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pro vyhledávání: '"beta-Thalassemia/blood"'
Cardiac complications are the leading cause of death in β-thalassemia major (TM) patients. The aim of this study was to investigate the impact of iron overload on ventricular functions using conventional and tissue Doppler imaging (TDI) in patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::a75cd51109370d37c597a5e92b240ed0
Autor:
Konstantinos L. Bourantas, Alexandres Chr. Makis, Anestis Mavridis, Aristidis Chaidos, Georgios N. Dalekos, Stavroula Tsiara
To identify a possible acute phase response during the steady state of sickle cell disease, we estimated the serum alterations of acute phase proteins, beta2-microglobulin (beta2M), kappa and lambda light chains, interleukins (ILs) and tumor necrosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c028adf6ec6344b16f752737abc8ad86
http://olympias.lib.uoi.gr/jspui/handle/123456789/24088
http://olympias.lib.uoi.gr/jspui/handle/123456789/24088
Anti delta IK17 monoclonal antibody was produced by fusing SP2/0/Ag 14 myeloma with spleen cells of BALB/c mice immunized with normal human thymocytes. a delta IK17 antibody recognizes a 44kD cell surface protein detected on human lymphocytes. delta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10561::ac86dfa906ce286f016aece8edea3d08
http://olympias.lib.uoi.gr/jspui/handle/123456789/7470
http://olympias.lib.uoi.gr/jspui/handle/123456789/7470
Publikováno v:
Acta haematologica. 92(2)
Six sickle cell/beta-thalassemia patients (3 males and 3 females) were treated with 500 U/kg body weight human recombinant erythropoietin (h-rEPO) along with 300 mg/day iron sulfate in two phases, for a period of 90 days. Fetal hemoglobin (HbF) was a
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