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Journal Abstract Search

192 related items for PubMed ID: 3109005

  • 1. C8 beta subunit deficiency in a patient with recurrent neisserial infections.
    Fontana L, Tedesco F, De Carolis C, Roncelli L, Teggi A, Paffetti A, Perricone R.
    Ric Clin Lab; 1987; 17(1):19-25. PubMed ID: 3109005
    [Abstract] [Full Text] [Related]

  • 2. Recurrent meningococcal infections associated with a functional deficiency of the C8 component of human complement.
    Matthews N, Stark JM, Harper PS, Doran J, Jones DM.
    Clin Exp Immunol; 1980 Jan; 39(1):53-9. PubMed ID: 6771072
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  • 3. The role of complement in anti-bacterial defence.
    D'Amelio R, Biselli R.
    Ann Ital Med Int; 1994 Jan; 9(3):173-7. PubMed ID: 7946895
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  • 4. Recurrent meningococcal meningitis associated with deficiencies of C8 and anti-meningococcal antibody.
    Cooke RP, Zafar M, Haeney MR.
    J Clin Lab Immunol; 1987 May; 23(1):53-6. PubMed ID: 3112405
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  • 5. [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
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  • 6. Inherited C8 beta subunit deficiency in a patient with recurrent meningococcal infections: in vivo functional kinetic analysis of C8.
    Rao CP, Minta JO, Laski B, Alper CA, Gelfand EW.
    Clin Exp Immunol; 1985 Apr 23; 60(1):183-90. PubMed ID: 3924449
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  • 7. Decreased C5b67-inhibitor activity in two families with hereditary functional deficiency of the eighth component of complement.
    Zeitz HJ, Zeff RA, Gewurz H, Lint TF.
    J Immunol; 1983 Jun 23; 130(6):2809-13. PubMed ID: 6854017
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  • 8. 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 23; 63(5):243-73. PubMed ID: 6433145
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  • 9. [Homozygote CB deficiency revealed by recurrent Neisseria meningitidis infections in an adolescent].
    Louaib D, Nathanson M, Lachassinne E, Huault G, Muller MH, Sauvion S, Gaudelus J, Perelman R.
    Arch Pediatr; 1994 Oct 23; 1(10):908-12. PubMed ID: 7842072
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  • 13. Hereditary complement deficiency in survivors of meningococcal disease: high prevalence of C7/C8 deficiency in Sephardic (Moroccan) Jews.
    Zimran A, Rudensky B, Kramer MR, Tedesco F, Ehrenfeld M, Raz R, Greif Z, Gelber M, Lishner M, Golan E.
    Q J Med; 1987 Apr 23; 63(240):349-58. PubMed ID: 3685247
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  • 15. Molecular, genetic, and functional analysis of homozygous C8 beta-chain deficiency in two siblings.
    Kotnik V, Luznik-Bufon T, Schneider PM, Kirschfink M.
    Immunopharmacology; 1997 Dec 23; 38(1-2):215-21. PubMed ID: 9476133
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  • 16. Prevalence of hereditary properdin, C7 and C8 deficiencies in patients with meningococcal infections.
    Schlesinger M, Nave Z, Levy Y, Slater PE, Fishelson Z.
    Clin Exp Immunol; 1990 Sep 23; 81(3):423-7. PubMed ID: 2397612
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  • 17. Normal bactericidal capacity against Neisseria meningitidis in serum from a patient with a hemolytically inactive complement factor 8 (C8).
    Strate M, Olsen H, Teisner B, Brandslund I.
    Acta Pathol Microbiol Immunol Scand B; 1983 Dec 23; 91(6):431-4. PubMed ID: 6424405
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  • 18. Complement C8 deficiency with recurrent meningococcemia: examination of meningococcal opsonization.
    Kemp AS, Vernon J, Muller-Eberhard HJ, Bau DC.
    Aust Paediatr J; 1985 Aug 23; 21(3):169-71. PubMed ID: 4062713
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  • 19. Inherited deficiency of C8 in a patient with recurrent meningococcal infections: further evidence for a dysfunctional C8 molecule and nonlinkage to the HLA system.
    Densen P, Brown EJ, O'Neill GJ, Tedesco F, Clark RA, Frank MM, Webb D, Myers J.
    J Clin Immunol; 1983 Jan 23; 3(1):90-9. PubMed ID: 6186685
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