Update on the Diagnostic and Therapeutic Landscape of Sporadic Inclusion Body Myositis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical)
Link
https://link.springer.com/content/pdf/10.1007/s11940-021-00681-5.pdf
Reference36 articles.
1. Keshishian A, Greenberg SA, Agashivala N, Baser O, Johnson K. Health care costs and comorbidities for patients with inclusion body myositis. Curr Med Res Opin. 2018;34:1679–85.
2. Callan A, Capkun G, Vasanthaprasad V, Freitas R, Needham M. A systematic review and meta-analysis of prevalence studies of sporadic inclusion body myositis. J Neuromuscul Dis. 2017;4(2):127–37. https://doi.org/10.3233/JND-160198.
3. Dobloug GC, Antal EA, Sveberg L, Garen T, Bitter H, Stjärne J, et al. High prevalence of inclusion body myositis in Norway; a population-based clinical epidemiology study. Eur J Neurol. 2015;22(4):672–e41. https://doi.org/10.1111/ene.12627 Epub 2014 Dec 21.
4. Needham M, James I, Corbett A, Day T, Christiansen F, Phillips B, et al. Sporadic inclusion body myositis: phenotypic variability and influence of HLA- DR3 in a cohort of 57 Australian cases. J Neurol Neurosurg Psychiatry. 2008;79:1056–60.
5. Cox FM, Verschuuren JJ, Verbist BM, Niks EH, Wintzen AR, Badrising UA. Detecting dysphagia in inclusion body myositis. J Neurol. 2009;256(12):2009–13. https://doi.org/10.1007/s00415-009-5229-9.
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