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

Year Number of Results
1838 1
1900 1
1903 3
1905 1
1907 1
1908 1
1910 3
1911 4
1912 3
1913 2
1915 1
1916 1
1917 3
1918 3
1920 1
1922 2
1923 3
1924 12
1925 2
1926 1
1927 1
1928 3
1930 1
1931 2
1932 4
1933 2
1934 2
1935 3
1936 5
1937 1
1939 1
1941 1
1945 8
1946 36
1947 39
1948 42
1949 33
1950 60
1951 63
1952 65
1953 65
1954 69
1955 72
1956 66
1957 76
1958 76
1959 81
1960 70
1961 74
1962 86
1963 155
1964 177
1965 141
1966 139
1967 166
1968 185
1969 181
1970 200
1971 213
1972 205
1973 199
1974 207
1975 202
1976 198
1977 231
1978 205
1979 219
1980 226
1981 220
1982 255
1983 288
1984 269
1985 283
1986 330
1987 330
1988 343
1989 402
1990 378
1991 394
1992 409
1993 469
1994 473
1995 489
1996 545
1997 503
1998 554
1999 543
2000 652
2001 699
2002 685
2003 733
2004 761
2005 874
2006 931
2007 957
2008 1068
2009 1159
2010 1170
2011 1282
2012 1387
2013 1397
2014 1528
2015 1573
2016 1660
2017 1808
2018 1811
2019 1896
2020 2205
2021 2461
2022 2469
2023 2247
2024 1756

