Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/86619
Full metadata record
DC FieldValueLanguage
dc.contributor.authorCrunelli, Vincenzo-
dc.contributor.authorLőrincz, Magor L.-
dc.contributor.authorMcCafferty, Cian P.-
dc.contributor.authorLambert, Régis C.-
dc.contributor.authorLeresche, Nathalie-
dc.contributor.authorDi Giovanni, Giuseppe-
dc.contributor.authorDavid, Francois-
dc.date.accessioned2022-01-10T13:42:17Z-
dc.date.available2022-01-10T13:42:17Z-
dc.date.issued2020-
dc.identifier.citationCrunelli, V., Lőrincz, M. L., McCafferty, C., Lambert, R. C., Leresche, N., Di Giovanni, G., & David, F. (2020). Clinical and experimental insight into pathophysiology, comorbidity and therapy of absence seizures. Brain, 143(8), 2341-2368.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar/handle/123456789/86619-
dc.description.abstractAbsence seizures in children and teenagers are generally considered relatively benign because of their non-convulsive nature and the large incidence of remittance in early adulthood. Recent studies, however, show that 30% of children with absence seizures are pharmaco-resistant and 60% are affected by severe neuropsychiatric comorbid conditions, including impairments in attention, cognition, memory and mood. In particular, attention deficits can be detected before the epilepsy diagnosis, may persist even when seizures are pharmacologically controlled and are aggravated by valproic acid monotherapy. New functional MRI-magnetoencephalography and functional MRI-EEG studies provide conclusive evidence that changes in blood oxygenation level-dependent signal amplitude and frequency in children with absence seizures can be detected in specific cortical networks at least 1 min before the start of a seizure, spike-wave discharges are not generalized at seizure onset and abnormal cortical network states remain during interictal periods. From a neurobiological perspective, recent electrical recordings and imaging of large neuronal ensembles with single-cell resolution in non-anaesthetized models show that, in contrast to the predominant opinion, cortical mechanisms, rather than an exclusively thalamic rhythmogenesis, are key in driving seizure ictogenesis and determining spike-wave frequency. [Excerpt from Abstract]en_GB
dc.language.isoenen_GB
dc.publisherOxford University Pressen_GB
dc.rightsinfo:eu-repo/semantics/openAccessen_GB
dc.subjectPetit mal epilepsy -- Treatmenten_GB
dc.subjectPetit mal epilepsy -- Drug therapyen_GB
dc.subjectPetit mal epilepsy -- Animal modelsen_GB
dc.subjectPetit mal epilepsy -- Alternative treatmenten_GB
dc.subjectBasal ganglia -- Pathophysiologyen_GB
dc.subjectLimbic systemen_GB
dc.titleClinical and experimental insight into pathophysiology, comorbidity and therapy of absence seizuresen_GB
dc.typearticleen_GB
dc.rights.holderThe copyright of this work belongs to the author(s)/publisher. The rights of this work are as defined by the appropriate Copyright Legislation or as modified by any successive legislation. Users may access this work and can make use of the information contained in accordance with the Copyright Legislation provided that the author must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the prior permission of the copyright holder.en_GB
dc.description.reviewedpeer-revieweden_GB
dc.identifier.doi10.1093/brain/awaa072-
dc.publication.titleBrainen_GB
Appears in Collections:Scholarly Works - FacM&SPB



Items in OAR@UM are protected by copyright, with all rights reserved, unless otherwise indicated.