References
- Leitao MF, Vilela MM, Rutz R, Grumach AS, Condino-Neto A, Kirschfink M. Complement factor I deficiency in a family with recurrent infections. Immunopharmacology 1997; 38: 207–13
- Floret D, Stamm D, Ponard D. Increased susceptibility to infection in children with congenital deficiency of factor I. Pediatr Infect Dis J 1991; 10: 615–8
- Amadei N, Baracho GV, Nudelman V, Bastos W, Florido MP, Isaac L. Inherited complete factor I deficiency associated with systemic lupus erythematosus, higher susceptibility to infection and low levels of factor H. Scand J Immunol 2001; 53: 615–21
- Solal-Celigny P, Laviolette M, Hebert J, Atkins PC, Sirois M, Brun G, et al. C3b inactivator deficiency with immune complex manifestations. Clin Exp Immunol 1982; 47: 197–205
- Vyse TJ, Späth PJ, Davies KA, Morley BJ, Philippe P, Athanassiou P, et al. Hereditary complement factor I deficiency. Quart J Med 1994; 87: 385–402
- Sjöholm AG, Truedsson L, Jensenius J. Complement pathway and meningococcal disease. Diagnostic aspects. Methods in Molecular Medicine, vol 67. Meningococcal: Disease Methods and Protocols, AJ Pollard, MCJ Maiden. Humana Press Inc, Totowa, NJUSA 2001; 529–47
- Johnson U, Truedsson L, Gustavii B. Complement components in 100 newborns and their mothers determined by electroimmunoassay. Acta Pathol Microbiol Immunol Scand [C] 1983; 91: 147–50
- Sturfelt G, Truedsson L. Complement factor D concentrations in normal sera: comparison of immunochemical and functional determinations. Acta Pathol Microbiol Immunol Scand [C] 1983; 91: 383–9
- Späth PJ, Sjöholm AG, Fredrikson GN, Misiano G, Rohner R, Scherz R, Schaad UB, et al. Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n). Clin Exp Immunol 1999; 118: 278–84
- Wahn V, Gobal U, Day NK. Restoration of complement function by plasma infusion in factor I (C3b inactivator) deficiency. J Pediatr 1984; 105: 673–4
- Sullivan KE, Winkelstein JA. Genetically determined deficiencies of the complement system. Primary Immunodeficiency Diseases, HD Ochs, CIE Smith, JM Puck. Oxford University Press, New York 1999; 397–416
- Naked GM, Florido MP, Ferreira de Paula P, Vinet AM, Inostroza JS, Isaac L. Deficiency of human complement factor I associated with lowered factor H. Clin Immunol 2000; 96: 162–7
- Rasmussen JM, Teisner B, Brandt J, Brandslund I, Gry H. Metabolism of C3 and factor B in patients with congenital factor I deficiency. J Clin Lab Immunol 1990; 31: 59–67
- Shiang R, Murray JC, Morton CC, Buetow KH, Wasmuth JJ, Olney AH, et al. Mapping of the human complement factor I gene to 4q25. Genomics 1989; 4: 82–6
- Vyse TJ, Morley BJ, Bartok I, Theodoridis EL, Davies KA, Webster ADB. The molecular basis of hereditary complement factor I deficiency. J Clin Invest 1996; 97: 925–33
- Baracho GV, Nudelman V, Isaac L. Molecular characterization of homozygous hereditary factor I deficiency. Clin Exp Immunol 2003; 131: 280–6
- Gonzales-Rubio C, Ferreria-Cerdan A, Ponce IM, Arpa J, Fontan G, Lopez-Trascasa M. Complement factor I deficiency associated with recurrent meningitis coinciding with menstruation. Arch Neurol 2001; 58: 1923–8
- Bonnin AJ, Zeitz HJ, Gewurz A. Complement factor I deficiency with recurrent aseptic meningitis. Arch Intern Med 1993; 153: 1380–3
- Rasmussen JM, Teisner B, Brandslund I, Svehag SE. A family with complement factor I deficiency. Scand J Immunol 1986; 23: 711–5
- Taylor PR, Carugati A, Fadok VA, Cook HT, Andrews M, Carroll MC, et al. A hierarchical role for classical pathway components in the clearance of apoptotic cells in vivo. J Exp Med 2000; 192: 359–66
- Ross SC, Densen P. Complement deficiency states and infection: epidemiology, pathogenesis and consequences of neisserial and other infections in an immune deficiency. Medicine (Baltimore) 1984; 63: 243–73
- Rasmussen MJ, Teisner B, Jepsen HH, Svehag SE, Knudsen F, Kirstein H, Buhl M. Three cases of factor I deficiency: the effect of treatment with plasma. Clin Exp Immunol 1988; 74: 131–6
- Sadallah S, Gudat F, Laissue JA, Spath PJ, Schifferli JA. Glomerulonephritis in a patient with complement factor I deficiency. Am J Kidney Dis 1999; 33: 1153–7