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Journal Abstract Search

119 related items for PubMed ID: 666136

  • 1. 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; 88(6):796-8. PubMed ID: 666136
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  • 2. Deficiency of the second complement component association with the HLA haplotype A10, B18 in a normal population.
    Rynes RI, Britten AF, Pickering RJ.
    Ann Rheum Dis; 1982 Feb; 41(1):93-6. PubMed ID: 6950690
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  • 3. 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; 46(2):420-4. PubMed ID: 7039890
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  • 4. [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
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  • 5. Simultaneous occurrence of hereditary C6 and C2 deficiency in a French-Canadian family.
    Delâge JM, Lehner-Netsch G, Lafleur R, Simard J, Brun G, Prochazka E.
    Immunology; 1979 Jun; 37(2):419-28. PubMed ID: 468307
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  • 6. [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; 35(10):1085-95. PubMed ID: 107905
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  • 7. HLA-linked C2 deficiency in a Dutch patient with systemic lupus erythematosus.
    Berrens L, de la Faille HB, Borst-Eilers E.
    J Clin Pathol; 1979 Jun; 32(6):528-33. PubMed ID: 469009
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  • 8. HLA antigen studies in a family with C2 deficiency.
    Opelz G, Glovsky MM.
    J Immunogenet; 1976 Oct; 3(5):303-6. PubMed ID: 137935
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  • 10. Studies on the C2-deficiency gene in man.
    Mortensen JP, Buskjaer L, Lamm LU.
    Immunology; 1980 Apr; 39(4):541-9. PubMed ID: 7380478
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  • 11. The spondylitis of inflammatory bowel disease. Evidence for a non-HLA linked axial arthropathy.
    Enlow RW, Bias WB, Arnett FC.
    Arthritis Rheum; 1980 Dec; 23(12):1359-65. PubMed ID: 6450595
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  • 12. Lack of association between the HLA-A10 (A25), B18 and C2o haplotype and anaphylactoid purpura (AP).
    Krüger J, Opferkuch W, Evers KG, Bosecker L, Haase W.
    Tissue Antigens; 1980 Jan; 15(1):68-74. PubMed ID: 12735335
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  • 15. Complement factor 2 deficiency: a clinical and serological family study.
    D'Cruz D, Taylor J, Ahmed T, Asherson R, Khamashta M, Hughes GR.
    Ann Rheum Dis; 1992 Nov; 51(11):1254-6. PubMed ID: 1361318
    [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; 12(3):132-6. PubMed ID: 389503
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  • 18. Lack of association of HLA B27 with radiographic sacroiliitis in inflammatory bowel disease.
    Hyla JF, Franck WA, Davis JS.
    J Rheumatol; 1976 Jun; 3(2):196-200. PubMed ID: 950636
    [Abstract] [Full Text] [Related]

  • 19. Hereditary C2 deficiency associated with immune complex disease.
    McPherson AJ, McKenzie I, Castaldi PA, Stewart GJ.
    Aust J Exp Biol Med Sci; 1978 Feb; 56(1):81-98. PubMed ID: 149533
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  • 20. Linkage relationship of C2 deficiency, HLA and glyoxalase I loci.
    Mahowald ML, Dalmasso AP, Petzel RA, Yunis EJ.
    Vox Sang; 1979 Feb; 37(6):321-8. PubMed ID: 161677
    [Abstract] [Full Text] [Related]

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