- Abstract Number: 1570
Deconvolution of the Lipidomic Signature of Very Early Diagnosis of Systemic Sclerosis (VEDOSS) and Established Disease: Lipid Biomarker Features That Predict Disease Progression in Skin and Lung
- Abstract Number: 0780
Deep B Cell Tissue Depletion Following Anti-CD19 CART Cells Therapy
- Abstract Number: 0921
Deep Immunologic Profiling of Trisomy 8-associated Autoinflammatory Disease (TRIAD)
- Abstract Number: 2107
Deep Immunophenotyping of Knee Osteoarthritis Patients Reveals Alterations in T Cell, Treg, and Monocyte Subpopulations
- Abstract Number: 1705
Deep Phenotyping Characterization of Peripheral Natural Killer Cells Reveals Impaired Cytotoxicity and Exhaustion During VEXAS Syndrome
- Abstract Number: 0444
Deep Serologic Profiling Identifies Novel Autoantibodies Associated with Fetal Atrioventricular Block
- Abstract Number: 2307
Deep Spatial Profiling Unveils Dominant Double Negative B Cells in Severe Forms of Sjögren’s Syndrome
- Abstract Number: 0036
Deep Topic Modeling Deconvolves Cell States in Spatial Transcriptomic Profiles of Rheumatoid Arthritis Synovial Tissue
- Abstract Number: 1141
Defining a Novel Type of Myositis: Immune Mediated Megaconial Myopathy (IMMM)
- Abstract Number: 2282
Defining a Personalized Treatment Approach to Rheumatoid Arthritis: Using Genetic Markers of TNFi Response
- Abstract Number: 0874
Defining a Protective Role for Mucosal-associated Invariant T (MAIT) Cells in Spontaneous Cutaneous Lupus Erythematosus
- Abstract Number: 0818
Defining BASDAI Cut-offs for Disease Activity States in Axial Spondylarthritis – Results from the EuroSpA Collaboration
- Abstract Number: 2649
Defining Clinical Subgroups of Patients with Relapsing Polychondritis: A Latent Class and Decision Tree Analysis in Two Independent Prospective Cohorts
- Abstract Number: 2638
Defining Sonographic Enthesitis in Psoriatic Arthritis: Developing a Data- and Expert-driven Diagnostic Criteria for Inflammatory Enthesitis at the Single Enthesis Level
- Abstract Number: 0904
Defining the Function of Disease Variants with CRISPR Editing and Multimodal Single Cell Sequencing
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