Editorial: A New Classification of Adult Autoimmune Myositis.

scientific article

Editorial: A New Classification of Adult Autoimmune Myositis. is …
instance of (P31):
editorialQ871232
scholarly articleQ13442814

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P356DOI10.1002/ART.40063
P698PubMed publication ID28382651

P50authorJean-Pierre RaynauldQ90067190
P2093author name stringJean-Luc Senécal
Yves Troyanov
P2860cites workHeterogeneity of autoantibodies in 100 patients with autoimmune myositis: insights into clinical features and outcomesQ33293736
Most patients with cancer-associated dermatomyositis have antibodies to nuclear matrix protein NXP-2 or transcription intermediary factor 1γ.Q33814323
Polymyositis and dermatomyositis (first of two parts)Q33911013
Polymyositis: an overdiagnosed entityQ34536136
Rituximab in the treatment of refractory adult and juvenile dermatomyositis and adult polymyositis: a randomized, placebo-phase trialQ34644962
Common and distinct clinical features in adult patients with anti-aminoacyl-tRNA synthetase antibodies: heterogeneity within the syndrome.Q34661961
The autoantibody repertoire: searching for orderQ35038302
Anti-signal recognition particle autoantibodies: marker of a necrotising myopathyQ35638565
An autoimmune myositis-overlap syndrome associated with autoantibodies to nuclear pore complexes: description and long-term follow-up of the anti-Nup syndromeQ36150817
Redefining dermatomyositis: a description of new diagnostic criteria that differentiate pure dermatomyositis from overlap myositis with dermatomyositis featuresQ36150826
Novel classification of idiopathic inflammatory myopathies based on overlap syndrome features and autoantibodies: analysis of 100 French Canadian patientsQ36190260
Clinical Spectrum Time Course in Anti Jo-1 Positive Antisynthetase Syndrome: Results From an International Retrospective Multicenter Study.Q36195131
Anti-Melanoma Differentiation-Associated Gene 5 Is Associated With Rapidly Progressive Lung Disease and Poor Survival in US Patients With Amyopathic and Myopathic DermatomyositisQ36893955
Anti-melanoma differentiation-associated protein 5-associated dermatomyositis: expanding the clinical spectrum.Q36947409
Number, characteristics, and classification of patients with dermatomyositis seen by dermatology and rheumatology departments at a large tertiary medical centerQ36965164
Predictors of clinical improvement in rituximab-treated refractory adult and juvenile dermatomyositis and adult polymyositisQ37704799
Correlation of clinicoserologic and pathologic classifications of inflammatory myopathies: study of 178 cases and guidelines for diagnosisQ37726608
Acquired immune and inflammatory myopathies: pathologic classificationQ37936148
A Comprehensive Overview on Myositis-Specific Antibodies: New and Old Biomarkers in Idiopathic Inflammatory Myopathy.Q38596370
The Clinical Features of Myositis-Associated Autoantibodies: a ReviewQ38603422
Immune-Mediated Necrotizing Myopathy: Update on Diagnosis and ManagementQ38619882
Statin-Associated Autoimmune MyopathyQ38737361
Autoantigens as Partners in Initiation and Propagation of Autoimmune Rheumatic Diseases.Q38747090
High risk of cancer in autoimmune necrotizing myopathies: usefulness of myositis specific antibody.Q40795767
2016 American College of Rheumatology/European League Against Rheumatism Criteria for Minimal, Moderate, and Major Clinical Response in Adult Dermatomyositis and Polymyositis: An International Myositis Assessment and Clinical Studies Group/PaediatriQ46815762
American College of Rheumatology. Preliminary definition of improvement in rheumatoid arthritisQ47643186
Autoantibody levels in myositis patients correlate with clinical response during B cell depletion with rituximab.Q52861037
Nuclear actin aggregation is a hallmark of anti-synthetase syndrome-induced dysimmune myopathy.Q52868984
Inflammatory Muscle DiseasesQ55953708
119th ENMC international workshop: Trial design in adult idiopathic inflammatory myopathies, with the exception of inclusion body myositis, 10–12 October 2003, Naarden, The NetherlandsQ57752724
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 sclQ58160729
A novel autoantibody to a 155-kd protein is associated with dermatomyositisQ58490778
P433issue5
P304page(s)878-884
P577publication date2017-04-06
P1433published inArthritis & RheumatologyQ4797636
P1476titleEditorial: A New Classification of Adult Autoimmune Myositis.
P478volume69

Reverse relations

cites work (P2860)
Q48285249Anti-aminoacyl-tRNA synthetase-related myositis and dermatomyositis: clues for differential diagnosis on muscle biopsy.
Q91059371Classification and management of adult inflammatory myopathies
Q54977148Current Classification and Management of Inflammatory Myopathies.
Q47235167Describing and expanding the clinical phenotype of anti-MDA5-associated rapidly progressive interstitial lung disease: case series of nine Canadian patients and literature review
Q52628910Immune-Mediated Necrotizing Myopathy.
Q55277507New Myositis Classification Criteria-What We Have Learned Since Bohan and Peter.
Q41111946RIG-I expression in perifascicular myofibers is a reliable biomarker of dermatomyositis
Q57814497Seronegative patients form a distinctive subgroup of immune-mediated necrotizing myopathy
Q92155590Statin-Associated Necrotizing Autoimmune Myositis Complicated by an Uncommon Adverse Effect to Treatment
Q92501690Statin-induced anti-HMGCR myopathy: successful therapeutic strategies for corticosteroid-free remission in 55 patients
Q64275961The PRINTO evidence-based proposal for glucocorticoids tapering/discontinuation in new onset juvenile dermatomyositis patients
Q59798184The Utilization of Autoantibodies in Approaches to Precision Health

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