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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. doi: 10.1681/ASN.V102281. J Am Soc Nephrol. 1999. PMID: 10215327
The factor H protein family.
Zipfel PF, Jokiranta TS, Hellwage J, Koistinen V, Meri S. Zipfel PF, et al. Immunopharmacology. 1999 May;42(1-3):53-60. doi: 10.1016/s0162-3109(99)00015-6. Immunopharmacology. 1999. PMID: 10408366 Review.
364 results