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Journal Abstract Search

130 related items for PubMed ID: 2398910

  • 1. [Fatal pneumococcal meningitis in a 1-year-old child with homozygous C2 deficiency].
    Glöckel U, Schneider PM, Beck JD, Brade V.
    Monatsschr Kinderheilkd; 1990 Jul; 138(7):399-402. PubMed ID: 2398910
    [Abstract] [Full Text] [Related]

  • 2. Deficiency of C2, the second complement component, in the family of a patient with SLE-like syndrome: the first case of hereditary C2 deficiency in Czechoslovakia.
    Starsia Z, Zitnan D, Loos M, Stefanovic J, Bosák V, Niks M, Tomanová H, Lukác J, Lulovicová M.
    Haematologia (Budap); 1987 Jul; 20(4):215-20. PubMed ID: 3428724
    [Abstract] [Full Text] [Related]

  • 3. HLA genotypes in a family with a case of homozygous C2 deficiency and discoid lupus erythematosus.
    Braathen LR, Bratlie A, Teisberg P.
    Acta Derm Venereol; 1986 Jul; 66(5):419-22. PubMed ID: 2431580
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 7. [Deficiency of C2 component in a 9-year old girl].
    Madaliński K, Prokopowicz K, Wygledowska G, Bogdanik I.
    Pol Tyg Lek; 1996 May 23; 51(19-22):293-4. PubMed ID: 9289715
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 11. Frequency in Spanish population of familial complement factor 2 type I deficits and associated HLA haplotypes.
    Antolín SC, Del Rey Cerros MJ, Sierra EM, Miñarro DO, Clemente J, Martínez LA, Peña PV, Panete MJ, Pérez PM, Paz-Artal E.
    Hum Immunol; 2005 Oct 23; 66(10):1093-8. PubMed ID: 16386652
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 13. [Role of the classical and alternative complement pathways in chemotaxis of human C2 deficiency (author's transl)].
    Pham Huu T, Buriot D, Griscelli C.
    Ann Immunol (Paris); 1980 Dec 23; 131C(1):69-77. PubMed ID: 7396417
    [Abstract] [Full Text] [Related]

  • 14. Inherited deficiency of second component of complement and HLA haplotype A10,B18 associated with inflammatory bowel disease.
    Slade JD, Luskin AT, Gewurz H, Kraft SC, Kirsner JB, Zeitz HJ.
    Ann Intern Med; 1978 Jun 23; 88(6):796-8. PubMed ID: 666136
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 17. Selective deficiencies in complement component : a family with hereditary C2 deficiency.
    Dantant M, Rivat C, Gilbert D, Fontaine M, Cavelier B, Godin M, Fillastre JP.
    Biomedicine; 1978 Sep 23; 28(3):185-90. PubMed ID: 698338
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 19. Hereditary deficiency of C2 in association with linear scleroderma 'en coup de sabre'.
    Hulsmans RF, Asghar SS, Siddiqui AH, Cormane RH.
    Arch Dermatol; 1986 Jan 15; 122(1):76-9. PubMed ID: 3942410
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

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