum-like lesions of the eye and skin are frequently observed in β-thalassaemia, and there has been speculation about associated vascular lesions. This led to our study of histopathological material from thalassaemic patients. Hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8b41b887737e2dbdc9ff58eb057a9a2
https://doi.org/10.1111/j.1600-0609.1999.tb01130.x
https://doi.org/10.1111/j.1600-0609.1999.tb01130.x
Autor:
K. Tsomi, Fotis Karabatsos, C. Van Vliet-Konstantinidou, Christina Fragodimitri, M. Karagiorga-Lagana, Evangelos Premetis, Alexandra Stamoulakatou
Publikováno v:
European Journal of Haematology. 67:135-141
Arterial and stromal elastorrhexis, an elastic tissue disorder, was recently described in β-thalassaemia major. Histopathological material from 10 patients with thalassaemia intermedia, 14 with sickle cell thalassaemia and 18 with hereditary spheroc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b835152a75f7c1948eb7f08db5dc363
https://doi.org/10.1034/j.1600-0609.2001.5790349.x
https://doi.org/10.1034/j.1600-0609.2001.5790349.x
Autor:
E, Kanavakis, I, Papassotiriou, M, Karagiorga, C, Vrettou, A, Metaxotou-Mavrommati, A, Stamoulakatou, C, Kattamis, J, Traeger-Synodinos
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::996693d9564ad216ea983e74e4a20840
https://doi.org/10.1046/j.1365-2141.2000.02448.x
https://doi.org/10.1046/j.1365-2141.2000.02448.x
Autor:
I, Papassotiriou, J, Traeger-Synodinos, E, Kanavakis, M, Karagiorga, A, Stamoulakatou, C, Kattamis
Publikováno v:
Journal of Pediatric Hematology/Oncology. 20:539-544
To determine serum immunoreactive erythropoietin (Epo) and soluble transferrin receptors (sTfR) levels in patients with hemoglobin H (HbH) disease and the correlation with HbH levels and alpha-globin genotype.Twenty patients with HbH disease were stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a78067778fee37ce1a631c2c719d23b1
https://doi.org/10.1097/00043426-199811000-00005
https://doi.org/10.1097/00043426-199811000-00005
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
Publikováno v:
European journal of haematology. 90(4)
Objectives Beta thalassaemia major (β-TM) and sickle-cell disease (SCD) are severe haemogobinopathies requiring life-lasting, advanced medical management. In the Mediterranean region, both conditions occur with high frequency. We assessed the effica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56926da93bc5aadc885c1379178fb7e2
https://pubmed.ncbi.nlm.nih.gov/23331260
https://pubmed.ncbi.nlm.nih.gov/23331260
Background: Portal vein system thrombosis (PVT) is an infrequent but potentially serious complication after laparoscopic splenectomy. Patients with β-thalassemia are at higher risk as they have splenomegaly and hypercoagulability. Subjects and Metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::368264c3e594b6e328c3b4fdb6befb4e
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3128151
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3128151
Autor:
Giorgos Chouliaras, Jacqueline Youssef, Antonis Kattamis, Vasilios Berdoukas, Fotis Karabatsos, Christina Fragodimitri, Antonia Chatziliami, M. Karagiorga-Lagana, Vassilis Ladis
Publikováno v:
Journal of magnetic resonance imaging : JMRI. 34(1)
Purpose: To evaluate whether the introduction of magnetic resonance imaging (MRI) in the management of thalassemia major (TM) patients has affected the risk of cardiac death. Materials and Methods: In all, 804 TM patients from two large reference uni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e274761c7935c05fcd1e5cd0cb02a883
https://pubmed.ncbi.nlm.nih.gov/21608067
https://pubmed.ncbi.nlm.nih.gov/21608067
Autor:
Fotis Karabatsos, H. Georgakis, Christina Fragodimitri, Helen Michelakakis, M. Karagiorga-Lagana, E. Dimitriou, J. Saraphidou, Evangelos Premetis
Publikováno v:
European Journal of Pediatrics. 156:602-604
The urinary levels of the lysosomal enzymes N-acetyl-beta-D-glucosaminidase (NAG) (EC 3.2.1.52) and alpha-mannosidase (EC 3.2.1.24) were evaluated in patients with beta-thalassaemia major and normal control subjects. Two groups of patients with diffe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1399f465b931de8db30bce231c66c620
https://doi.org/10.1007/s004310050673
https://doi.org/10.1007/s004310050673