Association of Henoch-Schönlein purpura glomerulonephritis with C4B deficiency

This publication has 15 references indexed in Scilit:

• Regional variation in C4 phenotype in patients with IgA nephropathy
  The Journal of Pediatrics, 1990
• Is Henoch-Schönlein Purpura the Systemic Form of IgA Nephropathy?
  American Journal of Kidney Diseases, 1988
• The Role of Complement and Its Receptor in the Elimination of Immune Complexes
  New England Journal of Medicine, 1986
• Hydralazine binds covalently to complement component C4
  FEBS Letters, 1985
• Complement phenotypes in glomerulonephritis: Increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpura
  Kidney International, 1984
• Henoch-Schönlein Nephritis: Prognostic Features and the Challenge of Therapy
  American Journal of Kidney Diseases, 1983
• Inherited structural polymorphism of the fourth component of human complement.
  Proceedings of the National Academy of Sciences, 1980
• IgA IMMUNE COMPLEXES IN HENOCH-SCHÖNLEIN PURPURA
  The Lancet, 1979
• Selective deficiency of the second component of complement in a patient with anaphylactoid purpura
  Clinical Immunology and Immunopathology, 1975
• Biosynthetic Defect in Monocytes from Human Beings with Genetic Deficiency of the Second Component of Complement
  New England Journal of Medicine, 1975