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165 related items for PubMed ID: 16499568

  • 1.
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  • 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
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  • 3. [Hereditary complement deficiencies].
    Fischer E.
    Hautarzt; 1982 Feb; 33(2):65-72. PubMed ID: 6281215
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  • 4. Systemic lupus erythematosus, partial lipodystrophy and hypocomplementemia.
    Jasin HE.
    J Rheumatol; 1979 Feb; 6(1):43-50. PubMed ID: 439110
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  • 7. Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H.
    Pickering MC, Cook HT, Warren J, Bygrave AE, Moss J, Walport MJ, Botto M.
    Nat Genet; 2002 Aug; 31(4):424-8. PubMed ID: 12091909
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  • 11. [Investigation of the complement system in clinical practice].
    Frémeaux-Bacchi V, Dragon-Durey MA, Blouin J, Mouthon L, Fridman WH.
    Ann Med Interne (Paris); 2003 Dec; 154(8):529-40. PubMed ID: 15037829
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  • 12. Laboratory detection of complement activation and complement deficiencies.
    Lint TF.
    Am J Med Technol; 1982 Sep; 48(9):743-8. PubMed ID: 6814254
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  • 13. Complement polymorphism, the major histocompatibility complex and associated diseases: a speculation.
    Porter RR.
    Mol Biol Med; 1983 Jul; 1(1):161-8. PubMed ID: 6679872
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  • 14. [Clinical aspects of the complement system].
    Tsukamoto H, Horiuchi T.
    Rinsho Byori; 2006 Jul; 54(7):757-62. PubMed ID: 16913667
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  • 15. Complement in human diseases: Lessons from complement deficiencies.
    Botto M, Kirschfink M, Macor P, Pickering MC, Würzner R, Tedesco F.
    Mol Immunol; 2009 Sep; 46(14):2774-83. PubMed ID: 19481265
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  • 16. The Seventh K Prathap Memorial Lecture. The pathogenesis of autoimmune immune complex disease.
    Lachmann PJ.
    Malays J Pathol; 1992 Jun; 14(1):1-5. PubMed ID: 1469911
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  • 17. Autoimmune manifestations in primary immune deficiencies.
    Bussone G, Mouthon L.
    Autoimmun Rev; 2009 Feb; 8(4):332-6. PubMed ID: 19028607
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  • 18. [Decrease of the 3rd fraction of serum complement. Study in a hospital population of 13000 patients].
    Laudet J, Frot JC, Baglin A, Parlier H, Giraudet P.
    Sem Hop; 1983 Nov 10; 59(41):2819-21. PubMed ID: 6316542
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  • 19. [An exceptional component C3 deficiency revealed by serum protein electrophoresis].
    Dejoie T, Audrain M, Bach-Ngohou K, Denis M, Legoue-Morillon S, Thomas C, Masson D.
    Ann Biol Clin (Paris); 2009 Nov 10; 67(6):715-9. PubMed ID: 19939777
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  • 20. The first confirmed case with C3 deficiency caused by compound heterozygous mutations in the C3 gene; a new aspect of pathogenesis for C3 deficiency.
    Kida M, Fujioka H, Kosaka Y, Hayashi K, Sakiyama Y, Ariga T.
    Blood Cells Mol Dis; 2008 Nov 10; 40(3):410-3. PubMed ID: 18201916
    [Abstract] [Full Text] [Related]

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