The DOI matches its Crossref record.
Deciphering the Clinical Presentations, Pathogenesis, and Treatment of the Idiopathic Inflammatory Myopathies
Open accessAbstract
The idiopathic inflammatory myopathies or myositis syndromes (the most common forms are polymyositis, dermatomyositis, and inclusion body myositis) are systemic autoimmune diseases defined by chronic muscle weakness and inflammation of unknown etiology and result in significant morbidity and mortality. Research suggests that categorizing heterogeneous myositis syndromes into mutually exclusive and stable phenotypes by using clinical and immune response features is useful for predicting clinical signs and symptoms, associated genetic and environmental risk factors, and responses to therapy and prognosis. Knowledge of myositis phenotypes should enhance clinicians' ability to recognize and manage these rare disorders.
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Citations
Cited by
Statin-Associated Autoimmune Myopathy
Mammen, A. L. (2016) · New England Journal of Medicine · doi:10.1056/nejmra1515161 · Cited by 366
The Myositis Autoantibody Phenotypes of the Juvenile Idiopathic Inflammatory Myopathies
Rider, L. G., Shah, M., Mamyrova, G., Huber, A. M., Rice, M. M., Targoff, I. N., & Miller, F. W. (2013) · Medicine · doi:10.1097/md.0b013e31829d08f9 · Cited by 288
Self-citationAn overview of polymyositis and dermatomyositis
Findlay, A. R., Goyal, N. A., & Mozaffar, T. (2015) · Muscle & Nerve · doi:10.1002/mus.24566 · Cited by 259
Metadata
- Authors
- Rider, L. G.
- Venue
- JAMA
- Publisher
- American Medical Association (AMA)
- Published
- 2011-01-12
- Volume
- 305
- Issue
- 2
- Pages
- 183
- ISSN
- 0002-9955 (ISSN-L)
- 0098-7484
- OpenAlex
- W2161967080
- Cited by
- 177
- References
- 0
- FWCI
- 8.00
- Type
- journal article
- Language
- en
- Open access
- green
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- Rider, L. G. (2011). Deciphering the Clinical Presentations, Pathogenesis, and Treatment of the Idiopathic Inflammatory Myopathies. JAMA. https://doi.org/10.1001/jama.2010.1977
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