Favorable outcome of COVID-19 infection in a patient with congenital myasthenic syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s10072-021-05057-w.pdf
Reference7 articles.
1. Guidon AC, Amato AA (2020) COVID-19 and neuromuscular disorders. Neurology 94(22):959–969. https://doi.org/10.1212/WNL.0000000000009566
2. Wolfe GI, Herbelin L, Nations SP, Foster B, Bryan WW, Barohn RJ (1999) Myasthenia gravis activities of daily living profile. Neurology 52(7):1487–1489. https://doi.org/10.1212/wnl.52.7.1487
3. Burns TM, Conaway M, Sanders DB, MG Composite and MG-QOL15 Study Group (2010) The MG composite: a valid and reliable outcome measure for myasthenia gravis. Neurology 74(18):1434–1440. https://doi.org/10.1212/WNL.0b013e3181dc1b1e
4. Alekseeva TM, Gavrilov YV, Kreis OA, Valko PO, Weber KP, Valko Y (2018) Fatigue in patients with myasthenia gravis. J Neurol 265(10):2312–2321. https://doi.org/10.1007/s00415-018-8995-4
5. Maggi L, Bernasconi P, D’Amico A et al (2019) Italian recommendations for diagnosis and management of congenital myasthenic syndromes. Neurol Sci 40(3):457–468. https://doi.org/10.1007/s10072-018-3682-x
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1. COVID-19 in a Cohort of Patients with Congenital Myasthenic Syndrome;Journal of Neuromuscular Diseases;2021-11-02
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