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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 67
1955 72
1956 66
1957 76
1958 73
1959 81
1960 69
1961 73
1962 86
1963 155
1964 177
1965 141
1966 138
1967 166
1968 185
1969 180
1970 197
1971 213
1972 200
1973 195
1974 204
1975 191
1976 187
1977 223
1978 192
1979 203
1980 209
1981 209
1982 238
1983 269
1984 249
1985 260
1986 290
1987 284
1988 303
1989 350
1990 322
1991 311
1992 332
1993 373
1994 372
1995 380
1996 396
1997 356
1998 406
1999 371
2000 438
2001 468
2002 454
2003 447
2004 458
2005 518
2006 556
2007 553
2008 620
2009 645
2010 663
2011 751
2012 795
2013 749
2014 843
2015 821
2016 895
2017 962
2018 1004
2019 1085
2020 1218
2021 1399
2022 1465
2023 1330
2024 614

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28,040 results

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Page 1
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 wit …
Idiopathic inflammatory myopathy and non-coding RNA.
Yang Y, GuangXuan H, GenMeng W, MengHuan L, Bo C, XueJie Y. Yang Y, et al. Front Immunol. 2023 Sep 6;14:1227945. doi: 10.3389/fimmu.2023.1227945. eCollection 2023. Front Immunol. 2023. PMID: 37744337 Free PMC article. Review.
Idiopathic inflammatory myopathies (IIMs) are common autoimmune diseases that affect skeletal muscle quality and function. The lack of an early diagnosis and treatment can lead to irreversible muscle damage. Non-coding RNAs (ncRNAs) play an important role in infl …
Idiopathic inflammatory myopathies (IIMs) are common autoimmune diseases that affect skeletal muscle quality and function. The …
Idiopathic inflammatory myopathies: a review.
Ashton C, Paramalingam S, Stevenson B, Brusch A, Needham M. Ashton C, et al. Intern Med J. 2021 Jun;51(6):845-852. doi: 10.1111/imj.15358. Intern Med J. 2021. PMID: 34155760 Review.
Idiopathic inflammatory myopathy (IIM) is the umbrella term including dermatomyositis (DM), polymyositis (PM), overlap myositis (OM), sporadic inclusion body myositis (IBM) and necrotising autoimmune myopathy (NAM), also known as immune-m …
Idiopathic inflammatory myopathy (IIM) is the umbrella term including dermatomyositis (DM), polymyositis (PM), overlap …
Murine models of idiopathic inflammatory myopathy.
Konishi R, Ichimura Y, Okiyama N. Konishi R, et al. Immunol Med. 2023 Mar;46(1):9-14. doi: 10.1080/25785826.2022.2137968. Epub 2022 Oct 25. Immunol Med. 2023. PMID: 36282924 Review.
Idiopathic inflammatory myopathies (IIMs) are characterized by inflammation of muscles and other organs. ...To investigate the pathogenesis of IIMs, several animal models of experimental myositis have been established. Classical murine models of autoimmune …
Idiopathic inflammatory myopathies (IIMs) are characterized by inflammation of muscles and other organs. ...To investigate the …
A Comprehensive Overview on Myositis-Specific Antibodies: New and Old Biomarkers in Idiopathic Inflammatory Myopathy.
Satoh M, Tanaka S, Ceribelli A, Calise SJ, Chan EK. Satoh M, et al. Clin Rev Allergy Immunol. 2017 Feb;52(1):1-19. doi: 10.1007/s12016-015-8510-y. Clin Rev Allergy Immunol. 2017. PMID: 26424665 Free PMC article. Review.
Autoantibodies specific for idiopathic inflammatory myopathy (myositis-specific autoantibodies (MSAs)) are clinically useful biomarkers to help the diagnosis of polymyositis/dermatomyositis (PM/DM). ...Several recent studies suggested heterogeneity in …
Autoantibodies specific for idiopathic inflammatory myopathy (myositis-specific autoantibodies (MSAs)) are clini …
Development of a New Classification System for Idiopathic Inflammatory Myopathies Based on Clinical Manifestations and Myositis-Specific Autoantibodies.
Mariampillai K, Granger B, Amelin D, Guiguet M, Hachulla E, Maurier F, Meyer A, Tohmé A, Charuel JL, Musset L, Allenbach Y, Benveniste O. Mariampillai K, et al. JAMA Neurol. 2018 Dec 1;75(12):1528-1537. doi: 10.1001/jamaneurol.2018.2598. JAMA Neurol. 2018. PMID: 30208379 Free PMC article.
IMPORTANCE: Idiopathic inflammatory myopathies are heterogeneous in their pathophysiologic features and prognosis. ...CONCLUSIONS AND RELEVANCE: These findings suggest a classification of idiopathic inflammatory myopathies with 4 subgroups: dermatomyos …
IMPORTANCE: Idiopathic inflammatory myopathies are heterogeneous in their pathophysiologic features and prognosis. ...CONCLUSI …
International Guideline for Idiopathic Inflammatory Myopathy-Associated Cancer Screening: an International Myositis Assessment and Clinical Studies Group (IMACS) initiative.
Oldroyd AGS, Callen JP, Chinoy H, Chung L, Fiorentino D, Gordon P, Machado PM, McHugh N, Selva-O'Callaghan A, Schmidt J, Tansley SL, Vleugels RA, Werth VP; International Myositis Assessment and Clinical Studies Group Cancer Screening Expert Group; Aggarwal R. Oldroyd AGS, et al. Nat Rev Rheumatol. 2023 Dec;19(12):805-817. doi: 10.1038/s41584-023-01045-w. Epub 2023 Nov 9. Nat Rev Rheumatol. 2023. PMID: 37945774 Review.
Adult-onset idiopathic inflammatory myopathy (IIM) is associated with an increased cancer risk within the 3 years preceding and following IIM onset. ...
Adult-onset idiopathic inflammatory myopathy (IIM) is associated with an increased cancer risk within the 3 years prece …
[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. ...The different IIM have been classified according to thei …
Idiopathic inflammatory myopathies (IIM) are a heterogeneous group of acquired immune-mediated diseases, which typically invol …
Classification of idiopathic inflammatory myopathies: pathology perspectives.
Tanboon J, Nishino I. Tanboon J, et al. Curr Opin Neurol. 2019 Oct;32(5):704-714. doi: 10.1097/WCO.0000000000000740. Curr Opin Neurol. 2019. PMID: 31369423 Review.
PURPOSE OF REVIEW: Idiopathic inflammatory myopathies (IIM) are rare diseases with heterogenous clinicopathological features. ...RECENT FINDINGS: Considering clinicoseropathological features, IIM are suggestively classified into four major subgroups: dermatomyositis …
PURPOSE OF REVIEW: Idiopathic inflammatory myopathies (IIM) are rare diseases with heterogenous clinicopathological features. …
Molecular signature of neutrophil extracellular trap mediating disease module in idiopathic inflammatory myopathy.
Moon SJ, Jung SM, Baek IW, Park KS, Kim KJ. Moon SJ, et al. J Autoimmun. 2023 Jul;138:103063. doi: 10.1016/j.jaut.2023.103063. Epub 2023 May 22. J Autoimmun. 2023. PMID: 37220716
The rarity and heterogeneity of idiopathic inflammatory myopathy (IIM) pose challenges for researching IIM in affected individuals. ...A transcriptomic dataset of muscle tissues from normal controls (n = 105) and patients with dermatomyositis (n = 89), polymy …
The rarity and heterogeneity of idiopathic inflammatory myopathy (IIM) pose challenges for researching IIM in affected …
28,040 results
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