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British Journal of Rheumatology|June 1, 1988
Successful treatment of Raynaud's syndrome with Iloprost, a chemically stable prostacyclin analogueD A Yardumian, D A Isenberg, M Rustin, et al.Journal of Immunology (Baltimore, Md. : 1950)|May 22, 2001
Accelerated nephrotoxic nephritis is exacerbated in C1q-deficient miceM G Robson, H T Cook, M Botto, et al.Journal of Immunology (Baltimore, Md. : 1950)|September 22, 1998
Multiple lupus susceptibility loci map to chromosome 1 in BXSB miceM B Hogarth, J H Slingsby, P J Allen, et al.Lupus|January 17, 2003
Disturbances in peripheral blood B cell subpopulations in autoimmune patientsK N Potter, C I Mockridge, A Rahman, et al.Lupus|August 30, 2003
The prevalence and clinical significance of autoantibodies to plasminogen activator inhibitor 1 in systemic lupus erythematosusR L Bates, S J Payne, S L Drury, et al.International Journal of Immunopharmacology|January 1, 1981
Cyclosporin A for the treatment of systemic lupus erythematosusD A Isenberg, M L Snaith, W J Morrow, et al.Clinical and Experimental Immunology|June 17, 2005
Natural killer cell activity in families of patients with systemic lupus erythematosus: demonstration of a killing defect in patientsM R J Green, A S M Kennell, M J Larche, et al.Annals of the Rheumatic Diseases|February 1, 1992
Fasting lipids and anticardiolipin antibodies as risk factors for vascular disease in systemic lupus erythematosusA J MacGregor, V B Dhillon, A Binder, et al.Clinical and Experimental Immunology|November 1, 1987
Family study of the major histocompatibility complex in HLA DR3 negative patients with systemic lupus erythematosusJ R Batchelor, A H Fielder, M J Walport, et al.Kidney International|August 1, 1996
Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish familyR Topaloglu, A Bakkaloglu, J H Slingsby, et al.Pageof 56