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Journal of Clinical Immunology|March 1, 1997
Combined heterozygous deficiency of the classical complement pathway proteins C2 and C4D Hartmann, V Fremeaux-Bacchi, L Weiss, et al.Human Genetics|December 1, 1987
The study of a French family with two duplicated C4A haplotypesC M Giles, B Uring-Lambert, W Boksch, et al.Complement (Basel, Switzerland)|January 1, 1985
Detection of the genetic polymorphism of human C2 (native protein and C2a fragment) by immunoblotting after polyacrylamide gel isoelectric focusingB Uring-Lambert, S Gas, J Goetz, et al.Immunogenetics|January 1, 1988
Antigenic determinants expressed by human C4 allotypes; a study of 325 families provides evidence for the structural antigenic modelC M Giles, B Uring-Lambert, J Goetz, et al.Journal of Immunoassay|August 1, 1996
Influence of anticoagulants on the level of soluble HLA class I and class II antigens measured in blood samplesS Hausmann, R Claus, U Falk, et al.Journal of Clinical Immunology|September 1, 1994
Complete inherited deficiency of the fourth complement component in a child with systemic lupus erythematosus and his disease-free brother in a north African familyV Fremeaux-Bacchi, B Uring-Lambert, L Weiss, et al.Clinical and Experimental Immunology|April 1, 1989
Familial properdin deficiency associated with chronic discoid lupus erythematosusE R Holme, J Veitch, A Johnston, et al.The Journal of Clinical Investigation|February 1, 1989
Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasiaY Morel, J André, B Uring-Lambert, et al.Complement and Inflammation|January 1, 1990
C4 reference typing reportG Mauff, M Brenden, M Braun-Stilwell, et al.Nephron|January 1, 1996
Complement C4 phenotypes in patients with end-stage renal diseaseK Lhotta, A Schlögl, B Uring-Lambert, et al.Pageof 20