"Myositis, Inclusion Body" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10)
Descriptor ID |
D018979
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MeSH Number(s) |
C05.651.594.600 C10.668.491.562.500
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Concept/Terms |
Myositis, Inclusion Body- Myositis, Inclusion Body
- Inclusion Body Myositides
- Myositides, Inclusion Body
- Inclusion Body Myositis
Inclusion Body Myopathy, Sporadic- Inclusion Body Myopathy, Sporadic
- Myositis, Inclusion Body, Sporadic
- Myopathy, Inclusion Body, Sporadic
- Inclusion Body Myositis, Sporadic
- Sporadic Inclusion Body Myositis
|
Below are MeSH descriptors whose meaning is more general than "Myositis, Inclusion Body".
Below are MeSH descriptors whose meaning is more specific than "Myositis, Inclusion Body".
This graph shows the total number of publications written about "Myositis, Inclusion Body" by people in this website by year, and whether "Myositis, Inclusion Body" was a major or minor topic of these publications.
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click here.
Year | Major Topic | Minor Topic | Total |
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1995 | 0 | 1 | 1 |
1996 | 4 | 0 | 4 |
1997 | 7 | 0 | 7 |
1998 | 5 | 0 | 5 |
1999 | 1 | 0 | 1 |
2000 | 5 | 1 | 6 |
2001 | 1 | 0 | 1 |
2002 | 2 | 0 | 2 |
2003 | 2 | 3 | 5 |
2004 | 3 | 1 | 4 |
2005 | 3 | 1 | 4 |
2006 | 2 | 2 | 4 |
2007 | 6 | 0 | 6 |
2008 | 2 | 0 | 2 |
2009 | 2 | 0 | 2 |
2010 | 3 | 0 | 3 |
2011 | 3 | 0 | 3 |
2012 | 2 | 0 | 2 |
2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Myositis, Inclusion Body" by people in Profiles.
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Dalakas MC. Autoimmune inflammatory myopathies. Handb Clin Neurol. 2023; 195:425-460.
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Scott AP, Laing NG, Mastaglia F, Dalakas M, Needham M, Allcock RJ. Investigation of NOTCH4 coding region polymorphisms in sporadic inclusion body myositis. J Neuroimmunol. 2012 Sep 15; 250(1-2):66-70.
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Schmidt J, Barthel K, Zschüntzsch J, Muth IE, Swindle EJ, Hombach A, Sehmisch S, Wrede A, Lühder F, Gold R, Dalakas MC. Nitric oxide stress in sporadic inclusion body myositis muscle fibres: inhibition of inducible nitric oxide synthase prevents interleukin-1ß-induced accumulation of ß-amyloid and cell death. Brain. 2012 Apr; 135(Pt 4):1102-14.
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Scott AP, Laing NG, Mastaglia F, Needham M, Walter MC, Dalakas MC, Allcock RJ. Recombination mapping of the susceptibility region for sporadic inclusion body myositis within the major histocompatibility complex. J Neuroimmunol. 2011 Jun; 235(1-2):77-83.
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Dalakas MC. Review: An update on inflammatory and autoimmune myopathies. Neuropathol Appl Neurobiol. 2011 Apr; 37(3):226-42.
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Dalakas MC. Pathophysiology of inflammatory and autoimmune myopathies. Presse Med. 2011 Apr; 40(4 Pt 2):e237-47.
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Sung RK, Ursell PC, Rame JE, Bailey H, Caleshu C, Nussbaum RL, Scheinman MM. QTc prolongation and family history of sudden death in a patient with desmin cardiomyopathy. Pacing Clin Electrophysiol. 2011 Dec; 34(12):e105-8.
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Dalakas MC. Inflammatory muscle diseases: a critical review on pathogenesis and therapies. Curr Opin Pharmacol. 2010 Jun; 10(3):346-52.
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Dalakas MC. Immunotherapy of myositis: issues, concerns and future prospects. Nat Rev Rheumatol. 2010 Mar; 6(3):129-37.
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Muth IE, Barthel K, Bähr M, Dalakas MC, Schmidt J. Proinflammatory cell stress in sporadic inclusion body myositis muscle: overexpression of alphaB-crystallin is associated with amyloid precursor protein and accumulation of beta-amyloid. J Neurol Neurosurg Psychiatry. 2009 Dec; 80(12):1344-9.