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Mutation of complement factor B causing massive fluid-phase dysregulation of the alternative complement pathway can result in atypical hemolytic uremic syndrome

Yuzhou Zhang, Robin Kremsdorf, C. John Sperati, Kammi Henriksen, Mari Mori, Renee X. Goodfellow, Gabriella R. Pitcher, Cindy Benson, Nicolò Ghiringhelli Borsa, Ronald P. Taylor,

Kidney International · 2020 · 15 citations · 16 references

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16

Genetics and Outcome of Atypical Hemolytic Uremic Syndrome

Véronique Frémeaux‐Bacchi, Fádi Fakhouri, Arnaud Garnier et al. · Clinical Journal of the American Society of Nephrology · 2013 · 713 citations

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Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference

Timothy H.J. Goodship, H. Terence Cook, Fádi Fakhouri et al. · Kidney International · 2016 · 695 citations · Full text

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Formation of the initial C3 convertase of the alternative complement pathway. Acquisition of C3b-like activities by spontaneous hydrolysis of the putative thioester in native C3.

Michael K. Pangburn, Robert D. Schreiber, Hans J. Müller‐Eberhard · The Journal of Experimental Medicine · 1981 · 443 citations · Full text

, , +10

Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype

Elena Bresin, Erica Rurali, Jessica Caprioli et al. · Journal of the American Society of Nephrology · 2013 · 350 citations

, , +17

Clinical Features of Anti-Factor H Autoantibody–Associated Hemolytic Uremic Syndrome

Marie‐Agnès Dragon‐Durey, Sidharth Kumar Sethi, Arvind Bagga et al. · Journal of the American Society of Nephrology · 2010 · 295 citations · Full text

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