Human genetics of Whipple’s disease
Purpose of review Whipple’s disease (WD), triggered by Tropheryma whipplei (T. whipplei), is a rare, chronic, inflammatory, systemic infectious disease […]
Rheumatology
JCR
Mortality Trends in Polymyositis and Dermatomyositis in Mexico: A General Population-Based Study From 2000 to 2019
Introduction Patients with polymyositis and dermatomyositis (PM/DM) are prone to multiple complications that may lead to increased mortality rates. Data
JCR
Noninfectious Uveitis in Pediatric Rheumatology: Long-term Follow-up at Tertiary Centers
Objectives Our study aimed to identify potential predictors for additional systemic involvement in patients with noninfectious uveitis, specifically focusing on
Rheumatology
AI am the future: artificial intelligence in pediatric rheumatology
Purpose of review There is a growing interest in the applications of artificial intelligence in pediatric rheumatology. Although concerns with
JCR
Validation of the ANCA-Associated Vasculitis Patient-Reported Outcomes Questionnaire in a Latin American Vasculitis Cohort
Background/Objectives The aim of this work is to validate the ANCA-associated vasculitis patient-reported outcome (AAV-PRO) questionnaire in a Latin American
JCR
Association Between Vascular Calcifications on Joint Radiographs and Calcium Pyrophosphate Crystal Arthritis: A Medical Records Review Study
Objective Previous studies have shown an association between chondrocalcinosis (CC) and vascular calcifications (VCs). This study aimed to investigate the
JCR
Early Axial Spondyloarthritis Detection: Two-Year Follow-up of the Sp-EYE Study on Acute Anterior Uveitis and Chronic Back Pain Screening
Objective In the previous Spondyloarthritis EYE study, we confirmed the potential of a screening strategy for early axial spondyloarthritis (axSpA)
JCR
Clinical Experience with TNF Inhibition and Longitudinal Image Monitoring in Osseous Sarcoidosis
Background In this case series, we present longitudinal imaging surveillance of 6 cases of osseous sarcoidosis, each of which was
Annals of Rheumatic Diseases
EULAR/PReS recommendations for the diagnosis and management of Stills disease, comprising systemic juvenile idiopathic arthritis and adult-onset Stills disease
Systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still’s disease (AOSD) are considered the same disease, but a common approach for
Annals of Rheumatic Diseases
Correction: AB0159 Health related quality of life among patients with rheumatoid arthritis at Tikur Anbessa specialized Hospital. A Hospital- based cross sectional study
Adugna BA. AB0159 HEALTH RELATED QUALITY OF LIFE AMONG PATIENTS WITH RHEUMATOID ARTHRITIS AT TIKUR ANBESSA SPECIALIZED HOSPITAL. A HOSPITAL-
Annals of Rheumatic Diseases
Development of international consensus on a standardised image acquisition protocol for diagnostic evaluation of the sacroiliac joints by MRI: an ASAS-SPARTAN collaboration
Background A range of sacroiliac joint (SIJ) MRI protocols are used in clinical practice but not all were specifically designed
Annals of Rheumatic Diseases
Clinical information on imaging referrals for suspected or known axial spondyloarthritis: recommendations from the Assessment of Spondyloarthritis International Society (ASAS)
Objectives This study aims to establish expert consensus recommendations for clinical information on imaging requests in suspected/known axial spondyloarthritis (axSpA),
Annals of Rheumatic Diseases
Journey through discovery of 75 years glucocorticoids: evolution of our knowledge of glucocorticoid receptor mechanisms in rheumatic diseases
For three-quarters of a century, glucocorticoids (GCs) have been used to treat rheumatic and autoimmune diseases. Over these 75 years,
Sage Journals
Glucocorticoid-induced osteoporosis in systemic lupus erythematosus
Rheumatology Practice and Research, Volume 3, Issue , January-December 2018. Improvement in survival of systemic lupus erythematosus has been brought
Sage Journals
Cognitive dysfunction in patients with systemic lupus erythematosus: The challenge in diagnosis and management
Rheumatology Practice and Research, Volume 3, Issue , January-December 2018. Cognitive dysfunction is one of the five psychiatric syndromes recognised
Sage Journals
Demographic features and clinical aspects of Behçet’s disease in Omani patients
Rheumatology Practice and Research, Volume 3, Issue , January-December 2018. Objectives:Behçet’s disease is a chronic, relapsing, multisystem vasculitis of unknown