HYPOCOMPLEMENTÆMIC MULTIPLE SCLEROSIS: HETEROZYGOUS C2 DEFICIENCY LINKED TO HLA A10, B18
- 1 November 1976
- journal article
- letter
- Published by Elsevier in The Lancet
- Vol. 308 (7993) , 1023
- https://doi.org/10.1016/s0140-6736(76)90859-x
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- MULTIPLE SCLEROSIS WITH HYPOCOMPLEMENTÆMIAThe Lancet, 1976
- MULTIPLE SCLEROSIS WITH HYPOCOMPLEMENTÆMIAThe Lancet, 1975
- ASSOCIATION OF C2 DEFICIENCY AND THE HL-A HAPLOTYPE 10,W18Transplantation, 1975
- Hereditary complement (C2) deficiency with dermatomyositisThe American Journal of Medicine, 1975
- EVIDENCE FOR LINKAGE BETWEEN HL-A HISTOCOMPATIBILITY GENES AND THOSE INVOLVED IN THE SYNTHESIS OF THE SECOND COMPONENT OF COMPLEMENTThe Journal of Experimental Medicine, 1974
- C2 Deficiency DEVELOPMENT OF LUPUS ERYTHEMATOSUSJournal of Clinical Investigation, 1973
- Hereditary C2 Deficiency with Some Manifestations of Systemic Lupus ErythematosusThe Journal of Immunology, 1972
- Pathways of complement activation in glomerulonephritisKidney International, 1972
- Methods for the separation, purification and measurement of nine components of hemolytic complement in guinea-pig serumImmunochemistry, 1966