[[Collins, AJ; Foley, Robert N.; Herzog, Charles; Chavers, Blanche M; Gilbertson, David; Ishani, Areef; Kasiske, Bertram L.; Liu, Jiannong; Mau, Lih-Wen; McBean, Marshall (2010). "Excerpts from the US Renal Data System 2009 annual report". Am J Kidney Dis 55: S1–S7. doi:10.1053/j.ajkd.2009.10.009.]]
asnjournals.org
cjasn.asnjournals.org
[[Noris, M; Caprioli, J; Bresin, E; Mossali, C; Pianetti, G; Gamba, S; Daina, E; Fenili, C; Castelletti, F; Sorosina, A.; Piras, R.; Donadelli, R.; Maranta, R.; Van Der Meer, I.; Conway, E. M.; Zipfel, P. F.; Goodship, T. H.; Remuzzi, G. (2010). "Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype". Clin J Am Soc Nephrol 5 (10): 1844–1859. doi:10.2215/CJN.02210310. PMC: 2974386. PMID20595690.]]
[[Loirat C, Noris M, Fremaux-Bacchi V, Chantal; Noris, M; Fremeaux-Bacchi, V (2008). "Complement and the atypical hemolytic uremia syndrome in children". Pediatr Nephrol 23 (11): 1957–1972. doi:10.1007/s00467-008-0872-4. PMID18594873.]]
[[Hosler GA, Cusumano AM, Hutchins GM, GA; Cusumano, AM; Hutchins, GM (2003). "Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome are distinct pathologic entities: a review of 56 autopsy cases". Arch Pathol Lab Med 127 (7): 834–839. doi:10.1043/1543-2165(2003)127<834:TTPAHU>2.0.CO;2 (inactive 2015-02-02). PMID12823037.]]
[[Noris, M; Caprioli, J; Bresin, E; Mossali, C; Pianetti, G; Gamba, S; Daina, E; Fenili, C; Castelletti, F; Sorosina, A.; Piras, R.; Donadelli, R.; Maranta, R.; Van Der Meer, I.; Conway, E. M.; Zipfel, P. F.; Goodship, T. H.; Remuzzi, G. (2010). "Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype". Clin J Am Soc Nephrol 5 (10): 1844–1859. doi:10.2215/CJN.02210310. PMC: 2974386. PMID20595690.]]
[[Caprioli, J; Noris, M; Brioschi, S; Pianetti, G; Castelletti, F; Bettinaglio, P; Mele, C; Bresin, E; Cassis, L; Gamba, S; Porrati, F; Bucchioni, S; Monteferrante, G; Fang, CJ; Liszewski, MK; Kavanagh, D; Atkinson, JP; Remuzzi, G; International Registry of Recurrent Familial HUS/TTP (2006). "Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome". Blood 108 (4): 1267–1279. doi:10.1182/blood-2005-10-007252Archived 2016년 5월 5일 - 웨이백 머신. PMC: 1895874. PMID16621965.]]
[[Stahl, AL; Vaziri-Sani, F; Heinen, S; Kristoffersson, AC; Gydell, KH; Raafat, R; Gutierrez, A; Beringer, O; Zipfel, PF; Karpman, D. (2008). "Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement depositionn on platelets and their activation". Blood 111 (11): 5307–5315. doi:10.1182/blood-2007-08-106153Archived 2018년 6월 2일 - 웨이백 머신. PMID18268093.]]
[[Dragon-Durey, M-A; Sethi, SK; Bagga, A; Blanc, C; Blouin, J; Ranchin, B; André, JL; Takagi, N; Cheong, HI; Hari, P.; Le Quintrec, M.; Niaudet, P.; Loirat, C.; Fridman, W. H.; Frémeaux-Bacchi, V. (2010). "Clinical features of anti-factor H autoantibody-associated hemolytic uremic syndrome". J Am Soc Nephrol 21 (12): 2180–2187. doi:10.1681/ASN.2010030315. PMC: 3014031. PMID21051740.]]
[[Zuber, J; Le Quintrec, Moglie; Sberro-Soussan, Rebecca; Loirat, Chantal; Frémeaux-Bacchi, Véronique; Legendre, Christophe (2011). "New insights into postrenal transplant hemolytic uremic syndrome". Nature Reviews Nephrology 7 (1): 23–25. doi:10.1038/nrneph.2010.155. PMID21102542.]]
