Abstract Number: 103 • 2026 Pediatric Rheumatology Symposium
Anifrolumab Use in Youngsters with Rheumatic Conditions: Case Series and a Review of the Evidence Base
Background/Purpose: Systemic lupus erythematosus (SLE) is a chronic, multisystem autoimmune disease that poses unique diagnostic and therapeutic challenges in children, given they experience more severe…Abstract Number: 079 • 2026 Pediatric Rheumatology Symposium
Still’s Disease Associated Lung Disease: Update From the European Registry
Background/Purpose: Lung disease (LD) is an emerging severe life-threatening complication of Still’s Disease (SD) characterized by peculiar features. Patients with SD complicated by LD are…Abstract Number: 099 • 2026 Pediatric Rheumatology Symposium
Clinical Features of Juvenile Antisynthetase Syndrome: A Single-Center Case Series
Background/Purpose: Anti-synthetase syndrome (ASyS) is a rare autoimmune myopathy in children characterized by a triad of myositis, arthritis, and interstitial lung disease (ILD), though not all manifestations may be present at disease onset. Pediatric data remain limited, and disease…Abstract Number: 001 • 2026 Pediatric Rheumatology Symposium
Longitudinal Cardiovascular Profiles of Youth with Childhood-onset Systemic Lupus Erythematosus
Background/Purpose: The cumulative impact of childhood-onset systemic lupus erythematosus (cSLE) on cardiovascular damage begins at disease onset. We sought to characterize longitudinal cardiovascular profiles of…Abstract Number: 012 • 2026 Pediatric Rheumatology Symposium
Prevalence and Impact of Adverse Childhood Experiences in Pediatric Systemic Lupus Erythematosus
Background/Purpose: Adverse childhood experiences (ACEs) have been linked to incident childhood-onset SLE (cSLE) and poorer patient-reported outcomes, raising the possibility that early-life stress may contribute…Abstract Number: 045 • 2026 Pediatric Rheumatology Symposium
Genotypes and Clinical Phenotypes of Monogenic Autoinflammatory Disorders in Michigan
Background/Purpose: Data regarding monogenic systemic autoinflammatory disorders (SAID) from the USA is scarce. Our study aims to report the spectrum of SAID and detail unique…Abstract Number: 086 • 2026 Pediatric Rheumatology Symposium
APOL1 Focal Segmental Glomerulosclerosis Requiring Renal Transplant, the Burden of Childhood onset Autoimmune and Autoinflammatory Disease
Background/Purpose: Apolipoprotein L1 (APOL1) mediated kidney disease with focal segmental glomerulosclerosis (FSGS) is a severe form of renal disease with risk of progressing towards end…Abstract Number: 041 • 2026 Pediatric Rheumatology Symposium
Pediatric Behçet’s Disease: A 13-Year Single-Center Experience Highlighting Diagnostic Delays and High Neurological Burden
Background/Purpose: Behçet's disease (BD) is a systemic vasculitis primarily characterized by recurrent oral and genital aphthous ulceration. It is reported that 15-20% of all BD…Abstract Number: 026 • 2026 Pediatric Rheumatology Symposium
Treatment strategies for articular flares in JIA patients receiving biologic therapy
Background/Purpose: Biologic agents form the cornerstone of therapy for Juvenile Idiopathic Arthritis (JIA); however, the optimal management of flares that occur during ongoing treatment remains…Abstract Number: 047 • 2026 Pediatric Rheumatology Symposium
Association of anti-DFS70 with autoimmune diseases in children
Background/Purpose: The ANA 23 panel is widely requested in patients with positive ANA to guide their association with autoimmune diseases; however, the anti-DFS70 antibody has…Abstract Number: 090 • 2026 Pediatric Rheumatology Symposium
Characterizing CNS MRI Abnormalities in Pediatric ANCA-Associated Vasculitis
Background/Purpose: CNS involvement in pediatric ANCA-associated vasculitis (AAV) is rare but can lead to significant neurological symptoms, including headaches, seizures, behavioral changes, and occasional cerebrovascular…Abstract Number: 036 • 2026 Pediatric Rheumatology Symposium
Giant Aneurysms in Kawasaki Disease: A Large Quarternary Single Center Experience
Background/Purpose: Kawasaki disease (KD) is an acute medium-vessel vasculitis predominantly affecting children younger than five years old. It is the most common cause of acquired…Abstract Number: 104 • 2026 Pediatric Rheumatology Symposium
Identification of Joints with Active Arthritis from Clinical Notes with High Fidelity using a Large Language Model
Background/Purpose: Accumulating evidence supports a new, biology-driven classification system for JIA diagnosis and prognosis, depending upon identification of patterns of arthritis involvement, rather than just…Abstract Number: 093 • 2026 Pediatric Rheumatology Symposium
HOW DO WE HANDLE STILL’S DISEASE? REAL-LIFE CLINICIANS’ CHOICES FROM THE METAPHOR PROJECT WORLDWIDE SURVEY
Background/Purpose: Despite continuous improvement in care and the recent update of international recommendations, relevant discrepancies in the approach to Still’s disease (SD) still exists.The study…Abstract Number: 106 • 2026 Pediatric Rheumatology Symposium
Clinical Characteristics and Safety Outcomes in Refractory Kawasaki Disease Treated with Second-Dose Infliximab
Background/Purpose: Infliximab is an effective treatment for Kawasaki Disease (KD) as part of intensified initial therapy in combination with intravenous immunoglobulin (IVIG) or as a…
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