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Journal Abstract Search

142 related items for PubMed ID: 313733

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  • 3. Linkage relationship of C2 deficiency, HLA and glyoxalase I loci.
    Mahowald ML, Dalmasso AP, Petzel RA, Yunis EJ.
    Vox Sang; 1979; 37(6):321-8. PubMed ID: 161677
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  • 5. Mixed lymphocyte culture determinants and C2 deficiency: LD-7a associated with C2 deficiency in four families.
    Fu SM, Stern R, Kunkel HG, Dupont B, Hansen JA, Day NK, Good RA, Jersild C, Fotino M.
    J Exp Med; 1975 Aug 01; 142(2):495-506. PubMed ID: 124762
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  • 6. [Hereditary C2 deficiency with systemic lupus erythematosus: clinical and immunologic studies in a family (author's transl)].
    Brouet JC, Fridman WH, Clauvel JP, Sasportes M, Danon F, Seligmann M.
    Nouv Presse Med; 1977 Oct 22; 6(35):3199-203. PubMed ID: 928048
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  • 7. C3 metabolism in a patient with deficiency of the second component of complement (C2) and discoid lupus erythematosus.
    Wild JH, Zvaifler NJ, Müller-Eberhard HJ, Wilson CB.
    Clin Exp Immunol; 1976 May 22; 24(2):238-48. PubMed ID: 1084239
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  • 8. Hereditary C2 deficiency associated with immune complex disease.
    McPherson AJ, McKenzie I, Castaldi PA, Stewart GJ.
    Aust J Exp Biol Med Sci; 1978 Feb 22; 56(1):81-98. PubMed ID: 149533
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  • 11. Hereditary C2 deficiency: diagnosis and HLA gene complex associations.
    Gibson DJ, Glass D, Carpenter CB, Schur PH.
    J Immunol; 1976 Apr 22; 116(4):1065-70. PubMed ID: 1082903
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  • 18. Studies on the C2-deficiency gene in man.
    Mortensen JP, Buskjaer L, Lamm LU.
    Immunology; 1980 Apr 22; 39(4):541-9. PubMed ID: 7380478
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  • 19. Oligoclonality, impaired class switch and B-cell memory responses in WHIM syndrome.
    Mc Guire PJ, Cunningham-Rundles C, Ochs H, Diaz GA.
    Clin Immunol; 2010 Jun 22; 135(3):412-21. PubMed ID: 20226738
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  • 20. 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 22; 37(2):419-28. PubMed ID: 468307
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