Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Despina Pantelidou"'
Autor:
Philippos Klonizakis, Noémi Roy, Ioanna Papatsouma, Maria Mainou, Ioanna Christodoulou, Despina Pantelidou, Smaro Kokkota, Michael Diamantidis, Alexandra Kourakli, Vasileios Lazaris, Dimitrios Andriopoulos, Apostolos Tsapas, Robert J. Klaassen, Efthymia Vlachaki
Publikováno v:
Healthcare, Vol 12, Iss 5, p 524 (2024)
The assessment of health-related quality of life (HRQoL) in thalassemia offers a holistic approach to the disease and facilitates better communication between physicians and patients. This study aimed to evaluate the HRQoL of transfusion-dependent th
Externí odkaz:
https://doaj.org/article/2b7b58604d1546f0b53387bbf45a0f12
Autor:
Varnavas Constantinou, Penelope‐Georgia Papayanni, Despina Mallouri, Ioannis Batsis, Asimina Bouinta, Despoina Papadopoulou, Vasiliki Papadimitriou, Maria Kammenou, Despina Pantelidou, Damianos Sotiropoulos, Ioanna Sakellari, Achilles Anagnostopoulos, Evangelia Yannaki
Publikováno v:
British Journal of Haematology. 196:1401-1404
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca165037b567bdd541bfbd09371f3b68
https://doi.org/10.1111/bjh.17965
https://doi.org/10.1111/bjh.17965
Autor:
Chrysoula Pourzitaki, Despina Pantelidou, Perla Eleftheriou, Dimitrios Kouvelas, Michael D. Diamantidis, Vasileios Tsolakidis, Maria Papaioannou, Efthymia Vlachaki
Publikováno v:
Hemoglobin. 45(3)
Sickle cell disease includes a group of congenital hemolytic anemias, all characterized by the predominance of Hb S (HBB: c.20A>T). The population movement due to economic migration or escape from ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5d94ed0f7517b7e8233eee3561756b7
https://pubmed.ncbi.nlm.nih.gov/34334096
https://pubmed.ncbi.nlm.nih.gov/34334096
Autor:
Vassilios Papadopoulos, Fotios Girtovitis, Anna Karagianni, Vaia Papageorgiou, Despina Pantelidou, M. Topalidou, Aristea-Lia Mpellou, Anna Kioumi, Panagiotis Patinakis
Publikováno v:
Open Journal of Blood Diseases. :36-42
Sickle-cell intrahepatic cholestasis (SCIC) is an uncommon complication of sickle-cell disease (SCD), which can be life-threating if left untreated. We present the case of a 28-year-old man with SCD, who presented with jaundice and abdominal pain, on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efcf63fe409b77c54b35ca5ea9a49f30
https://doi.org/10.4236/ojbd.2013.31008
https://doi.org/10.4236/ojbd.2013.31008
Publikováno v:
British Journal of Haematology. 121:605-613
Research is required to determine the optimal approach for prophylactic platelet transfusions in patients with haematological malignant disorders. It has been suggested that thresholds for prophylactic platelet transfusions of platelet counts below 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6dcd0f0506dfac2866d6ab018e16a0fb
https://doi.org/10.1046/j.1365-2141.2003.04312.x
https://doi.org/10.1046/j.1365-2141.2003.04312.x
Autor:
Zafiris Kartasis, Ioannis Manavis, Ioannis Kotsianidis, Alexandros Polychronidis, Despina Pantelidou, Emanuel Spanoudakis, Anastasios J. Karayiannakis, Costas Tsatalas, Vasiliki Kaloutsi, Dimitris Margaritis, George Bourikas
Publikováno v:
Acta Haematologica. 110:193-196
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare disorder characterized by pancytopenia, hemolysis, and thrombosis. Abdominal vein thrombosis is a life-threatening manifestation of this disease. We present a patient with complete spleen necrosis d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::579d047d46052b8a1d2ed1ae3dbe2548
https://doi.org/10.1159/000074224
https://doi.org/10.1159/000074224
Publikováno v:
Annals of Hematology
Annals of Hematology, Springer Verlag, 2009, 89 (6), pp.641-642. 〈10.1007/s00277-009-0852-1〉
Annals of Hematology, Springer Verlag, 2009, 89 (6), pp.641-642. 〈10.1007/s00277-009-0852-1〉
Dear Editor, The cytogenetic hallmark of chronic myeloid leukemia (CML) is the Philadelphia chromosome (Ph), the consequence of the reciprocal translocation t(9;22)(q34;q11.2) that results in the BCR-ABL1 fusion gene, located in the Ph chromosome [1]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c01fe927be55faf67b9341281a7686ec
https://hal.archives-ouvertes.fr/hal-00486566/file/PEER_stage2_10.1007%2Fs00277-009-0852-1.pdf
https://hal.archives-ouvertes.fr/hal-00486566/file/PEER_stage2_10.1007%2Fs00277-009-0852-1.pdf
Publikováno v:
British journal of haematology. 121(4)
Research is required to determine the optimal approach for prophylactic platelet transfusions in patients with haematological malignant disorders. It has been suggested that thresholds for prophylactic platelet transfusions of platelet counts below 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3c9c311f960a509d38eec0bbbb58bab6
https://pubmed.ncbi.nlm.nih.gov/14616988
https://pubmed.ncbi.nlm.nih.gov/14616988
Autor:
Emmanuel Spanoudakis, Vasiliki Kaloutsi, George Bourikas, Costas Tsatalas, Dimitris Margaritis, Despina Pantelidou
Publikováno v:
The Hematology Journal. 5:546-547
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c8680c94b3fd393f76412a74b0c4457
https://doi.org/10.1038/sj.thj.6200554
https://doi.org/10.1038/sj.thj.6200554
Publikováno v:
British Journal of Haematology. 123:751-752
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58622aa9b006c7a216ad62f241be8dba
https://doi.org/10.1046/j.1365-2141.2003.04693.x
https://doi.org/10.1046/j.1365-2141.2003.04693.x