[[Ariceta, G; Besbas, N; Johnson, S; Karpman, D; Landau, D; Licht, C; Loirat, C; Pecoraro, C; Taylor, CM; Van De Kar, Nicole; Vandewalle, Johan; Zimmerhackl, Lothar B.; European Paediatric Study Group for HUS (2009). "Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome". Pediatr Nephrol 24 (4): 687–696. doi:10.1007/s00467-008-0964-1. PMID18800230.]]
[[Sellier-Leclerc, AL; Fremeaux-Bacchi, V; Dragon-Durey, MA; Macher, MA; Niaudet, P; Guest, G; Boudailliez, B; Bouissou, F; Deschenes, G; Gie, S.; Tsimaratos, M.; Fischbach, M.; Morin, D.; Nivet, H.; Alberti, C.; Loirat, C.; French Society of Pediatric Nephrology (2007). "Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome". J Am Soc Nephrol 18 (8): 2392–2400. doi:10.1681/ASN.2006080811. PMID17599974.]]
[[Sallee, M; Daniel, L; Piercecchi, MD; Jaubert, D; Fremeaux-Bacchi, V; Berland, Y; Burtey, S (2010). "Myocardial infarction is a complication of factor H-associated atypical HUS". Nephrol Dial Transplant 25 (6): 2028–2032. doi:10.1093/ndt/gfq160. PMID20305136.]]
[[
Noris, M; Remuzzi, G (2009). "Atypical hemolytic-uremic syndrome". N Engl J Med 361 (17): 1676–1687. doi:10.1056/NEJMra0902814. PMID19846853.]]
[[Benz, K; Amann, K (2010). "Thrombotic microangiopathy: new insights". Current Opinion in Nephrology and Hypertension 19 (3): 242–247. doi:10.1097/MNH.0b013e3283378f25. PMID20186056.]]
[[Zipfel, PF; Heinen, S; Skerka, C (2010). "Thrombotic microangiopathies:new insights and new challenges". Current Opinion in Nephrology and Hypertension 19 (4): 372–378. doi:10.1097/MNH.0b013e32833aff4a. PMID20539230.]]
[[Fang CJ, Fremeaux-Bacchi V, Liszewski MK, et al. (2008). "Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome". Blood 111 (2): 624–632. doi:10.1182/blood-2007-04-084533Archived 2018년 6월 2일 - 웨이백 머신. PMC: 2200836. PMID17914026.]]
[[Bitzan, M; Schaefer, Franz; Reymond, Didier (2010). "Treatment of typical (enteropathic) hemolytic uremic syndrome". Semin Thromb Hemostas 36 (6): 594–610. doi:[1]Archived 2018년 6월 7일 - 웨이백 머신 10.1055/s-0030-1262881Archived 2018년 6월 7일 - 웨이백 머신. PMID20865636.]]
[[Szczepiorkowski, ZM; Winters, Jeffrey L.; Bandarenko, Nicholas; Kim, Haewon C.; Linenberger, Michael L.; Marques, Marisa B.; Sarode, Ravindra; Schwartz, Joseph; Weinstein, Robert; Shaz, Beth H.; Apheresis Applications Committee of the American Society for Apheresis (2010). "Guidelines on the use of therapeutic apheresis in clinical practice- evidence based approach from the Apheresis Applications Committee of the American Society of Apheresis". J Clin SPheresis 25 (3): 83–177. doi:10.1002/jca.20240. PMID20568098.]]
[[Michon, B; Moghrabi, A; Winikoff, R; Barrette, S; Bernstein, ML; Champagne, J; David, M; Duval, M; Hume, HA; Robitaille, Nancy; Bélisle, André; Champagne, Martin A. (2007). "Complications of apheresis in children". Transfusion 47 (10): 1837–1842. doi:10.1111/j.1537-2995.2007.01405.x. PMID17880609.]]
[[Licht, C; Pluthero, FG; Li, L; Christensen, H; Habbig, S; Hoppe, B; Geary, DF; Zipfel, PF; Kahr, WH (2009). "Platelet-associated complement factor H in healthy persons and patients with atypical HUS". Blood 114 (20): 4538–4545. doi:10.1182/blood-2009-03-205096Archived 2018년 6월 1일 - 웨이백 머신. PMID19704120.]]
[[Keating, GM (December 2013). "Eculizumab: a review of its use in atypical haemolytic uraemic syndrome.". Drugs 73 (18): 2053–66. doi:10.1007/s40265-013-0147-7. PMID24249647.]]
