Search research articles
Contact Us
Filters
Showing results (91-100 of 125) with videos related to
Page
of 13
Sort By:
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 relationship
M 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 deficiency
N 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 muscle
C 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 disease
P 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 population
V 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 factor
K 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 mechanism
B 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 profiles
A 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 interchange
G 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 mutations
L Schejbel, L Skattum, S Hagelberg, et al.
Page
of 13
Search research articles
Search
Showing results (91-100 of 125) with videos related to
Sort By:
Page
of 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 relationship
M 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 deficiency
N 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 muscle
C 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 disease
P 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 population
V 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 factor
K 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 mechanism
B 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 profiles
A 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 interchange
G 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 mutations
L Schejbel, L Skattum, S Hagelberg, et al.
Page
of 13