Genetic Insights into Pyridoxine-Dependent Epilepsy in Children
Researchers studied six Chinese children diagnosed with pyridoxine-dependent epilepsy (PDE) to understand the clinical features and genetic changes related to this condition.
Researchers studied six Chinese children diagnosed with pyridoxine-dependent epilepsy (PDE) to understand the clinical features and genetic changes related to this condition.
Researchers studied a patient with severe muscle weakness, a condition known as arthrogryposis, and epilepsy that did not respond to treatment.
This study looked at how effective the ketogenic diet therapy (KDT) is for children with drug-resistant epilepsy caused by specific genetic mutations.
This study looked at the experiences of a child named Ethan who has Dravet syndrome, a severe form of epilepsy that starts in infancy.
This study focused on understanding the brain structure in a specific condition called focal cortical dysplasia (FCD), which is a common cause of epilepsy that does not respond well to medication.
This study looked at sudden unexpected death in epilepsy (SUDEP), which is a major cause of death related to epilepsy.
Researchers studied children with drug-resistant epilepsy (DRE) to find better ways to predict the success of epilepsy surgery.
This study looked at how effective cell therapy is in reducing seizures in animals that have chronic epilepsy.
Researchers studied the effectiveness and safety of two medications, levetiracetam (LEV) and phenobarbital (PB), for treating seizures in newborns.