Surgery May Help Some Kids with SYNGAP1 Epilepsy
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.
Latest on EEG and imaging in epilepsy, how tests predict outcomes and guide treatment, all presented in plain English for normal people.
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.
Researchers studied the connection between enlarged perivascular spaces (ePVS) in the brain and certain markers of epilepsy in patients undergoing a specific type of brain monitoring called stereo-electroencephalography (SEEG).
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 four children who had mutations in a specific gene called BCKDK.
Researchers conducted a systematic review to explore how advanced imaging techniques can identify neuro-inflammatory biomarkers in people with epilepsy who do not respond to medication.
This study looked at how well ultra-high field 7T MRI works for children with drug-resistant focal epilepsy.
Researchers studied a method called transcranial temporal interference stimulation (tTIS) to see how it could help people with neurological and psychiatric disorders.
This study focused on a genetic variant in a gene called CCDC82 and its link to neurodevelopmental disorders, particularly in a young boy with serious health issues.
This study focused on children with tuberous sclerosis complex (TSC) who experience epilepsy.