Perampanel as a novel treatment for subcortical myoclonus in myoclonus-dystonia syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10072-023-06803-y.pdf
Reference17 articles.
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2. Obeso JA, Rothwell JC, Lang AE, Marsden CD (1983) Myoclonic dystonia. Neurology 33:825–830. https://doi.org/10.1212/WNL.33.7.825
3. Quinn NP (1996) Essential myoclonus and myoclonic dystonia. Mov Disord 11:119–124. https://doi.org/10.1002/MDS.870110202
4. Peall KJ, Kurian MA, Wardle M, Waite AJ, Hedderly T, Lin JP et al (2014) SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype. J Neurol 261:2296–2304. https://doi.org/10.1007/S00415-014-7488-3
5. Grabowski M, Zimprich A, Lorenz-Depiereux B, Kalscheuer V, Asmus F, Gasser T et al (2003) The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted. Eur J Hum Genet 11:138–144. https://doi.org/10.1038/SJ.EJHG.5200938
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1. Myoclonus: an update;Current Opinion in Neurology;2024-05-24
2. Improvement in Myoclonus–Dystonia Syndrome during Treatment with Gonadotropin‐Releasing Hormone Agonist;Movement Disorders Clinical Practice;2023-09-25
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