ReviewEpileptic disorders : international epilepsy journal with videotape2016
The history of progressive myoclonus epilepsies.
Review in Epileptic disorders : international epilepsy journal with videotape, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
14 citing papers in PubMed.
- When gene replacement becomes a double-edged sword: Guardrails for precision neurotherapeutics in Lafora disease.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026Article
- Assessing the diagnostic performance of investigations in pediatric myoclonic epilepsies: A retrospective cohort study.Epilepsia · 2025Article
- Myoclonus: Differential diagnosis and current management.Epilepsia open · 2024Review
- History of familial adult myoclonus epilepsy/benign adult familial myoclonic epilepsy around the world.Epilepsia · 2023Article
- A novelFrontiers in genetics · 2023Article
- Article
- Adult-onset Krabbe disease presenting with progressive myoclonic epilepsy and asymmetric occipital lesions: A case report.Frontiers in neurology · 2022Article
- A novel homozygous splice-site mutation in SCARB2 is associated with progressive myoclonic epilepsy with renal failure.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021Article
- Article
- Reversing Accumulation of Polyglucosan Bodies by Virally Delivered CRISPR/Cas9 Genome Editing.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2021Article
- Novel Truncating and Missense Variants inFrontiers in cell and developmental biology · 2021Article
- Drug Treatment of Progressive Myoclonic Epilepsy.Paediatric drugs · 2020Review
- Review
- Progressive Myoclonic Epilepsy Due to Lafora Body Disease with a Novel Mutation.Journal of pediatric neurosciencesArticle
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
The history of the progressive myoclonus epilepsies (PMEs) spans more than a century. However, the recent history of PMEs begins with a consensus statement published in the wake of the Marseille PME workshop in 1989 (Marseille Consensus Group, 1990). This consensus helped define the various types of PME known at the time and set the agenda for a new era of genetic research which soon lead to the discovery of many PME genes. Prior to the Marseille meeting, and before the molecular era, there had been much confusion and controversy. Because investigators had but limited and biased experience with these rare disorders due to the uneven, skewed distribution of PMEs around the world, opinions and nosologies were based on local expertise which did not match well with the experiences of other researchers and clinicians. The three major areas of focus included: (1) the nature and limits of the concept of PME in varying scopes, which was greatly debated; (2) the description of discrete clinical entities by clinicians; and (3) the description of markers (pathological, biological, neurophysiological, etc.) which could lead to a precise diagnosis of a given PME type, with, in the best cases, a reliable correlation with clinical findings. In this article, we shall also examine the breakthroughs achieved in the wake of the 1989 Marseille meeting and recent history in the field, following the identification of several PME genes. As in other domains, the molecular and genetic approach has challenged some established concepts and has led to the description of new PME types. However, as may already be noted, this approach has also confirmed the existence of the major, established types of PME, which can now be considered as true diseases.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.