부산대학교 도서관

Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications. ANA-positive patients with persistent oligoarticular, extended oligoarticular, or polyarticular JIA have the same disease entity and differ only in disease severity.[4] Corroborating studies suggest that HLA associations and peripheral blood transcriptomic signatures differ at the boundary of 6 years old. Familial aggregation of juvenile idiopathic arthritis with other autoimmune diseases: impact on clinical characteristics, disease activity status and disease damage. Juvenile idiopathic arthritis (JIA) refers to a group of heterogeneous diseases sharing unknown original chronic inflammatory arthritis over 6 weeks. [Extracted from the article]