Effect of membrane composition and structure on solute removal and biocompatibility in hemodialysis.
暂无分享,去创建一个
M J Lysaght | W R Clark | W. Clark | M. Lysaght | R. Hamburger | R J Hamburger | William R. Clark | Richard J. Hamburger | Michael J. Lysaght
[1] M. Daha,et al. Biocompatibility and Performance of a Modified Cellulosic and a Synthetic High Flux Dialyzer: A Randomized Crossover Comparison Between Cellulose Triacetate and Polysulphon , 1995, ASAIO journal.
[2] K. Nolph,et al. Ultrafiltration: a mechanism for removal of intermediate molecular weight substances in coil dialyzers. , 1974, Kidney international.
[3] C Ronco,et al. Impact of Spacing Filaments External to Hollow Fibers on Dialysate flow Distribution and Dialyzer Performance , 1997, The International journal of artificial organs.
[4] M. Kazatchkine,et al. Induction of IL-1 during hemodialysis: transmembrane passage of intact endotoxins (LPS). , 1990, Kidney international.
[5] D. Lane,et al. The scientific basis for selection of measures of thrombogenicity. , 1994, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[6] A. Dalmasso,et al. Hemodialysis leukopenia. Pulmonary vascular leukostasis resulting from complement activation by dialyzer cellophane membranes. , 1977, The Journal of clinical investigation.
[7] C. Ronco,et al. Beta 2-microglobulin Removal by Synthetic Dialysis Membranes. Mechanisms and Kinetics of the Molecule , 1997, The International journal of artificial organs.
[8] E. Klein,et al. Endotoxin and Bacterial Contamination of Dialysis Center Water and Dialysate; a Cross Sectional Survey , 1990, The International journal of artificial organs.
[9] K. Jindal,et al. A study of the basic principles determining the performance of several high-flux dialyzers. , 1989, American journal of kidney diseases : the official journal of the National Kidney Foundation.
[10] G. Lonnemann. Dialysate bacteriological quality and the permeability of dialyzer membranes to pyrogens. , 1993, Kidney international. Supplement.
[11] E. Lee,et al. Pharmacokinetics of Intravenous Vancomycin in Patients with End‐Stage Renal Failure , 1990, Therapeutic drug monitoring.
[12] M. Seitz,et al. Biocompatibility Differences with Respect to the Dialyzer Sterilization Method , 1998, Nephron.
[13] K. Schaefer,et al. Different handling of beta 2-microglobulin during hemodialysis and hemofiltration. , 1988, Nephron.
[14] E. Ritz,et al. Bioincompatibility of dialysis membranes: factor H binding correlates inversely with complement activation indicating a local imbalance of involved proteases/anti-proteases. , 1988, Advances in experimental medicine and biology.
[15] N. Hoenich,et al. Clinical comparison of high-flux cellulose acetate and synthetic membranes. , 1994, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[16] C. Ronco,et al. Haemodialysers and Associated Devices , 1996 .
[17] M. Goldman,et al. Adsorption of ß2-Microglobulin on Dialysis Membranes: Comparison of Different Dialyzers and Effects of Reuse Procedures , 1989, The International journal of artificial organs.
[18] W. Hörl,et al. Immune dysfunction in uremia. , 1997, Kidney international. Supplement.
[19] M. Lysaght. Hemodialysis membranes in transition. , 1988, Contributions to nephrology.
[20] H. Strathmann,et al. Basic features of the polyamide membranes. , 1992, Contributions to nephrology.
[21] J. Floege,et al. β2-Microglobulin Kinetics During Haemofiltration , 1988 .
[22] C. Dinarello,et al. Transcription, not synthesis, of interleukin-1 and tumor necrosis factor by complement. , 1990, Kidney international.
[23] A. Cheung,et al. Effects of Hemodialyzer Reuse on Clearances of Urea and β2-Microglobulin , 1999 .
[24] J. Rotschafer,et al. Vancomycin pharmacokinetics in patients with various degrees of renal function , 1988, Antimicrobial Agents and Chemotherapy.
[25] L. Henderson,et al. Biophysics of Ultrafiltration and Hemofiltration , 1996 .
[26] B. Branger,et al. β2-Microglobulin Kinetics During Haemodialysis and Haemofiltration , 1987 .
[27] B. Pereira. Cytokine production in patients on dialysis. , 1995, Blood purification.
[28] L. Smeby,et al. Microdomain structure of polymeric surfaces--potential for improving blood treatment procedures. , 1998, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[29] B. Jaber,et al. Effect of formaldehyde/bleach reprocessing on in vivo performances of high-efficiency cellulose and high-flux polysulfone dialyzers. , 1998, Journal of the American Society of Nephrology : JASN.
[30] A. Cheung,et al. Activation of complement by hemodialysis membranes: polyacrylonitrile binds more C3a than cuprophan. , 1990, Kidney international.
[31] J. Hertel,et al. Permeability and secondary membrane formation of a high flux polysulfone hemofilter. , 1986, Kidney international.
[32] J T Daugirdas,et al. Hemodialyzer mass transfer-area coefficients for urea increase at high dialysate flow rates. The Hemodialysis (HEMO) Study. , 1997, Kidney international.
[33] R. Ward,et al. A comparison of dialysers with low-flux membranes: significant differences in spite of many similarities. , 1997, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[34] M J Lysaght,et al. Kinetics of hemodiafiltration. I. In vitro transport characteristics of a hollow-fiber blood ultrafilter. , 1975, The Journal of laboratory and clinical medicine.