[[Klevens, RM; Edwards, JR; Andrus, ML; Peterson, KD; Dudeck, MA; Horan, TC; NHSN Participants in Outpatient Dialysis Surveillance (2008). "Dialysis surveillance report: National Healthcare Safety Network (NHSN)- data summary for 2006". Semin Dial 21 (1): 24–28. doi:10.1111/j.1525-139X.2007.00379.x. PMID18251954.]]
[[Kavanagh, D; Richards, A; Goodship, T; Jalanko, H (2010). "Transplantation in atypical hemolytic uremic syndrome". Semin Thromb Hemost 36 (6): 653–659. doi:[2]Archived 2018년 6월 6일 - 웨이백 머신 10.1055/s-0030-1262887Archived 2018년 6월 6일 - 웨이백 머신. PMID20865642.]]
[[Nester, C; Stewart, Z; Myers, D; Jetton, J; Nair, R; Reed, A; Thomas, C; Smith, R; Brophy, P (2011). "Pre-emptive eculizumab and plasmapheresis for renal transplant in atypical hemolytic syndrome". Clin J Am Soc Nephrol 6 (6): 1488–1494. doi:10.2215/CJN.10181110. PMC: 3109948. PMID21617085.]]
[[Bresin, E; Daina, E; Noris, M; Castelletti, F; Stefanov, R; Hill, P; Goodship, TH; Remuzzi, G; International Registry of Recurrent Familial HUS/TTP (2006). "Outcome of renal transplantation in patients with non- Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic background". Clin J Am Soc Nephrol 1 (1): 88–99. doi:10.2215/CJN.00050505. PMID17699195.]]
[[Zimmerhackl, LR; Besbas, N; Jungraithmayr, T; Van De Kar, N; Karch, H; Karpman, D; Landau, D; Loirat, C; Proesmans, W; Prüfer, Friederike; Rizzoni, Gianfranco; Taylor, Mark; European Study Group for Haemolytic Uraemic Syndromes Related Disorders (2006). "Epidemiology, clinical presentation, and pathophysiology of atypical and recurrent hemolytic uremic syndrome". Semin Thromb Hemost 32 (2): 113–120. doi:[3]Archived 2018년 6월 7일 - 웨이백 머신 10.1055/s-2006-939767Archived 2018년 6월 7일 - 웨이백 머신. PMID16575686.]]
oxfordjournals.org
ndt.oxfordjournals.org
[[Sallee, M; Daniel, L; Piercecchi, MD; Jaubert, D; Fremeaux-Bacchi, V; Berland, Y; Burtey, S (2010). "Myocardial infarction is a complication of factor H-associated atypical HUS". Nephrol Dial Transplant 25 (6): 2028–2032. doi:10.1093/ndt/gfq160. PMID20305136.]]
[[Loirat C, Noris M, Fremaux-Bacchi V, Chantal; Noris, M; Fremeaux-Bacchi, V (2008). "Complement and the atypical hemolytic uremia syndrome in children". Pediatr Nephrol 23 (11): 1957–1972. doi:10.1007/s00467-008-0872-4. PMID18594873.]]
[[Ariceta, G; Besbas, N; Johnson, S; Karpman, D; Landau, D; Licht, C; Loirat, C; Pecoraro, C; Taylor, CM; Van De Kar, Nicole; Vandewalle, Johan; Zimmerhackl, Lothar B.; European Paediatric Study Group for HUS (2009). "Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome". Pediatr Nephrol 24 (4): 687–696. doi:10.1007/s00467-008-0964-1. PMID18800230.]]
[[Keating, GM (December 2013). "Eculizumab: a review of its use in atypical haemolytic uraemic syndrome.". Drugs 73 (18): 2053–66. doi:10.1007/s40265-013-0147-7. PMID24249647.]]
[[Bitzan, M; Schaefer, Franz; Reymond, Didier (2010). "Treatment of typical (enteropathic) hemolytic uremic syndrome". Semin Thromb Hemostas 36 (6): 594–610. doi:[1]Archived 2018년 6월 7일 - 웨이백 머신 10.1055/s-0030-1262881Archived 2018년 6월 7일 - 웨이백 머신. PMID20865636.]]
