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Journal Abstract Search

125 related items for PubMed ID: 2088459

  • 21. Genetically determined low C4: a predisposing factor to autoimmune chronic active hepatitis.
    Vergani D, Wells L, Larcher VF, Nasaruddin BA, Davies ET, Mieli-Vergani G, Mowat AP.
    Lancet; 1985 Aug 10; 2(8450):294-8. PubMed ID: 2862466
    [Abstract] [Full Text] [Related]

  • 22. Letter: Haemolytic-uraemic syndrome: evidence for intravascular C3 activation.
    Stühlinger W, Kourilsky O, Kanfer A, Sraer JD.
    Lancet; 1974 Sep 28; 2(7883):788-9. PubMed ID: 4143056
    [No Abstract] [Full Text] [Related]

  • 23. Atypical hemolytic uremic syndrome due to factor H autoantibody.
    Uslu-Gökceoğlu A, Doğan CS, Comak E, Koyun M, Akman S.
    Turk J Pediatr; 2013 Sep 28; 55(1):86-9. PubMed ID: 23692839
    [Abstract] [Full Text] [Related]

  • 24. Systemic complement activation and complement gene analysis in enterohaemorrhagic Escherichia coli-associated paediatric haemolytic uraemic syndrome.
    Ahlenstiel-Grunow T, Hachmeister S, Bange FC, Wehling C, Kirschfink M, Bergmann C, Pape L.
    Nephrol Dial Transplant; 2016 Jul 28; 31(7):1114-21. PubMed ID: 27190382
    [Abstract] [Full Text] [Related]

  • 25. Complement factor I: Regulatory nexus, driver of immunopathology, and therapeutic.
    Hallam TM, Sharp SJ, Andreadi A, Kavanagh D.
    Immunobiology; 2023 Sep 28; 228(5):152410. PubMed ID: 37478687
    [Abstract] [Full Text] [Related]

  • 26. Complement-mediated injury and protection of endothelium: lessons from atypical haemolytic uraemic syndrome.
    Kerr H, Richards A.
    Immunobiology; 2012 Feb 28; 217(2):195-203. PubMed ID: 21855165
    [Abstract] [Full Text] [Related]

  • 27. A novel C3 mutation causing increased formation of the C3 convertase in familial atypical hemolytic uremic syndrome.
    Sartz L, Olin AI, Kristoffersson AC, Ståhl AL, Johansson ME, Westman K, Fremeaux-Bacchi V, Nilsson-Ekdahl K, Karpman D.
    J Immunol; 2012 Feb 15; 188(4):2030-7. PubMed ID: 22250080
    [Abstract] [Full Text] [Related]

  • 28. Serological and genetic complement alterations in infection-induced and complement-mediated hemolytic uremic syndrome.
    Westra D, Volokhina EB, van der Molen RG, van der Velden TJ, Jeronimus-Klaasen A, Goertz J, Gracchi V, Dorresteijn EM, Bouts AH, Keijzer-Veen MG, van Wijk JA, Bakker JA, Roos A, van den Heuvel LP, van de Kar NC.
    Pediatr Nephrol; 2017 Feb 15; 32(2):297-309. PubMed ID: 27718086
    [Abstract] [Full Text] [Related]

  • 29. Immunoglobulins and complement factor C4 in adult rhinosinusitis.
    Seppänen M, Suvilehto J, Lokki ML, Notkola IL, Järvinen A, Jarva H, Seppälä I, Tahkokallio O, Malmberg H, Meri S, Valtonen V.
    Clin Exp Immunol; 2006 Aug 15; 145(2):219-27. PubMed ID: 16879240
    [Abstract] [Full Text] [Related]

  • 30. Studies on the haemolytic activity of circulating C1q-C3/C4 complexes.
    Wouters D, Brouwer MC, Daha MR, Hack CE.
    Mol Immunol; 2008 Apr 15; 45(7):1893-9. PubMed ID: 18054386
    [Abstract] [Full Text] [Related]

  • 31. Complement C3F allotype synthesized by liver recipient modifies transplantation outcome independently from donor hepatic C3.
    Valero-Hervás DM, Sánchez-Zapardiel E, Castro MJ, Gallego-Bustos F, Cambra F, Justo I, Laguna-Goya R, Jiménez-Romero C, Moreno E, López-Medrano F, San Juan R, Fernández-Ruiz M, Aguado JM, Paz-Artal E.
    Clin Transplant; 2017 Jan 15; 31(1):. PubMed ID: 27801525
    [Abstract] [Full Text] [Related]

  • 32. The low C5 convertase activity of the C4A6 allotype of human complement component C4.
    Kinoshita T, Dodds AW, Law SK, Inoue K.
    Biochem J; 1989 Aug 01; 261(3):743-8. PubMed ID: 2803239
    [Abstract] [Full Text] [Related]

  • 33. Hypomorphic variant of the slow allele of C3 associated with hypocomplementemia and hematuria.
    McLean RH, Bryan RK, Winkelstein J.
    Am J Med; 1985 May 01; 78(5):865-8. PubMed ID: 3993666
    [Abstract] [Full Text] [Related]

  • 34. A mutation in factor I that is associated with atypical hemolytic uremic syndrome does not affect the function of factor I in complement regulation.
    Nilsson SC, Karpman D, Vaziri-Sani F, Kristoffersson AC, Salomon R, Provot F, Fremeaux-Bacchi V, Trouw LA, Blom AM.
    Mol Immunol; 2007 Mar 01; 44(8):1835-44. PubMed ID: 17084897
    [Abstract] [Full Text] [Related]

  • 35. C4, BF, C3 allele distribution and complement activity in healthy aged people and centenarians.
    Bellavia D, Fradà G, Di Franco P, Feo S, Franceschi C, Sansoni P, Brai M.
    J Gerontol A Biol Sci Med Sci; 1999 Apr 01; 54(4):B150-3. PubMed ID: 10219002
    [Abstract] [Full Text] [Related]

  • 36. Atypical haemolytic uraemic syndrome.
    Kavanagh D, Goodship TH, Richards A.
    Br Med Bull; 2006 Apr 01; 77-78():5-22. PubMed ID: 16968692
    [Abstract] [Full Text] [Related]

  • 37. C3, BF and C4 polymorphisms in Tunisians.
    Ayed K, Gorgi Y.
    Hum Hered; 1990 Apr 01; 40(6):363-7. PubMed ID: 2083950
    [Abstract] [Full Text] [Related]

  • 38. Molecular basis of complement factor I deficiency in Tunisian atypical haemolytic and uraemic syndrome patients.
    Jlajla H, Dehman F, Jallouli M, Khedher R, Ayadi I, Zerzeri Y, Laadhar L, Sfar I, Mahfoudh A, Gorgi Y, Cheour E, Zouaghi K, Gargah T, Kallel Sellami M.
    Nephrology (Carlton); 2019 Mar 01; 24(3):357-364. PubMed ID: 29292855
    [Abstract] [Full Text] [Related]

  • 39. Breakdown products of C3 and factor B in hemolytic-uremic syndrome.
    Kim Y, Miller K, Michael AF.
    J Lab Clin Med; 1977 Apr 01; 89(4):845-50. PubMed ID: 845484
    [Abstract] [Full Text] [Related]

  • 40. Treatment of human complement components C4 and C3 with amines or chaotropic ions. Evidence of a functional and structural change that provides uncleaved C4 and C3 with properties of their soluble activated froms, C4b and C3b.
    von Zabern I, Nolte R, Vogt W.
    Scand J Immunol; 1981 Apr 01; 13(5):413-31. PubMed ID: 6171865
    [Abstract] [Full Text] [Related]

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