Conclusions: This study showed that amino acids may be involved in mechanisms underlying myasthenia gravis pathogenesis and may also be considered as potential indicators of certain pathways altered in myasthenia. However, given the multifactorial, heterogeneous and complex nature of this disease, further work with a larger study group is...

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Conclusions: The plasma myokine profile was significantly altered in patients with MG. FABP3 concentration may be useful in assessing disease severity and predicting the treatment response.

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Conclusions/Relevance: Adequate management of the newborn resulted in a positive outcome and evident withdrawal of the symptoms. Although TNMG is one of the rare neuromuscular disorders in newborns that can be treated, a multidisciplinary approach in the management of pregnant women with MG and newborns through timely diagnosis and early...

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Conclusions: The 10-year PRs of hereditary polyneuropathies, HD, MG, and inherited muscle diseases in young South Korean males have been reported. These data could be valuable to understanding each neuromuscular disease in the young male population of South Korea.

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Conclusions/Relevance: The substantial and durable improvements in HRQoL end points in this study demonstrate the broader benefit of treatment with efgartigimod beyond relief of immediate signs and symptoms of gMG.

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