Background Idiopathic inflammatory myopathies (IIMs) are rare autoimmune diseases with limited epidemiological data from Latin America. Objective To characterize IIMs […]
Objective The prevalence of juvenile-onset systemic lupus erythematosus (JSLE) differs by race/ethnicity with environmental, genetic, and social factors implicated in
Background/Objective This study assessed the outcomes of patients with antineutrophil cytoplasm antibody–associated vasculitis glomerulonephritis (AAV-GN). Methods This historical cohort study
Objectives Our study aimed to identify potential predictors for additional systemic involvement in patients with noninfectious uveitis, specifically focusing on
Introduction Patients with polymyositis and dermatomyositis (PM/DM) are prone to multiple complications that may lead to increased mortality rates. Data
Purpose of review Whipple’s disease (WD), triggered by Tropheryma whipplei (T. whipplei), is a rare, chronic, inflammatory, systemic infectious disease
Purpose of review There is a growing interest in the applications of artificial intelligence in pediatric rheumatology. Although concerns with
Background/Objectives The aim of this work is to validate the ANCA-associated vasculitis patient-reported outcome (AAV-PRO) questionnaire in a Latin American
Objective Previous studies have shown an association between chondrocalcinosis (CC) and vascular calcifications (VCs). This study aimed to investigate the
Objective In the previous Spondyloarthritis EYE study, we confirmed the potential of a screening strategy for early axial spondyloarthritis (axSpA)
Background In this case series, we present longitudinal imaging surveillance of 6 cases of osseous sarcoidosis, each of which was
Adugna BA. AB0159 HEALTH RELATED QUALITY OF LIFE AMONG PATIENTS WITH RHEUMATOID ARTHRITIS AT TIKUR ANBESSA SPECIALIZED HOSPITAL. A HOSPITAL-
For three-quarters of a century, glucocorticoids (GCs) have been used to treat rheumatic and autoimmune diseases. Over these 75 years,
Systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still’s disease (AOSD) are considered the same disease, but a common approach for
Background A range of sacroiliac joint (SIJ) MRI protocols are used in clinical practice but not all were specifically designed
Objectives This study aims to establish expert consensus recommendations for clinical information on imaging requests in suspected/known axial spondyloarthritis (axSpA),
Rheumatology Practice and Research, Volume 3, Issue , January-December 2018. Improvement in survival of systemic lupus erythematosus has been brought
Rheumatology Practice and Research, Volume 3, Issue , January-December 2018. Cognitive dysfunction is one of the five psychiatric syndromes recognised
Rheumatology Practice and Research, Volume 3, Issue , January-December 2018. Objectives:Behçet’s disease is a chronic, relapsing, multisystem vasculitis of unknown
