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Clinical and Experimental Immunology
|
March 24, 2009
Complement classical pathway components are all important in clearance of apoptotic and secondary necrotic cells
B Gullstrand, U Mårtensson, G Sturfelt, et al.
Clinical and Experimental Rheumatology
|
September 1, 1995
Prospective analysis of C1 dissociation and complement activation in patients with systemic lupus erythematosus
H Jonsson, G Sturfelt, U Mårtensson, et al.
Clinical Immunology (Orlando, Fla.)
|
August 1, 2008
Serum bactericidal activity against Neisseria meningitidis in patients with C3 nephritic factors is dependent on IgG allotypes
L Skattum, B Gullstrand, E Holmström, et al.
Journal of Clinical Immunology
|
January 14, 2000
Circulating immune complexes and complement C4 null alleles in patients in patients operated on for premature atherosclerotic peripheral vascular disease
S Nityanand, L Truedsson, A Mustafa, et al.
The Journal of Rheumatology
|
February 1, 1996
C1 inhibitor deficiency in a patient with rheumatoid arthritis--increased risk of adverse effects of penicillamine?
G Sturfelt, L Rydgren, L Truedsson, et al.
Scandinavian Journal of Immunology
|
June 1, 1992
Western blot analysis of human IgG reactive with the collagenous portion of C1q: evidence of distinct binding specificities
U Mårtensson, A G Sjöholm, G Sturfelt, et al.
Scandinavian Journal of Gastroenterology
|
June 8, 2004
Postoperative on-line monitoring with intraperitoneal microdialysis is a sensitive clinical method for measuring increased anaerobic metabolism that correlates to the cytokine response
K Jansson, B Redler, L Truedsson, et al.
Experimental and Clinical Immunogenetics
|
January 1, 1991
C4 polymorphism and major histocompatibility complex haplotypes in IgA deficiency: association with C4A null haplotypes
D Bućin, L Truedsson, L Hammarström, et al.
Genomics
|
September 1, 1995
Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency
J Westberg, G N Fredrikson, L Truedsson, et al.
Molecular Immunology
|
July 20, 2005
Complement deficiency and disease: an update
A G Sjöholm, G Jönsson, J H Braconier, et al.
Page
of 13
Search research articles
Search
Showing results (61-70 of 125) with videos related to
Sort By:
Page
of 13
Clinical and Experimental Immunology
|
March 24, 2009
Complement classical pathway components are all important in clearance of apoptotic and secondary necrotic cells
B Gullstrand, U Mårtensson, G Sturfelt, et al.
Clinical and Experimental Rheumatology
|
September 1, 1995
Prospective analysis of C1 dissociation and complement activation in patients with systemic lupus erythematosus
H Jonsson, G Sturfelt, U Mårtensson, et al.
Clinical Immunology (Orlando, Fla.)
|
August 1, 2008
Serum bactericidal activity against Neisseria meningitidis in patients with C3 nephritic factors is dependent on IgG allotypes
L Skattum, B Gullstrand, E Holmström, et al.
Journal of Clinical Immunology
|
January 14, 2000
Circulating immune complexes and complement C4 null alleles in patients in patients operated on for premature atherosclerotic peripheral vascular disease
S Nityanand, L Truedsson, A Mustafa, et al.
The Journal of Rheumatology
|
February 1, 1996
C1 inhibitor deficiency in a patient with rheumatoid arthritis--increased risk of adverse effects of penicillamine?
G Sturfelt, L Rydgren, L Truedsson, et al.
Scandinavian Journal of Immunology
|
June 1, 1992
Western blot analysis of human IgG reactive with the collagenous portion of C1q: evidence of distinct binding specificities
U Mårtensson, A G Sjöholm, G Sturfelt, et al.
Scandinavian Journal of Gastroenterology
|
June 8, 2004
Postoperative on-line monitoring with intraperitoneal microdialysis is a sensitive clinical method for measuring increased anaerobic metabolism that correlates to the cytokine response
K Jansson, B Redler, L Truedsson, et al.
Experimental and Clinical Immunogenetics
|
January 1, 1991
C4 polymorphism and major histocompatibility complex haplotypes in IgA deficiency: association with C4A null haplotypes
D Bućin, L Truedsson, L Hammarström, et al.
Genomics
|
September 1, 1995
Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency
J Westberg, G N Fredrikson, L Truedsson, et al.
Molecular Immunology
|
July 20, 2005
Complement deficiency and disease: an update
A G Sjöholm, G Jönsson, J H Braconier, et al.
Page
of 13