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Journal Abstract Search

151 related items for PubMed ID: 389503

  • 21. Association of systemic lupus erythematosus and SLE-like syndromes with hereditary and acquired complement deficiency states.
    Agnello V.
    Arthritis Rheum; 1978 Jun; 21(5 Suppl):S146-52. PubMed ID: 666879
    [Abstract] [Full Text] [Related]

  • 22. Glomerulonephritis with mesangial deposits of IgA unassociated with systemic disease.
    Katz A, Underdown BJ, Minta JO, Lepow IH.
    Can Med Assoc J; 1976 Feb 07; 114(3):209-15. PubMed ID: 801796
    [Abstract] [Full Text] [Related]

  • 23. Hereditary C2 deficiency associated with cutaneous lupus erythematosus: clinical, laboratory, and genetic studies.
    Levy SB, Pinnell SR, Meadows L, Snyderman R, Ward FE.
    Arch Dermatol; 1979 Jan 07; 115(1):57-61. PubMed ID: 760659
    [Abstract] [Full Text] [Related]

  • 24. Inherited deficiency of the second component of complement. Rheumatic disease associations.
    Glass D, Raum D, Gibson D, Stillman JS, Schur PH.
    J Clin Invest; 1976 Oct 07; 58(4):853-61. PubMed ID: 965492
    [Abstract] [Full Text] [Related]

  • 25. Membranoproliferative glomerulonephritis in childhood cirrhosis associated with alpha1-antitrypsin deficiency.
    Moroz SP, Cutz E, Balfe JW, Sass-Kortsak A.
    Pediatrics; 1976 Feb 07; 57(2):232-8. PubMed ID: 1082572
    [Abstract] [Full Text] [Related]

  • 26. Deficiencies of the complement system in man.
    Day NK, Good RA.
    Birth Defects Orig Artic Ser; 1975 Feb 07; 11(1):306-11. PubMed ID: 807272
    [Abstract] [Full Text] [Related]

  • 27. [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 07; 138(7):399-402. PubMed ID: 2398910
    [Abstract] [Full Text] [Related]

  • 28. 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 Jul 07; 13(2):104-11. PubMed ID: 9063702
    [Abstract] [Full Text] [Related]

  • 29. Lupus erythematosus-like syndrome with a familial deficiency of C2.
    Douglass MC, Lamberg SI, Lorincz AL, Good RA, Day NK.
    Arch Dermatol; 1976 May 07; 112(5):671-4. PubMed ID: 1275522
    [Abstract] [Full Text] [Related]

  • 30. [Familial and hereditary mesangial glomerulonephritis with IgA deposits (author's transl)].
    Gutiérrez Millet V, Navas Palacios JJ, Ortega Ruano R, Barrientos Guzmán A, Usera Sarraga G, Prieto Carles C, Montalbán MA, Rodicio JL.
    Med Clin (Barc); 1981 Jan 10; 76(1):1-7. PubMed ID: 7012469
    [Abstract] [Full Text] [Related]

  • 31. The chromosomal order of genes controlling the major histocompatibility complex, properdin factor B, and deficiency of the second component of complement.
    Raum D, Glass D, Carpenter CB, Alper CA, Schur PH.
    J Clin Invest; 1976 Nov 10; 58(5):1240-8. PubMed ID: 993342
    [Abstract] [Full Text] [Related]

  • 32. Hereditary C2 deficiency: association with skin lesions resembling the discoid lesion of systemic lupus erythematosus.
    Stern R, Fu SM, Fotino M, Agnello V, Kunkel HG.
    Arthritis Rheum; 1976 Nov 10; 19(3):517-22. PubMed ID: 132935
    [Abstract] [Full Text] [Related]

  • 33. 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 10; 37(2):419-28. PubMed ID: 468307
    [Abstract] [Full Text] [Related]

  • 34. Mesangial disposal of glomerular immune deposits in acute malarial glomerulonephritis of rats.
    Sterzel RB, Ehrich JH, Lucia H, Thomson D, Kashgarian M.
    Lab Invest; 1982 Feb 10; 46(2):209-14. PubMed ID: 7038293
    [Abstract] [Full Text] [Related]

  • 35. 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 10; 66(10):1093-8. PubMed ID: 16386652
    [Abstract] [Full Text] [Related]

  • 36. Lobular form idiopathic glomerulonephritis with massive subendothelial and paramesangial immune deposits, a three-year follow-up case.
    Ito H, Moriki T, Nishiya K, Yasuoka N, Chijiwa T, Nakamura T, Arii K, Hisakawa N, Hashimoto K, Uesugi N, Takebayashi S.
    Clin Nephrol; 1997 Nov 10; 48(5):321-6. PubMed ID: 9403218
    [Abstract] [Full Text] [Related]

  • 37. Evidence for activation of the alternate pathway in glomerulonephritis.
    Michael AF, McLean RH.
    Adv Nephrol Necker Hosp; 1974 Nov 10; 4():49-66. PubMed ID: 4219999
    [No Abstract] [Full Text] [Related]

  • 38. Hereditary C2 deficiency associated with common variable immunodeficiency.
    Seligmann M, Brouet JC, Sasportes M.
    Ann Intern Med; 1979 Aug 10; 91(2):216-7. PubMed ID: 313733
    [Abstract] [Full Text] [Related]

  • 39. Inherited deficiency of the second component of complement (C2) with membranoproliferative glomerulonephritis.
    Kim Y, Friend PS, Dresner IG, Yunis EJ, Michael AF.
    Am J Med; 1977 May 10; 62(5):765-71. PubMed ID: 860727
    [Abstract] [Full Text] [Related]

  • 40. Lupus nephritis: correlation between light, electron microscopic and immunofluorescent findings and renal function.
    Sinniah R, Feng PH.
    Clin Nephrol; 1976 Aug 10; 6(2):340-51. PubMed ID: 782752
    [Abstract] [Full Text] [Related]

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