Structural brain MRI abnormalities in SCN1A-, SCN2A-, SCN3A-, and SCN8A-related epilepsies: a cohort study [PDF]
Frontiers in NeurologyPurposeTo characterize the prevalence and patterns of structural brain magnetic resonance imaging (MRI) abnormalities in children with genetically confirmed SCN1A-, SCN2A-, SCN3A-, or SCN8A-related epilepsy and to identify genotype-specific imaging ...
Daewoong Ahn +13 more
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Saudi Journal of Anaesthesia, 2022 Postoperative myoclonic movement (PMM) is an uncommon side effect after general anesthesia (GA), and the exact cause of this neurologic complication is still unknown.
Alaa Ali M. Elzohry +3 more
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Nonketotic hyperglycemia with epileptic seizure: one case report
Chinese Journal of Contemporary Neurology and Neurosurgery, 2021 doi：10.3969/j.issn.1672⁃6731.2021.12 ...
GAO Yu⁃tian +3 more
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Caring for Children with Dravet Syndrome: Exploring the Daily Challenges of Family Caregivers
Children, 2023 While Polish studies focus on the symptoms, causes and treatment of people suffering from Dravet syndrome (DS), much less is known about the situation of the family caregivers of DS children.
Jan Domaradzki, Dariusz Walkowiak
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Thalamic nuclei volumes and intrinsic thalamic network in patients with occipital lobe epilepsy
Brain and Behavior, 2023 Introduction This study aimed to investigate the alterations in individual thalamic nuclei volumes in patients with occipital lobe epilepsy (OLE) compared with those of healthy controls, and to analyze the intrinsic thalamic network based on these ...
Dong Ah Lee +2 more
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Transient lesion in the splenium of the corpus callosum and a sudden antiepileptic drugs withdrawal: A case with focal epilepsy in presurgical evaluation [PDF]
Vojnosanitetski Pregled, 2010 Introduction. A sudden withdrawal of antiepileptic drugs gives higher rate of epileptic seizures in the settings of video electroencephalography (vEEG), monitoring that is a subject to further registration and analysis.
Ristić Aleksandar +7 more
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Cessation of еpileptic seizures series using peroral valproate in an adult patient with partial epilepsy [PDF]
Vojnosanitetski Pregled, 2007 Introduction. Golden rule for the initiation of antiepileptic therapy in the majority of epileptic syndromes is "start low and go slow", a principle after the second unprovoked seizure. There are certain clinical situations however when fast titration of
Spasić Mirjana, Lukić Stevo
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Genetic generalized epilepsy and generalized onset seizures with focal evolution (GOFE)
Epilepsy & Behavior Reports, 2022 “Generalized Onset with Focal Evolution” (GOFE) is an underrecognized seizure type defined by an evolution from generalized onset to focal activity during the same ictal event. We aimed to discuss electroclinical aspects of GOFE and to emphasize its link
Florian Lamy +8 more
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Epilepsia Open, 2020 Mutations in SYNGAP1 are associated with developmental delay, epilepsy, and autism spectrum disorder (ASD). Epilepsy is often drug‐resistant in this syndrome with frequent drop attacks.
Mathieu Kuchenbuch +5 more
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Idiopathic and symptomatic forms of genetic epilepsy
Эпилепсия и пароксизмальные состояния, 2022 According to the new classification of the epilepsies proposed in 2017 by The International League Against Epilepsy, idiopathic epilepsies are recommended to refer to genetic epilepsy, suggesting to consider the term “idiopathic” as outdated.
A. G. Malov
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