H deficiency in two brothers with atypical dense intramembranous deposit disease
- 1 December 1986
- journal article
- research article
- Published by Elsevier in Kidney International
- Vol. 30 (6), 949-956
- https://doi.org/10.1038/ki.1986.278
Abstract
No abstract availableThis publication has 30 references indexed in Scilit:
- Genetically determined variation in the complement system: Relationship to diseaseThe Journal of Pediatrics, 1984
- Dense intramembranous deposit disease: New pathologic featuresKidney International, 1984
- Inherited complement component deficiencies in membranoproliferative glomerulonephritisKidney International, 1983
- An inherited defect in the C3 convertase, C3b,Bb, associated with glomerulonephritisKidney International, 1983
- Immunohistochemical study of the human glomerular C3b receptor in normal kidney and in seventy-five cases of renal diseases: loss of C3b receptor antigen in focal hyalinosis and in proliferative nephritis of systemic lupus erythematosus.Journal of Clinical Investigation, 1982
- Recurrence of dense deposits in transplanted kidney: II. Serum complement and nephritic factor profilesKidney International, 1979
- Mechanism of action of factor D of the alternative complement pathway.The Journal of Experimental Medicine, 1978
- Immunopathology of membranoproliferative glomerulonephritis with subendothelial deposits (Type I MPGN)Clinical Immunology and Immunopathology, 1978
- Human complement C3b inactivator: isolation, characterization, and demonstration of an absolute requirement for the serum protein beta1H for cleavage of C3b and C4b in solution.The Journal of Experimental Medicine, 1977
- Nephritic factor: Description of a new quantitative assay and findings in glomerulonephritisKidney International, 1976