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  1. 5781
    “…Kawasaki disease (KD) is a diffuse and acute small-vessel vasculitis observed in children and has genetic and autoimmune components. …”
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    High-density Genotyping of Immune Loci in Kawasaki Disease and IVIG Treatment Response in European-American Case-parent Trio Study
  2. 5782
    “…An inflammatory aetiology is plausible such as a subclinical retinal vasculitis, possibly with altered local microvascular autoregulation, and warrants further investigation. …”
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    Retinal changes in visceral leishmaniasis by retinal photography
  3. 5783
    “…Two adult female patients also showed late onset autoimmune inflammatory responses characterized by alopecia, skin ulcers secondary to inflammatory vasculitis, interstitial lung disease, and Raynaud’s phenomenon. …”
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    Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
  4. 5784
    por Cheung, Yiu-Fai
    Publicado 2014
    “…Kawasaki disease (KD), an acute vasculitis that primarily affects young children, is the most common acquired paediatric cardiovascular disease in developed countries. …”
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    Vascular health late after Kawasaki disease: implications for accelerated atherosclerosis
  5. 5785
    “…The most commonly associated skin lesions without classical lupus changes are cutaneous vasculitis, oral ulcers and diffuse non-scarring alopecia. …”
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    Mucocutaneous manifestations in juvenile-onset systemic lupus erythematosus: a review of literature
  6. 5786
    “…Some individuals experienced spontaneous regression of their JMML but developed vasculitis later in life. Importantly, JMML specimens from affected children show loss of the normal CBL allele through acquired isodisomy. …”
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    Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia
  7. 5787
    “…INTRODUCTION: Behçet’s disease (BD) is a rare vasculitis in sub-Saharan Africa. Vascular thrombosis, especially venous, is common in this condition and also constitutes a basic diagnostic criterion. …”
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    Superior vena cava syndrome revealing a Behçet’s disease
  8. 5788
    “…Objective: Kawasaki disease (KD) clinically presents as a systemic vasculitis syndrome with significant cardiovascular involvement. …”
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    Distribution and Protective Role of HLAB40 in Iranian Patients with Kawasaki Disease; a Report from Southern Iran
  9. 5789
    “…Henoch-Schönlein purpura (HSP) is a common systemic vasculitis in children. Animal models of HSP are needed to better understand the mechanism of HSP. …”
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    Hematologic and immunological characteristics of Henoch-Schönlein purpura in rat and rabbit models induced with ovalbumin based on type III hypersensitivity
  10. 5790
    “…INTRODUCTION: Kawasaki disease is an acute necrotising vasculitis of the medium- and small-sized vessels, occurring mainly in Japanese and Korean babies and children, aged 6 months to 5 years. …”
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    Adult Kawasaki disease in a European patient: a case report and review of the literature
  11. 5791
    “…Fluorescein angiography revealed delayed venous filling with neither leakage nor vasculitis. A comprehensive work-up that included infectious, inflammatory, and hypercoagulability studies was unremarkable, and magnetic resonance imaging of the orbits was unrevealing. …”
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    Central retinal vein occlusion resulting from anomalous retinal vascular anatomy in a 24-year-old man
  12. 5792
    “…A skin biopsy obtained 5 cm above the left lateral malleolus revealed medium-sized dermal vasculitis with dense mononuclear infiltrate. Electromyography showed peripheral neuropathy. …”
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    Non-Systemic Vasculitic Neuropathy: An Enigmatic Clinical Entity
  13. 5793
    “…OBJECTIVES: Behçet’s disease (BD) is a chronic, recurring vasculitis of unknown etiology. Patients with BD may use a lot of medications associated with the clinical symptoms. …”
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    Mandibular bone mineral density in patients with Behçet’s disease
  14. 5794
    “…Details of patients who were considered as treatment unresponsive psychosis and later turned out to be due to vasculitis were entered in excel sheet and analyzed. …”
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    New Onset Psychosis as The First Manifestation of Neuro-Psychiatric Lupus. A Situation Causing Diagnostic Dilemma
  15. 5795
    “…DISCUSSION: PAN is a vasculitis that predominantly involves small to medium-sized vessels. …”
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    Widespread lytic lesions—A metastatic or vasculitic process?
  16. 5796
    “…Lung lesions were characterized by vasculitis, necrosis, and increased presence of macrophages and neutrophils, relative to uninfected animals. …”
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    Morphological characterization and immunohistochemical detection of the proinflammatory cytokines IL-1β, IL-17A, and TNF-α in lung lesions associated with contagious bovine pleuropneumonia
  17. 5797
    “…Other intracranial artery diseases, such as dissection and vasculitis, also have distinctive characteristics in HR-MRI. …”
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    High-resolution Magnetic Resonance Imaging of Moyamoya Disease
  18. 5798
    “…However, subsequent skin biopsy results demonstrated neutrophilic infiltration into the dermis without vasculitis, and subsequent human leukocyte antigen typing was positive for Cw1 and negative for B51 and the patient was diagnosed with NSD. …”
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    Neuro-Sweet disease with positive modified acid-fast staining of the cerebrospinal fluid: A case report
  19. 5799
    “…BACKGROUND: Kawasaki disease (KD) is a systemic vasculitis with an acute and self-limited course. The incidence of KD differs widely among ethnic groups and is higher in the Asian population. …”
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    Kawasaki disease: an epidemiological study in central Italy
  20. 5800
    “…BACKGROUND: Behçet’s disease is a progressive diffuse inflammatory vasculitis characterized by recurrent oral and genital ulceration and ocular inflammation. …”
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    Complete heart block in a Caucasian woman with Behçet’s disease: a case report
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