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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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Pulmonary involvement in antineutrophil cytoplasmic antibody‐associated vasculitides: A single center experience from Turkey

International journal of rheumatic diseases, 2023-08, Vol.26 (8), p.1495-1503

2023

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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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A comparative analysis of different biofluids using Raman spectroscopy to determine disease activity in ANCA‐associated vasculitis

Journal of biophotonics, 2021-04, Vol.14 (4), p.n/a

2021

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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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Distinct HLA and non‐HLA associations in different subtypes of ANCA‐associated vasculitides in North India

International journal of rheumatic diseases, 2020-07, Vol.23 (7), p.958-965

2020

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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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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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Indian Rheumatology Association guidelines for the management of ANCA associated vasculitis

Autoimmunity reviews, 2024-11, Vol.23 (11), p.103647, Article 103647

2024

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Two cases of refractory eosinophilic granulomatosis with polyangiitis wherein mepolizumab was effective against pulmonary and ear lesions

Modern rheumatology case reports, 2021-04, Vol.5 (2), p.327-332

2021

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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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Unmasking eosinophilic granulomatosis with polyangiitis (EGPA)

European journal of internal medicine, 2024-10, Vol.128, p.34-35

2024

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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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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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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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Tocilizumab monotherapy uncovered the role of the CCL22/17‐CCR4+ Treg axis during remission of crescentic glomerulonephritis

Clinical & translational immunology, 2020, Vol.9 (11), p.e1203-n/a

2020

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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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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

Pulmonary involvement in antineutrophil cytoplasmic antibody‐associated vasculitides: A single center experience from Turkey

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

A comparative analysis of different biofluids using Raman spectroscopy to determine disease activity in ANCA‐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

Distinct HLA and non‐HLA associations in different subtypes of ANCA‐associated vasculitides in North India

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

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

Indian Rheumatology Association guidelines for the management of ANCA associated vasculitis

Two cases of refractory eosinophilic granulomatosis with polyangiitis wherein mepolizumab was effective against pulmonary and ear lesions

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

Unmasking eosinophilic granulomatosis with polyangiitis (EGPA)

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

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

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

Tocilizumab monotherapy uncovered the role of the CCL22/17‐CCR4+ Treg axis during remission of crescentic glomerulonephritis

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

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