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Journal Abstract Search

134 related items for PubMed ID: 2398910

  • 21. Homozygous C2 deficiency: association with defective alternative pathway function and immunoglobulin deficiency.
    Sanal O, Yel L, Tezcan I, Ersoy F, Berkel AI.
    Int Arch Allergy Immunol; 1996 Jun; 110(2):195-8. PubMed ID: 8645999
    [Abstract] [Full Text] [Related]

  • 22. 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
    [Abstract] [Full Text] [Related]

  • 23. [Complete deficiency in the C2 fraction of complement associated with a glomerular nephropathy: apropos of 2 cases].
    Ayed K, Bardi R, Sassi F, Gorgi Y, Ben Maiz H, Haddad S, Ben Ayed H.
    Nephrologie; 1988 Feb; 9(5):239-44. PubMed ID: 3216945
    [Abstract] [Full Text] [Related]

  • 24. Hereditary C2 deficiency: diagnosis and HLA gene complex associations.
    Gibson DJ, Glass D, Carpenter CB, Schur PH.
    J Immunol; 1976 Apr; 116(4):1065-70. PubMed ID: 1082903
    [Abstract] [Full Text] [Related]

  • 25. Human histocompatibility leukocyte antigen (HLA) haplotype frequencies estimated from the data on HLA class I, II, and III antigens in 111 Japanese narcoleptics.
    Matsuki K, Juji T, Tokunaga K, Naohara T, Satake M, Honda Y.
    J Clin Invest; 1985 Dec; 76(6):2078-83. PubMed ID: 3865934
    [Abstract] [Full Text] [Related]

  • 26. Recurrent pyogenic infections in individuals with absence of the second component of complement.
    Sampson HA, Walchner AM, Baker PJ.
    J Clin Immunol; 1982 Jan; 2(1):39-45. PubMed ID: 6980226
    [Abstract] [Full Text] [Related]

  • 27. Complement-human histocompatibility antigen haplotypes in C2 deficiency.
    Awdeh ZL, Raum DD, Glass D, Agnello V, Schur PH, Johnston RB, Gelfand EW, Ballow M, Yunis E, Alper CA.
    J Clin Invest; 1981 Feb; 67(2):581-3. PubMed ID: 7462431
    [Abstract] [Full Text] [Related]

  • 28. Vasculitis simulating eczematous dermatitis due to C2 deficiency.
    Irestedt M, Månsson T, Svensson A.
    Acta Derm Venereol; 1987 Feb; 67(3):265-7. PubMed ID: 2442945
    [Abstract] [Full Text] [Related]

  • 29. [Genetic deficiency of C2 associated with haplotype A25, B18 in familial systemic lupus erythematosus].
    Gantes MA, González T.
    Med Clin (Barc); 1987 Feb; 79(7):295-8. PubMed ID: 7176738
    [No Abstract] [Full Text] [Related]

  • 30. HLA antigen studies in a family with C2 deficiency.
    Opelz G, Glovsky MM.
    J Immunogenet; 1976 Oct; 3(5):303-6. PubMed ID: 137935
    [Abstract] [Full Text] [Related]

  • 31. Incomplete functional deficiencies of the fourth (C4) and second (C2) components of complement in a patient with linear frontoparietal scleroderma and his family. Deficiencies determined by a gene not linked to human leukocyte antigen system.
    Venneker GT, van Meegen M, de Kok-Nazaruk M, Hulsmans RF, de Waall LP, Bos JD, Asghar SS.
    Exp Clin Immunogenet; 1996 Oct; 13(2):104-11. PubMed ID: 9063702
    [Abstract] [Full Text] [Related]

  • 32. Defective activation of the alternative pathway of complement in patients with homozygous C2 deficiency: studies in two unrelated families.
    Schwertz R, Esser E, Seger RA, Rubinstein A, Hauptmann G, Wahn V.
    Eur J Pediatr; 1991 Jul; 150(9):647-51. PubMed ID: 1915518
    [Abstract] [Full Text] [Related]

  • 33. C2 deficiency, moderately low IgG2 concentrations and lack of the G2m(23) allotype marker in a child with repeated bacterial infections.
    Sjöholm AG, Hallberg T, Oxelius VA, Hammarström L, Smith CI, Lindgren F.
    Acta Paediatr Scand; 1987 May; 76(3):533-8. PubMed ID: 3604675
    [Abstract] [Full Text] [Related]

  • 34. 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
    [Abstract] [Full Text] [Related]

  • 35. 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
    [Abstract] [Full Text] [Related]

  • 36. Homozygosity for the IgG2 subclass allotype G2M(n) protects against severe infection in hereditary C2 deficiency.
    Jönsson G, Oxelius VA, Truedsson L, Braconier JH, Sturfelt G, Sjöholm AG.
    J Immunol; 2006 Jul 01; 177(1):722-8. PubMed ID: 16785571
    [Abstract] [Full Text] [Related]

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  • 38. Serum concentrations of C4 isotypes and factor B in type I C2 deficiency suggest haplotype-dependent quantitative expression of MHC class III complement genes.
    Truedsson L, Gullstrand B, Jönsson T, Klint C.
    Exp Clin Immunogenet; 1995 Jul 01; 12(2):66-73. PubMed ID: 7576717
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