A hospital based registry of juvenile idiopathic arthritis in Norway
نویسندگان
چکیده
Objectives To evaluate clinical characteristics in patients with JIA registered in the hospital based registry. Methods The registry is based on written informed consent. JIA patients were classified using ICD-10 codes and they were registered once. Gender, date of registration and year for disease onset was recorded, in addition to onset type, number of active joints and physician’s global assessment of disease activity (VAS 0-100 mm).
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عنوان ژورنال:
دوره 12 شماره
صفحات -
تاریخ انتشار 2014