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Rheumatology International|January 1, 1992
Abnormal galactosylation of serum IgG in patients with systemic lupus erythematosus and members of families with high frequency of autoimmune diseasesM Tomana, R E Schrohenloher, J D Reveille, et al.
Southern Medical Journal|August 1, 1996
Systemic lupus erythematosus diagnosed during interferon alfa therapyL F Morris, N A Lemak, F C Arnett, et al.
Immunogenetics|January 1, 1985
Null alleles of the fourth component of complement and HLA haplotypes in familial systemic lupus erythematosusJ D Reveille, F C Arnett, R W Wilson, et al.
Immunogenetics|January 1, 1989
C4A gene deletion and HLA associations in black Americans with systemic lupus erythematosusM L Olsen, R Goldstein, F C Arnett, et al.
Annals of Internal Medicine|December 1, 1984
Primary Sjögren's syndrome and other autoimmune diseases in families. Prevalence and immunogenetic studies in six kindredsJ D Reveille, R W Wilson, T T Provost, et al.
The Journal of Rheumatology|March 1, 1982
Ro(SSA) and La(SSB) antibodies in the clinical spectrum of Sjögren's syndromeE L Alexander, T J Hirsch, F C Arnett, et al.
The Journal of Rheumatology|December 1, 1985
Multicentric reticulohistiocytosis and Sjögren's syndromeR N Carey, J W Blotzer, I D Wolfe, et al.
Arthritis and Rheumatism|November 30, 2006
SPARC, an upstream regulator of connective tissue growth factor in response to transforming growth factor beta stimulationX D Zhou, M M Xiong, F K Tan, et al.
The American Journal of Medicine|August 1, 1986
Relationship between C4 null genes, HLA-D region antigens, and genetic susceptibility to systemic lupus erythematosus in Caucasian and black AmericansP F Howard, M C Hochberg, W B Bias, et al.
Lupus|July 26, 2011
Clinical presentations and molecular basis of complement C1r deficiency in a male African-American patient with systemic lupus erythematosusY L Wu, B P Brookshire, R R Verani, et al.
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