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Myositis-specific autoantibodies (MSAs) are increasingly used to delineate distinct subgroups of JDM. The aim of our study was to explore without a priori hypotheses whether MSAs are associated with distinct clinical-pathological changes and severity in a monocentric JDM cohort.

Muscle ischaemia associated with NXP2 autoantibodies: a severe subtype of juvenile dermatomyositis