Recurrent meningococcal septicaemia and properdin deficiency.

[1]  Z. Fishelson,et al.  Hereditary properdin deficiency in three families of Tunisian Jews , 1993, Acta paediatrica.

[2]  O. Mellbye,et al.  Low Prevalence of Complement Deficiencies among Patients with Meningococcal Disease in Norway , 1993, Scandinavian journal of immunology.

[3]  J. Weiler,et al.  Properdin: Approaching four decades of research , 1993, Immunologic research.

[4]  P. Densen.  COMPLEMENT DEFICIENCIES AND MENINGOCOCCAL DISEASE , 1991, Clinical and experimental immunology.

[5]  P. Densen,et al.  Infectious diseases associated with complement deficiencies , 1991, Clinical Microbiology Reviews.

[6]  Z. Fishelson,et al.  Prevalence of hereditary properdin, C7 and C8 deficiencies in patients with meningococcal infections , 1990, Clinical and experimental immunology.

[7]  P. Magnussen,et al.  Complement and immunoglobulin studies in 15 cases of chronic meningococcemia: properdin deficiency and hypoimmunoglobulinemia. , 1990, Scandinavian Journal of Infectious Diseases.

[8]  C. Koch,et al.  Congenital properdin deficiency and meningococcal infection. , 1987, Clinical immunology and immunopathology.

[9]  P. Densen,et al.  Complement Deficiency States and Infection: Epidemiology, Pathogenesis and Consequences of Neisserial and Other Infections in an Immune Deficiency , 1984, Medicine.

[10]  A. Sjöholm,et al.  Properdin deficiency in a family with fulminant meningococcal infections. , 1982, Clinical and experimental immunology.

[11]  T. Platts-Mills,et al.  Activation of the alternate pathway of human complements by rabbit cells. , 1974, Journal of immunology.