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L Truedsson

Showing results (91-100 of 125) with videos related to

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Clinical and Experimental Immunology|January 19, 2005
Deficiency of the mannan-binding lectin pathway of complement and poor outcome in cystic fibrosis: bacterial colonization may be decisive for a relationshipM Carlsson, A G Sjöholm, L Eriksson, et al.
Journal of Investigational Allergology & Clinical Immunology|July 20, 2010
Homozygosity for a novel mutation in the C1q C chain gene in a Turkish family with hereditary C1q deficiencyN Gulez, F Genel, F Atlihan, et al.
Rheumatology (Oxford, England)|December 26, 2001
Increased endothelial expression of HLA-DQ and interleukin 1alpha in extra-articular rheumatoid arthritis. Results from immunohistochemical studies of skeletal muscleC Turesson, P Englund, L T Jacobsson, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|January 4, 2001
Response of inflammatory markers to balloon angioplasty in peripheral arterial occlusive diseaseP Danielsson, P Schatz, P Swartbol, et al.
Arthritis and Rheumatism|April 13, 2004
Polymorphisms of the Fc gamma receptor type IIB gene are not associated with systemic lupus erythematosus in the Swedish populationV Magnusson, R Zunec, J Odeberg, et al.
Annals of the Rheumatic Diseases|November 1, 1990
Disease activity and joint damage progression in early rheumatoid arthritis: relation to IgG, IgA, and IgM rheumatoid factorK B Eberhardt, L Truedsson, H Pettersson, et al.
Scandinavian Journal of Immunology|December 22, 1999
Low concentrations of immunoglobulin G antibodies to Salmonella serogroup C in C2 deficiency: suggestion of a mannan-binding lectin pathway-dependent mechanismB Selander, A Weintraub, E Holmström, et al.
Lupus|December 12, 2003
The heterogeneity of neuropsychiatric systemic lupus erythematosus is reflected in lack of association with cerebrospinal fluid cytokine profilesA Jönsen, A A Bengtsson, O Nived, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 15, 1996
Molecular characterization of properdin deficiency type III: dysfunction produced by a single point mutation in exon 9 of the structural gene causing a tyrosine to aspartic acid interchangeG N Fredrikson, J Westberg, E J Kuijper, et al.
Genes and Immunity|June 10, 2011
Molecular basis of hereditary C1q deficiency--revisited: identification of several novel disease-causing mutationsL Schejbel, L Skattum, S Hagelberg, et al.
Pageof 13

Showing results (91-100 of 125) with videos related to

Sort By:
Pageof 13
Clinical and Experimental Immunology|January 19, 2005
Deficiency of the mannan-binding lectin pathway of complement and poor outcome in cystic fibrosis: bacterial colonization may be decisive for a relationshipM Carlsson, A G Sjöholm, L Eriksson, et al.
Journal of Investigational Allergology & Clinical Immunology|July 20, 2010
Homozygosity for a novel mutation in the C1q C chain gene in a Turkish family with hereditary C1q deficiencyN Gulez, F Genel, F Atlihan, et al.
Rheumatology (Oxford, England)|December 26, 2001
Increased endothelial expression of HLA-DQ and interleukin 1alpha in extra-articular rheumatoid arthritis. Results from immunohistochemical studies of skeletal muscleC Turesson, P Englund, L T Jacobsson, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|January 4, 2001
Response of inflammatory markers to balloon angioplasty in peripheral arterial occlusive diseaseP Danielsson, P Schatz, P Swartbol, et al.
Arthritis and Rheumatism|April 13, 2004
Polymorphisms of the Fc gamma receptor type IIB gene are not associated with systemic lupus erythematosus in the Swedish populationV Magnusson, R Zunec, J Odeberg, et al.
Annals of the Rheumatic Diseases|November 1, 1990
Disease activity and joint damage progression in early rheumatoid arthritis: relation to IgG, IgA, and IgM rheumatoid factorK B Eberhardt, L Truedsson, H Pettersson, et al.
Scandinavian Journal of Immunology|December 22, 1999
Low concentrations of immunoglobulin G antibodies to Salmonella serogroup C in C2 deficiency: suggestion of a mannan-binding lectin pathway-dependent mechanismB Selander, A Weintraub, E Holmström, et al.
Lupus|December 12, 2003
The heterogeneity of neuropsychiatric systemic lupus erythematosus is reflected in lack of association with cerebrospinal fluid cytokine profilesA Jönsen, A A Bengtsson, O Nived, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 15, 1996
Molecular characterization of properdin deficiency type III: dysfunction produced by a single point mutation in exon 9 of the structural gene causing a tyrosine to aspartic acid interchangeG N Fredrikson, J Westberg, E J Kuijper, et al.
Genes and Immunity|June 10, 2011
Molecular basis of hereditary C1q deficiency--revisited: identification of several novel disease-causing mutationsL Schejbel, L Skattum, S Hagelberg, et al.
Pageof 13