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Multicolor flow cytometric analysis of TLR2 and TLR9 expression and function in NK cells from patients with ANCA‐associated vasculitis

Cytometry. Part B, Clinical cytometry, 2018-05, Vol.94 (3), p.412-422

2018

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At the Bench: Neutrophil extracellular traps (NETs) highlight novel aspects of innate immune system involvement in autoimmune diseases

Journal of leukocyte biology, 2016-02, Vol.99 (2), p.253-264

2016

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Long-term outcomes and prognostic factors for survival of patients with ANCA-associated vasculitis

Nephrology, dialysis, transplantation, 2023-06, Vol.38 (7), p.1655-1665

2023

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Comparison of agranulocytosis and anti‐neutrophil cytoplasmic antibody‐associated vasculitis caused by two antithyroid drugs: A pharmacovigilance study using the WHO international database

Fundamental & clinical pharmacology, 2024-08, Vol.38 (4), p.780-788

2024

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Altered follicular regulatory T (Tfr)‐ and helper T (Tfh)‐cell subsets are associated with autoantibody levels in microscopic polyangiitis patients

European journal of immunology, 2021-07, Vol.51 (7), p.1809-1823

2021

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Patients of 75 years and over with ANCA‐associated vasculitis have a lower relapse risk than younger patients: A multicentre cohort study

Journal of internal medicine, 2022-03, Vol.291 (3), p.350-363

2022

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Cutaneous manifestations of microscopic polyangiitis successfully controlled with avacopan alone

Journal of dermatology, 2023-07, Vol.50 (7), p.e206-e207

2023

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Antineutrophil cytoplasmic antibody-associated vasculitis, update on molecular pathogenesis, diagnosis, and treatment

International journal of nephrology and renovascular disease, 2018-01, Vol.11, p.313-319

2018

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Frequency, risk factors and prophylaxis of infection in ANCA-associated vasculitis

European journal of clinical investigation, 2015-03, Vol.45 (3), p.346-368

2015

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Plasmapheresis for systemic vasculitis

Therapeutic apheresis and dialysis, 2022-06, Vol.26 (3), p.493-506

2022

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Recent advances in the treatment strategy for AAV improved outcomes with intensive GC tapering

International journal of rheumatic diseases, 2024-01, Vol.27 (1), p.e15009-n/a

2024

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Cutaneous manifestations of antineutrophil cytoplasmic antibody‐associated vasculitis (AAV): a concise review with emphasis on clinical and histopathologic correlation

International journal of dermatology, 2022-12, Vol.61 (12), p.1442-1451

Gibson, Lawrence E.

2022

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Comparison of characteristics of muscle magnetic resonance imaging findings in patients with antineutrophilic cytoplasmic antibody‐associated vasculitis and polyarteritis nodosa

International journal of rheumatic diseases, 2024-03, Vol.27 (3), p.e15116-n/a

2024

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Allograft failure in kidney transplant recipients who developed kidney failure secondary to ANCA‐associated vasculitis

Clinical transplantation, 2021-04, Vol.35 (4), p.e14235-n/a

2021

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Experience of double plasma purification in 603 patients from a single center in Shanghai, China

Therapeutic apheresis and dialysis, 2023-06, Vol.27 (3), p.488-494

2023

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Systematic Review and Metaanalysis of Worldwide Incidence and Prevalence of Antineutrophil Cytoplasmic Antibody (ANCA) Associated Vasculitis

Journal of clinical medicine, 2022-05, Vol.11 (9), p.2573

2022

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Skewing toward Treg and Th2 responses is a characteristic feature of sustained remission in ANCA‐positive granulomatosis with polyangiitis

European journal of immunology, 2017-04, Vol.47 (4), p.724-733

2017

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Aortic aneurysm as a complication of myeloperoxidase-antineutrophil cytoplasmic antibody-associated vasculitis

Open medicine (Warsaw, Poland), 2017-01, Vol.12 (1), p.468-473

2017

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Organisation of lymphocytic infiltrates in ANCA‐associated glomerulonephritis

Histopathology, 2018-06, Vol.72 (7), p.1093-1101

2018

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Incidence of Systemic Vasculitis and Clinical Outcomes in Systemic Sclerosis: 2-Years Follow-Up of Asymptomatic Positive for Anti-Neutrophilic Cytoplasmic Antibody

Clinical, cosmetic and investigational dermatology, 2024-01, Vol.17, p.301-309

2024

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Primary Vasculitis in Childhood: GPA and MPA in Childhood

Frontiers in pediatrics, 2018-08, Vol.6, p.226

2018

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Proteinase 3: the odd one out that became an autoantigen

Journal of leukocyte biology, 2017-09, Vol.102 (3), p.689-698

2017

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Diagnostic d’une granulomatose éosinophilique avec polyangéite sous benralizumab

Revue des maladies respiratoires, 2022-09, Vol.39 (7), p.621-625

2022

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Alterations in circulating lymphoid cell populations in systemic small vessel vasculitis are non‐specific manifestations of renal injury

Clinical and experimental immunology, 2018-02, Vol.191 (2), p.180-188

2018

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Th17 and Treg lymphocytes as cellular biomarkers of disease activity in Granulomatosis with Polyangiitis

European journal of immunology, 2017-04, Vol.47 (4), p.633-636

Cosmi, Lorenzo

2017

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