[35] W. Hörl,et al. Ofloxacin clearance during hemodialysis: a comparison of polysulfone and cellulose acetate hemodialyzers. , 1998, American journal of kidney diseases : the official journal of the National Kidney Foundation.
[36] B. Descamps-Latscha,et al. Permeability of cellulosic and non-cellulosic membranes to endotoxin subunits and cytokine production during in-vitro haemodialysis. , 1992, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[37] G. Lonnemann,et al. The role of plasma coating on the permeation of cytokine-inducing substances through dialyser membranes. , 1995, Nephrology, Dialysis and Transplantation.
[38] D Luehmann,et al. Technical requirements for rapid high-efficiency therapies. , 1986, Artificial organs.
[39] N A Hoenich,et al. Clinical characterization of Dicea a new cellulose membrane for haemodialysis. , 1997, Clinical nephrology.
[40] L. Henderson,et al. Kinetics of hemodiafiltration. II. Clinical characterization of a new blood cleansing modality. , 1975, The Journal of laboratory and clinical medicine.
[41] D. Walb,et al. Transmembranous Transport and Adsorption of Beta-2-microglobulin during Hemodialysis using Polysulfone, polyacrylonitrile, polymethylmethacrylate and Cuprammonium Rayon Membranes , 1989, The International journal of artificial organs.
[42] D. Churchill,et al. Effects of two low-flux cellulose acetate dialysers on plasma lipids and lipoproteins--a cross-over trial. , 1998, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[43] S. Barnum,et al. Renal filtration and catabolism of complement protein D. , 1985, The New England journal of medicine.
[44] W. Hörl,et al. Isolation of a granulocyte inhibitory protein from uraemic patients with homology of beta 2-microglobulin. , 1994, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[45] L. Chiarantini,et al. Bioreactivity and biocompatibility of a vitamin E-modified multi-layer hemodialysis filter. , 1998, Kidney international.
[46] D. Fearon,et al. Biocompatibility of dialysis membranes: effects of chronic complement activation. , 1984, Kidney international.
[47] I Ledebo,et al. Principles and practice of hemofiltration and hemodiafiltration. , 1998, Artificial organs.
[48] W R Clark,et al. Membrane adsorption of beta 2-microglobulin: equilibrium and kinetic characterization. , 1994, Kidney International.
[49] B. Branger,et al. High-flux synthetic versus cellulosic membranes for beta 2-microglobulin removal during hemodialysis, hemodiafiltration and hemofiltration. , 1989, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[50] J. Volanakis,et al. Metabolism of complement factor D in renal failure. , 1988, Kidney international.
[51] B. Descamps-Latscha,et al. Influence of Haemodialysis Membranes on β2-Microlobulin Kinetics:In Vivo and In Vitro Studies , 1988 .
[52] M. Lysaght. Evolution of hemodialysis membranes. , 1995, Contributions to nephrology.
[53] W. Clark,et al. Vancomycin mass transfer characteristics of high-flux cellulosic dialysers. , 1997, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[54] K. Sakai,et al. Removal of beta-2-microglobulin by diffusion alone is feasible using highly permeable dialysis membranes. , 1988, ASAIO transactions.
[55] E. Ritz,et al. Fluid phase generation of terminal complement complex as a novel index of bioincompatibility. , 1990, Kidney international.
[56] J. Floege,et al. Detection of endotoxin-like interleukin-1-inducing activity during in vitro dialysis. , 1988, Kidney international.
[57] P. Södersten,et al. Middle-sized molecule fractions isolated from uremic ultrafiltrate and normal urine inhibit ingestive behavior in the rat. , 1996, Journal of the American Society of Nephrology : JASN.
[58] S. Goldfarb,et al. Proinflammatory cytokines and hemofiltration membranes. , 1994, Journal of the American Society of Nephrology : JASN.
[59] B. Molitoris,et al. Plasma protein adsorption to highly permeable hemodialysis membranes. , 1995, Kidney international.
[60] M. Daha,et al. Cytokine profiles during clinical high-flux dialysis: no evidence for cytokine generation by circulating monocytes. , 1997, Journal of the American Society of Nephrology : JASN.
[61] I. Lauder,et al. Treatment of hyperlipidaemia in patients with non-insulin-dependent diabetes mellitus with progressive nephropathy. , 1997, Contributions to nephrology.
[62] T Akizawa,et al. Classification of dialysis membranes by performance. , 1995, Contributions to nephrology.
[63] T. Balstad,et al. Removal, generation and adsorption of beta-2-microglobulin during hemofiltration with five different membranes. , 1988, Blood purification.
[64] M. Favero,et al. Microbial contamination of renal dialysis systems and associated health risks. , 1974, Transactions - American Society for Artificial Internal Organs.
[65] E Lusvarghi,et al. Improved biocompatibility by modified cellulosic membranes: the case of hemophan. , 2008, Artificial organs.
[66] J. Schifferli,et al. Adsorption of complement factor D by polyacrylonitrile dialysis membranes. , 1993, Kidney international.
[67] R. Cronin,et al. Heterogeneity in gentamicin clearance between high-efficiency hemodialyzers. , 1994, American journal of kidney diseases : the official journal of the National Kidney Foundation.
[68] W. Clark,et al. Dialyzer-dependent changes in solute and water permeability with bleach reprocessing. , 1999, American journal of kidney diseases : the official journal of the National Kidney Foundation.