Titlebook: Artificial Kidney, Artificial Liver, and Artificial Cells; Thomas Ming Swi Chang (Professor of Physiology, Pr Book 1978 Springer Science+B

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Feldanalyse als Forschungsprogrammal, London, U.K., my colleagues and I claim no credit as innovators. Indeed, we are mindful of the sound basis to haemoperfusion that was hewn out by Yatsidis and, above all, by Professor Chang here in Montreal, to whom as host I should like to take this opportunity to express my appreciation and gr

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Christian Baier,Andreas Schmitzence has been brought forward that uremic patients accumulate these substances in their body fluids (2–6). Serum middle molecule levels determined by gel filtration were reported by Chang et al. (7) to be more reduced following 2 hours of hemoperfusion than after hemodialysis for 6 to 10 hours as fo

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Evaluation of Charcoal Hemoperfusion in Uremia on a short-time basis (1, 2), and no long term studies of the particular charcoal hemoperfusion device used in these studies have been performed. Chang, et al (3, 4) have published the only long-term studies of charcoal hemoperfusion in the management of uremia.

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Hemoperfusion and Removal of Endogenous Uremic Middle Moleculesence has been brought forward that uremic patients accumulate these substances in their body fluids (2–6). Serum middle molecule levels determined by gel filtration were reported by Chang et al. (7) to be more reduced following 2 hours of hemoperfusion than after hemodialysis for 6 to 10 hours as found by Dzurik et al. (8).

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