A case of mixed hereditary gelsolin amyloidosis and hydroxychloroquine induced myopathy
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s13760-024-02607-9.pdf
Reference7 articles.
1. Kiuru-Enari A, Haltia M (2013) Hereditary gelsolin amyloidosis. Handb Clin Neurol 115:659–668. https://doi.org/10.1016/B978-0-444-52902-2.00039-4
2. Mustonen T, Schmidt EK, Valori M, Tienari PJ, Atula S et al (2018) Common origin of the gelsolin gene variant in 62 Finnish AGel amyloidosis families. Eur J Hum Genet Jan 26(1):117–123. https://doi.org/10.1038/s41431-017-0026-x
3. Namiranian D, Geisler S (2022) Neuromuscular complications of systemic amyloidosis. Am J Med Apr 135(Suppl 1). https://doi.org/10.1016/j.amjmed.2022.01.006. S13-S19
4. Margaretten M (2017) Neurologic manifestations of primary Sjogren syndrome. Rheum Dis Clin North Am Nov 43(4):519–529. https://doi.org/10.1016/j.rdc.2017.06.002
5. Biguetti CC, Junior JFS, Fiedler MW, Marrelli MT, Brotto M (2021) The toxic effects of chloroquine and hydroxychloroquine on skeletal muscle: a systematic review and meta-analysis. Sci Rep Mar 23(1):6589. https://doi.org/10.1038/s41598-021-86079-4
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