Familial Clustering and Immunogenetic Aspects of IgA Nephropathy
- 1 November 1988
- journal article
- review article
- Published by Elsevier in American Journal of Kidney Diseases
- Vol. 12 (5), 366-370
- https://doi.org/10.1016/s0272-6386(88)80026-x
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Relation of mesangial IgA glomerulonephritis to polymorphism of immunoglobulin heavy chain switch region.Journal of Clinical Investigation, 1988
- Epidemic Renal Disease of Unknown Etiology in the Zuni IndiansAmerican Journal of Kidney Diseases, 1987
- Relationship between C4 null genes, HLA-D region antigens, and genetic susceptibility to systemic lupus erythematosus in Caucasian and Black AmericansThe American Journal of Medicine, 1986
- Familial IgA NephropathyNew England Journal of Medicine, 1985
- Complement phenotypes in glomerulonephritis: Increased frequency of homozygous null C4 phenotypes in IgA nephropathy and Henoch-Schönlein purpuraKidney International, 1984
- Strong association between IgA nephropathy and HLA-DR4 antigenKidney International, 1982
- Genetic investigation in mesangial IgA nephropathyTissue Antigens, 1982
- Strong Association of HLA-DR4 with Benign IgA NephropathyNephron, 1982
- HLA Antigens and Berger's DiseaseTissue Antigens, 1980
- IGA NEPHROPATHY IN HLA-IDENTICAL SIBLINGSTransplantation, 1978