Clinical Features, Treatment, and Outcome of Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A Multinational, Multicenter Study of 362 PatientsFrancesca Minoia, Angelo Ravelli, Sergio Davì et al.|Arthritis & Rheumatology|2014Cited by 430
Functional rare and low frequency variants in BLK and BANK1 contribute to human lupusSimon Jiang, Carola G. Vinuesa, Kathryn McKeon et al.|Nature Communications|2019Cited by 122
Development and initial validation of the MS score for diagnosis of macrophage activation syndrome in systemic juvenile idiopathic arthritisFrancesca Minoia, Angelo Ravelli, Francesca Bovis et al.|Annals of the Rheumatic Diseases|2019Cited by 109
Different histological classifications for Henoch-Schönlein purpura nephritis: which one should be used?Marija Jelušić, Seza Özen, Mario Šestan et al.|Pediatric Rheumatology|2019Cited by 94
Clinical characteristics and genetic analyses of 187 patients with undefined autoinflammatory diseasesNienke M. ter Haar, Marco Gattorno, Charlotte Eijkelboom et al.|Annals of the Rheumatic Diseases|2019Cited by 77