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  1. 7001
    “…Pathology of AoA and AoS suggests an initial subclinical endothelialitis or vasculitis, which is exacerbated by thrombogenesis and atherogenic factors and ultimately resulting in AoA and AoS. …”
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    Aortic Atherosclerosis in Systemic Lupus Erythematosus
  2. 7002
    “…METHODS: We analyzed contemporaneous blood and urine samples of patients with active LN (n = 19), other Systemic Lupus Erythematosus (SLE) patients (n = 79) and urine samples of patients with diabetic nephropathy (DN; n = 14) and anti-neutrophil cytoplasmatic antibody (ANCA) associated vasculitis (AAV; n = 11) by flow cytometry. RESULTS: Numbers of urinary T cells, B cells and macrophages correlated with disease activity and were significantly higher in the active LN group. …”
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    The cellular signature of urinary immune cells in Lupus nephritis: new insights into potential biomarkers
  3. 7003
    por Geier, David A., Geier, Mark R.
    Publicado 2014
    “…It was observed that cases with the SAAE outcomes of gastroenteritis (odds ratio (OR) = 4.6, 95 % confidence interval (CI) = 1.3–18.5), arthritis (OR = 2.5, 95 % CI = 1.4–4.3), systemic lupus erythematosus (OR = 5.3, 95 % CI = 1.5–20.5), vasculitis (OR = 4, 95 % CI = 1.01–16.4), alopecia (OR = 8.3, 95 % CI = 4.5–15.9), or CNS conditions (OR = 1.8, 95 % CI = 1.04–2.9) were significantly more likely than controls to have received HPV4 vaccine (median onset of SAAE symptoms from 6 to 55 days post-HPV4 vaccination). …”
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    A case–control study of quadrivalent human papillomavirus vaccine-associated autoimmune adverse events
  4. 7004
    “…There were no statistically significant differences in laboratory data, symptoms and signs, Birmingham Vasculitis Activity Score, or CT findings between the two groups. …”
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    Comparative investigation of respiratory tract involvement in granulomatosis with polyangiitis between PR3-ANCA positive and MPO-ANCA positive cases: a retrospective cohort study
  5. 7005
    “…They were compared with ANCA-negative IgAN patients (n = 40) and ANCA-associated systemic vasculitis (AASV) patients (n = 40) with a randomly selected and matched proportion of crescentic glomeruli. …”
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    Clinical features of IgA nephropathy with serum ANCA positivity: a retrospective case–control study
  6. 7006
    “…Kawasaki disease (KD) is an acute, inflammatory, and self-limited vasculitis affecting infants and young children. Coronary artery aneurysm (CAA) formation is the major complication of KD and the leading cause of acquired cardiovascular disease among children. …”
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    Genetic variants in PLCB4/PLCB1 as susceptibility loci for coronary artery aneurysm formation in Kawasaki disease in Han Chinese in Taiwan
  7. 7007
    “…Clinical features included early presentation (prominent vitritis, localized retinitis, and vasculitis) in 7/13 (53.85%) patients and late presentation (attenuation of vessels, retinal pigment epithelium atrophic changes, and optic atrophy) in 6/13 (46.15%) patients. …”
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    Clinical experience in treatment of diffuse unilateral subretinal neuroretinitis
  8. 7008
    “…RESULTS: Our cohort of patients included 84 with juvenile idiopathic arthritis (JIA), 21 with systemic lupus erythematosus (SLE), 6 with systemic vasculitis, 2 with juvenile scleroderma, 2 with idiopathic uveitis, 1 with mixed connective tissue disease and 1 with SLE/scleroderma overlap syndrome. …”
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    Primary complement and antibody deficiencies in autoimmune rheumatologic diseases with juvenile onset: a prospective study at two centers
  9. 7009
    “…Twelve children had atypical haemolytic uraemic syndrome, two had anti-glomerular basement disease and one each had lupus nephritis with neurological manifestation and anti-nuclear cytoplasmic antibody–associated vasculitis. The mean serum creatinine at presentation was 6.52 [interquartile range (IQR) 4.96–7.85] mg/dL with a mean eGFR of 43 (IQR 27.54–56.7) mL/min/1.73 m(2). …”
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    Plasma exchange for paediatric kidney disease—indications and outcomes: a single-centre experience*
