Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Loukia Evliati"'
Autor:
Sophia Delicou, Konstantinos Manganas, Aikaterini Xydaki, Loukia Evliati, Ioanna Myrilla, Leonidas Rubatis, Stavroula Kostaridou
Publikováno v:
Therapeutic Advances in Vaccines and Immunotherapy, Vol 12 (2024)
Background: Hemoglobinopathies, such as sickle cell disease and thalassemia, are genetic disorders that affect hemoglobin structure or production, leading to various health complications, including an increased risk of infections. Vaccinations play a
Externí odkaz:
https://doaj.org/article/6c35e8414a3146e0902f0b9e31a99d9c
Autor:
Antonis Kattamis, Ersi Voskaridou, Sophia Delicou, Evangelos Klironomos, Ioannis Lafiatis, Foteini Petropoulou, Michael D. Diamantidis, Stylianos Lafioniatis, Loukia Evliati, Eleni Kapsali, Kiki Karvounis‐Marolachakis, Despoina Timotheatou, Chrysoula Deligianni, Panagiotis Viktoratos, Alexandra Kourakli
Publikováno v:
eJHaem, Vol 4, Iss 3, Pp 569-581 (2023)
Abstract Patients with transfusion‐dependent beta (β)‐thalassaemia experience a broad range of complications. ULYSSES, an epidemiological, multicentre, retrospective cross‐sectional study, aimed to assess the prevalence and severity of treatme
Externí odkaz:
https://doaj.org/article/5531c3281aa74871a9933de3259920cb
Autor:
Sophia Delicou, Aikaterini Xydaki, Konstantinos Manganas, Emmanouil Koullias, Loukia Evliati, Chryssoula Kalkana, Michael D. Diamantidis, Achilles Manafas, Marianna Katsatou, Leonidas Roumpatis, Theodoros Aforozis
Publikováno v:
Thalassemia Reports, Vol 12, Iss 2, Pp 39-45 (2022)
During a pandemic, people are fearful of becoming infected with the virus, which causes anxiety, loss of purpose, and depression. This study aimed to evaluate the social and psychological impact, as well as the impact on homecare, of patients with he
Externí odkaz:
https://doaj.org/article/a83d2507027f484382ded59336844e7b
Autor:
Polyxeni Delaporta, Alexandra Kourakli, Sophia Delicou, Michael D. Diamantidis, Chrysoula Kalkana, Efthymia Vlachaki, Eftychios Eftychiadis, Ioannis Lafiatis, Despoina Pantelidou, Argiris Symeonidis, Vasileios Lazaris, Aikaterini Xydaki, Achilles Manafas, Loukia Evliati, Filippos Klonizakis, Ioanna Manika, Despoina Papadopoulou, Marianna Chatzieleftheriou, Konstantina Toutoudaki, Dimitra Kyriakopoulou, Antonis Kattamis
Publikováno v:
Blood. 140:8205-8207
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33210638ea2e105cc480c7ef3e7aefef
https://doi.org/10.1182/blood-2022-167675
https://doi.org/10.1182/blood-2022-167675
Autor:
Konstantinos Manganas, Sophia Delicou, Aikaterini Xydaki, Alexandra Kourakli, Loukia Evliati, Euthimia Vlahaki, Evangelos Klironomos, Michail Diamantidis, Ioannis Lafiatis, Antonis Kattamis, Ioannis-Georgios Koskinas
Publikováno v:
Journal of Hepatology. 77:S472
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eee3403deac20e0774f82d8b08699523
https://doi.org/10.1016/s0168-8278(22)01273-9
https://doi.org/10.1016/s0168-8278(22)01273-9
Autor:
Alexandra Kourakli, Loukia Evliati, Ioannis Lafiatis, Ersi Voskaridou, Kiki Karvounis-Marolachakis, Stylianos Lafioniatis, Sophia Delicou, Despoina Timotheatou, Fotini Petropoulou, Eleni Kapsali, Antonis Kattamis, Michael D. Diamantidis, Evangelos Klironomos
Publikováno v:
Blood. 136:5-6
Subtitle Notification: The first and the second author have equally contributed to this project Introduction: Transfusion-dependent β-thalassemia (TDT) confers substantial burden on both patients and the healthcare system, attributable to disease- a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ace42f9f33a4e68000d8cac90fd55e9
https://doi.org/10.1182/blood-2020-138533
https://doi.org/10.1182/blood-2020-138533
Autor:
Aikaterini Xydaki, Despoina Papadopoulou, Ioannis Lafiatis, Despoina Pantelidou, Konstantinos Manganas, Vassiliki Bartzi, Argiris Symeonidis, Dimitra Kyriakopoulou, Sophia Delicou, Antonis Kattamis, Vasileios Lazaris, Eftychios Eftychiadis, Loukia Evliati, Chrysoula Apostolou, Michael D. Diamantidis, Evangelos Klironomos, Efthymia Vlachaki, Alexandra Kourakli
Publikováno v:
Blood. 134:4838-4838
Background: Sickle cell disease (SCD) is an autosomal recessive disorder caused by a point mutation in the β-globin chain of hemoglobin that forms hemoglobin S. It is clinically characterized by complicated episodes of veno-occlusive crises (VOC), e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f064621d4a927251a73cc60a37d6b67
https://doi.org/10.1182/blood-2019-127966
https://doi.org/10.1182/blood-2019-127966