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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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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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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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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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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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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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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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Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and fibromyalgia: PR3-versus MPO-ANCA-associated vasculitis, an exploratory cross-sectional studyResearch in context

Lancet Regional Health - Americas (Online), 2023-04, Vol.20, p.100460

2023

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Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and fibromyalgia: PR3-versus MPO-ANCA-associated vasculitis, an exploratory cross-sectional study

Lancet Regional Health - Americas (Online), 2023-04, Vol.20, p.100460-100460, Article 100460

2023

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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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ANCA‐associated vasculitis with scleritis, corneal melt, and perforation rescued by rituximab: Case report and literature review

Clinical case reports, 2023-06, Vol.11 (6), p.e7595-n/a

2023

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COPA syndrome caused by a novel p.Arg227Cys COPA gene variant

Molecular genetics & genomic medicine, 2024-01, Vol.12 (1), p.e2309-n/a

2024

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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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Sequential development of ANCA‐associated vasculitis and anti‐GBM disease: A report of two cases

Clinical case reports, 2021-07, Vol.9 (7), p.e04553-n/a

2021

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ANCA-Associated Vasculitis Clinical Presentation and Clinical Predictors of Relapse in Saudi Arabia

Open access rheumatology: research and reviews, 2021-01, Vol.13, p.213-220

2021

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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

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

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

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

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

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

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

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and fibromyalgia: PR3-versus MPO-ANCA-associated vasculitis, an exploratory cross-sectional studyResearch in context

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and fibromyalgia: PR3-versus MPO-ANCA-associated vasculitis, an exploratory cross-sectional study

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

ANCA‐associated vasculitis with scleritis, corneal melt, and perforation rescued by rituximab: Case report and literature review

COPA syndrome caused by a novel p.Arg227Cys COPA gene variant

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

Sequential development of ANCA‐associated vasculitis and anti‐GBM disease: A report of two cases

ANCA-Associated Vasculitis Clinical Presentation and Clinical Predictors of Relapse in Saudi Arabia

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