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Journal Abstract Search

134 related items for PubMed ID: 2398910

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  • 4. [C2 deficiency discovered in pneumococcal meningitis].
    Monfort-Gouraud M, Le Gall MA, Nicot F, Badoual J.
    Arch Fr Pediatr; 1993 Feb; 50(2):139-41. PubMed ID: 8343021
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  • 5. [Systemic lupus erythematosus associated with homozygous C2 deficiency. Apropos of a case report and literature review].
    Borradori L, Gueissaz F, Frenk E, Rohner R, Scherz R, Lantin JP, Späth PJ.
    Schweiz Med Wochenschr; 1991 Mar 23; 121(12):418-23. PubMed ID: 2028245
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  • 6. Renal transplantation in a patient with hereditary deficiency of the second component of complement.
    Zeitz HJ, Gewurz A, Jonasson O, Geis WP, Gewurz H.
    Clin Exp Immunol; 1981 Nov 23; 46(2):420-4. PubMed ID: 7039890
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  • 8. [Homozygous C7 defect in a German family].
    Pietsch H, Raab K, Lalyko K, Wahn V.
    Monatsschr Kinderheilkd; 1993 May 23; 141(5):412-5. PubMed ID: 8326961
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  • 9. Complementing the patient: a complement component deficiency in a patient with recurrent infections and glomerulonephritis.
    Sinclair D, Wilde G, Bex S, Peters S.
    Clin Lab; 2005 May 23; 51(9-10):505-7. PubMed ID: 16285472
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  • 10. Studies on the C2-deficiency gene in man.
    Mortensen JP, Buskjaer L, Lamm LU.
    Immunology; 1980 Apr 23; 39(4):541-9. PubMed ID: 7380478
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  • 12. [Familial glomerulonephritis and hereditary deficiency of C2].
    Genin C, Freycon MT, Berthoux FC, Lepetit JC, Bétuel H, Freidel C, Freycon F.
    Arch Fr Pediatr; 1978 Dec 23; 35(10):1085-95. PubMed ID: 107905
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  • 15. [Lupus erythematosus and hereditary lack of complement. Review of about one case of C2 deficit (author's transl)].
    Morel P, Sohier J, Peltier AP, Cottenot F, Civatte J.
    Ann Dermatol Venereol; 1977 Dec 23; 104(12):831-9. PubMed ID: 613949
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  • 16. Hereditary C2 deficiency associated with non-systemic glomerulonephritis.
    Sobel AT, Moisy M, Hirbec G, Tournesac A, Berry JP, Mannoni P, Peltier AP, Lagrue G.
    Clin Nephrol; 1979 Sep 23; 12(3):132-6. PubMed ID: 389503
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  • 18. IgG and complement-mediated tissue damage in the absence of C2: evidence of a functionally active C2-bypass pathway in a guinea pig model.
    Wagner E, Platt JL, Howell DN, Marsh HC, Frank MM.
    J Immunol; 1999 Sep 15; 163(6):3549-58. PubMed ID: 10477630
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  • 20. Inherited deficiency of properdin and C2 in a patient with recurrent bacteremia.
    Gelfand EW, Rao CP, Minta JO, Ham T, Purkall DB, Ruddy S.
    Am J Med; 1987 Mar 23; 82(3 Spec No):671-5. PubMed ID: 3826129
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