Blau syndrome is a monogenic disease resulting from mutations in the pattern recognition
receptor NOD2, and is phenotypically characterized by the triad of granulomatous polyarthritis…

We used the Immunochip array to analyze 2,816 individuals with juvenile idiopathic arthritis
(JIA), comprising the most common subtypes (oligoarticular and rheumatoid factor–negative …

… Dr Rose is a Co-investigator on that grant. … Rose CD, Martin TM. Caspase recruitment
domain 15 mutations and rheumatic diseases. Curr Opin Rheumatol 2005; 17:579–585 …

… , we analyzed the 3 mutations associated with CD: R702W, G908R, and 1007frameshift. …
CD to our knowledge. Clinical data were not available on the parent in either family with the CD …

Objective To test for associations between non–major histocompatibility complex susceptibility
loci previously reported in autoimmune diseases and juvenile idiopathic arthritis (JIA). …

Objective. To report baseline articular, functional and ocular findings of the first international
prospective cohort study of Blau syndrome (BS). Methods. Three-year, multicentre, …

… histology of the synovium in CD. The actual frequency of granuloma in CD synovium may be
… There are at least two reports of synovial granulomata in CD synovium with one case where …

… 373 Rose, et al: Blau mutation in granulomatous arthritis … Saini SK, Rose CD. Liver
involvement in familial granulomatous arthritis (Blau syndrome). J Rheumatol 1996;23:396-9. …

… and a national cohort in spain - Rosé - 2009 - Arthritis & Rheumatism - Wiley Online Library
… Rosé had full access to all of the data in the study and takes responsibility for the integrity of …

Objective In a genome‐wide association study of Caucasian patients with juvenile idiopathic
arthritis (JIA), we have previously described findings limited to autoimmunity loci shared by …