Management/Treatment of Lambert-Eaton Myasthenic Syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical)
Link
https://link.springer.com/content/pdf/10.1007/s11940-021-00690-4.pdf
Reference77 articles.
1. •• Sanders DB, Juel VC, Harati Y, et al. 3,4-Diaminopyridine base effectively treats the weakness of Lambert-Eaton myasthenia. Muscle Nerve 2018;57:561–568. A randomized double-blind placebo-controlled withdrawal study that showed the efficacy of amifampridine in patients with LEMS.
2. Deenen JC, Horlings CG, Verschuuren JJ, Verbeek AL, van Engelen BG. The epidemiology of neuromuscular disorders: a comprehensive overview of the literature. Journal of neuromuscular diseases. 2015;2:73–85.
3. Abenroth DC, Smith AG, Greenlee JE, Austin SD, Clardy SL. Lambert-Eaton myasthenic syndrome: epidemiology and therapeutic response in the national veterans affairs population. Muscle Nerve. 2017;56:421–6.
4. Wirtz PW, van Dijk JG, van Doorn PA, et al. The epidemiology of the Lambert-Eaton myasthenic syndrome in the Netherlands. Neurology. 2004;63:397–8.
5. • Kesner VG, Oh SJ, Dimachkie MM, Barohn RJ. Lambert-Eaton myasthenic syndrome. Neurol Clin 2018;36:379–394. A review article discussing the history, epidemiology, clinical features, diagnosis, and management of LEMS.
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