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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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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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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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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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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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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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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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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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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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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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Do ANCA‐associated vasculitides and IgG4‐related disease really overlap or not?

International journal of rheumatic diseases, 2019-10, Vol.22 (10), p.1926-1932

2019

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Clinical and pathological features of anti‐neutrophil cytoplasmic antibody‐associated vasculitis in patients with minor urinary abnormalities

Nephrology (Carlton, Vic.), 2018-11, Vol.23 (11), p.1007-1012

2018

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Multivariable index for assessing the activity and predicting all‐cause mortality in antineutrophil cytoplasmic antibody‐associated vasculitis

Journal of clinical laboratory analysis, 2020-01, Vol.34 (1), p.e23022-n/a

2020

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IgA‐ and SIgA anti‐PR3 antibodies in serum versus organ involvement and disease activity in PR3‐ANCA‐associated vasculitis

Clinical and experimental immunology, 2016-05, Vol.184 (2), p.208-215

2016

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Neutrophils from vasculitis patients exhibit an increased propensity for activation by anti‐neutrophil cytoplasmic antibodies

Clinical and experimental immunology, 2014-06, Vol.176 (3), p.363-372

2014

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The avidity of PR3‐ANCA in patients with granulomatosis with polyangiitis during follow‐up

Clinical and experimental immunology, 2016-08, Vol.185 (2), p.141-147

2016

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Patients with ANCA‐associated vasculitis' experiences of informational needs: A qualitative interview study

Journal of renal care, 2022-06, Vol.48 (2), p.84-92

English ed., 2022

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Immunoglobulin (Ig)M antibodies to proteinase 3 in granulomatosis with polyangiitis and microscopic polyangiitis

Clinical and experimental immunology, 2017-04, Vol.188 (1), p.174-181

2017

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Hypertrophic pachymeningitis is a characteristic manifestation of granulomatosis with polyangiitis: A retrospective study of anti‐neutrophil cytoplasmic antibody‐associated vasculitis

International journal of rheumatic diseases, 2017-04, Vol.20 (4), p.489-496

2017

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Anti‐neutrophil cytoplasmic antibody (ANCA)‐associated vasculitis: where to go?

Clinical and experimental immunology, 2011-05, Vol.164 (Supplement_1), p.1-3

Kallenberg, C. G. M.

2011

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Clinical features and prognosis of microscopic polyangiitis with usual interstitial pneumonia compared with idiopathic pulmonary fibrosis

The clinical respiratory journal, 2019-07, Vol.13 (7), p.460-466

2019

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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

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

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

Plasmapheresis for systemic vasculitis

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

Cutaneous manifestations of microscopic polyangiitis successfully controlled with avacopan alone

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

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

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

Proteinase 3: the odd one out that became an autoantigen

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

Do ANCA‐associated vasculitides and IgG4‐related disease really overlap or not?

Clinical and pathological features of anti‐neutrophil cytoplasmic antibody‐associated vasculitis in patients with minor urinary abnormalities

Multivariable index for assessing the activity and predicting all‐cause mortality in antineutrophil cytoplasmic antibody‐associated vasculitis

IgA‐ and SIgA anti‐PR3 antibodies in serum versus organ involvement and disease activity in PR3‐ANCA‐associated vasculitis

Neutrophils from vasculitis patients exhibit an increased propensity for activation by anti‐neutrophil cytoplasmic antibodies

The avidity of PR3‐ANCA in patients with granulomatosis with polyangiitis during follow‐up

Patients with ANCA‐associated vasculitis' experiences of informational needs: A qualitative interview study

Immunoglobulin (Ig)M antibodies to proteinase 3 in granulomatosis with polyangiitis and microscopic polyangiitis

Hypertrophic pachymeningitis is a characteristic manifestation of granulomatosis with polyangiitis: A retrospective study of anti‐neutrophil cytoplasmic antibody‐associated vasculitis

Anti‐neutrophil cytoplasmic antibody (ANCA)‐associated vasculitis: where to go?

Clinical features and prognosis of microscopic polyangiitis with usual interstitial pneumonia compared with idiopathic pulmonary fibrosis

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