Children with epilepsy have a higher risk of also having autism spectrum disorder (ASD). A new study in Developmental ...
Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder is a rare, genetically determined developmental and epileptic encephalopathy characterized by early-onset refractory seizures and severe ...
Gene editing can repair a DNA error in mice that causes Dravet syndrome, a rare, incurable, and potentially deadly form of ...
The prevalence of ASD is higher in children with epilepsy, and co-occurring ASD in epilepsy is associated with an elevated rate of intellectual disability.
The purpose of the CNC Epilepsy and Epilepsy Disorders Pillar is to foster collaborative research projects between basic and clinical scientists that will lead to better and improved approaches for ...
CORPUS CHRISTI, Texas — National Epilepsy Awareness Month isn't until November, but the Epilepsy Foundation of Central and South Texas (EFCST) are getting a head start. The Purple Pumpkin Project is ...
ORLANDO — Sleep disorders in people with epilepsy are linked to a significantly higher risk for sudden unexplained death in epilepsy (SUDEP) and all-cause mortality, new research shows. Marion Lazaj, ...
Researchers demonstrated that individuals who had childhood epilepsy have an increased accumulation of brain amyloid later in life, potentially predisposing them to late-onset brain amyloid disorders, ...
In a large-scale study of electronic health records investigators determined the prevalence of functional seizures and characterized comorbidities associated with them. Functional seizures are sudden ...
Families, friends and advocates will come together on Saturday for Midland's 19th annual Stroll for Epilepsy.
CMP-002 administration resulted in a statistically significant improvement in seizure phenotypes and parameters in a SYNGAP1 haploinsufficient mouse model Results build upon prior preclinical evidence ...
Gina Dewald’s unique experience as a mother helps her connect with families expecting medically complex children.