New Myositis Classification Criteria-What We Have Learned Since Bohan and Peter.

scientific article published on 17 March 2018

New Myositis Classification Criteria-What We Have Learned Since Bohan and Peter. is …
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scholarly articleQ13442814
review articleQ7318358

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P6179Dimensions Publication ID1101557100
P356DOI10.1007/S11926-018-0726-4
P932PMC publication ID5857275
P698PubMed publication ID29550929

P2093author name stringIngrid E Lundberg
Valérie Leclair
P2860cites workMeasures of adult and juvenile dermatomyositis, polymyositis, and inclusion body myositis: Physician and Patient/Parent Global Activity, Manual Muscle Testing (MMT), Health Assessment Questionnaire (HAQ)/Childhood Health Assessment Questionnaire (C-Q27021322
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A novel autoantibody to a 155-kd protein is associated with dermatomyositisQ58490778
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Would a new name hasten the acceptance of amyopathic dermatomyositis (dermatomyositis siné myositis) as a distinctive subset within the idiopathic inflammatory dermatomyopathies spectrum of clinical illness?Q77802015
Classification criteria for psoriatic arthritis: development of new criteria from a large international studyQ80001900
Classification criteria for rheumatic diseases: why and how?Q81377286
Combining MRI and muscle biopsy improves diagnostic accuracy in subacute-onset idiopathic inflammatory myopathyQ88013139
Classifying idiopathic inflammatory myopathies: comparing the performance of six existing criteriaQ95365536
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International consensus outcome measures for patients with idiopathic inflammatory myopathies. Development and initial validation of myositis activity and damage indices in patients with adult onset disease.Q35179618
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
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Comparative analyses of muscle MRI and muscular function in anti-synthetase syndrome patients and matched controls: a cross-sectional studyQ37604939
Idiopathic inflammatory myopathies and the anti-synthetase syndrome: a comprehensive reviewQ37674765
Correlation of clinicoserologic and pathologic classifications of inflammatory myopathies: study of 178 cases and guidelines for diagnosisQ37726608
Acquired immune and inflammatory myopathies: pathologic classificationQ37936148
The clinical phenotype associated with myositis-specific and associated autoantibodies: a meta-analysis revisiting the so-called antisynthetase syndromeQ38202468
Distinctions between diagnostic and classification criteria?Q38380153
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
Myositis-specific autoantibodies: an important tool to support diagnosis of myositisQ38646384
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Anti-HMGCR antibodies as a biomarker for immune-mediated necrotizing myopathies: A history of statins and experience from a large international multi-center studyQ38834515
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/PaediatriQ38849144
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The role of magnetic resonance imaging techniques in evaluation and management of the idiopathic inflammatory myopathies.Q39088767
State of the art on nailfold capillaroscopy in dermatomyositis and polymyositisQ39408875
Clinical manifestations and long-term outcome of anti-Jo1 antisynthetase patients in a large cohort of Spanish patients from the GEAS-IIM group.Q39800399
Testing for myositis specific autoantibodies: Comparison between line blot and immunoprecipitation assays in 57 myositis seraQ39975993
Inclusion body myositis: A distinct variety of idiopathic inflammatory myopathyQ40119689
A new approach to the classification of idiopathic inflammatory myopathy: myositis-specific autoantibodies define useful homogeneous patient groupsQ40743626
Computer-assisted analysis of 153 patients with polymyositis and dermatomyositisQ40783082
Classification criteria for the idiopathic inflammatory myopathiesQ41647350
Major histocompatibility complex class I antigen expression, immunolocalization of interferon subtypes, and T cell-mediated cytotoxicity in myopathiesQ45112924
2017 European League Against Rheumatism/American College of Rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups.Q47699498
2016 American College of Rheumatology/European League Against Rheumatism Criteria for Minimal, Moderate, and Major Clinical Response in Juvenile Dermatomyositis: An International Myositis Assessment and Clinical Studies Group/Paediatric RheumatologyQ47924181
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue4
P407language of work or nameEnglishQ1860
P921main subjectglobulinsQ321710
blood proteinsQ425056
myositisQ1433212
P5008on focus list of Wikimedia projectScienceSourceQ55439927
P304page(s)18
P577publication date2018-03-17
P1433published inCurrent Rheumatology ReportsQ23930052
P1476titleNew Myositis Classification Criteria-What We Have Learned Since Bohan and Peter.
P478volume20

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cites work (P2860)
Q96137016Assessment of Optimal Screening Tests for the Detection of an Inflammatory Myositis-associated Interstitial Lung Disease
Q92801301Increased Serum Matrix Metalloproteinase-9 Levels are Associated with Anti-Jo1 but not Anti-MDA5 in Myositis Patients
Q99630519Paraneoplastic dermatomyositis associated with metastatic leiomyosarcoma of unknown primary
Q98292008Role of Myokines in Myositis Pathogenesis and Their Potential to be New Therapeutic Targets in Idiopathic Inflammatory Myopathies
Q93164366The clinical phenotype associated with antisynthetase autoantibodies

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