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Epilepsy and Seizures: Archives News of the month

Recognising the neurological burden of onchocerciasis: the need to include onchocerciasis-associated epilepsy in onchocerciasis global health metrics

 Published on 02/04/2025 |  Original article (Abstract)  | Amaral Luís-Jorge et al. | Infectious Diseases of Poverty 2025; 14(1): 26

Using data from the 2021 Global Burden of Disease (GBD) study, Zhu and colleagues [1] assessed the prevalence and health burdens of vector-borne parasitic infectious diseases associated with poverty, revealed a statistically significant decrease in the overall burden of onchocerciasis since 1990. The...

Immunological factors in pediatric generalized and focal epilepsy: interplay with anti-seizure medications

 Published on 26/03/2025 |  Original article (Abstract)  | Zhang Dongyan et al. | BMC Pediatrics 2025; 25(1): 210

Epilepsy is a chronic neurological disorder characterized by an enduring predisposition to generate epileptic seizures, affecting approximately 50 million people worldwide, with a higher prevalence in pediatric populations [1, 2]. Pediatric epilepsy encompasses diverse seizure types, including generalized...

Adjunctive Brivaracetam in People with Epilepsy and Intellectual Disability: Evidence from the BRIVAracetam Add-On First Italian netwoRk Study

 Published on 19/03/2025 |  Original article (Abstract)  | Simona Lattanzi   et al. | Neurology and Therapy 2025; aop: 10.1007/s40120-025-00717-x

Epilepsies are among the most common chronic disorders of the brain and affect around 55 million people worldwide in absence of geographical, social, or racial boundaries [1]. In people with an intellectual disability, epilepsy is significantly more common than in the general population. Community-based...

Exploring the causal relationship between serum EFNB2 levels and epilepsy: a bidirectional Mendelian randomization and co-localization analysis

 Published on 12/03/2025 |  Original article (Abstract)  | Zhang Xudong et al. | BMC Neurology 2025; 25(1): 84

Epilepsy represents a severe neurological disorder that not only affects neural function but also significantly impedes cognitive and developmental progress, presenting considerable challenges for affected individuals and families globally [1]. Characterized by persistent seizures and profound neurodevelopmental...

Catatonia and Maintenance Electroconvulsive Therapy in a 15-Year-Old Patient With MED13L Haploinsufficiency Syndrome in the Context of Epilepsy Diathesis

 Published on 05/03/2025 |  Original article (Abstract)  | Ince, H.Yavuz MD et al. | Journal of ECT 2024; 40(3): 201-2

The MED13L gene encodes a component of the mediator complex, a group of proteins that operates as a transcriptional coactivator for the majority of genes transcribed by RNA polymerase II.1 It is implicated in the initial formation of the heart and brain.1 MED13L haploinsufficiency syndrome has been shown...