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The Journal of Clinical Investigation
|
October 1, 1992
A unique recombination event resulting in a C4A*Q0,C4B*Q0 double null haplotype
M B Fasano, J A Winkelstein, T LaRosa, et al.
Journal of Clinical Immunology
|
April 1, 1982
Partial H (beta 1H) deficiency and glomerulonephritis in two families
R J Wyatt, B A Julian, A Weinstein, et al.
Tissue Antigens
|
February 1, 1990
Characterization of two hybrid C4 allotypes (C4A*12 and C4B*3) by electrophoretic, serological and restriction fragment length polymorphism analyses
R H McLean, W B Bias, C Giles, et al.
The Journal of Pediatrics
|
February 1, 1982
Serum hemolytic factor D values in children with steroid-responsive idiopathic nephrotic syndrome
M Ballow, T L Kennedy, K M Gaudio, et al.
The American Journal of Medicine
|
August 1, 1986
Relationship between C4 null genes, HLA-D region antigens, and genetic susceptibility to systemic lupus erythematosus in Caucasian and black Americans
P F Howard, M C Hochberg, W B Bias, et al.
Pediatrics
|
June 1, 1981
Meningococcal meningitis in familial deficiency of the fifth component of complement
G Peter, M B Weigert, A R Bissel, et al.
Pediatric Research
|
August 1, 1977
Decreased serum factor B concentration associated with decreased opsonization of Escherichia coli in the idiopathic nephrotic syndrome
R H McLean, A Forsgren, B Björkstén, et al.
Clinical Immunology and Immunopathology
|
October 1, 1981
Familial deficiency of C5 in humans: intact but deficient alternative complement pathway activity
R H McLean, G Peter, R Gold, et al.
Immunogenetics
|
January 1, 1985
Null alleles of the fourth component of complement and HLA haplotypes in familial systemic lupus erythematosus
J D Reveille, F C Arnett, R W Wilson, et al.
Seminars in Nephrology
|
December 1, 1987
Immunogenetic markers as prognostic features in patients from Kentucky with IgA nephropathy
R J Wyatt, B A Julian, S Y Woodford, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 76) with videos related to
Sort By:
Page
of 8
The Journal of Clinical Investigation
|
October 1, 1992
A unique recombination event resulting in a C4A*Q0,C4B*Q0 double null haplotype
M B Fasano, J A Winkelstein, T LaRosa, et al.
Journal of Clinical Immunology
|
April 1, 1982
Partial H (beta 1H) deficiency and glomerulonephritis in two families
R J Wyatt, B A Julian, A Weinstein, et al.
Tissue Antigens
|
February 1, 1990
Characterization of two hybrid C4 allotypes (C4A*12 and C4B*3) by electrophoretic, serological and restriction fragment length polymorphism analyses
R H McLean, W B Bias, C Giles, et al.
The Journal of Pediatrics
|
February 1, 1982
Serum hemolytic factor D values in children with steroid-responsive idiopathic nephrotic syndrome
M Ballow, T L Kennedy, K M Gaudio, et al.
The American Journal of Medicine
|
August 1, 1986
Relationship between C4 null genes, HLA-D region antigens, and genetic susceptibility to systemic lupus erythematosus in Caucasian and black Americans
P F Howard, M C Hochberg, W B Bias, et al.
Pediatrics
|
June 1, 1981
Meningococcal meningitis in familial deficiency of the fifth component of complement
G Peter, M B Weigert, A R Bissel, et al.
Pediatric Research
|
August 1, 1977
Decreased serum factor B concentration associated with decreased opsonization of Escherichia coli in the idiopathic nephrotic syndrome
R H McLean, A Forsgren, B Björkstén, et al.
Clinical Immunology and Immunopathology
|
October 1, 1981
Familial deficiency of C5 in humans: intact but deficient alternative complement pathway activity
R H McLean, G Peter, R Gold, et al.
Immunogenetics
|
January 1, 1985
Null alleles of the fourth component of complement and HLA haplotypes in familial systemic lupus erythematosus
J D Reveille, F C Arnett, R W Wilson, et al.
Seminars in Nephrology
|
December 1, 1987
Immunogenetic markers as prognostic features in patients from Kentucky with IgA nephropathy
R J Wyatt, B A Julian, S Y Woodford, et al.
Page
of 8