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Rheumatology (Oxford, England)
|
June 29, 2007
Association between SLE nephritis and polymorphic variants of the CRP and FcgammaRIIIa genes
A Jönsen, I Gunnarsson, B Gullstrand, et al.
Scandinavian Journal of Rheumatology
|
March 2, 2016
CD81 and CD48 show different expression on blood eosinophils in systemic sclerosis: new markers for disease and pulmonary inflammation?
D M Wuttge, A Andreasson, E Tufvesson, et al.
Immunopharmacology
|
February 26, 1998
Human properdin deficiency has a heterogeneous genetic background
L Truedsson, J Westberg, G N Fredrikson, et al.
Human Immunology
|
January 23, 1998
Relationship between protein complotypes and DNA variant haplotypes: complotype-RFLP constellations (CRC)
S Simon, L Truedsson, D Marcus-Bagley, et al.
Human Immunology
|
October 31, 1998
Characterization of non-expressed C4 genes in a case of complete C4 deficiency: identification of a novel point mutation leading to a premature stop codon
G N Fredrikson, B Gullstrand, P M Schneider, et al.
Tissue Antigens
|
November 5, 1998
HLA-Cw alleles associated with HLA extended haplotypes and C2 deficiency
O P Clavijo, J C Delgado, Z L Awdeh, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery
|
July 1, 1996
Biological responses differ considerably between endovascular and conventional aortic aneurysm surgery
P Swartbol, L Norgren, U Albrechtsson, et al.
Tissue Antigens
|
August 23, 2007
A polymorphic variant in the MHC2TA gene is not associated with systemic lupus erythematosus
M V Prasad Linga-Reddy, I Gunnarsson, E Svenungsson, et al.
Scandinavian Journal of Rheumatology
|
March 19, 2013
Low diagnostic and predictive value of anti-dsDNA antibodies in unselected patients with recent onset of rheumatic symptoms: results from a long-term follow-up Scandinavian multicentre study
M Compagno, S Jacobsen, O P Rekvig, et al.
Experimental and Clinical Immunogenetics
|
January 1, 1995
Fluorescent detection of microsatellite polymorphisms: properdin deficiency linked to PFC microsatellite
D Agardi, M Pigg, A G Sjöholm, et al.
Page
of 13
Search research articles
Search
Showing results (101-110 of 125) with videos related to
Sort By:
Page
of 13
Rheumatology (Oxford, England)
|
June 29, 2007
Association between SLE nephritis and polymorphic variants of the CRP and FcgammaRIIIa genes
A Jönsen, I Gunnarsson, B Gullstrand, et al.
Scandinavian Journal of Rheumatology
|
March 2, 2016
CD81 and CD48 show different expression on blood eosinophils in systemic sclerosis: new markers for disease and pulmonary inflammation?
D M Wuttge, A Andreasson, E Tufvesson, et al.
Immunopharmacology
|
February 26, 1998
Human properdin deficiency has a heterogeneous genetic background
L Truedsson, J Westberg, G N Fredrikson, et al.
Human Immunology
|
January 23, 1998
Relationship between protein complotypes and DNA variant haplotypes: complotype-RFLP constellations (CRC)
S Simon, L Truedsson, D Marcus-Bagley, et al.
Human Immunology
|
October 31, 1998
Characterization of non-expressed C4 genes in a case of complete C4 deficiency: identification of a novel point mutation leading to a premature stop codon
G N Fredrikson, B Gullstrand, P M Schneider, et al.
Tissue Antigens
|
November 5, 1998
HLA-Cw alleles associated with HLA extended haplotypes and C2 deficiency
O P Clavijo, J C Delgado, Z L Awdeh, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery
|
July 1, 1996
Biological responses differ considerably between endovascular and conventional aortic aneurysm surgery
P Swartbol, L Norgren, U Albrechtsson, et al.
Tissue Antigens
|
August 23, 2007
A polymorphic variant in the MHC2TA gene is not associated with systemic lupus erythematosus
M V Prasad Linga-Reddy, I Gunnarsson, E Svenungsson, et al.
Scandinavian Journal of Rheumatology
|
March 19, 2013
Low diagnostic and predictive value of anti-dsDNA antibodies in unselected patients with recent onset of rheumatic symptoms: results from a long-term follow-up Scandinavian multicentre study
M Compagno, S Jacobsen, O P Rekvig, et al.
Experimental and Clinical Immunogenetics
|
January 1, 1995
Fluorescent detection of microsatellite polymorphisms: properdin deficiency linked to PFC microsatellite
D Agardi, M Pigg, A G Sjöholm, et al.
Page
of 13