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Journal Abstract Search

155 related items for PubMed ID: 3997207

  • 21. Age of onset in vitiligo: relationship with HLA supratypes.
    Finco O, Cuccia M, Martinetti M, Ruberto G, Orecchia G, Rabbiosi G.
    Clin Genet; 1991 Jan; 39(1):48-54. PubMed ID: 1997215
    [Abstract] [Full Text] [Related]

  • 22. Molecular analysis of the IGHA and MHC class III region genes in one family with IgA and C4 deficiencies.
    Keyeux G, Lefranc MP, Chevailler A, Lefranc G.
    Exp Clin Immunogenet; 1990 Jan; 7(3):170-80. PubMed ID: 1974449
    [Abstract] [Full Text] [Related]

  • 23. Gm allotypes in IgA deficiency.
    Hammarström L, Grubb R, Smith CI.
    J Immunogenet; 1985 Jun; 12(3):125-30. PubMed ID: 3867712
    [Abstract] [Full Text] [Related]

  • 24. Molecular heterogeneity of second and fourth components of complement and their genes in systemic sclerosis and association of HLA alleles A1, B8 and DR3 with limited and DR5 with diffuse systemic sclerosis.
    Venneker GT, van den Hoogen FH, van Meegen M, de Kok-Nazaruk M, Hulsmans RF, Boerbooms AM, de Waal LP, Bos JD, Asghar SS.
    Exp Clin Immunogenet; 1998 Jun; 15(2):90-9. PubMed ID: 9691203
    [Abstract] [Full Text] [Related]

  • 25. Selective IgA deficiency and the HLA-B8 antigen. Report of two cases with familial data.
    Perez-Jimenez F, Lopez PB, Tallo EP, Guzman JR, Molina JS, Pereperez JA.
    Arch Intern Med; 1981 Mar; 141(4):509-10. PubMed ID: 7212894
    [Abstract] [Full Text] [Related]

  • 26. Major histocompatibility complex haplotypes and complement C4 alleles in systemic lupus erythematosus. Results of a multicenter study.
    Hartung K, Baur MP, Coldewey R, Fricke M, Kalden JR, Lakomek HJ, Peter HH, Schendel D, Schneider PM, Seuchter SA.
    J Clin Invest; 1992 Oct; 90(4):1346-51. PubMed ID: 1401069
    [Abstract] [Full Text] [Related]

  • 27. Increased frequency of HLA-A1 and -B8 in association with total lack, but not with deficiency of serum IgA.
    Heikkilä M, Koistinen J, Lohman M, Koskimies S.
    Tissue Antigens; 1984 May; 23(5):280-3. PubMed ID: 6611606
    [Abstract] [Full Text] [Related]

  • 28. Evidence for linkage of IgA deficiency with the major histocompatibility complex.
    Lakhanpal S, O'Duffy JD, Homburger HA, Moore SB.
    Mayo Clin Proc; 1988 May; 63(5):461-5. PubMed ID: 3361955
    [Abstract] [Full Text] [Related]

  • 29. Association of HLA-Bw65 with two major complotypes.
    Darke C, O'Neill GJ.
    Tissue Antigens; 1987 Jul; 30(1):11-7. PubMed ID: 3672489
    [Abstract] [Full Text] [Related]

  • 30. Comparative analysis of the disease-associated complement C4 gene from the HLA-A1, B8, DR3 haplotype.
    Ulgiati D, Abraham LJ.
    Exp Clin Immunogenet; 1996 Jul; 13(1):43-54. PubMed ID: 8854088
    [Abstract] [Full Text] [Related]

  • 31. The [HLA-B18, F1C30, DR3] conserved extended haplotype carries a susceptibility gene for IgD deficiency.
    Calvo B, Castaño L, Marcus-Bagley D, Fici DA, Awdeh Z, Alper CA.
    J Clin Immunol; 2000 May; 20(3):216-20. PubMed ID: 10941830
    [Abstract] [Full Text] [Related]

  • 32. Heterogeneity in the structural basis of the human complement C4A null allele (C4A Q0) as revealed by HindIII restriction fragment length polymorphism analysis.
    Uring-Lambert B, Vegnaduzzi N, Carroll MC, Tongio MM, Goetz J, Hauptmann G.
    FEBS Lett; 1987 Jun 08; 217(1):65-8. PubMed ID: 2885219
    [Abstract] [Full Text] [Related]

  • 33. Complement and HLA. Further definition of high-risk haplotypes in insulin-dependent diabetes.
    Rich S, O'Neill G, Dalmasso AP, Nerl C, Barbosa J.
    Diabetes; 1985 May 08; 34(5):504-9. PubMed ID: 3987976
    [Abstract] [Full Text] [Related]

  • 34. Molecular genetics of C4B deficiency in IgA nephropathy.
    Welch TR, Beischel LS, Choi EM.
    Hum Immunol; 1989 Dec 08; 26(4):353-63. PubMed ID: 2573592
    [Abstract] [Full Text] [Related]

  • 35. Long PCR detection of the C4A null allele in B8-C4AQ0-C4B1-DR3.
    Grant SF, Kristjánsdóttir H, Steinsson K, Blöndal T, Yuryev A, Stefansson K, Gulcher JR.
    J Immunol Methods; 2000 Oct 20; 244(1-2):41-7. PubMed ID: 11033017
    [Abstract] [Full Text] [Related]

  • 36. HLA A1, B8, DR3 extended haplotypes in autoimmune chronic hepatitis.
    Tait B, Mackay IR, Board P, Coggan M, Emery P, Eckardt G.
    Gastroenterology; 1989 Aug 20; 97(2):479-81. PubMed ID: 2787258
    [Abstract] [Full Text] [Related]

  • 37. HLA and complement allotypes in Type 1 (insulin-dependent) diabetes.
    McCluskey J, McCann VJ, Kay PH, Zilko PJ, Christiansen FT, O'Neill GJ, Dawkins RL.
    Diabetologia; 1983 Mar 20; 24(3):162-5. PubMed ID: 6573286
    [Abstract] [Full Text] [Related]

  • 38. Human MHC class III (Bf, C2, C4) genes and GLO: their association with other HLA antigens and extended haplotypes in the Spanish population.
    Regueiro JR, Arnaiz-Villena A.
    Tissue Antigens; 1988 Jan 20; 31(1):14-25. PubMed ID: 3341017
    [Abstract] [Full Text] [Related]

  • 39. Susceptibility locus for IgA deficiency and common variable immunodeficiency in the HLA-DR3, -B8, -A1 haplotypes.
    Schroeder HW, Zhu ZB, March RE, Campbell RD, Berney SM, Nedospasov SA, Turetskaya RL, Atkinson TP, Go RC, Cooper MD, Volanakis JE.
    Mol Med; 1998 Feb 20; 4(2):72-86. PubMed ID: 9508785
    [Abstract] [Full Text] [Related]

  • 40. [Polymorphism of C4 and factor B in type I diabetes].
    Blickle JF, Hauptmann G, Goetz J, Tongio MM, Mayer S, Brogard JM, Dorner M.
    Pathol Biol (Paris); 1988 Jun 20; 36(6):791-4. PubMed ID: 3047638
    [Abstract] [Full Text] [Related]

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