Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Michalis Samarkos"'
Autor:
Panagiotis T Diamantopoulos, Amalia Anastasopoulou, Maria Dimopoulou, Michalis Samarkos, Helen Gogas
Publikováno v:
Therapeutic Advances in Hematology, Vol 14 (2023)
Patients with sickle cell disease (SCD) suffer from complications due to anemia, inflammation, and vaso-occlusion. Factors that trigger sickling and/or inflammation may initiate such complications, while treatment with hydroxyurea (HU) reduces their
Externí odkaz:
https://doaj.org/article/58f90757d6364a30953ddfe06cfe443d
Autor:
Dimitris Basoulis, Pantelis Avramopoulos, Maria Aggelara, Georgios Karamanakos, Pantazis-Michail Voutsinas, Amalia Karapanou, Mina Psichogiou, Michalis Samarkos, Foteini Ntziora, Nikolaos V. Sipsas
Publikováno v:
Canadian Respiratory Journal, Vol 2023 (2023)
Background. High-flow nasal cannula (HFNC) is an oxygen delivery method shown to reduce the risk of intubation and mortality in patients with type 1 respiratory failure. The ROX-index score can predict HFNC failure. This study aims to evaluate sequen
Externí odkaz:
https://doaj.org/article/2a47c13d88d94093a708f1dad3bfdf8b
Autor:
Olga Benopoulou, Irene Kourbeti, Mina Psichogiou, Fani Athanassouli, Eva Kassi, Ilias Giovanopoulos, Nikos Asonitis, Marina Mantzourani, Akrivi Savelli, Fotini Petychaki, Michalis Samarkos, Helen Gogas, Evangelos Cholongitas, Anna Angelousi
Publikováno v:
Endocrine Abstracts.
Autor:
Dimitris Loukopoulos, Maria Dalekou, Effie Apostolidou, Christos Meletis, Michalis Samarkos, Konstantinos Korovesis, Evangelos Terpos, John Meletis, Veroniki Komninaka, Eleni Variami, Efstathios Paravasiliou, Konstantinos Konstantopoulos, Olga Benopoulou
Publikováno v:
Hematology (Amsterdam, Netherlands). 5(6)
During bone marrow engraftment following BMT there is a re-establishment of fetal erythropoiesis, expressed by the increase of F-cells. This seems to depend on several factors such as underlying disease, conditioning before therapy and other mechanis
Autor:
Michalis Samarkos, Nora Viniou, Konstantinos Korovesis, Evangelos Terpos, Effie Apostolidou, Christos Meletis, Despina Mavrogianni, Maria Tsironi, John Meletis
Publikováno v:
International Journal of Hematology. 78:344-348
Paroxysmal nocturnal hemoglobinuria (PNH) clones deficient in glycosylphosphatidylinositol-anchored molecules, including CD55 and CD59, have been previously described in patients with multiple myeloma (MM). The aim of this study was to investigate th
Autor:
Veroniki Komninaka, Konstantinos Konstantopoulos, Nora Viniou, Michalis Samarkos, Effie Apostolidou, Christos Meletis, Eleni Variami, John Meletis, Konstantinos Anargyrou, Despina Mavrogianni, Olga Benopoulou, Evangelos Terpos, Konstantinos Korovesis
Publikováno v:
International Journal of Hematology. 75:40-44
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal disorder characterized by a decrease or absence of glycosylphosphatidylinositol (GPI)-anchored molecules such as CD55 and CD59 from the surface of affected cells, resulting in intravascu
Autor:
Despina Mavrogianni, Effie Apostolidou, Veroniki Komninaka, Konstantinos Anargyrou, Christos Meletis, Nora Viniou, Konstantinos Konstantopoulos, Evangelos Terpos, Michalis Samarkos, Eleni Variami, Konstantinos Korovesis, John Meletis
Publikováno v:
Hematology. 7:69-74
CD55 and CD59 are complement regulatory proteins that are linked to the cell membrane via a glycosyl-phosphatidylinositol anchor. They are reduced mainly in paroxysmal nocturnal hemoglobinuria (PNH) and in other hematological disorders. However, ther
Autor:
E Terpos, Konstantinos Korovesis, Dimitris Loukopoulos, Effie Apostolidou, Michalis Samarkos, Konstantinos Konstantopoulos, Eleni Variami, Olga Benopoulou, Despina Mavrogianni, Xenophon Yataganas, Veroniki Komninaka, John Meletis, Christos Meletis
Publikováno v:
Haematologia. 31:7-16
Paroxysmal nocturnal haemoglobinuria (PNH) is an acquired clonal stem cell disorder characterized by intravascular haemolysis, venous thrombosis, marrow hypoplasia, frequent episodes of infection, and rarely leukaemic conversion. At the cellular leve
Autor:
Kostas Korovesis, Nora Viniou, Effie Apostolidou, Christos Meletis, Eleni Variami, Dimitris Boutsis, Despina Mavrogianni, Dimitris Loukopoulos, Evangelos Terpos, Veroniki Komninaka, Michalis Samarkos, John Meletis, Kostas Konstantopoulos
Publikováno v:
The Hematology Journal. 2:33-37
Introduction Paroxysmal nocturnal hemoglobinuria is an acquired clonal stem cell disorder characterized by the decrease or absence of glycosylphosphatidylinositol-anchored molecules from the surface of the affected cells, such as CD55 and CD59, resul
Autor:
Niki Stavrogianni, Christos Poziopoulos, Christos Meletis, Evi Michali, Stathis Vavourakis, John Meletis, Kostas Konstantopoulos, George Vaiopoulos, Michalis Samarkos, Xenophon Yataganas, Dimitris Loukopoulos
Publikováno v:
British Journal of Haematology. 89:911-913
A case of adult osteopetrosis Type I was diagnosed in a 22-year-old female. She presented for investigation of anaemia with 'myelophthisic' characteristics and extramedullary haemopoiesis which was resistant to haematinics, nandrolone and low-dose co