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  1. 6921
    “…RESULTS: Twenty eyes of 20 patients with UME were studied: anterior uveitis (n = 3), anterior + intermediate uveitis (n = 5), posterior uveitis (n = 3), retinal vasculitis (n = 3), and panuveitis (n = 6). Mean CMT at the presentation was 423.3 µm (range: 270–604 µm), which improved at 1 month (n = 16), 2 months (n = 10), and ≥3 months (n = 11) follow-up, to 415.3 µm (range: 247–579 mm) (P = 0.411), 364.4 mm (range: 258–566 µm) (P = 0.099), 344 µm (range: 258–484 µm) (P = 0.001), respectively. …”
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    Topical interferon therapy in uveitic macular edema
  2. 6922
    “…Non-occlusive retinal vasculitis, peripheral vessel occlusions, cataract and elevated intraocular pressure were found more commonly among juvenile-onset eyes. …”
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    Ocular Behçet Disease—Clinical Manifestations, Treatments and Outcomes According to Age at Disease Onset
  3. 6923
    “…The risk of progression to end-stage kidney disease (ESKD) in patients with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) and glomerulonephritis (AAV-GN) remains high. …”
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    PLEX in AAV-GN: insights from the meta-analysis results and impact on remission induction treatment recommendations
  4. 6924
    “…CASE REPORT - INTRODUCTION: Behçet’s disease (BD) is a systemic inflammatory, variable-vessel vasculitis manifesting most commonly with recurrent oral or genital ulcers and uveitis. …”
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    O16 A diagnosis of BehÇet’s Disease with secondary antiphospholipid syndrome
  5. 6925
    “…The SLE-TB patients had a significant increase in the clinical and laboratory features of disease activity (arthritis, mucocutaneous lesions, renal involvement, vasculitis, low complement, raised ds-DNA antibodies), and cumulative prednisone use over the preceding 3 months. …”
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    Tuberculosis remains a major burden in systemic lupus erythematosus patients in Durban, South Africa
  6. 6926
    “…Our case demonstrates the involvement of kidneys and vasculitis of the skin, sclera, and lungs by COVID-19. …”
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    Atypical Immunologic Manifestations of COVID-19: a Case Report and Narrative Review
  7. 6927
    “…Behçet disease (BD) is a chronic systemic vasculitis that is clinically characterized by recurrent oral ulcers, genital ulcers, uveitis, and skin lesions. …”
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    The proportion of C1q-high and ISG15-high monocytes in the skin of patients with Behçet disease
  8. 6928
    “…Variable signs or sequelae of intraocular inflammation were observed in 9 patients, including keratic precipitates, band keratopathy, trace to 2+ anterior chamber cells, cystoid macular edema, and retinal vasculitis on fluorescein angiography. Ten patients were observed to show optic disc elevation and demonstrated peripapillary thickening on OCT. …”
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    Ophthalmic Manifestations of ROSAH (Retinal Dystrophy, Optic Nerve Edema, Splenomegaly, Anhidrosis, and Headache) Syndrome, an Inherited NF κB–Mediated Autoinflammatory Disease with Retinal Dystrophy
  9. 6929
    “…BACKGROUND: Takayasu arteritis (TA) is a chronic granulomatous vasculitis with unknown pathophysiology. TA with severe aortic obstruction has a poor prognosis. …”
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    Case report: Aggressive progression of acute heart failure due to juvenile tuberculosis-associated Takayasu arteritis with aortic stenosis and thrombosis
  10. 6930
    “…BACKGROUND: Kawasaki disease (KD) is a form of pediatric systemic vasculitis. Although the etiology remains unclear, infections have been identified as possible triggers. …”
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    Evaluation of the association of birth order and group childcare attendance with Kawasaki disease using data from a nationwide longitudinal survey
  11. 6931
    “…BACKGROUND: Renal involvement is a common and severe complication of anti-neutrophil cytoplasmic antibody-(ANCA)-associated vasculitis potentially resulting in pauci-immune necrotizing and crescentic ANCA glomerulonephritis (GN) with rapid deterioration of kidney function, progression to end stage kidney disease or, if left untreated, lethal exitus. …”
