Pediatric epilepsy research translated for parents into normal language, including summaries about diagnosis, treatments, school, safety, and safety.
This study looked at children with a specific genetic condition called SYNGAP1-related developmental and epileptic encephalopathy (DEE), which causes severe developmental issues and epilepsy.
This study looked at 37 children who had changes in a specific part of their DNA called the 15q11.2 region.
This study looked at a rare genetic disorder called spinocerebellar ataxia type 13 (SCAR13) in two families from Pakistan.
Researchers studied how often unreported information about genetic changes, known as variants of uncertain significance (VUS), is found in children with epilepsy.
This study looked at children with a condition called acute encephalopathy with biphasic seizures and late reduced diffusion (AESD), which can occur after infections.
This study looked at how parents of children and youth with epilepsy (CYE) view their child’s cognitive abilities and how this affects their experiences with moving from pediatric to adult healthcare.
Researchers studied the effects of vitamin E as an additional treatment for epilepsy by reviewing 11 randomized controlled trials that included a total of 824 patients.
This study looked at four children who had mutations in a specific gene called BCKDK.
A group of 22 experts from Nordic countries studied how to improve the use of Vagus Nerve Stimulation (VNS) therapy for people with drug-resistant epilepsy.