Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Vasilis Ladis"'
Autor:
Nikolaos Kelekis, Olympia Papakonstantinou, Nikos Economopoulos, Efstathios P. Efstathopoulos, Athanassios Gouliamos, Efthymia Alexopoulou, Stavroula Kostaridou, Vasilis Ladis, Odysseas Benekos, Antonis Kattamis
Publikováno v:
Journal of Magnetic Resonance Imaging. 29:853-859
Purpose To investigate the correlation between the degree of hepatic, splenic, pancreatic, vertebral bone marrow (VBM), and myocardial siderosis, as expressed by relaxation rate (R2 = 1/T2) values, in patients with thalassemia. Materials and Methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eed7c310be57108274bb53ea3fab8ae0
https://doi.org/10.1002/jmri.21707
https://doi.org/10.1002/jmri.21707
Publikováno v:
Vaccine. 24:3050-3053
Natural and vaccine-induced immunity and immunological memory to Haemophilus influenzae type b (Hib) were evaluated in adolescents and adults with β-thalassemia. At baseline 10/23 (43%) unvaccinated patients had naturally acquired anticapsular antib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e522595fefecf5863b771feeeb69e92
https://doi.org/10.1016/j.vaccine.2006.01.034
https://doi.org/10.1016/j.vaccine.2006.01.034
Autor:
Antonis Kattamis, Alexis Kelekis, Panagiotis Baras, Nikolaos Kelekis, Vasilis Ladis, Ioannis Seimenis, Fotini Stripeli, Efstathios P. Efstathopoulos, Efthymia Alexopoulou, Elias Brountzos
Publikováno v:
Journal of Magnetic Resonance Imaging. 23:163-170
Purpose To evaluate the usefulness of a time-efficient MRI method for the quantitative determination of tissue iron in the liver and heart of β-thalassemic patients using spin-spin relaxation rate, R2, measurements. Materials and Methods Images were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27674a40d48b30f70447c981597cfa00
https://doi.org/10.1002/jmri.20489
https://doi.org/10.1002/jmri.20489
Autor:
Emmanuel Kanavakis, Irini Orfanou, Antonis Kattamis, Anna Metaxotou-Mavrommati, Fotini Psichou, Evangelia Lagona, Vasilis Ladis, Christos Kattamis
Publikováno v:
Pediatric Hematology and Oncology. 21:335-342
The authors studied the long-term clinical and hematological response to hydroxyurea (HU) therapy in young patients, with either S/beta-thalassemia (beta(thal)) (8 patients) or SS (6 patients). All patients with S/beta(thal) responded well to treatme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0406796368e70be55921718ee9963cc1
https://doi.org/10.1080/08880010490440473
https://doi.org/10.1080/08880010490440473
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:
Stilianos Lafioniatis, Maria Theohari, Antonis Kattamis, Ioannis Lafiatis, Athanasios Anastasiadis, Athanasios Galanopoulos, Maria Kalmanti, Artemis Basileiadi, Kallistheni Farmaki, Eftihios Eftihiadis, Eleni Vrettou, Marina Economou, Ioannis Davros, Agapi Mprimi, Polixeni Maili, Markisia Karagiorga, Georgios Xanthopoulidis, Antigoni Tsirka, Efthimia Dimitriadou, Andreas Mihos, Maria Stamatopoulou, Maria Aggelaki, Evaggelia Panori, Ersi Voskaridou, Alexandros Papadakis, Zafeiris Kartasis, Dionisia Dionisopoulou, Peristera Dimoxenou, Ioannis Adamopoulos, Ourania Papageorgiou, Konstantinos Maragkos, Elanso Damba Haile, Androniki Ntalamaga, Margarita Papadopoulou, Kalliopi Kontogianni, Maria Tsironi, Dimitrios Georgakopoulos, Vasilis Ladis, Alexandra Kourakli, Eleni Hassapopoulou, Freideriki Koutsouka, Georgia Tapaki, Marouso Drosou, Pantelis Drandrakis
Publikováno v:
Annals of hematology. 91(9)
Haemoglobinopathies are the most common hereditary disorders in Greece. Although there is a successful national prevention program, established 35 years ago, there is lack of an official registry and collection of epidemiological data for haemoglobin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76016dadb16e7163cf1d5a8883ab65db
https://pubmed.ncbi.nlm.nih.gov/22526366
https://pubmed.ncbi.nlm.nih.gov/22526366
Autor:
Vasilis Ladis, Joanne Traeger-Synodinos, Alexandra Stamoulakatou, Emmanuel Kanavakis, Tania Siahanidou, Ioannis Papassotiriou, Varvara Douna, Irine Fylaktou
Publikováno v:
Hemoglobin. 34(5)
Hb Agrinio [α29(B10)Leu→Pro] is a highly unstable variant, classified as a nondeletional α-thalassemia (α-thal) mutation. To date it has only been described in individuals of Greek and Cypriot origin. Evaluation of the phenotypic presentation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74de79646bd9d93bbcb009b7f34f4830
https://pubmed.ncbi.nlm.nih.gov/20854116
https://pubmed.ncbi.nlm.nih.gov/20854116
Autor:
Vana I. Spoulou, Vasilis Ladis, Maria Theodoridou, George V. Orthopoulos, Dimitris K. Tsousis
Publikováno v:
Vaccine. 27(3)
The effect of the 23-valent pneumococcal polysaccharide vaccine (PPV) on the 7-valent conjugate (PCV) vaccine-induced priming was evaluated in 35 splenectomised beta-thalassemics [median (range) age: 30 (12-41) years] vaccinated with either PCV/PPV o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f46064061dfae3de96771ec8d1e3d0dd
https://pubmed.ncbi.nlm.nih.gov/19010369
https://pubmed.ncbi.nlm.nih.gov/19010369
Autor:
Efthymia Alexopoulou, Nikolaos Kelekis, Elias Brountzos, Angeliki Boussiotou, Vasilis Ladis, Dimitrios A. Kelekis
Publikováno v:
Journal of magnetic resonance imaging : JMRI. 18(5)
Giant adrenal myelolipoma is an uncommon entity. We present the atypical MR imaging findings of a giant adrenal myelolipoma in a patient with homozygous beta-thalassemia with histopathology correlation. The tumor showed a drop in signal on the oppose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e21cd66e79028f64118dd1d11ff8c052
https://pubmed.ncbi.nlm.nih.gov/14579404
https://pubmed.ncbi.nlm.nih.gov/14579404
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
https://pubmed.ncbi.nlm.nih.gov/11764096