Academic literature on the topic 'Membrane plasmapheresis'

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Journal articles on the topic "Membrane plasmapheresis"

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POPOVICH, ROBERT, ZENGZHI HE, and JACK MONCRIEF. "Peritoneal Membrane Plasmapheresis." ASAIO Journal 38, no. 3 (1992): M668—M672. http://dx.doi.org/10.1097/00002480-199207000-00121.

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Nosé, Y., and P. S. Malchesky. "Therapeutic Membrane Plasmapheresis." Therapeutic Apheresis 4, no. 1 (2000): 3–9. http://dx.doi.org/10.1046/j.1526-0968.2000.00231.x.

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Popovich, Robert, Zengzhi He, and Jack Moncrief. "Peritoneal Membrane Plasmapheresis." Peritoneal Dialysis International: Journal of the International Society for Peritoneal Dialysis 13, no. 2_suppl (1993): 82–84. http://dx.doi.org/10.1177/089686089301302s20.

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Lambrecht, L., R. Vanholder, and S. Ringoir. "Single-Needle Membrane Plasmapheresis." Blood Purification 6, no. 2 (1988): 77–84. http://dx.doi.org/10.1159/000169487.

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Baldini, G. M., E. Baldini, and M. De Palma. "Donor Plasmapheresis: Plasma Membrane Separators." International Journal of Artificial Organs 16, no. 5_suppl (1993): 143–44. http://dx.doi.org/10.1177/039139889301605s29.

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McVey, D. Scott, and Raymond W. Loan. "Total and antigen-specific serum immunoglobulin isotype concentrations in hyperimmunized cattle that have undergone plasmapheresis." American Journal of Veterinary Research 50, no. 5 (1989): 758–61. https://doi.org/10.2460/ajvr.1989.50.05.758.

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SUMMARY The effects of prolonged plasmapheresis of cattle on total and antigen-specific immunoglobulin production were evaluated. Five adult cows were hyperimmunized by repeated iv administration of live, logarithmic-phase Pasteurella haemolytica A1 organisms. Three of the cows underwent plasmapheresis daily for 3 weeks. From 2 cows, serum was only obtained periodically. Anti-P haemolytica antibody was assayed by indirect hemagglutination and a kinetic-augmented, antigen-capture elisa for capsular polysaccharide and lipopolysaccharide/outer membrane protein antigens. Total serum immunoglobulin
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Stepner, Tova A., Christian S. Vassilieff, and Edward F. Leonard. "Cell-plasma interactions during membrane plasmapheresis." Clinical Hemorheology and Microcirculation 5, no. 1 (2016): 15–26. http://dx.doi.org/10.3233/ch-1985-5104.

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Yokoyama, Shigeki, Retsuji Yamanaka, Manabu Oki, and Takemitsu Hosoi. "Donor plasmapheresis using automated membrane devices." Journal of the Japan Society of Blood Transfusion 36, no. 1 (1990): 5–9. http://dx.doi.org/10.3925/jjtc1958.36.5.

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Faber, J. C., A. J. Reppucci, J. M. Mathias, and J. P. Hoffmann. "Automated plasmapheresis with a nylon membrane." Plasma Therapy and Transfusion Technology 9, no. 4 (1988): 347–50. http://dx.doi.org/10.1016/0278-6222(88)90013-7.

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Stromberg, R. R., L. I. Friedman, D. R. Boggs, and M. J. Lysaght. "Membrane technology applied to donor plasmapheresis." Journal of Membrane Science 44, no. 1 (1989): 131–43. http://dx.doi.org/10.1016/s0376-7388(00)82345-5.

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Dissertations / Theses on the topic "Membrane plasmapheresis"

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Zydney, Andrew Lawrence. "Cross-flow membrane plasmapheresis : an analysis of flux and hemolysis." Thesis, Massachusetts Institute of Technology, 1985. http://hdl.handle.net/1721.1/15235.

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Yan, Feng. "Synthese et adsorption de polymeres biocompatibles destines a moduler les proprietes de membranes utilisees en plasmapherese et en dialyse renale." Université Louis Pasteur (Strasbourg) (1971-2008), 1987. http://www.theses.fr/1987STR13242.

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Des polymacromeres biocompatibles destines a moduler les proprietes des membranes de plasmapherese et de dialyse renale ont ete synthetisees puis caracterises en solution et a l'etat solide. Leur adsorption sur ces membranes a ete etudiee en detail. L'effort de recherche a porte principalement sur les points suivants: obtention d'homopolymeres de l'acrylate et du methacrylate de monomethoxy-poly(ethylene glycol) (monomere a), de fortes masses moleculaires; etude du phenomene de gelification au cours de la polymerisation en phase homogene; analyse de la cinetique de copolymerisation radicalaire
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Books on the topic "Membrane plasmapheresis"

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Maciej, Nałęcz, Klinkmann Horst, International Centre for Biocybernetics, World Health Organization. Collaborating Centre for Research and Training in Biocybernetics and Biomedical Engineering., and International Centre of Biocybernetics. Seminar 3.2., eds. Theory and application of membranes in hemodialysis and plasmapheresis, Jabłonna, April 1990. ICB, 1992.

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Cui, Zhao, Neil Turner, and Ming-hui Zhao. Antiglomerular basement membrane disease. Edited by Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0073_update_001.

