Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Ioannis, Rombos"'
Autor:
Iakovos Armenis, Vassiliki Kalotychou, Revekka Tzanetea, Panagoula Kollia, Zoi Kontogeorgiou, Dimitra Anastasopoulou, Marina Mantzourani, Michael Samarkos, Konstantinos Pantos, Kostas Konstantopoulos, Ioannis Rombos
Publikováno v:
Data in Brief, Vol 10, Iss C, Pp 192-197 (2017)
In this article, we present data on endothelial Nitric Oxide Synthase (eNOS) gene T786C and G894T polymorphisms in Greek steady-state Sickle Cell Disease patients in comparison to healthy controls. Moreover, eNOS mRNA levels were determined in periph
Externí odkaz:
https://doaj.org/article/2487c195e7af4898b575722ea4902f0d
Autor:
Kostas Konstantopoulos, Revekka Tzanetea, Ioannis Rombos, Iakovos Armenis, Vassiliki Kalotychou
Publikováno v:
Nitric oxide : biology and chemistry.
Hypoxia-Inducible Factor-1α (HIF-1α) expression is upregulated in Sickle Cell Disease (SCD) and correlates with various laboratory markers of disease severity. Nitric Oxide plays a pivotal role in SCD pathophysiology and endothelial Nitric Oxide Sy
Autor:
Dimitra Anastasopoulou, Kostas Konstantopoulos, Ioannis Moyssakis, C. Pantos, Vassiliki Kalotychou, Ioannis Rombos, Revekka Tzanetea, Iakovos Armenis
Publikováno v:
Annals of hematology. 98(7)
Sickle cell disease (SCD), a hereditary form of chronic hemolytic anemia, is characterized by acute vascular occlusion and chronic complications as pulmonary hypertension (PH), a hallmark of higher mortality. This study aimed to determine peripheral
Autor:
Michael Samarkos, Konstantinos Pantos, Ioannis Rombos, Revekka Tzanetea, Panagoula Kollia, Vassiliki Kalotychou, Dimitra Anastasopoulou, Kostas Konstantopoulos, Zoi Kontogeorgiou, Marina Mantzourani, Iakovos Armenis
Publikováno v:
Nitric oxide : biology and chemistry. 62
Endothelial Nitric Oxide Synthase (eNOS) is crucial for vascular homeostasis. Polymorphisms T786C and G894T affect eNOS regulation and have been related to various diseases. Sickle Cell Disease (SCD), a clinically diverse chronic hemolytic anemia, im
Autor:
Christina Lazaropoulou, Ioannis Rombos, Periklis Makrythanasis, Vassiliki Kalotychou, Ino Kanavaki, Ioannis Papassotiriou, Antonis Kattamis, Revekka Tzanetea
Publikováno v:
European Journal of Clinical Investigation. 42:27-33
Eur J Clin Invest 2012; 42 (1): 27–33 Abstract Background and aim The primary symptoms of sickle cell disease (SCD) arise from vaso-occlusive crises. The pathogenesis of these crises is complex phenomenon where endothelial activation and damage has
Autor:
Kostas Konstantopoulos, Ioannis Papassotiriou, Vassiliki Kalotychou, Ioannis Rombos, Revekka Tzanetea
Publikováno v:
Hemoglobin. 34:383-388
A 40-year-old Greek male was admitted to the hospital because of acute respiratory infection. The patient has been undergoing regular venesection for erythrocytosis for 20 years; he has also been taking oral anticoagulants for thrombosis for 15 years
Autor:
Ioannis Rombos, Maria Tsironi, Periklis Makrythanasis, Antonis Kattamis, Christina Lazaropoulou, Ioannis Papassotiriou, Ino Kanavaki
Publikováno v:
Blood Cells, Molecules, and Diseases. 43:230-234
The term thalassemia intermedia, indicates a clinical condition of intermediate severity between thalassaemia minor, the asymptomatic carrier, and thalassaemia major, the transfusion-dependent, severe form. Thromboembolic events frequently complicate
Autor:
Maria Karakosta, Kalliopi N. Manola, Alkiviadis Kostakis, Gabriel E. Pantelias, Ioannis Rombos, Gregory Kouraklis, Vassiliki Kalotychou
Publikováno v:
Acta haematologica. 132(1)
Chronic lymphocytic leukemia (CLL) has been recently attributed to a combination of genetic predisposition and exposure to environmental factors. UDP-glucuronosyltransferase (UGT)1A1*28 is an inborn polymorphism that results in significant downregula
Autor:
Ino, Kanavaki, Periklis, Makrythanasis, Christina, Lazaropoulou, Antonis, Kattamis, Revekka, Tzanetea, Vassiliki, Kalotychou, Ioannis, Rombos, Ioannis, Papassotiriou
Publikováno v:
European journal of clinical investigation. 42(1)
The primary symptoms of sickle cell disease (SCD) arise from vaso-occlusive crises. The pathogenesis of these crises is complex phenomenon where endothelial activation and damage has a major role. Chronic inflammation also plays an important role in
Autor:
Antonios Kattamis, Ioannis Papassotiriou, Emmanuel Kanavakis, Filia Apostolakou, Ino Kanavaki, Christina Lazaropoulou, Maria Papastamataki, Evgenios Goussetis, Vassiliki Kalotychou, Anna Gizi, Ioannis Rombos
Publikováno v:
Blood cells, moleculesdiseases. 46(3)
Continuous reactive oxygen species (ROS) production in individuals with sickle cell disease (SCD) may alter their overall redox status and cause tissue damage. The aim of this study was to evaluate oxidative stress in patients with SCD using two new