Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Niki Vgontza"'
Autor:
Aspasia Argyrou, Serena Valsami, Abraham Pouliakis, Maria Gavalaki, Antonis Aggelidis, Vasiliki Voulgaridou, Vasiliki Pliatsika, Theofanis Adraktas, Andreas Papachronis, Chrysoula Alepi, Vasiliki Giannopoulou, Panagiotis Siourounis, Sofia Tsagia, Georges Martinis, Eftihia Kontekaki, Eleftheria Zervou, Spiridon Koliofotis, Elias Kyriakou, Athina Mougiou, Lempousi Dimitra, Afrodite Chairopoulou, Aggeliki Tsakania, Maria Baka, Ioanna Apostolidou, Dimitra Moschandreou, Anastasia Livada, Marianna Politou, Fragoula Roussinou, Christina Pappa, Vasiliki Koika, Niki Vgontza, Anthippi Gafou, Ioanna Dendrinou, Fotini Sakellaridi, Lampothea Labrianou, Zafeiria Alexandropoulou, Vasiliki Sochali, Kostas Malekas, Areti Skordilaki, Georgia Kakava, Konstantinos Lebesopoulos, Konstantinos Stamoulis, Elisavet Grouzi
Publikováno v:
Turkish Journal of Hematology, Vol 38, Iss 1, Pp 22-32 (2021)
Objective: Fresh frozen plasma (FFP) transfusion is widely used in modern clinical settings. Practices regarding its use vary due to lack of guidelines from randomized trials. The aim of this study was to assess both the current practices regarding F
Externí odkaz:
https://doaj.org/article/856e28b3191146318980af524dcb6a3e
Autor:
Serena Valsami, Elisavet Grouzi, Abraham Pouliakis, Leontini Fountoulaki - Paparisos, Elias Kyriakou, Maria Gavalaki, Elias Markopoulos, Ekaterini Kontopanou, Ioannis Tsolakis, Argyrios Tsantes, Alexandra Tsoka, Anastasia Livada, Vassiliki Rekari, Niki Vgontza, Dimitra Agoritsa, Marianna Politou, Stavros Nousis, Aspasia Argyrou, Ekaterini Manaka, Maria Baka, Maria Mouratidou, Stavroula Tsitlakidou, Konstantinos Malekas, Dimitrios Maltezos, Paraskevi Papadopoulou, Vassiliki Pournara, Ageliki Tirogala, Emmanouil Lysikatos, Sousanna Pefani, Konstantinos Stamoulis
Publikováno v:
Turkish Journal of Hematology, Vol 34, Iss 1, Pp 52-58 (2017)
Objective: Greece is ranked as the second highest consumer of blood components in Europe. For an effective transfusion system and in order to reduce variability of transfusion practice by implementing evidence-based transfusion guidelines it is neces
Externí odkaz:
https://doaj.org/article/2ba2f37dc2fa40cf81cf4c758f39ba5d
Autor:
Maria Baka, Paraskevi Papadopoulou, Dimitrios Maltezo, Elisavet Grouzi, Emmanouil Lysikatos, Sousanna Pefani, Elias Markopoulos, Anastasia Livada, Niki Vgontza, Maria Gavalaki, Dimitra Agoritsa, Ageliki Tirogala, Alexandra Tsoka, Argyrios Tsantes, Stavros Nousis, Abraham Pouliakis, Stavroula Tsitlakidou, Serena Valsami, Ioannis Tsolakis, Leontini Fountoulaki-Paparisos, Vassiliki Rekari, Aspasia Argyrou, Ekaterini Kontopanou, Vassiliki Pournara, Marianna Politou, Konstantinos E. Stamoulis, Maria Mouratidou, Konstantinos Malekas, Ekaterini Manaka, Elias Kyriakou
Publikováno v:
Turkish Journal of Hematology, Vol 34, Iss 1, Pp 52-58 (2017)
Turkish Journal of Hematology
Turkish Journal of Hematology
Greece is ranked as the second highest consumer of blood components in Europe. For an effective transfusion system and in order to reduce variability of transfusion practice by implementing evidence-based transfusion guidelines it is necessary to stu
Autor:
Athanasios Lagiandreou, Efthimios Dalagiorgos, John Koskinas, Helen Berdoussi, Nikolaos J. Tsagarakis, Evanthia Diamanti-Kandarakis, Niki Vgontza, Ersi Voskaridou, Konstantinos Kaligeros, Dimitrios Kountouras, Paraskevi Roussou, Evangelia Fatourou, Nikolaos Chrysanthos, Markissia Karagiorga
Publikováno v:
Liver International. 33:420-427
Background Iron overload and hepatitis-C virus (HCV) infection, have been implicated in the evolution of liver disease, in patients with transfusion-dependent beta-thalassaemia major (BTM). However, the impact of these factors in late stages of liver
Autor:
Konstantinos Sialevris, Niki Vgontza, Melanie Deutsch, Spyridon Tsikrikas, Dimitrios Vassilopoulos, Athanasios J. Archimandritis, Emmanuel Tsochatzis
Publikováno v:
Annals of Hematology. 87:499-500
Dear Editor, We present a case of an adult patient with sickle cell βthalassemia and a severe episode of recurrent acute splenic sequestration crisis (ASSC). A 21-year-old white man with sickle cell β-thalassemia was admitted to our hospital with h