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L Truedsson

Showing results (61-70 of 125) with videos related to

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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 cellsB 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 erythematosusH 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 allotypesL 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 diseaseS 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 specificitiesU 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 responseK 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 haplotypesD 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 immunodeficiencyJ Westberg, G N Fredrikson, L Truedsson, et al.
Molecular Immunology|July 20, 2005
Complement deficiency and disease: an updateA G Sjöholm, G Jönsson, J H Braconier, et al.
Pageof 13

Showing results (61-70 of 125) with videos related to

Sort By:
Pageof 13
Clinical and Experimental Immunology|March 24, 2009
Complement classical pathway components are all important in clearance of apoptotic and secondary necrotic cellsB 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 erythematosusH 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 allotypesL 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 diseaseS 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 specificitiesU 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 responseK 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 haplotypesD 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 immunodeficiencyJ Westberg, G N Fredrikson, L Truedsson, et al.
Molecular Immunology|July 20, 2005
Complement deficiency and disease: an updateA G Sjöholm, G Jönsson, J H Braconier, et al.
Pageof 13