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    Leukocyturia and hematuria enable non-invasive differentiation of Bowman’s capsule rupture severity in PR3-ANCA glomerulonephritis
  12. 6932
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    Validation of the Turkish Version of the Sarcoidosis Health Questionnaire: a cross-sectional study
  13. 6933
    “…Despite apparent virological remission, lung pathology was similar to that observed in acute COVID‐19 individuals, including micro‐ and macro‐vascular thrombosis (67% of cases), vasculitis (24%), squamous metaplasia of the respiratory epithelium (30%), frequent cytological abnormalities and syncytia (67%), and the presence of dysmorphic features in the bronchial cartilage (44%). …”
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    Persistent SARS‐CoV‐2 infection in patients seemingly recovered from COVID‐19
  14. 6934
    “…Henoch-Schonlein purpura (HSP), a recurrent and immunoglobulin (Ig)A-mediated vasculitis, presents not only as skin lesions but also as systemic involvement that can be life-threatening. …”
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    Proanthocyanidins: A novel approach to Henoch‑Schonlein purpura through balancing immunity and arresting oxidative stress via TLR4/MyD88/NF‑κB signaling pathway (Review)
  15. 6935
    “…The most frequent underlying diseases were ANCA-associated vasculitis (29%) and rheumatoid arthritis (23%). Median anti-S antibody titers at RTX initiation, 3 months, and 6 months were 1620 (589–2080), 1055 (467–2080), and 407 (186–659) BAU/mL, respectively. …”
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    Impact of rituximab on humoral response to SARS-CoV-2 vaccination in previously vaccinated patients with autoimmune diseases
  16. 6936
    “…Seventy-five patients with clinically suspected autoimmune vasculitis (AIV) and 25 healthy volunteers were also tested for anti-myeloperoxidase and anti-proteinase 3 antibodies using IIF, the AtheNA Multi-Lyte(®) AIV system, and enzyme-linked immunosorbent assay (ELISA). …”
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    Performance of two multiplex flow cytometric assays for antibody detection in Egyptian patients
  17. 6937
    “…CONCLUSION: We present the case of a young adult with diagnosis of DADA2 as a cause for recurrent strokes due to vasculitis. This stroke etiology is rare but should be considered as a cause of recurrent stroke of unknown origin in young patients to avoid a disabling disease course by disease-specific treatment options.…”
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    Brainstem Infarction in Immunodeficiency Identified as Adenosine Deaminase 2 Deficiency: Case Report
  18. 6938
    “…METHODS: A steering committee (SC) was formed that included clinicians, patients, patient advocates, and researchers associated with rheumatic diseases (psoriatic arthritis, rheumatoid arthritis, vasculitis), inflammatory bowel disease, and multiple sclerosis. …”
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    Engaging Multistakeholder Perspectives to Identify Patient‐Centered Research Priorities Regarding Vaccine Uptake Among Adults With Autoimmune Conditions
  19. 6939
    “…In this systematic review, SLE was proven to have a strong relationship with diverse CVDs, including rare ones scarcely discussed in the literature, such as vasculitis and aortic dissection. All eight of the final papers indicated a connection between SLE and CVDs, based on the systematic analysis of these articles, which revealed that most recent research supports a higher risk of peripheral arterial occlusive disease (PAOD), MI, pericarditis, myocarditis, and other cardiovascular disorders in individuals with SLE. …”
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    Systemic Lupus Erythematosus and Cardiovascular Diseases: A Systematic Review
  20. 6940
    “…To be diagnosed with FIRS placenta must contain chorionic vasculitis and/or funisitis. Children had to be in study period for at least 5 years. …”
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    Fetal inflammatory response and risk for psychiatric disorders
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