Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/3922
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dc.contributor.authorStevanovic, Galinaen_US
dc.contributor.authorJovic, Nebojsaen_US
dc.contributor.authorKecmanović, Miljanaen_US
dc.date.accessioned2020-12-09T17:29:33Z-
dc.date.available2020-12-09T17:29:33Z-
dc.date.issued2020-
dc.identifier.issn0042-8450-
dc.identifier.issn2406-0720-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/3922-
dc.description.abstractBackgrund/Aim. Lafora disease (LD) is progressive myoclonus epilepsy, characterized by intractable myoclonus and seizures, inevitable neurological deterioration, brutal cognitive decline and poor prognosis. The treatment still remains purely symptomatic. Recently, two single-case studies and one case series study reported the favourable effects of perampanel in LD. Our study aimed to test the benefits reported in three separate case studies. Methods. We performed an open label, prospective study of 4 patients aged between 22 and 34 years with mutation in NHLRC1 (EPM2B) gene, treated with perampanel (6–8 mg/day) as add-on therapy. Follow-up period comprised 14–26 months. Seizure frequency, myoclonus, functional disability and cognitive performance were analysed. Results. In 3 patients, both, seizures and myoclonus, showed remarkable improvement after the drug introduction (> 50% reduction). No significant effect was seen in one case. The functional and cognitive impairment maintained at the same level, though all patients were at the later stage of the disease. Psychiatric side effects were dose related. Conclusion. Our study supports the rare, previously reported observations that perampanel is beneficial in treating LD patients.en_US
dc.relation.ispartofVojnosanitetski pregleden_US
dc.relation.ispartofseries77 (5);539-544-
dc.subjectlafora diseaseen_US
dc.subjectdiagnosisen_US
dc.subjectanticolvusantsen_US
dc.subjectperampanelen_US
dc.subjecttreatment outcomeen_US
dc.titleIs adjunctive perampanel beneficial for lafora disease?en_US
dc.typeArticleen_US
dc.identifier.doi10.2298/VSP170416013S-
dc.description.rankM23-
dc.description.impact0.418-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.orcid0000-0002-0182-8817-
Appears in Collections:Journal Article
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