C3 glomerulopathy and atypical hemolytic uremic syndrome: an updated review of the literature on alternative complement pathway disorders
Author:
Publisher
Springer Science and Business Media LLC
Subject
Urology,Nephrology
Link
https://link.springer.com/content/pdf/10.1007/s11255-020-02729-y.pdf
Reference53 articles.
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2. Goodship TH, Cook HT, Fakhouri F, Fervenza FC, Fremeaux-Bacchi V, Kavanagh D, Nester CM, Noris M, Pickering MC, Rodriguez de Cordoba S, Roumenina LT, Sethi S, Smith RJ, Conference P (2017) Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference. Kidney Int 91(3):539–551. https://doi.org/10.1016/j.kint.2016.10.005
3. Catikkas M, Demir E, Ozluk Y, Caliskan Y, Badur RM, Turkmen A (2018) Case report: C3 glomerulopathy advancing atypical hemolytic uremic syndrome. Nefrologia 38(4):450–452. https://doi.org/10.1016/j.nefro.2017.09.010
4. Cook HT (2018) Evolving complexity of complement-related diseases: C3 glomerulopathy and atypical haemolytic uremic syndrome. Curr Opin Nephrol Hypertens 27(3):165–170. https://doi.org/10.1097/MNH.0000000000000412
5. Fervenza FC, Sethi S, Glassock RJ (2012) Idiopathic membranoproliferative glomerulonephritis: does it exist? Nephrol Dial Transplant 27(12):4288–4294. https://doi.org/10.1093/ndt/gfs288
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1. The favorable outcome of subsequent pregnancy in a patient with a history of obstetric atypical hemolytic uremic syndrome;Almanac of Clinical Medicine;2022-07-22
2. C3glomerulopathy: Understanding an ultra‐rare complement‐mediated renal disease;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2022-06-23
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