[[Kavanagh, D; Richards, A; Goodship, T; Jalanko, H (2010). "Transplantation in atypical hemolytic uremic syndrome". Semin Thromb Hemost 36 (6): 653–659. doi:[2]Archived 2018년 6월 6일 - 웨이백 머신 10.1055/s-0030-1262887Archived 2018년 6월 6일 - 웨이백 머신. PMID20865642.]]
[[Zimmerhackl, LR; Besbas, N; Jungraithmayr, T; Van De Kar, N; Karch, H; Karpman, D; Landau, D; Loirat, C; Proesmans, W; Prüfer, Friederike; Rizzoni, Gianfranco; Taylor, Mark; European Study Group for Haemolytic Uraemic Syndromes Related Disorders (2006). "Epidemiology, clinical presentation, and pathophysiology of atypical and recurrent hemolytic uremic syndrome". Semin Thromb Hemost 32 (2): 113–120. doi:[3]Archived 2018년 6월 7일 - 웨이백 머신 10.1055/s-2006-939767Archived 2018년 6월 7일 - 웨이백 머신. PMID16575686.]]
web.archive.org
[[Caprioli, J; Noris, M; Brioschi, S; Pianetti, G; Castelletti, F; Bettinaglio, P; Mele, C; Bresin, E; Cassis, L; Gamba, S; Porrati, F; Bucchioni, S; Monteferrante, G; Fang, CJ; Liszewski, MK; Kavanagh, D; Atkinson, JP; Remuzzi, G; International Registry of Recurrent Familial HUS/TTP (2006). "Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome". Blood 108 (4): 1267–1279. doi:10.1182/blood-2005-10-007252Archived 2016년 5월 5일 - 웨이백 머신. PMC: 1895874. PMID16621965.]]
[[Stahl, AL; Vaziri-Sani, F; Heinen, S; Kristoffersson, AC; Gydell, KH; Raafat, R; Gutierrez, A; Beringer, O; Zipfel, PF; Karpman, D. (2008). "Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement depositionn on platelets and their activation". Blood 111 (11): 5307–5315. doi:10.1182/blood-2007-08-106153Archived 2018년 6월 2일 - 웨이백 머신. PMID18268093.]]
[[Fang CJ, Fremeaux-Bacchi V, Liszewski MK, et al. (2008). "Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome". Blood 111 (2): 624–632. doi:10.1182/blood-2007-04-084533Archived 2018년 6월 2일 - 웨이백 머신. PMC: 2200836. PMID17914026.]]
[[Bitzan, M; Schaefer, Franz; Reymond, Didier (2010). "Treatment of typical (enteropathic) hemolytic uremic syndrome". Semin Thromb Hemostas 36 (6): 594–610. doi:[1]Archived 2018년 6월 7일 - 웨이백 머신 10.1055/s-0030-1262881Archived 2018년 6월 7일 - 웨이백 머신. PMID20865636.]]
[[Licht, C; Pluthero, FG; Li, L; Christensen, H; Habbig, S; Hoppe, B; Geary, DF; Zipfel, PF; Kahr, WH (2009). "Platelet-associated complement factor H in healthy persons and patients with atypical HUS". Blood 114 (20): 4538–4545. doi:10.1182/blood-2009-03-205096Archived 2018년 6월 1일 - 웨이백 머신. PMID19704120.]]
[[Kavanagh, D; Richards, A; Goodship, T; Jalanko, H (2010). "Transplantation in atypical hemolytic uremic syndrome". Semin Thromb Hemost 36 (6): 653–659. doi:[2]Archived 2018년 6월 6일 - 웨이백 머신 10.1055/s-0030-1262887Archived 2018년 6월 6일 - 웨이백 머신. PMID20865642.]]
[[Zimmerhackl, LR; Besbas, N; Jungraithmayr, T; Van De Kar, N; Karch, H; Karpman, D; Landau, D; Loirat, C; Proesmans, W; Prüfer, Friederike; Rizzoni, Gianfranco; Taylor, Mark; European Study Group for Haemolytic Uraemic Syndromes Related Disorders (2006). "Epidemiology, clinical presentation, and pathophysiology of atypical and recurrent hemolytic uremic syndrome". Semin Thromb Hemost 32 (2): 113–120. doi:[3]Archived 2018년 6월 7일 - 웨이백 머신 10.1055/s-2006-939767Archived 2018년 6월 7일 - 웨이백 머신. PMID16575686.]]
