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Treating people donating their own blood before surgery.
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Biggs JC, Atkinson KA, Booker V et al (1995) Prospective randomised double-blind trial of the in vivo use of recombinant human erythropoietin in bone marrow transplantation from HLA-identical sibling donors.
In their editorial, Ingelfinger and Remuzzi note the recommendations "are not based on persuasive randomized, controlled trials.
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In connection with the June 2011 ESA label changes, we also agreed to conduct additional clinical trials examining the use of ESAs in CKD.
EPO concentration and red blood cell volume after a few weeks.
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Erythropoietin-induced thrombosis as a result of increased inflammation and thrombin activatable fibrinolytic inhibitor.
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Mice were bled 0, 2, 8, 32, 56 and 80 h after the passive transfer of mouse serum.
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In this review, we have outlined the considerations that need to be taken into account when prescribing ESA for the treatment of anemia in CKD.
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Randomized clinical trials seemed to support an increased mortality with ESA therapy, although more recent ones have not.
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Frequency of administration of recombinant human erythropoietin for anaemia of end-stage renal disease in dialysis patients.
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By comparing the entries at regular intervals, for instance, every 3 months, the directions that the projects take can be visualized.
Poster 843, Supportive Care Session: Prevention of anaemia in patients with solid tumours receiving platinum-based chemotherapy: the NeoPrevent study.
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The toxins produced by the body can cause ulceration.
Tracking the Aftermath of a Corporate Scandal from a Network Perspective: The Case of Roche in Turkey, in Amjad Hadjikhani, Ulf Elg, Pervez Ghauri (ed.
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Toma, only about half of MDS patients (40 percent to 50 percent) respond to ESA treatment.
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MedWatch Safety Information and Adverse Event Reporting.
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G-CSF may shorten the period of neutropenia after chemotherapy, helping the JW patient by limiting septic episodes that exacerbate bleeding and shorten red cell survival.
Euclidean cluster analysis for patients before and after erythropoietin treatment.
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Conclusions High-dose EPO administered as an adjunct to PPCI failed to reduce MI size.
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