  10. 7010
    “…She later developed cerebral vasculitis, indicating refractory disease, and was treated with second-line rituximab with excellent response. …”
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    Blindness in a Sri Lankan woman with bilateral breast lumps: a case report
  11. 7011
    “…BACKGROUND: Kawasaki disease is an acute, systemic vasculitis that affects the coronary arteries. However, the relationship between myocardial fibrosis and Kawasaki disease has been completely unknown until now. …”
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    Quantitative evaluation of myocardial fibrosis by cardiac integrated backscatter analysis in Kawasaki disease
  12. 7012
    “…Kawasaki disease (KD; MIM#61175) is a systemic vasculitis syndrome with unknown etiology which predominantly affects infants and children. …”
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    Variations in ORAI1 Gene Associated with Kawasaki Disease
  13. 7013
    “…BACKGROUND: Kawasaki disease (KD) is a form of self-limiting vasculitis that causes coronary artery abnormality in children. …”
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    Monoclonal antibody therapy for Kawasaki disease: a protocol for systematic reviews and meta-analysis
  14. 7014
    “…Prevalences were 9.2% for pure sensory neuropathy, 5.3% for sensorimotor neuropathy, 1.3% for cerebral vasculitis and 1.0% for myelitis. Neurological manifestations were associated with greater pSS activity as assessed using the ESSDAI (9.4±6.8 vs 4.3±4.8; p<0.001) and proportion of patients taking immunomodulatory/immunosuppressive drugs (32.4% (24/74) versus 13.8% (44/318), p=0003). …”
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    Epidemiology of neurological manifestations in Sjögren's syndrome: data from the French ASSESS Cohort
  15. 7015
    “…The child underwent surgical resection of the tumor, and the histologic examination of the lung specimens revealed lymphoplasmacytic infiltrates with fibrosis and vasculitis correlating with IgG4-related lung disease. …”
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    Pulmonary manifestation of immunoglobulin G4-related disease in a 7-year-old immunodeficient boy with Epstein-Barr virus infection: a case report
  16. 7016
    “…Patients were included if they fulfilled at least 3 American College of Rheumatology criteria for GCA, or 2 criteria associated with extratemporal biopsy-proven giant-cell vasculitis; they underwent at least 1 FDG-PET/CT scan at diagnosis or during follow-up; and the morphology of the aorta was assessed by medical imaging at diagnosis. …”
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    (18)F-fluorodeoxyglucose positron emission tomography and the risk of subsequent aortic complications in giant-cell arteritis: A multicenter cohort of 130 patients
  17. 7017
    “…Competences with lower self-reported ability included managing patients with vasculitis, identifying crystals and performing an ultrasound. …”
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    Rheumatology training experience across Europe: analysis of core competences
  18. 7018
    “…Coronary artery involvement is the most serious feature of this vasculitis syndrome. Timely diagnosis of coronary artery involvement is of utmost importance since it can prevent long-term morbidity and mortality. …”
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    Novel Echocardiographic Indices for Assessing the Left Main Coronary Artery in Children With Kawasaki Disease
  19. 7019
    “…This dose regimen is being tested in clinical trials in patients with anti-neutrophil cytoplasmic antibody-associated vasculitis. Trial Registration ISRCTN registry with trial ID ISRCTN13564773.…”
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    Characterization of Pharmacologic and Pharmacokinetic Properties of CCX168, a Potent and Selective Orally Administered Complement 5a Receptor Inhibitor, Based on Preclinical Evaluation and Randomized Phase 1 Clinical Study
  20. 7020
    “…An important number of cases present with seizures and the most frequent findings in neuroimaging are changes in basal ganglia and cerebral vasculitis. A defective CP, because of non-functional C1q, does not protect against NP involvement in SLE. …”
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    C1q Deficiency and Neuropsychiatric Systemic Lupus Erythematosus
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