[[Loirat C, Noris M, Fremaux-Bacchi V, Chantal; Noris, M; Fremeaux-Bacchi, V (2008). "Complement and the atypical hemolytic uremia syndrome in children". Pediatr Nephrol 23 (11): 1957–1972. doi:10.1007/s00467-008-0872-4. PMID18594873.]]
[[Hosler GA, Cusumano AM, Hutchins GM, GA; Cusumano, AM; Hutchins, GM (2003). "Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome are distinct pathologic entities: a review of 56 autopsy cases". Arch Pathol Lab Med 127 (7): 834–839. doi:10.1043/1543-2165(2003)127<834:TTPAHU>2.0.CO;2 (inactive 2015-02-02). PMID12823037.]]
[[Noris, M; Caprioli, J; Bresin, E; Mossali, C; Pianetti, G; Gamba, S; Daina, E; Fenili, C; Castelletti, F; Sorosina, A.; Piras, R.; Donadelli, R.; Maranta, R.; Van Der Meer, I.; Conway, E. M.; Zipfel, P. F.; Goodship, T. H.; Remuzzi, G. (2010). "Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype". Clin J Am Soc Nephrol 5 (10): 1844–1859. doi:10.2215/CJN.02210310. PMC: 2974386. PMID20595690.]]
[[Caprioli, J; Noris, M; Brioschi, S; Pianetti, G; Castelletti, F; Bettinaglio, P; Mele, C; Bresin, E; Cassis, L; Gamba, S; Porrati, F; Bucchioni, S; Monteferrante, G; Fang, CJ; Liszewski, MK; Kavanagh, D; Atkinson, JP; Remuzzi, G; International Registry of Recurrent Familial HUS/TTP (2006). "Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome". Blood 108 (4): 1267–1279. doi:10.1182/blood-2005-10-007252Archived 2016년 5월 5일 - 웨이백 머신. PMC: 1895874. PMID16621965.]]
[[Hoffman, R; Benz, EJ; Silberstein, LE; Heslop, H; Weitz J; Anastasi, J. (2012). Hematology: Basic Principles and Practice (6th ed.). Elsevier. ISBN978-1-4377-2928-3.]]
[[Stahl, AL; Vaziri-Sani, F; Heinen, S; Kristoffersson, AC; Gydell, KH; Raafat, R; Gutierrez, A; Beringer, O; Zipfel, PF; Karpman, D. (2008). "Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement depositionn on platelets and their activation". Blood 111 (11): 5307–5315. doi:10.1182/blood-2007-08-106153Archived 2018년 6월 2일 - 웨이백 머신. PMID18268093.]]
[[Dragon-Durey, M-A; Sethi, SK; Bagga, A; Blanc, C; Blouin, J; Ranchin, B; André, JL; Takagi, N; Cheong, HI; Hari, P.; Le Quintrec, M.; Niaudet, P.; Loirat, C.; Fridman, W. H.; Frémeaux-Bacchi, V. (2010). "Clinical features of anti-factor H autoantibody-associated hemolytic uremic syndrome". J Am Soc Nephrol 21 (12): 2180–2187. doi:10.1681/ASN.2010030315. PMC: 3014031. PMID21051740.]]
[[Zuber, J; Le Quintrec, Moglie; Sberro-Soussan, Rebecca; Loirat, Chantal; Frémeaux-Bacchi, Véronique; Legendre, Christophe (2011). "New insights into postrenal transplant hemolytic uremic syndrome". Nature Reviews Nephrology 7 (1): 23–25. doi:10.1038/nrneph.2010.155. PMID21102542.]]
[[Ariceta, G; Besbas, N; Johnson, S; Karpman, D; Landau, D; Licht, C; Loirat, C; Pecoraro, C; Taylor, CM; Van De Kar, Nicole; Vandewalle, Johan; Zimmerhackl, Lothar B.; European Paediatric Study Group for HUS (2009). "Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome". Pediatr Nephrol 24 (4): 687–696. doi:10.1007/s00467-008-0964-1. PMID18800230.]]
[[Sellier-Leclerc, AL; Fremeaux-Bacchi, V; Dragon-Durey, MA; Macher, MA; Niaudet, P; Guest, G; Boudailliez, B; Bouissou, F; Deschenes, G; Gie, S.; Tsimaratos, M.; Fischbach, M.; Morin, D.; Nivet, H.; Alberti, C.; Loirat, C.; French Society of Pediatric Nephrology (2007). "Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome". J Am Soc Nephrol 18 (8): 2392–2400. doi:10.1681/ASN.2006080811. PMID17599974.]]
