Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Helen Berdousi"'
Publikováno v:
British Journal of Haematology. 151:504-508
Abnormal iron regulation in patients with thalassaemia intermedia may lead to iron overload even in the absence of transfusions. There are limited data on iron chelator use in patients with thalassaemia intermedia and no guidelines exist for the mana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c881c41666dd7da8ea88a51b57636183
https://doi.org/10.1111/j.1365-2141.2010.08346.x
https://doi.org/10.1111/j.1365-2141.2010.08346.x
Autor:
Helen Berdousi, Olympia Papakonstantinou, Nicholas Gourtsoyiannis, Thomas G. Maris, Vasilios Ladis, Stavroula Kostaridou, Christos Kattamis
Publikováno v:
European Radiology. 17:1535-1543
The study aims at describing the MR features of pancreas in beta-thalassemia major, investigating the relations between MR findings and glucose disturbances and between hepatic and pancreatic siderosis. Signal intensity ratios of the pancreas and liv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::617ad188172cee611dbb6b24fdf8cf81
https://doi.org/10.1007/s00330-006-0507-8
https://doi.org/10.1007/s00330-006-0507-8
Publikováno v:
American Journal of Hematology. 68:221-224
We studied the changing pattern of the distribution of ferritin levels in 430 regularly-transfused patients with thalassemia in an attempt to evaluate compliance of chelation with deferoxamine. The study covered 15 years and was divided in three peri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e4a528ebea226a4d8caed317b6c7e86
https://doi.org/10.1002/ajh.1185
https://doi.org/10.1002/ajh.1185
Publikováno v:
British journal of haematology. 151(5)
Abnormal iron regulation in patients with thalassaemia intermedia may lead to iron overload even in the absence of transfusions. There are limited data on iron chelator use in patients with thalassaemia intermedia and no guidelines exist for the mana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ee28292212914e0a99d84aeb09910b79
https://pubmed.ncbi.nlm.nih.gov/20950401
https://pubmed.ncbi.nlm.nih.gov/20950401
Publikováno v:
Annals of the New York Academy of Sciences. 1054
Iron-induced organ degeneration is the main factor of mortality in patients with thalassemia major. Since chelation therapy is at a turning point, from the laborious parenteral route to the use of new promising oral agents, we investigated the curren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::130b5fd5d8341197736423f071ca1be9
https://pubmed.ncbi.nlm.nih.gov/16339695
https://pubmed.ncbi.nlm.nih.gov/16339695
Autor:
Vassilios Ladis, Antonis Kattamis, Efthymia Alexopoulou, Nikolaos Kelekis, Helen Berdousi, Kalliopi Drakaki, Christos Kattamis, Ioannis Papasotiriou, Aggeliki Galani, Irini Kaloumenou
Publikováno v:
Blood cells, moleculesdiseases. 36(1)
The simultaneous use of deferioxamine (DFO) and deferiprone (DFP) has an additive effect in iron excretion in transfusion-dependent thalassemic patients. In a prospective study, we evaluated the safety and effectiveness of combined therapy with these
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b18e52d82c293d0b5888f1ca41081eee
https://pubmed.ncbi.nlm.nih.gov/16386928
https://pubmed.ncbi.nlm.nih.gov/16386928
Autor:
Helen Berdousi, Fani Palamidou, Spyros Frissiras, Charalambos Theodorides, Christos Kattamis, Vasilis Ladis
Publikováno v:
Annals of the New York Academy of Sciences. 850
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::277868ecd0b00c068dbccb6a987fa8e0
https://pubmed.ncbi.nlm.nih.gov/9668588
https://pubmed.ncbi.nlm.nih.gov/9668588
Autor:
Christos Kattamis, Stylianos Chatzipanagiotou, E. Kourti, N.J. Legakis, Vassilis Ladis, Helen Berdousi, Fani Palamidou
Publikováno v:
Clinical Microbiology and Infection. (2):67-72
Objective To evaluate the prevalence of class-specific antibodies (G, A, M) to Yersinia enterocolitica plasmid-encoded outer proteins (Yops), in a closely followed multitransfused population of patients with thalassemia. Methods Sera from 408 β-thal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::056b5f3cdc167ae2d60c8db87a6976cb