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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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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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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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Primary Vasculitis in Childhood: GPA and MPA in Childhood

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

2018

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

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

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

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

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

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

Cutaneous manifestations of microscopic polyangiitis successfully controlled with avacopan alone

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

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

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

Plasmapheresis for systemic vasculitis

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

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

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

Primary Vasculitis in Childhood: GPA and MPA in Childhood

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

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

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

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

Organisation of lymphocytic infiltrates in ANCA‐associated glomerulonephritis

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

Proteinase 3: the odd one out that became an autoantigen

Diagnostic d’une granulomatose éosinophilique avec polyangéite sous benralizumab

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

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

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