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• W2004995700 endingPage "248" @default.
• W2004995700 startingPage "239" @default.
• W2004995700 abstract "The progressive myoclonic epilepsies (PMEs) are a group of symptomatic generalised epilepsies caused by rare disorders, most of which have a genetic component, a debilitating course, and a poor outcome. Challenges with PME arise from difficulty with diagnosis, especially in the early stages of the illness, and further problems of management and drug treatment. Recent advances in molecular genetics have helped achieve better understanding of the different disorders that cause PME. We review the PMEs with emphasis on updated genetics, diagnosis, and therapeutic options." @default.
• W2004995700 created "2016-06-24" @default.
• W2004995700 creator A5029049310 @default.
• W2004995700 creator A5033042596 @default.
• W2004995700 creator A5064074861 @default.
• W2004995700 date "2005-04-01" @default.
• W2004995700 modified "2023-10-07" @default.
• W2004995700 title "Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects" @default.
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• W2004995700 doi "https://doi.org/10.1016/s1474-4422(05)70043-0" @default.
• W2004995700 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15778103" @default.
• W2004995700 hasPublicationYear "2005" @default.
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