Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Evaggelia Vetsiou"'
Autor:
Panagiotis Andreadis, Stamatia Theodoridou, Marily Pasakiotou, Stergios Arapoglou, Eleni Gigi, Evaggelia Vetsiou, Efthymia Vlachaki
Publikováno v:
Case Reports in Hematology, Vol 2015 (2015)
We herein would like to report an interesting case of a patient who presented with anemia and thrombocytopenia combined with high serum Lactic Dehydrogenase where Thrombotic Thrombocytopenic Purpura was originally considered. As indicated a central v
Externí odkaz:
https://doaj.org/article/eaaec3e8e68c4b8ea7751ed8442ca7b9
Autor:
Efthymia Vlachaki, Panagiotis Andreadis, Nikolaos Neokleous, Aleka Agapidou, Evaggelia Vetsiou, Panagiotis Katsinelos, Panagiota Boura
Publikováno v:
Case Reports in Hematology, Vol 2014 (2014)
Sickle cell/β+ thalassemia (Hb S/β+thal) is considered as a variant form of sickle cell disease. Acute episodes of vasoocclusive pain crisis are characteristic for sickle cell disorders and may be complicated by an acute or chronic life-threatening
Externí odkaz:
https://doaj.org/article/30e4ca02d982438ebf001f59f17535fc
Autor:
Maria Sarigianni, Efthymia Vlachaki, Sofia Chissan, Filippos Klonizakis, Evaggelia Vetsiou, Kyriaki I. Anastasiadou, Elissavet Ioannidou-Papagiannaki, Ioannis Klonizakis
Publikováno v:
Hematology Reports, Vol 3, Iss 3, Pp e25-e25 (2011)
We report a case of a bone marrow aspiration and trephine biopsy (BMATB) associated haematoma in an 85 years old male without any predisposing risk factors. Six days after BMATB, he suffered from a massive thigh and buttock haematoma and a fall in ha
Externí odkaz:
https://doaj.org/article/2b72d17303944e30962ee38bacb3281a
Autor:
Efthymia Vlachaki, Vaia Papageorgiou, Filippos Klonizakis, Maria Spandonidou, Sofia Chisan, Evaggelia Vetsiou, Elissavet Ioannidou
Publikováno v:
Hematology Reports, Vol 3, Iss 3, Pp e20-e20 (2011)
Immune thrombocytopenia (ITP) in adults is an acquired chronic immune-mediated disorder defined by isolated thrombocytopenia. In recent years, an improved understanding of the pathophysiology of ITP has been achieved and is now accepted that the diso
Externí odkaz:
https://doaj.org/article/d2586569791843278380566de7aca5f8
Autor:
Alexandra Agapidou, Evaggelia Vetsiou, Efthymia Vlachaki, Stamatia Theodoridou, Despoina Adamidou, Georgios Spanos, Nikolaos Sousos, Kyriakos Psarras, Philippos Klonizakis, Timoleon-Achilleas Vyzantiadis
Publikováno v:
Acta Haematologica. 137:175-182
Extramedullary hematopoiesis (EMH) results from the extension of hematopoietic tissue beyond the confines of the bones. Since the initiation of regular transfusion programs from an early age for all thalassemia major (ΤΜ) patients, EMH has not been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67a72699a72917ab7ec8bbdd7616bff5
https://doi.org/10.1159/000463919
https://doi.org/10.1159/000463919
Autor:
Michael D. Diamantidis, Paraskevi Fotiou, Nikolaos Neokleous, Evaggelia Vetsiou, Achilles Manafas, Aleka Agapidou, Efthymia Vlachaki
Publikováno v:
International Journal of Hematology. 103:537-544
The life expectancy of thalassemic patients has increased, and now approaches that of healthy individuals, thanks to improved treatment regimens. However, pregnancy in women with β-Thalassemia Μajor remains a challenging condition. Recent advances
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b907191b1e0ef08dbbb822231c8c9ab9
https://doi.org/10.1007/s12185-016-1945-y
https://doi.org/10.1007/s12185-016-1945-y
Autor:
Sofia Hissan, Efthymia Vlachaki, Elias Onoufriadis, Sofia Vakalopoulou, Evaggelia Vetsiou, Dimitra Paspali, Nikolaos Neokleous, Vasilia Garypidou, Panagiota Boura, Nicolaos Sousos
Publikováno v:
Hemoglobin. 39:169-172
β-Thalassemia major (β-TM) is a chronic, genetic blood disorder. Patients are considered to be vulnerable to emotional and behavioral problems. The aim of this study was to assess mental health and somatic pain of patients with homozygous β-TM, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02cac8e09a55afd2e2dd0c111eebdbd8
https://doi.org/10.3109/03630269.2015.1031244
https://doi.org/10.3109/03630269.2015.1031244
Autor:
E. Gigi, Efthymia Vlachaki, Panagiotis Andreadis, Marily Pasakiotou, Stergios Arapoglou, Evaggelia Vetsiou, Stamatia Theodoridou
Publikováno v:
Case Reports in Hematology
Case Reports in Hematology, Vol 2015 (2015)
Case Reports in Hematology, Vol 2015 (2015)
We herein would like to report an interesting case of a patient who presented with anemia and thrombocytopenia combined with high serum Lactic Dehydrogenase where Thrombotic Thrombocytopenic Purpura was originally considered. As indicated a central v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fe97d9b40aef3982be61d38ad9780f8
https://doi.org/10.1155/2015/478151
https://doi.org/10.1155/2015/478151
Autor:
Eudokia Mandala, Konstantina Tsioni, Evaggelia Vetsiou, Emmanouil Sinakos, E. Gigi, Angelos Daniilidis, Efthymia Vlachaki, Philippos Klonizakis, Nikolaos Sousos, Despoina Adamidou
Publikováno v:
British journal of haematology. 181(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27c74631ee713a6aa00cdc53652da1d0
https://pubmed.ncbi.nlm.nih.gov/28106901
https://pubmed.ncbi.nlm.nih.gov/28106901
Publikováno v:
Hemoglobin. 37:94-100
Deferasirox (DFRA) is a novel oral chelator agent for treatment of iron overload. Although well established in the treatment of β-thalassemia major (β-TM), it has not yet been fully investigated in patients with sickle cell disease. The aim of this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98fed860d93a189d7df4359e01d9c16b
https://doi.org/10.3109/03630269.2012.746696
https://doi.org/10.3109/03630269.2012.746696