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Cyclophosphamide and plasma exchange are the standard of care in rapidly progressive glomerulonephritis or lung haemorrhage caused by antiglomerular basement membrane (anti-GBM) disease, and it is unusual to encounter patients at earlier stages. Steroids are universally used in addition. There is some evidence that plasma exchange may not be a critical part of treatment at an earlier stage. There is no more than anecdotal evidence for other therapies. Slower-onset therapies such as antibodies to B cells are rarely appropriate. If untreated, patients with severe anti-GBM disease will not recove
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Sternbach, Marion. Apheresis in the ICU. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0268.

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This chapter describes therapeutic plasma exchange, as well as cytapheresis for hyperleukocytosis and essential thrombocythemia, as well as harvesting haematological stem cells (HSC) for transplantation. Instrumentation and techniques are mostly density centrifugation, much less column adsorption for antibodies or membrane filtration for noxious molecules. Pathophysiology of apheresis is dealt with in great detail with emphasis on prevention and treatment of side effects, much more critical in the intensive care unit (ICU) setting. Main manifestations are: hypocalcaemia due to chelation by ant
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Book chapters on the topic "Membrane plasmapheresis"

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Jaffrin, M. Y., and L. H. Ding. "High Performance Systems for Membrane Plasmapheresis." In Advances in haemapheresis. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3904-9_3.

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Verbrugh, Henri A. "The Biology of the Peritoneal Membrane During Chronic Peritoneal Dialysis." In New Perspectives in Hemodialysis, Peritoneal Dialysis, Arteriovenous Hemofiltration, and Plasmapheresis. Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-5718-6_13.

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Goyal, Venkat, and Pranay Oza. "Plasmapheresis." In Manual of Extracorporeal Membrane Oxygenation (ECMO) in the ICU. Jaypee Brothers Medical Publishers (P) Ltd., 2014. http://dx.doi.org/10.5005/jp/books/12297_24.

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Sun, Shudong, Yupei Li, Lunhao Zhi, Weifeng Zhao, and Changsheng Zhao. "Blood Purification Membranes Used in Liquid–Liquid Environments." In Blood Purification Materials. Royal Society of Chemistry, 2025. https://doi.org/10.1039/9781839165412-00101.

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Currently, the majority of blood purification membranes, including those applied in hemodialysis, hemofiltration, and plasma separation, are used in liquid–liquid environments, where both sides of the membrane contact liquid. This type of membrane material has strict requirements regarding permselectivity function, antifouling performance, and blood compatibility (especially anticoagulant properties). In this chapter, first the materials used for this type of blood purification membrane are introduced briefly, then the fouling of membranes and relevant improvement strategies are discussed. Sub
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Kubisz, Peter, Pavol Holly, and Jan Stasko. "Bleeding in Patients with Antiphospholipid Antibodies." In Antiphospholipid Syndrome - Recent Advances in Basic and Clinical Aspects [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.97856.

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The antiphospholipid antibodies (aPL) are commonly associated with thrombotic events and obstetric complications. However, apart from the bleeding complications of antithrombotic therapy, the acquired coagulopathy caused by the aPL, particularly by lupus anticoagulant and anticardiolipin antibodies, might be occasionally manifested as a hemorrhagic syndrome with various clinical severity. Bleeding symptoms vary from mild (mucocutaneous) up to life-threatening (gastrointestinal, intracranial). The bleeding may be the first manifestation of aPL or appear concomitantly with thrombosis. The underl
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Morkos, Michael, and Daniel Cormican. "Myasthenia Gravis." In Advanced Anesthesia Review, edited by Alaa Abd-Elsayed. Oxford University PressNew York, 2023. http://dx.doi.org/10.1093/med/9780197584521.003.0198.

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Abstract Myasthenia gravis is the result of autoimmune antibodies targeted against acetylcholine receptors on postsynaptic membranes of the neuromuscular junction. The majority of patients will describe drooping of the eyelids and blurred vision as their initial symptoms with worsening weakness associated with continued muscle use. Typically treated with pyridostigmine, other options such as intravenous immunoglobulin and plasmapheresis, exist for severe symptoms associated with myasthenic syndrome. The anesthetic plan must be thoughtfully considered, taking into account premedication, inducti
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Conference papers on the topic "Membrane plasmapheresis"

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Chesta, F., and T. Vossler. "Navigating the Grey: Extracorporeal Membrane Oxygenation and Plasmapheresis in Severe Diffuse Alveolar Hemorrhage Due to Microscopic Polyangiitis." In American Thoracic Society 2024 International Conference, May 17-22, 2024 - San Diego, CA. American Thoracic Society, 2024. http://dx.doi.org/10.1164/ajrccm-conference.2024.209.1_meetingabstracts.a5786.

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Cumming, A. M., R. T. Wensley, S. E. Cottrell, and I. W. Delamore. "A STUDY ON THE RECOVERY OF FACTOR VIII PROCOAGULANT ACTIVITY FROM RECALCIFIED, HEPARINISED, CITRATED PLASMA." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644156.

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This study has been carried out to investigate the potential for increasing the recovery of factor VIII procoagulant activity (factor VIII:C),in cryoprecipitates and concentrates, by the use of heparin anticoagulant. Jhctor VIII:C in citrated plasmahas been shown to be stabilised by recalcification and heparinisation of the plasma. Donations of substantially platelet-free and platelet-product-free plasma, anticoagulated by acid citrate dextrose formula A anticoagulant (ACD A), were collected using a combined membrane filtration/centrifugation plasmapheresis device (the HemaSciences "Autopheres
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