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Criteria for the pathogenicity of anticentromere (anti–CENP‐B) autoantibodies in systemic sclerosis: comment on the article by van Leeuwen et al

Arthritis & rheumatology (Hoboken, N.J.), 2022-09, Vol.74 (9), p.1606-1607

2022

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Editorial: A New Classification of Adult Autoimmune Myositis

Arthritis & rheumatology (Hoboken, N.J.), 2017-05, Vol.69 (5), p.878-884

2017

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Scleromyositis: A distinct novel entity within the systemic sclerosis and autoimmune myositis spectrum. Implications for care and pathogenesis

Frontiers in immunology, 2023-01, Vol.13, p.974078-974078

2023

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Treatment Algorithms in Systemic Lupus Erythematosus

Arthritis care & research (2010), 2015-09, Vol.67 (9), p.1237-1245

2015

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Histopathological features of systemic sclerosis-associated myopathy: A scoping review

Autoimmunity reviews, 2021-07, Vol.20 (7), p.102851, Article 102851

2021

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Autoantibodies to a novel Rpp38 (Th/To) derived B-cell epitope are specific for systemic sclerosis and associate with a distinct clinical phenotype

Rheumatology (Oxford, England), 2019-10, Vol.58 (10), p.1784-1793

2019

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Pathogenic roles of autoantibodies in systemic sclerosis: Current understandings in pathogenesis

Journal of Scleroderma and Related Disorders, 2020-06, Vol.5 (2), p.103-129

2020

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Early-Life Antibiotic Exposure Causes Intestinal Dysbiosis and Exacerbates Skin and Lung Pathology in Experimental Systemic Sclerosis

Journal of investigative dermatology, 2017-11, Vol.137 (11), p.2316-2325

2017

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Heterogeneity of autoantibodies in 100 patients with autoimmune myositis: insights into clinical features and outcomes

Arthritis research & therapy, 2007-01, Vol.9 (4), p.R78-R78

2007

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Prevalence of Systemic Sclerosis in Primary Biliary Cholangitis Using the New ACR/EULAR Classification Criteria

Journal of rheumatology, 2017-01, Vol.44 (1), p.33

2017

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Redefining dermatomyositis: a description of new diagnostic criteria that differentiate pure dermatomyositis from overlap myositis with dermatomyositis features

Medicine (Baltimore), 2014-11, Vol.93 (24), p.318-332

2014

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Myositis with prominent B cell aggregates may meet classification criteria for sporadic inclusion body myositis

Neuromuscular disorders : NMD, 2023-02, Vol.33 (2), p.169-182

2023

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Atorvastatin-induced necrotizing autoimmune myositis: An emerging dominant entity in patients with autoimmune myositis presenting with a pure polymyositis phenotype

Medicine (Baltimore), 2017-01, Vol.96 (3), p.e5694

2017

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Predictive value of antinuclear autoantibodies: The lessons of the systemic sclerosis autoantibodies

Autoimmunity reviews, 2008-09, Vol.7 (8), p.588-593

2008

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Topoisomerase I peptide-loaded dendritic cells induce autoantibody response as well as skin and lung fibrosis

Autoimmunity (Chur, Switzerland), 2016-12, Vol.49 (8), p.503-513

2016

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Anti-SMN autoantibodies in mixed connective tissue disease are associated with a severe systemic sclerosis phenotype

Rheumatic & musculoskeletal diseases open, 2023-10, Vol.9 (4), p.e003431

2023

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Recognising the spectrum of scleromyositis: HEp-2 ANA patterns allow identification of a novel clinical subset with anti-SMN autoantibodies

Rheumatic & musculoskeletal diseases open, 2020-09, Vol.6 (2), p.e001357

2020

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Decreased secretion of MMP by non-lesional late-stage scleroderma fibroblasts after selection via activation of the apoptotic fas-pathway

Journal of cellular physiology, 2011-07, Vol.226 (7), p.1907-1914

2011

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fibrotic phenotype of systemic sclerosis fibroblasts varies with disease duration and severity of skin involvement: reconstitution of skin fibrosis development using a tissue engineering approach

The Journal of pathology, 2009-03, Vol.217 (4), p.534-542

2009

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An autoimmune myositis-overlap syndrome associated with autoantibodies to nuclear pore complexes: description and long-term follow-up of the anti-Nup syndrome

