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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1899 2
1945 6
1946 18
1947 15
1948 23
1949 15
1950 33
1951 24
1952 35
1953 46
1954 39
1955 43
1956 42
1957 48
1958 43
1959 56
1960 43
1961 42
1962 57
1963 101
1964 110
1965 85
1966 80
1967 92
1968 99
1969 103
1970 125
1971 128
1972 126
1973 118
1974 130
1975 118
1976 96
1977 141
1978 116
1979 131
1980 117
1981 115
1982 131
1983 147
1984 139
1985 167
1986 157
1987 154
1988 192
1989 200
1990 177
1991 188
1992 199
1993 214
1994 225
1995 230
1996 221
1997 212
1998 220
1999 206
2000 241
2001 240
2002 273
2003 243
2004 255
2005 280
2006 277
2007 280
2008 321
2009 331
2010 329
2011 376
2012 421
2013 361
2014 417
2015 382
2016 467
2017 434
2018 470
2019 487
2020 546
2021 579
2022 575
2023 529
2024 459
2025 129

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14,668 results

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Page 1
An overview of polymyositis and dermatomyositis.
Findlay AR, Goyal NA, Mozaffar T. Findlay AR, et al. Muscle Nerve. 2015 May;51(5):638-56. doi: 10.1002/mus.24566. Muscle Nerve. 2015. PMID: 25641317 Free article. Review.
Polymyositis and dermatomyositis are inflammatory myopathies that differ in their clinical features, histopathology, response to treatment, and prognosis. ...In this review we address the current knowledge of the epidemiology, clinical characteristics, diagnostic evaluatio …
Polymyositis and dermatomyositis are inflammatory myopathies that differ in their clinical features, histopathology, response to trea …
Polymyositis and dermatomyositis.
Dalakas MC, Hohlfeld R. Dalakas MC, et al. Lancet. 2003 Sep 20;362(9388):971-82. doi: 10.1016/S0140-6736(03)14368-1. Lancet. 2003. PMID: 14511932 Review.
On the basis of unique clinical, histopathological, immunological, and demographic features, they can be differentiated into three major and distinct subsets: dermatomyositis, polymyositis, and inclusion-body myositis. Use of new diagnostic criteria is essential to discrim …
On the basis of unique clinical, histopathological, immunological, and demographic features, they can be differentiated into three major and …
Current diagnosis and treatment of polymyositis and dermatomyositis.
Sasaki H, Kohsaka H. Sasaki H, et al. Mod Rheumatol. 2018 Nov;28(6):913-921. doi: 10.1080/14397595.2018.1467257. Epub 2018 May 9. Mod Rheumatol. 2018. PMID: 29669460 Review.
Idiopathic inflammatory myopathies (IIMs) are heterogeneous disorders that affect the skeletal muscles. Polymyositis, dermatomyositis, and inclusion body myositis are major IIM subsets. Immune-mediated necrotizing myopathy became recognized as a potentially new IIM subset. …
Idiopathic inflammatory myopathies (IIMs) are heterogeneous disorders that affect the skeletal muscles. Polymyositis, dermatomyositis …
Clinical and Radiological Features of Interstitial Lung Diseases Associated with Polymyositis and Dermatomyositis.
Palmucci S, Di Mari A, Cancemi G, Pennisi I, Mauro LA, Sambataro G, Sambataro D, Galioto F, Fazio G, Ferlito A, Pino F, Basile A, Vancheri C. Palmucci S, et al. Medicina (Kaunas). 2022 Nov 30;58(12):1757. doi: 10.3390/medicina58121757. Medicina (Kaunas). 2022. PMID: 36556960 Free PMC article. Review.
Polymyositis and dermatomyositis are autoimmune idiopathic systemic inflammatory diseases, characterized by various degrees of muscle inflammation and typical cutaneous lesions-the latter found in dermatomyositis. ...The interstitial lung disease occurs in one-third of …
Polymyositis and dermatomyositis are autoimmune idiopathic systemic inflammatory diseases, characterized by various degrees of muscle …
Polymyositis and dermatomyositis: ocular manifestations and potential sight-threatening complications.
