BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 6103091)

  • 1. Complement deficiency and nephritis. A report of a family.
    Pussell BA; Bourke E; Nayef M; Morris S; Peters DK
    Lancet; 1980 Mar; 1(8170):675-7. PubMed ID: 6103091
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inherited C3 deficiency with recurrent infections and glomerulonephritis.
    Borzy MS; Gewurz A; Wolff L; Houghton D; Lovrien E
    Am J Dis Child; 1988 Jan; 142(1):79-83. PubMed ID: 2963536
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The first confirmed case with C3 deficiency caused by compound heterozygous mutations in the C3 gene; a new aspect of pathogenesis for C3 deficiency.
    Kida M; Fujioka H; Kosaka Y; Hayashi K; Sakiyama Y; Ariga T
    Blood Cells Mol Dis; 2008; 40(3):410-3. PubMed ID: 18201916
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Homozygous C3 deficiency associated with IgA nephropathy.
    Imai K; Nakajima K; Eguchi K; Miyazaki M; Endoh M; Tomino Y; Nomoto Y; Sakai H; Hyodo Y
    Nephron; 1991; 59(1):148-52. PubMed ID: 1944729
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Complement breakdown products in plasma from patients with systemic lupus erythematosus and patients with membranoproliferative or other glomerulonephritis.
    Perrin LH; Lambert PH; Miescher PA
    J Clin Invest; 1975 Jul; 56(1):165-76. PubMed ID: 1141431
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inherited C3 deficiency of the complement system.
    Grumach AS; Vilela MM; Gonzalez CH; Starobinas N; Pereira AB; Dias-da-Silva W; Carneiro-Sampaio MM
    Braz J Med Biol Res; 1988; 21(2):247-57. PubMed ID: 3264513
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hereditary glomerulonephritis of non-Alport type.
    Doherty CC; Middleton DT; Hill CM
    Proc Eur Dial Transplant Assoc; 1983; 19():575-81. PubMed ID: 6878256
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Compound heterozygous complement C3 deficiency.
    Katz Y; Wetsel RA; Schlesinger M; Fishelson Z
    Immunology; 1995 Jan; 84(1):5-7. PubMed ID: 7890305
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inherited deficiency of the third component of complement associated with recurrent pyogenic infections, circulating immune complexes, and vasculitis in a Dutch family.
    Roord JJ; Daha M; Kuis W; Verbrugh HA; Verhoef J; Zegers BJ; Stoop JW
    Pediatrics; 1983 Jan; 71(1):81-7. PubMed ID: 6848983
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel CFI mutation in a patient with leukocytoclastic vasculitis may redefine the clinical spectrum of Complement Factor I deficiency.
    Bay JT; Katzenstein TL; Kofoed K; Patel D; Skjoedt MO; Garred P; Schejbel L
    Clin Immunol; 2015 Oct; 160(2):315-8. PubMed ID: 25988862
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular analysis of hereditary deficiency of the third component of complement (C3) in two sisters.
    Matsuyama W; Nakagawa M; Takashima H; Muranaga F; Sano Y; Osame M
    Intern Med; 2001 Dec; 40(12):1254-8. PubMed ID: 11813855
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Complement and serum immunoglobulins in homozygous and heterozygous sickle cell anemia in Senegal].
    Dieye TN; Ndiaye O; Ndiaye AB; Thiam D; Fall-Seck K; Diop S; Diop BM; Fall M; Diakhaté L
    Dakar Med; 1999; 44(2):175-9. PubMed ID: 11957280
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 24(2):238-48. PubMed ID: 1084239
    [TBL] [Abstract][Full Text] [Related]  

  • 14. C3, C4, factor B and HLA-DR alpha mRNA expression in renal biopsy specimens from patients with IgA nephropathy.
    Oren R; Laufer J; Goldberg I; Kopolovic J; Waldherr R; Passwell JH
    Immunology; 1995 Dec; 86(4):575-83. PubMed ID: 8567024
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The complement abnormalities of lipodystrophy.
    Sissons JG; West RJ; Fallows J; Williams DG; Boucher BJ; Amos N; Peters DK
    N Engl J Med; 1976 Feb; 294(9):461-5. PubMed ID: 1246331
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [An exceptional component C3 deficiency revealed by serum protein electrophoresis].
    Dejoie T; Audrain M; Bach-Ngohou K; Denis M; Legoue-Morillon S; Thomas C; Masson D
    Ann Biol Clin (Paris); 2009; 67(6):715-9. PubMed ID: 19939777
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A silent gene (C3-) producing partial deficiency of the third component of human complement.
    Hoppe HH; Goedde HW; Agarwal DP; Benkmann H-G ; Hirth L; Janssen W
    Hum Hered; 1978; 28(2):141-6. PubMed ID: 621088
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial partial deficiency of the third component of complement (C3) and the hypocomplementemic cutaneous vasculitis syndrome.
    McLean RH; Weinstein A; Chapitis J; Lowenstein M; Rothfield NF
    Am J Med; 1980 Apr; 68(4):549-58. PubMed ID: 7369233
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Homozygous human C3 deficiency. The role of C3 in antibody production, C-1s-induced vasopermeability, and cobra venom-induced passive hemolysis.
    Alper CA; Colten HR; Gear JS; Rabson AR; Rosen FS
    J Clin Invest; 1976 Jan; 57(1):222-9. PubMed ID: 1107355
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.