Abstract
In 1999 a registry of patients with juvenile idiopathic arthritis (JIA) and juvenile onset connective tissue diseases was established at Rikshospitalet, Oslo University Hospital. The purpose of the registry is to initiate clinical, epidemiologic and laboratory research projects.
Highlights
In 1999 a registry of patients with juvenile idiopathic arthritis (JIA) and juvenile onset connective tissue diseases was established at Rikshospitalet, Oslo University Hospital
When comparing physician’s global between JIA subgroups, polyarthritis had higher than both pauciarticular arthritis; p=0.001, and systemic arthritis; p=0.024
The register should have been based on the ILAR criteria instead of the ICD-10 codes
Summary
In 1999 a registry of patients with juvenile idiopathic arthritis (JIA) and juvenile onset connective tissue diseases was established at Rikshospitalet, Oslo University Hospital. The purpose of the registry is to initiate clinical, epidemiologic and laboratory research projects
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