Ruiz-Lozano RE, Velazquez-Valenzuela F, Roman-Zamudio M, Andrade-Leal SK, Rodriguez-Garcia A. Ruiz-Lozano RE, et al. Rheumatol Int. 2022 Jul;42(7):1119-1131. doi: 10.1007/s00296-021-05035-7. Epub 2021 Oct 21. Rheumatol Int. 2022. PMID: 34674015 Review.
Dermatomyositis (DM) and polymyositis (PM) are idiopathic inflammatory myopathies characterized by progressive, symmetric, mainly proximal muscle weakness. ...
Dermatomyositis (DM) and polymyositis (PM) are idiopathic inflammatory myopathies characterized by progressive, symmetric, mainly pro …
Measures 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-HAQ), Childhood Myositis Assessment Scale (CMAS), Myositis Disease Activity Assessment Tool (MDAAT), Disease Activity Score (DAS), Short Form 36 (SF-36), Child Health Questionnaire (CHQ), physician global damage, Myositis Damage Index (MDI), Quantitative Muscle Testing (QMT), Myositis Functional Index-2 (FI-2), Myositis Activities Profile (MAP), Inclusion Body Myositis Functional Rating Scale (IBMFRS), Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI), Cutaneous Assessment Tool (CAT), Dermatomyositis Skin Severity Index (DSSI), Skindex, and Dermatology Life Quality Index (DLQI).
Rider LG, Werth VP, Huber AM, Alexanderson H, Rao AP, Ruperto N, Herbelin L, Barohn R, Isenberg D, Miller FW. Rider LG, et al. Arthritis Care Res (Hoboken). 2011 Nov;63 Suppl 11(0 11):S118-57. doi: 10.1002/acr.20532. Arthritis Care Res (Hoboken). 2011. PMID: 22588740 Free PMC article. Review. No abstract available.
Subcutaneous Edema in Polymyositis and Dermatomyositis.
Yoshimi R, Nakajima H. Yoshimi R, et al. Intern Med. 2023;62(15):2161-2162. doi: 10.2169/internalmedicine.1199-22. Epub 2023 Aug 1. Intern Med. 2023. PMID: 37532512 Free PMC article. No abstract available.
Burkholderia-associated polymyositis.
Kumar S, Kumar N, Panda PK, Jandrasupalli KK. Kumar S, et al. BMJ Case Rep. 2024 Jan 16;17(1):e255782. doi: 10.1136/bcr-2023-255782. BMJ Case Rep. 2024. PMID: 38232996
A diagnosis of polymyositis can readily be made when there is a typical history of proximal muscle weakness together with clinical findings, and there is corroboratory evidence in the form of elevated creatine kinase lactate dehydrogenase, aldolase, and serum glutamic-oxal …
A diagnosis of polymyositis can readily be made when there is a typical history of proximal muscle weakness together with clinical fi …
Interstitial Lung Disease in Polymyositis and Dermatomyositis.
Long K, Danoff SK. Long K, et al. Clin Chest Med. 2019 Sep;40(3):561-572. doi: 10.1016/j.ccm.2019.05.004. Clin Chest Med. 2019. PMID: 31376891 Review.
The idiopathic inflammatory myopathies (IIMs), including polymyositis (PM) and dermatomyositis (DM), are autoimmune connective tissue diseases with variable degrees of muscle inflammation and systemic involvement. ...
The idiopathic inflammatory myopathies (IIMs), including polymyositis (PM) and dermatomyositis (DM), are autoimmune connective tissue …
Current Classification and Management of Inflammatory Myopathies.
Schmidt J. Schmidt J. J Neuromuscul Dis. 2018;5(2):109-129. doi: 10.3233/JND-180308. J Neuromuscul Dis. 2018. PMID: 29865091 Free PMC article. Review.
Inflammatory disorders of the skeletal muscle include polymyositis (PM), dermatomyositis (DM), (immune mediated) necrotizing myopathy (NM), overlap syndrome with myositis (overlap myositis, OM) including anti-synthetase syndrome (ASS), and inclusion body myositis (IBM). .. …
Inflammatory disorders of the skeletal muscle include polymyositis (PM), dermatomyositis (DM), (immune mediated) necrotizing myopathy …
14,668 results
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