Progressive myoclonic epilepsy: myoclonic epilepsy and ataxia due to KCNC1 mutation (MEAK): a case report and review of the literature
Author:
Publisher
John Libbey Eurotext
Subject
Clinical Neurology,Neurology,General Medicine
Cited by 13 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Myoclonus improvement after seizures in progressive myoclonic epilepsy type 7: a case report;BMC Neurology;2024-05-23
2. Progressive myoclonic epilepsy as an expanding phenotype of NGLY1-associated congenital deglycosylation disorder: A case report and review of the literature;European Journal of Medical Genetics;2024-02
3. Myoclonus improvement after seizures in progressive myoclonic epilepsy type 7: a case report;2024-01-02
4. Epilepsies;Handbook of Clinical Neurology;2024
5. Potential Benefit of Channel Activators in Loss-of-Function Primary Potassium Channelopathies Causing Heredoataxia;The Cerebellum;2023-07-17
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