Case of anti-RuvBL1/2 antibody-positive morphea and polymyositis
Author:
Affiliation:
1. Department of Dermatology; Shiga University of Medical Science; Otsu Japan
2. Department of Dermatology; Graduate School of Medical Science; Kanazawa University; Kanazawa Japan
Publisher
Wiley
Subject
Dermatology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/1346-8138.13656/fullpdf
Reference5 articles.
1. 2013 classification criteria for systemic sclerosis: an American College of Rheumatology/European League against Rheumatism collaborative initiative;Hoogen;Arthritis Rheum,2013
2. Polymyositis and dermatomyositis (first of two parts);Bohan;N Engl J Med,1975
3. Linear scleroderma with prominent multiple lymphadenopathy followed by the development of polymyositis: a case report and review of published work;Takahashi;J Dermatol,2016
4. Autoantibodies to RuvBL1 and RuvBL2: a novel systemic sclerosis-related antibody associated with diffuse cutaneous and skeletal muscle involvement;Kaji;Arthritis Care Res (Hoboken),2014
5. Childhood-onset anti-ku antibody-positive generalized morphea with polymyositis: a Japanese Case Study;Kishi;Pediatr Dermatol,2015
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1. Anti-RuvBL1/2 Autoantibodies Detection in a Patient with Overlap Systemic Sclerosis and Polymyositis;Antibodies;2023-02-03
2. Anti-RuvBL1/2 autoantibodies in patients with systemic sclerosis or idiopathic inflammatory myopathy and a nuclear speckled pattern;Annals of the Rheumatic Diseases;2022-01-13
3. Bench to bedside review of myositis autoantibodies;Clinical and Molecular Allergy;2018-03-07
4. Presence of anti-eukaryotic initiation factor-2B, anti-RuvBL1/2 and anti-synthetase antibodies in patients with anti-nuclear antibody negative systemic sclerosis;Rheumatology;2017-12-22
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