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43,281 results

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Page 1
Inflammatory muscle disease - An update.
Baig S, Paik JJ. Baig S, et al. Best Pract Res Clin Rheumatol. 2020 Feb;34(1):101484. doi: 10.1016/j.berh.2019.101484. Epub 2020 Feb 8. Best Pract Res Clin Rheumatol. 2020. PMID: 32046904 Review.
Idiopathic inflammatory myopathies (IIM) are a heterogeneous group of inflammatory myopathies whose common feature is immune-mediated muscle injury. There are distinct subgroups including dermatomyositis (DM), polymyositis (PM), inclusion body myositis …
Idiopathic inflammatory myopathies (IIM) are a heterogeneous group of inflammatory myopathies whose common feature is immune-m …
Idiopathic inflammatory myopathies.
Lundberg IE, Fujimoto M, Vencovsky J, Aggarwal R, Holmqvist M, Christopher-Stine L, Mammen AL, Miller FW. Lundberg IE, et al. Nat Rev Dis Primers. 2021 Dec 2;7(1):86. doi: 10.1038/s41572-021-00321-x. Nat Rev Dis Primers. 2021. PMID: 34857798 Review.
Idiopathic inflammatory myopathies (IIM), also known as myositis, are a heterogeneous group of autoimmune disorders with varying clinical manifestations, treatment responses and prognoses. Muscle weakness is usually the classical clinical manifestation but ot …
Idiopathic inflammatory myopathies (IIM), also known as myositis, are a heterogeneous group of autoimmune disorders with varyi …
Joint and muscle inflammatory disease: A scoping review of the published evidence.
Lekieffre M, Gallay L, Landon-Cardinal O, Hot A. Lekieffre M, et al. Semin Arthritis Rheum. 2023 Aug;61:152227. doi: 10.1016/j.semarthrit.2023.152227. Epub 2023 May 13. Semin Arthritis Rheum. 2023. PMID: 37210805 Review.
Thirteen different diagnoses were found to associate myositis with polyarthritis: antisynthetase syndrome (29.6%, n=83), overlap myositis with rheumatoid arthritis (16.1%, n=45), drug-induced myositis (20.0%, n=56), rheumatoid myositis (7.5%, n=21), in …
Thirteen different diagnoses were found to associate myositis with polyarthritis: antisynthetase syndrome (29.6%, n=83), overlap m …
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 bo …
Inflammatory disorders of the skeletal muscle include polymyositis (PM), dermatomyositis (DM), (immune mediated) necrotizing m …
Classification and management of adult inflammatory myopathies.
Selva-O'Callaghan A, Pinal-Fernandez I, Trallero-Araguás E, Milisenda JC, Grau-Junyent JM, Mammen AL. Selva-O'Callaghan A, et al. Lancet Neurol. 2018 Sep;17(9):816-828. doi: 10.1016/S1474-4422(18)30254-0. Lancet Neurol. 2018. PMID: 30129477 Review.
Inflammatory myopathies, collectively known as myositis, are heterogeneous disorders characterised by muscle inflammation, and frequently accompanied by extramuscular manifestations that affect the skin, lung, and joints. ...Five main types of inflammatory …
Inflammatory myopathies, collectively known as myositis, are heterogeneous disorders characterised by muscle inflammati …
Immune-mediated necrotizing myopathy: clinical features and pathogenesis.
Allenbach Y, Benveniste O, Stenzel W, Boyer O. Allenbach Y, et al. Nat Rev Rheumatol. 2020 Dec;16(12):689-701. doi: 10.1038/s41584-020-00515-9. Epub 2020 Oct 22. Nat Rev Rheumatol. 2020. PMID: 33093664 Review.
Immune-mediated necrotizing myopathy (IMNM) is a group of inflammatory myopathies that was distinguished from polymyositis in 2004. ...IMNMs are frequently rapidly progressive and severe, displaying high serum creatine kinase levels, and failure to treat IMNMs effectively …
Immune-mediated necrotizing myopathy (IMNM) is a group of inflammatory myopathies that was distinguished from polymyositis in 2004. . …
Orbital Myositis: A Comprehensive Review and Reclassification.
McNab AA. McNab AA. Ophthalmic Plast Reconstr Surg. 2020 Mar/Apr;36(2):109-117. doi: 10.1097/IOP.0000000000001429. Ophthalmic Plast Reconstr Surg. 2020. PMID: 31261163 Review.
The commonest associated autoimmune condition is inflammatory bowel disease. Immunoglobulin G4-related ophthalmic disease often affects extraocular muscle. Drug reactions and rarely paraneoplastic disease may also cause extraocular muscle …
The commonest associated autoimmune condition is inflammatory bowel disease. Immunoglobulin G4-related ophthalmic disease …
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 Review.
Polymyositis and dermatomyositis are inflammatory myopathies that differ in their clinical features, histopathology, response to treatment, and prognosis. Although their clinical pictures differ, they both present with symmetrical, proximal muscle weakness. Treatmen …
Polymyositis and dermatomyositis are inflammatory myopathies that differ in their clinical features, histopathology, response to trea …
Classification of myositis.
Lundberg IE, de Visser M, Werth VP. Lundberg IE, et al. Nat Rev Rheumatol. 2018 May;14(5):269-278. doi: 10.1038/nrrheum.2018.41. Epub 2018 Apr 12. Nat Rev Rheumatol. 2018. PMID: 29651121 Review.
The idiopathic inflammatory myopathies (IIMs; also known as myositis) are a heterogeneous group of disorders in which a common feature is chronic inflammation of skeletal muscle, leading to muscle weakness. ...A new way of subgrouping patients could be …
The idiopathic inflammatory myopathies (IIMs; also known as myositis) are a heterogeneous group of disorders in which a common …
[Idiopathic inflammatory myopathies. A review].
Acosta I, Matamala JM, Jara P, Pino F, Gallardo A, Verdugo R. Acosta I, et al. Rev Med Chil. 2019 Mar;147(3):342-355. doi: 10.4067/S0034-98872019000300342. Rev Med Chil. 2019. PMID: 31344172 Free article. Review. Spanish.
Idiopathic inflammatory myopathies (IIM) are a heterogeneous group of acquired immune-mediated diseases, which typically involve the striated muscle with a variable involvement of the skin and other organs. Clinically, they are characterized by proximal muscle …
Idiopathic inflammatory myopathies (IIM) are a heterogeneous group of acquired immune-mediated diseases, which typically involve the …
43,281 results
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