Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Eleni Yfanti"'
Autor:
Sofia Chissan, Paschalis Evangelidis, Nikolaos Evangelidis, Nikolaos Kotsiou, Eleni Gavriilaki, Sofia Vakalopoulou, Eleni Yfanti, Stamatia Theodoridou
Publikováno v:
HemaSphere, Vol 7, p e6540436 (2023)
Externí odkaz:
https://doaj.org/article/8d0de137f94143a19f88ac86db6f0c54
Autor:
Stamatia Theodoridou, Evaggelia-Eleni Delaki, Eleni Yfanti, Aikaterini Teli, Genovefa Mantzou, Christina Karipidou, Maria Dimopoulou
Publikováno v:
HemaSphere, Vol 7, p e22018fd (2023)
Externí odkaz:
https://doaj.org/article/2e94bf79165b469bbf4b4a59e6287c8f
Autor:
Elena Alhazidou, Maria Androulaki, Michail Panagiotopoulos, Dimitrios Boudouvas, Dionysia Lampropoulou, Eleni Yfanti, Evangelia-Eleni Delaki, Konstantina Repa, Georgios Petrakos
Publikováno v:
Case Reports in Women's Health, Vol 28, Iss , Pp e00265- (2020)
Introduction: This case report describes a fetus with compound heterozygosity for Hb G-Hsi-Tsou and beta thalassemia, diagnosed in a healthy pregnancy. To the best of our knowledge, this is the first documented case of compound heterozygosity and the
Externí odkaz:
https://doaj.org/article/09d9b5cee9cc45ad8bcdd2dd8cf9e7bd
Autor:
Panayoula C. Tsiotra, Constantine Tsigos, Eleni Anastasiou, Eleni Yfanti, Eleni Boutati, Emmanouil Souvatzoglou, Ioannis Kyrou, Sotirios A. Raptis
Publikováno v:
Mediators of Inflammation, Vol 2008 (2008)
Resistin has been shown to cause insulin resistance and to impair glucose tolerance in rodents, but in humans its physiological role still remains elusive. The aim of this study was to examine whether resistin mRNA expression in human peripheral mono
Externí odkaz:
https://doaj.org/article/3b0d43b6c1c34da08e4ce27d382f6b9a
Autor:
Evangelia Zarkada, Eleni Yfanti, Aikaterini Teli, Angeliki Balassopoulou, Klio Sinopoulou, Stamatia Theodoridou
Publikováno v:
Hemoglobin. 46:140-142
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cc22b5a448565381f59e190dfab895e
https://doi.org/10.1080/03630269.2022.2096462
https://doi.org/10.1080/03630269.2022.2096462
Autor:
Evangelia, Zarkada, Eleni, Yfanti, Aikaterini, Teli, Angeliki, Balassopoulou, Klio, Sinopoulou, Stamatia, Theodoridou
Publikováno v:
Hemoglobin. 46(2)
We report the hematological data of the codon 7 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0a1419bf063a76383edd52e9b97ec059
https://pubmed.ncbi.nlm.nih.gov/36000573
https://pubmed.ncbi.nlm.nih.gov/36000573
Autor:
Konstantina Repa, Dimitrios Boudouvas, Dionysia Lampropoulou, Evangelia-Eleni Delaki, Elena Alhazidou, Georgios Petrakos, Michail Panagiotopoulos, Maria Androulaki, Eleni Yfanti
Publikováno v:
Case Reports in Women's Health
Case Reports in Women's Health, Vol 28, Iss, Pp e00265-(2020)
Case Reports in Women's Health, Vol 28, Iss, Pp e00265-(2020)
Introduction This case report describes a fetus with compound heterozygosity for Hb G-Hsi-Tsou and beta thalassemia, diagnosed in a healthy pregnancy. To the best of our knowledge, this is the first documented case of compound heterozygosity and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00d133f3a49575e7302601a09f2d0338
http://europepmc.org/articles/PMC7607242
http://europepmc.org/articles/PMC7607242
Autor:
Ersi Voskaridou, Evangelia Vetsiou, Effrossyni Boutou, Efthymia Vlachaki, Eleni Yfanti, Stamatia Theodoridou, Angeliki Balassopoulou, Evangelia-Eleni Delaki, Timoleon-Achilleas Vyzantiadis
Publikováno v:
Journal of pediatric hematology/oncology. 42(8)
Greece is a country of ~11 million people, where hemoglobinopathies are the most common genetic diseases. The reported data describe the clinical phenotype of cases with coinheritance of triplicated α-globin (anti-α3.7 kb) and β-globin gene mutati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed8129062bd83e0b6917043b3b354dcd
https://pubmed.ncbi.nlm.nih.gov/32032239
https://pubmed.ncbi.nlm.nih.gov/32032239
Autor:
Olga Karakasidou, Despoina Adamidou, Timoleon-Achilleas Vyzantiadis, Eleni Yfanti, Stamatia Theodoridou, Ersi Voskaridou, Angeliki Balassopoulou, Marina Economou, Theodoros Theodoridis, Effrossyni Boutou, Evangelia Skatharoudi, Nikolaos Prapas, Αikaterini Teli, Evangelia-Eleni Delaki
Publikováno v:
Hemoglobin. 42:257-263
Hemoglobinopathies constitute the most frequent monogenic disorders worldwide and in Greece. In Greece, carrier frequency is estimated at about 8.0%, resulting in a heavy disease burden in the past. Therefore, the implementation of a national prevent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5af4a17172365ca9b8827b239ab856bb
https://doi.org/10.1080/03630269.2018.1528986
https://doi.org/10.1080/03630269.2018.1528986
Autor:
Timoleon-Achilleas Vyzantiadis, Stamatia Theodoridou, Aikaterini Teli, Marina Economou, Theodoros Theodoridis, Eleni Yfanti
Publikováno v:
Hemoglobin. 42:129-131
Hb Adana (HBA2: c.179G>A) is found worldwide but is extremely rare and carriers are asymptomatic, with red cell indices similar to α+-thalassemia (α+-thal) carriers. First line screening tests are unable to detect the unstable hemoglobin (Hb). Coin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b54335c39ec6dfce0a4cbdd795d59cf
https://doi.org/10.1080/03630269.2018.1466711
https://doi.org/10.1080/03630269.2018.1466711