Prominent mitochondrial pathology in a case of refractory dermatomyositis: coincidence or concause?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10072-023-07035-w.pdf
Reference11 articles.
1. Liang L, Zhang Y-M, Chen H, Ye L-F, Li S-S, Lu X et al (2020) Anti-Mi-2 antibodies characterize a distinct clinical subset of dermatomyositis with favourable prognosis. Eur J Dermatol. https://doi.org/10.1684/ejd.2020.3750
2. Alhatou MI, Sladky JT, Bagasra O, Glass JD (2004) Mitochondrial abnormalities in dermatomyositis: characteristic pattern of neuropathology. J Mol Histol 35:615–619. https://doi.org/10.1007/s10735-004-2194-6
3. Garibaldi M, Fionda L, Vanoli F, Leonardi L, Loreti S, Bucci E et al (2020) Muscle involvement in myasthenia gravis: expanding the clinical spectrum of Myasthenia-Myositis association from a large cohort of patients. Autoimmun Rev 19:102498. https://doi.org/10.1016/j.autrev.2020.102498
4. Kim H, Dill S, O’Brien M, Vian L, Li X, Manukyan M et al (2021) Janus kinase (JAK) inhibition with baricitinib in refractory juvenile dermatomyositis. Ann Rheum Dis 80:406–408. https://doi.org/10.1136/annrheumdis-2020-218690
5. Lundberg IE, Fujimoto M, Vencovsky J, Aggarwal R, Holmqvist M, Christopher-Stine L et al (2021) Idiopathic inflammatory myopathies. Nat Rev Dis Primers 7:86. https://doi.org/10.1038/s41572-021-00321-x
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