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  1. 6381
    “…Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive disease associated with a highly variable clinical presentation, such as vasculitis, inflammation, and hematologic manifestations. …”
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    Case Report: Deficiency of Adenosine Deaminase 2 Presenting With Overlapping Features of Autoimmune Lymphoproliferative Syndrome and Bone Marrow Failure
  2. 6382
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    Roflumilast (Daliresp®) to reduce acute pulmonary events in fibrotic sarcoidosis: a multi-center, double blind, placebo controlled, randomized clinical trial
  3. 6383
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    Scout – sarcoidosis outcomes taskforce. A systematic review of outcomes to inform the development of a core outcome set for pulmonary sarcoidosis
  4. 6384
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    Frailty and chronic respiratory disease: the need for a multidisciplinary care model
  5. 6385
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    Raising awareness on physician-patient communication in IPF: an Italian multicenter study exploring the pulmonologist’s perspective
  6. 6386
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    Impulse Oscillometry as a measure of airway dysfunction in Sarcoidosis
  7. 6387
    “…OBJECTIVES: Takayasu arteritis (TAK) is a rare autoimmune rheumatic disease causing large-vessel vasculitis. Onset is typically between the ages of 20 and 30 years. …”
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    A systematic review and meta-analysis of the incidence rate of Takayasu arteritis
  8. 6388
    “…These include anterior uveitis, retinitis, chorioretinitis, retinal vasculitis, and optic nerve involvement. Proper clinical diagnosis of any of these infectious diseases is primarily based on epidemiological data, history, systemic symptoms and signs, and the pattern of ocular involvement. …”
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    Ocular Manifestations of Emerging Arthropod-Borne Infectious Diseases
  9. 6389
    por Dowsett, Thomas, Oni, Louise
    Publicado 2021
    “…It is classified as an autoimmune, small-vessel vasculitis caused by autoantibody formation against the alpha-3 chain in type IV collagen found in the glomerular basement membrane. …”
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    Anti-glomerular basement membrane disease in children: a brief overview
  10. 6390
    “…ABSTRACT: HCV is a virus that can cause chronic infection which can result in a systemic disease that may include many rheumatologic manifestations such as arthritis, myalgia, sicca syndrome, cryoglobulinemia vasculitis as well as other non-rheumatological disorders (renal failure, onco-haematological malignancies). …”
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    Autoantibodies and Rheumatologic Manifestations in Hepatitis C Virus Infection
  11. 6391
    “…Patients with HCV after a sustained virologic response (SVR) by DAA treatment have a lower risk than non-responders of developing cryoglobulinemic vasculitis and B-cell non-Hodgkin’s lymphomas. Furthermore, the SVR by DAA also reduces the risk of acute coronary syndrome, cardiovascular disease, insulin resistance and type 2 diabetes, and it improves atherosclerosis. …”
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    A Review on Extrahepatic Manifestations of Chronic Hepatitis C Virus Infection and the Impact of Direct-Acting Antiviral Therapy
  12. 6392
    “…Background: Kawasaki disease (KD) is a form of febrile vasculitis that primarily occurs in children. It can cause inflammation of the coronary arteries, which leads to aneurysms. …”
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    Increased Expression of Pyroptosis in Leukocytes of Patients with Kawasaki Disease
  13. 6393
    “…BACKGROUND: Childhood Polyarteritis nodosa (PAN) is a systemic vasculitis with necrotizing inflammation of medium- and small-sized arteries. …”
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    A young girl with severe polyarteritis nodosa successfully treated with tocilizumab: a case report
  14. 6394
    “…CONCLUSION: The comparison of clinical profiles of IOI or non-IOI cases in IVBr treatment for AMD suggests that the risk factors for IOI are old age, female sex, and history of diabetes; however, IOI with vasculitis or vascular occlusion in this cohort does not seem to cause severe visual impairment. …”
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    Risk factors for emerging intraocular inflammation after intravitreal brolucizumab injection for age-related macular degeneration
  15. 6395
    “…BACKGROUND: Behçet’s disease is a chronic multisystemic vasculitis affecting vessels of different sizes in various organs. …”
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    Imaging Features of Thoracic Manifestations of Behçet’s Disease: Beyond Pulmonary Artery Involvement
  16. 6396
    “…Background: Behçet’s disease (BD) is a rare chronic multisystemic vasculitis of unknown etiology. It is usually diagnosed between the 2(nd) and 4(th) decades of life, so its association with pregnancy is not unusual. …”
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    Behçet’s Disease and Pregnancy: A Retrospective Case-control Study
  17. 6397
    por Hu, Jinling, Ren, Weidong
    Publicado 2021
    “…Abstract: Kawasaki disease (KD) is one of the most common forms of systemic vasculitis in children. Pathological features include extensive inflammation of small and medium blood vessels throughout the body. …”
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    Analysis of the Risk Factors in Prognosis of Kawasaki Disease With Coronary Artery Lesions
  18. 6398
    “…The cases reported were three herpetic keratitis, two anterior scleritis, five anterior uveitis (AU), three toxoplasma retinochoroiditis, two Vogt-Koyanagi-Harada (VKH) disease reactivations, two pars planitis, two retinal vasculitis, one bilateral panuveitis in new-onset Behçet’s disease, three multiple evanescent white dot syndromes (MEWDS), one acute macular neuroretinopathy (AMN), five retinal vein occlusions (RVO), one non-arteritic ischemic optic neuropathy (NAION), three activations of quiescent choroidal neovascularization (CNV) secondary to myopia or uveitis, and one central serous chorioretinopathy (CSCR). …”
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    Uveitis and Other Ocular Complications Following COVID-19 Vaccination
  19. 6399
    “…BACKGROUND: Behcet’s disease (BD) is a chronic inflammatory disease that involves systemic vasculitis and mainly manifests as oral and genital ulcers, uveitis, and skin damage as the first clinical symptoms, leading to gastrointestinal, aortic, or even neural deterioration. …”
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    Novel Insights Into Gene Signatures and Their Correlation With Immune Infiltration of Peripheral Blood Mononuclear Cells in Behcet’s Disease
  20. 6400
    “…In human samples with acute glomerular injury (e.g., antineutrophil cytoplasmic autoantibody vasculitis), high VISTA expression in tubulointerstitial immune cells was associated with low tubulointerstitial fibrosis and good prognosis. …”
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    Kidney VISTA prevents IFN-γ/IL-9 axis–mediated tubulointerstitial fibrosis after acute glomerular injury
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