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Journal Abstract Search

181 related items for PubMed ID: 27744619

  • 21.
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  • 22. An international consensus approach to the management of atypical hemolytic uremic syndrome in children.
    Loirat C, Fakhouri F, Ariceta G, Besbas N, Bitzan M, Bjerre A, Coppo R, Emma F, Johnson S, Karpman D, Landau D, Langman CB, Lapeyraque AL, Licht C, Nester C, Pecoraro C, Riedl M, van de Kar NC, Van de Walle J, Vivarelli M, Frémeaux-Bacchi V, HUS International.
    Pediatr Nephrol; 2016 Jan; 31(1):15-39. PubMed ID: 25859752
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  • 28. A novel atypical hemolytic uremic syndrome-associated hybrid CFHR1/CFH gene encoding a fusion protein that antagonizes factor H-dependent complement regulation.
    Valoti E, Alberti M, Tortajada A, Garcia-Fernandez J, Gastoldi S, Besso L, Bresin E, Remuzzi G, Rodriguez de Cordoba S, Noris M.
    J Am Soc Nephrol; 2015 Jan; 26(1):209-19. PubMed ID: 24904082
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  • 29. Genotype/phenotype correlations in complement factor H deficiency arising from uniparental isodisomy.
    Wilson V, Darlay R, Wong W, Wood KM, McFarlane J, Schejbel L, Schmidt IM, Harris CL, Tellez J, Hunze EM, Marchbank K, Goodship JA, Goodship TH.
    Am J Kidney Dis; 2013 Nov; 62(5):978-83. PubMed ID: 23870792
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  • 31. Liver-kidney transplantation to cure atypical hemolytic uremic syndrome.
    Saland JM, Ruggenenti P, Remuzzi G, Consensus Study Group.
    J Am Soc Nephrol; 2009 May; 20(5):940-9. PubMed ID: 19092117
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  • 35. [Genetics of aHUS and transplant recurrence].
    Bresin E.
    G Ital Nefrol; 2015 May; 32 Suppl 64():. PubMed ID: 26479051
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  • 36. Severe atypical HUS caused by CFH S1191L--case presentation and review of treatment options.
    De S, Waters AM, Segal AO, Trautmann A, Harvey EA, Licht C.
    Pediatr Nephrol; 2010 Jan; 25(1):97-104. PubMed ID: 19856002
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  • 38. The importance of genetic mutation screening to determine retransplantation following failed kidney allograft from recurrent atypical haemolytic ureamic syndrome.
    Chua S, Wong G, Lim WH.
    BMJ Case Rep; 2014 Mar 26; 2014():. PubMed ID: 24671321
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  • 40. The development of atypical hemolytic uremic syndrome depends on complement C5.
    de Jorge EG, Macor P, Paixão-Cavalcante D, Rose KL, Tedesco F, Cook HT, Botto M, Pickering MC.
    J Am Soc Nephrol; 2011 Jan 26; 22(1):137-45. PubMed ID: 21148255
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