Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Revekka Tzanetea"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffff3b6d833e15ff09af0cb0df0a82cd
https://pubmed.ncbi.nlm.nih.gov/33812003
https://pubmed.ncbi.nlm.nih.gov/33812003
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::781c9ee8faa7beafb36457c7cb0c369f
https://pubmed.ncbi.nlm.nih.gov/31098737
https://pubmed.ncbi.nlm.nih.gov/31098737
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::125e5f0156e9fc5f8ccd0b7d821ec1d1
https://pubmed.ncbi.nlm.nih.gov/27871907
https://pubmed.ncbi.nlm.nih.gov/27871907
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a9aab666b45c1796fb80b2a34112078
https://doi.org/10.1111/j.1365-2362.2011.02551.x
https://doi.org/10.1111/j.1365-2362.2011.02551.x
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2da21406ca28e8ff86f36db79e13cb7
https://doi.org/10.3109/03630269.2010.486331
https://doi.org/10.3109/03630269.2010.486331
Autor:
Thomas Tassiopoulos, Kostas Konstantopoulos, Revekka Tzanetea, Vassiliki Kalotychou, Yannis Rombos, Phaedon Fessas, Athanasios Aessopos, Spyros Simitzis
Publikováno v:
Blood Cells, Molecules, and Diseases. 28:283-287
ABSTRACT Sickle cell disease patients who acquire iron deficiency may experience a degree of amelioration from painful crises in terms of frequency, severity, and duration. This observation prompted us to identify the potential utility of iron load r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::956a636ac63e6a79a98ebeacdffe90ad
https://doi.org/10.1006/bcmd.2002.0489
https://doi.org/10.1006/bcmd.2002.0489
Autor:
Aleka Stamoulakatou, Revekka Tzanetea, Yannis Rombos, Vassiliki Kalotychou, Kostas Konstantopoulos, Maria Karakosta
Gilbert’s syndrome is characterized by a benign indirect hyperbilirubinemia. It has often been underestimated and undiagnosed because of its mild symptoms; although it is not as rare as was once believed when its frequency was estimated using data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69ddbc108fb3c8b3ae736fc9d17b360a
https://europepmc.org/articles/PMC3205121/
https://europepmc.org/articles/PMC3205121/
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b09ec6f6878827628a0e5544f1fa6283
https://pubmed.ncbi.nlm.nih.gov/21615396
https://pubmed.ncbi.nlm.nih.gov/21615396
Autor:
Yannis Rombos, Vassiliki Kalotychou, Revekka Tzanetea, Dimitris Loukopoulos, Katerina Antonatou, E. Terpos
Publikováno v:
Blood cells, moleculesdiseases. 31(1)
Gilbert's syndrome is characterized by mild unconjugated hyperbilirubinemia. The molecular basis of this syndrome usually concerns an additional dinucleotide insertion (TA) in the A(TA)(n)TAA configuration residing in the promoter region of the UGT1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a53617409e1146c3f4e3a38f231b4813
https://pubmed.ncbi.nlm.nih.gov/12850481
https://pubmed.ncbi.nlm.nih.gov/12850481