A Phase 3 Trial of Upadacitinib for Giant-Cell Arteritis
In this randomized, placebo-controlled trial involving patients with giant-cell arteritis, the oral Janus kinase inhibitor upadacitinib (15 mg) significantly improved […]
In this randomized, placebo-controlled trial involving patients with giant-cell arteritis, the oral Janus kinase inhibitor upadacitinib (15 mg) significantly improved […]
Autoimmune congenital heart block occurs in around 1–2% of anti-Sjögren’s syndrome-related antigen A (SSA)/Ro antibody-positive pregnancies.1 Despite the rarity of
Purpose of review This review outlines the development of the axial spondyloarthritis disease activity score (ASDAS) as a composite index
Rheumato, Vol. 5, Pages 6: Comparison of Hip Abductor Muscle Composition and Its Age-Related Alterations Between Female Patients with Unilateral
Purpose of review To provide an overview of the most recent updates in the pathogenesis of juvenile idiopathic arthritis (JIA).
Background Axial spondyloarthritis (axSpA) is a chronic inflammatory disease primarily affecting the spine and sacroiliac joints, with anterior uveitis (AU)
Rheumato, Vol. 5, Pages 5: Hemophilic Arthropathy—Pathophysiology and Advances in Treatment Rheumato doi: 10.3390/rheumato5020005 Authors: Katarina Kovač Ivan Ljudevit Caktaš
Background Project ECHO (Extension for Community Healthcare Outcomes) links experts with community providers through video teleconferences that include both didactics
Background Janus kinase (JAK) inhibitors have been approved for treating psoriatic arthritis (PsA); however, the comparative efficacy of different JAK
Objective The prevalence of juvenile-onset systemic lupus erythematosus (JSLE) differs by race/ethnicity with environmental, genetic, and social factors implicated in
Background Idiopathic inflammatory myopathies (IIMs) are rare autoimmune diseases with limited epidemiological data from Latin America. Objective To characterize IIMs
Background/Objective This study assessed the outcomes of patients with antineutrophil cytoplasm antibody–associated vasculitis glomerulonephritis (AAV-GN). Methods This historical cohort study
Purpose of review Whipple’s disease (WD), triggered by Tropheryma whipplei (T. whipplei), is a rare, chronic, inflammatory, systemic infectious disease
Introduction Patients with polymyositis and dermatomyositis (PM/DM) are prone to multiple complications that may lead to increased mortality rates. Data
Objectives Our study aimed to identify potential predictors for additional systemic involvement in patients with noninfectious uveitis, specifically focusing on
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
Systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still’s disease (AOSD) are considered the same disease, but a common approach for
Adugna BA. AB0159 HEALTH RELATED QUALITY OF LIFE AMONG PATIENTS WITH RHEUMATOID ARTHRITIS AT TIKUR ANBESSA SPECIALIZED HOSPITAL. A HOSPITAL-
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),
For three-quarters of a century, glucocorticoids (GCs) have been used to treat rheumatic and autoimmune diseases. Over these 75 years,