[[Sallee, M; Daniel, L; Piercecchi, MD; Jaubert, D; Fremeaux-Bacchi, V; Berland, Y; Burtey, S (2010). "Myocardial infarction is a complication of factor H-associated atypical HUS". Nephrol Dial Transplant 25 (6): 2028–2032. doi:10.1093/ndt/gfq160. PMID20305136.]]
[[
Noris, M; Remuzzi, G (2009). "Atypical hemolytic-uremic syndrome". N Engl J Med 361 (17): 1676–1687. doi:10.1056/NEJMra0902814. PMID19846853.]]
[[Benz, K; Amann, K (2010). "Thrombotic microangiopathy: new insights". Current Opinion in Nephrology and Hypertension 19 (3): 242–247. doi:10.1097/MNH.0b013e3283378f25. PMID20186056.]]
[[Zipfel, PF; Heinen, S; Skerka, C (2010). "Thrombotic microangiopathies:new insights and new challenges". Current Opinion in Nephrology and Hypertension 19 (4): 372–378. doi:10.1097/MNH.0b013e32833aff4a. PMID20539230.]]
[[Fang CJ, Fremeaux-Bacchi V, Liszewski MK, et al. (2008). "Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome". Blood 111 (2): 624–632. doi:10.1182/blood-2007-04-084533Archived 2018년 6월 2일 - 웨이백 머신. PMC: 2200836. PMID17914026.]]
[[Bitzan, M; Schaefer, Franz; Reymond, Didier (2010). "Treatment of typical (enteropathic) hemolytic uremic syndrome". Semin Thromb Hemostas 36 (6): 594–610. doi:[1]Archived 2018년 6월 7일 - 웨이백 머신 10.1055/s-0030-1262881Archived 2018년 6월 7일 - 웨이백 머신. PMID20865636.]]
[[Szczepiorkowski, ZM; Winters, Jeffrey L.; Bandarenko, Nicholas; Kim, Haewon C.; Linenberger, Michael L.; Marques, Marisa B.; Sarode, Ravindra; Schwartz, Joseph; Weinstein, Robert; Shaz, Beth H.; Apheresis Applications Committee of the American Society for Apheresis (2010). "Guidelines on the use of therapeutic apheresis in clinical practice- evidence based approach from the Apheresis Applications Committee of the American Society of Apheresis". J Clin SPheresis 25 (3): 83–177. doi:10.1002/jca.20240. PMID20568098.]]
[[Michon, B; Moghrabi, A; Winikoff, R; Barrette, S; Bernstein, ML; Champagne, J; David, M; Duval, M; Hume, HA; Robitaille, Nancy; Bélisle, André; Champagne, Martin A. (2007). "Complications of apheresis in children". Transfusion 47 (10): 1837–1842. doi:10.1111/j.1537-2995.2007.01405.x. PMID17880609.]]
[[Licht, C; Pluthero, FG; Li, L; Christensen, H; Habbig, S; Hoppe, B; Geary, DF; Zipfel, PF; Kahr, WH (2009). "Platelet-associated complement factor H in healthy persons and patients with atypical HUS". Blood 114 (20): 4538–4545. doi:10.1182/blood-2009-03-205096Archived 2018년 6월 1일 - 웨이백 머신. PMID19704120.]]
[[Keating, GM (December 2013). "Eculizumab: a review of its use in atypical haemolytic uraemic syndrome.". Drugs 73 (18): 2053–66. doi:10.1007/s40265-013-0147-7. PMID24249647.]]
[[Collins, AJ; Foley, Robert N.; Herzog, Charles; Chavers, Blanche M; Gilbertson, David; Ishani, Areef; Kasiske, Bertram L.; Liu, Jiannong; Mau, Lih-Wen; McBean, Marshall (2010). "Excerpts from the US Renal Data System 2009 annual report". Am J Kidney Dis 55: S1–S7. doi:10.1053/j.ajkd.2009.10.009.]]
[[Klevens, RM; Edwards, JR; Andrus, ML; Peterson, KD; Dudeck, MA; Horan, TC; NHSN Participants in Outpatient Dialysis Surveillance (2008). "Dialysis surveillance report: National Healthcare Safety Network (NHSN)- data summary for 2006". Semin Dial 21 (1): 24–28. doi:10.1111/j.1525-139X.2007.00379.x. PMID18251954.]]
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