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130 related items for PubMed ID: 3679285

  • 1. Deficiency of the sixth component of complement and susceptibility to Neisseria meningitidis infections: studies in 10 families and five isolated cases.
    Orren A, Potter PC, Cooper RC, du Toit E.
    Immunology; 1987 Oct; 62(2):249-53. PubMed ID: 3679285
    [Abstract] [Full Text] [Related]

  • 2. Complement deficiency states and infection: epidemiology, pathogenesis and consequences of neisserial and other infections in an immune deficiency.
    Ross SC, Densen P.
    Medicine (Baltimore); 1984 Sep; 63(5):243-73. PubMed ID: 6433145
    [Abstract] [Full Text] [Related]

  • 3. Recurrent meningococcal meningitis with absence of the sixth component of complement: an evaluation of underlying immunologic mechanisms.
    Vogler LB, Newman SL, Stroud RM, Johnston RB.
    Pediatrics; 1979 Oct; 64(4):465-7. PubMed ID: 492812
    [Abstract] [Full Text] [Related]

  • 4. Complete deficiency of the sixth complement component (C6Q0), susceptibility to Neisseria meningitidis infections and analysis of the frequencies of C6Q0 gene defects in South Africans.
    Orren A, Owen EP, Henderson HE, van der Merwe L, Leisegang F, Stassen C, Potter PC.
    Clin Exp Immunol; 2012 Mar; 167(3):459-71. PubMed ID: 22288589
    [Abstract] [Full Text] [Related]

  • 5. Recurrent bacterial meningitis in patients with genetic defects of terminal complement components.
    Haeney MR, Thompson RA, Faulkner J, Mackintosh P, Ball AP.
    Clin Exp Immunol; 1980 Apr; 40(1):16-24. PubMed ID: 7389212
    [Abstract] [Full Text] [Related]

  • 6. The role of complement in anti-bacterial defence.
    D'Amelio R, Biselli R.
    Ann Ital Med Int; 1994 Apr; 9(3):173-7. PubMed ID: 7946895
    [Abstract] [Full Text] [Related]

  • 7. Molecular defects leading to human complement component C6 deficiency in an African-American family.
    Zhu ZB, Totemchokchyakarn K, Atkinson TP, Volanakis JE.
    Clin Exp Immunol; 1998 Jan; 111(1):91-6. PubMed ID: 9472666
    [Abstract] [Full Text] [Related]

  • 8. Human deficiency of the sixth component of complement in a patient with meningococcal meningitis and no haemostasis abnormality.
    Kernbaum S, Bastin R, Wautier JL, Bure A, Gougerot M, Peltier AP.
    Biomedicine; 1980 Jan; 33(6):197-201. PubMed ID: 6783144
    [Abstract] [Full Text] [Related]

  • 9. [Occurrence of complement defects in meningococcal disease: who should be examined?].
    Nielsen HE, Magnussen P, Lind I.
    Ugeskr Laeger; 1991 Apr 15; 153(16):1113-6. PubMed ID: 1902602
    [Abstract] [Full Text] [Related]

  • 10. Prevalence of mutations leading to complete C6 deficiency (C6Q0) in the Western Cape, South Africa and detection of novel mutations leading to C6Q0 in an Irish family.
    Parham KL, Roberts A, Thomas A, Würzner R, Henderson HE, Potter PC, Morgan BP, Orren A.
    Mol Immunol; 2007 Apr 15; 44(10):2756-60. PubMed ID: 17257682
    [Abstract] [Full Text] [Related]

  • 11. Prophylaxis against Neisseria meningitidis infections and antibody responses in patients with deficiency of the sixth component of complement.
    Potter PC, Frasch CE, van der Sande WJ, Cooper RC, Patel Y, Orren A.
    J Infect Dis; 1990 May 15; 161(5):932-7. PubMed ID: 2109021
    [Abstract] [Full Text] [Related]

  • 12. Combined hereditary deficiency of the sixth component of complement and factor VIII coagulant activity in a Dutch family.
    Daha MR, Bertina RM, Thompson J, Kauffmann RH, Nicholson-Weller A, Veltkamp JJ, Briët E.
    Clin Exp Immunol; 1982 Jun 15; 48(3):733-8. PubMed ID: 6811172
    [Abstract] [Full Text] [Related]

  • 13. Meningococcal meningitis in familial deficiency of the fifth component of complement.
    Peter G, Weigert MB, Bissel AR, Gold R, Kreutzer D, McLean RH.
    Pediatrics; 1981 Jun 15; 67(6):882-6. PubMed ID: 6785713
    [Abstract] [Full Text] [Related]

  • 14. Restricted genetic defects underlie human complement C6 deficiency.
    Dragon-Durey MA, Fremeaux-Bacchi V, Blouin J, Barraud D, Fridman WH, Kazatchkine MD.
    Clin Exp Immunol; 2003 Apr 15; 132(1):87-91. PubMed ID: 12653841
    [Abstract] [Full Text] [Related]

  • 15. Association between combined properdin and mannose-binding lectin deficiency and infection with Neisseria meningitidis.
    Bathum L, Hansen H, Teisner B, Koch C, Garred P, Rasmussen K, Wang P.
    Mol Immunol; 2006 Feb 15; 43(5):473-9. PubMed ID: 16337490
    [Abstract] [Full Text] [Related]

  • 16. Assessment of complement deficiency in patients with meningococcal disease in The Netherlands.
    Fijen CA, Kuijper EJ, te Bulte MT, Daha MR, Dankert J.
    Clin Infect Dis; 1999 Jan 15; 28(1):98-105. PubMed ID: 10028078
    [Abstract] [Full Text] [Related]

  • 17. [Recurrent meningitis in a familial defect of the beta-subunit of the 8th complement component].
    Nürnberger W, Pietsch H, Kobler P, Schwandt C, Seger R, Wahn V.
    Dtsch Med Wochenschr; 1989 Jun 23; 114(25):989-92. PubMed ID: 2737093
    [Abstract] [Full Text] [Related]

  • 18. A complement C5 gene mutation, c.754G>A:p.A252T, is common in the Western Cape, South Africa and found to be homozygous in seven percent of Black African meningococcal disease cases.
    Owen EP, Würzner R, Leisegang F, Rizkallah P, Whitelaw A, Simpson J, Thomas AD, Harris CL, Giles JL, Hellerud BC, Mollnes TE, Morgan BP, Potter PC, Orren A.
    Mol Immunol; 2015 Mar 23; 64(1):170-6. PubMed ID: 25534848
    [Abstract] [Full Text] [Related]

  • 19. Genetic detection of the silent allele (*Q0) in hereditary deficiencies of the human complement C6, C7, and C9 components.
    Alvarez V, Coto E, Setién F, Spath PJ, López-Larrea C.
    Am J Med Genet; 1995 Feb 13; 55(4):408-13. PubMed ID: 7762578
    [Abstract] [Full Text] [Related]

  • 20. Neisseria meningitidis. Early treatment and complement deficiency.
    Vega C, Quinby PM.
    J Ky Med Assoc; 1994 Jun 13; 92(6):227-9. PubMed ID: 8051497
    [No Abstract] [Full Text] [Related]

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