Medicine (Baltimore), 2014-11, Vol.93 (24), p.383-394

2014

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Etiology-Specific Endothelin-1 Clearance in Human Precapillary Pulmonary Hypertension

Chest, 2006-03, Vol.129 (3), p.689-695

2006

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Novel classification of idiopathic inflammatory myopathies based on overlap syndrome features and autoantibodies: analysis of 100 French Canadian patients

Medicine (Baltimore), 2005-07, Vol.84 (4), p.231-249

2005

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Thromboembolism complicating the treatment of lupus anticoagulant hypoprothrombinemia syndrome

Journal of rheumatology, 2006-10, Vol.33 (10), p.2088

2006

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Autoantibodies and microvascular damage are independent predictive factors for the progression of Raynaud's phenomenon to systemic sclerosis: A twenty‐year prospective study of 586 patients, with validation of proposed criteria for early systemic sclerosis

Arthritis and rheumatism, 2008-12, Vol.58 (12), p.3902-3912

2008

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Myositis with prominent B-cell aggregates causing shrinking lung syndrome in systemic lupus erythematosus: a case report

BMC rheumatology, 2022-02, Vol.6 (1), p.11-6, Article 11

2022

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Criteria for the pathogenicity of anticentromere (anti–CENP‐B) autoantibodies in systemic sclerosis: comment on the article by van Leeuwen et al

Editorial: A New Classification of Adult Autoimmune Myositis

Scleromyositis: A distinct novel entity within the systemic sclerosis and autoimmune myositis spectrum. Implications for care and pathogenesis

Treatment Algorithms in Systemic Lupus Erythematosus

Histopathological features of systemic sclerosis-associated myopathy: A scoping review

Autoantibodies to a novel Rpp38 (Th/To) derived B-cell epitope are specific for systemic sclerosis and associate with a distinct clinical phenotype

Pathogenic roles of autoantibodies in systemic sclerosis: Current understandings in pathogenesis

Early-Life Antibiotic Exposure Causes Intestinal Dysbiosis and Exacerbates Skin and Lung Pathology in Experimental Systemic Sclerosis

Heterogeneity of autoantibodies in 100 patients with autoimmune myositis: insights into clinical features and outcomes

Prevalence of Systemic Sclerosis in Primary Biliary Cholangitis Using the New ACR/EULAR Classification Criteria

Redefining dermatomyositis: a description of new diagnostic criteria that differentiate pure dermatomyositis from overlap myositis with dermatomyositis features

Myositis with prominent B cell aggregates may meet classification criteria for sporadic inclusion body myositis

Atorvastatin-induced necrotizing autoimmune myositis: An emerging dominant entity in patients with autoimmune myositis presenting with a pure polymyositis phenotype

Predictive value of antinuclear autoantibodies: The lessons of the systemic sclerosis autoantibodies

Topoisomerase I peptide-loaded dendritic cells induce autoantibody response as well as skin and lung fibrosis

Anti-SMN autoantibodies in mixed connective tissue disease are associated with a severe systemic sclerosis phenotype

Recognising the spectrum of scleromyositis: HEp-2 ANA patterns allow identification of a novel clinical subset with anti-SMN autoantibodies

Decreased secretion of MMP by non-lesional late-stage scleroderma fibroblasts after selection via activation of the apoptotic fas-pathway

fibrotic phenotype of systemic sclerosis fibroblasts varies with disease duration and severity of skin involvement: reconstitution of skin fibrosis development using a tissue engineering approach

An autoimmune myositis-overlap syndrome associated with autoantibodies to nuclear pore complexes: description and long-term follow-up of the anti-Nup syndrome

Etiology-Specific Endothelin-1 Clearance in Human Precapillary Pulmonary Hypertension

Novel classification of idiopathic inflammatory myopathies based on overlap syndrome features and autoantibodies: analysis of 100 French Canadian patients

Thromboembolism complicating the treatment of lupus anticoagulant hypoprothrombinemia syndrome

Autoantibodies and microvascular damage are independent predictive factors for the progression of Raynaud's phenomenon to systemic sclerosis: A twenty‐year prospective study of 586 patients, with validation of proposed criteria for early systemic sclerosis

Myositis with prominent B-cell aggregates causing shrinking lung syndrome in systemic lupus erythematosus: a case report

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