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Where next with atypical hemolytic uremic syndrome?
Jokiranta TS, Zipfel PF, Fremeaux-Bacchi V, Taylor CM, Goodship TJ, Noris M. Jokiranta TS, et al. Among authors: zipfel pf. Mol Immunol. 2007 Sep;44(16):3889-900. doi: 10.1016/j.molimm.2007.06.003. Mol Immunol. 2007. PMID: 17768107 Review.
Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities. Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopenic Purpura.
Noris M, Ruggenenti P, Perna A, Orisio S, Caprioli J, Skerka C, Vasile B, Zipfel PF, Remuzzi G. Noris M, et al. Among authors: zipfel pf. J Am Soc Nephrol. 1999 Feb;10(2):281-93. J Am Soc Nephrol. 1999. PMID: 10215327
Complement factor H and hemolytic uremic syndrome.
Zipfel PF, Skerka C, Caprioli J, Manuelian T, Neumann HH, Noris M, Remuzzi G. Zipfel PF, et al. Int Immunopharmacol. 2001 Mar;1(3):461-8. doi: 10.1016/s1567-5769(00)00047-3. Int Immunopharmacol. 2001. PMID: 11367530 Review.
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