Mitochondrial disorder should be considered as a differential of late-onset myasthenia gravis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s13760-020-01345-y.pdf
Reference5 articles.
1. Oliveira R, Landeiro L, Lauterbach M (2020) Very late onset of myasthenia gravis: case report and brief review of the literature. Acta Neurol Belg. https://doi.org/10.1007/s13760-020-01290-w
2. Finsterer J (2010) Mitochondrial disorder mimicking ocular myasthenia. Acta Neurol Belg 110:110–112
3. Kannaditharayil D, Napier F, Granit V, Bieri P, Herskovitz S (2017) Abnormal spontaneous activity on needle electromyography in myasthenia gravis. Muscle Nerve 56:E11–E12
4. Samuraki M, Furui E, Komai K, Takamori M, Yamada M (2007) Myasthenia gravis presenting with unusual neurogenic muscle atrophy. Muscle Nerve 36:394–399
5. Berrih-Aknin S (2014) Myasthenia Gravis: paradox versus paradigm in autoimmunity. J Autoimmun 52:1–28
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