Understanding Illness Perceptions in Epilepsy Across All Ages
This study looked at how people with epilepsy understand their illness and how these perceptions affect their health and emotions.
-
-
Epilepsy Research Summaries | Genetics | Imaging & EEG | Lifestyle & Sleep | Pediatrics | Recent Research
Suspect GNAO1 Gene Defect in Movement Disorders in Children
Researchers studied a 9-year-old girl with a rare movement disorder linked to a mutation in the GNAO1 gene.
-
Drug-Resistant Epilepsy | Epilepsy Research Summaries | Genetics | Ketogenic Diet | Pediatrics | Recent Research
Understanding Pediatric Epilepsy Challenges in Palestine
This study looked at pediatric epilepsy in Palestine, focusing on children aged 2 months to 18 years who were diagnosed between 2019 and 2024.
-
Suicidality Rates in Teens With New Focal Epilepsy
Researchers studied adolescents who were newly diagnosed with focal epilepsy to understand how often they experience thoughts of suicide, known as suicidality.
-
Suicidality Rates in Teens With New Focal Epilepsy
Researchers studied the mental health of adolescents who were newly diagnosed with focal epilepsy.
-
Drug-Resistant Epilepsy | Epilepsy Research Summaries | Genetics | Imaging & EEG | Pediatrics | Recent Research
Understanding Seizure Risks in Leukodystrophy Patients
This study looked at the occurrence of seizures and epilepsy in children diagnosed with leukodystrophies, which are rare brain disorders that affect the white matter of the brain.
-
High Risk of Epilepsy After Neonatal Seizures Found
A recent study from Sweden looked at the risk of developing epilepsy after infants experienced seizures shortly after birth.
-
Child Neurologists Need Better Training on Reproductive Health Counseling
This study looked at how child neurologists talk to female patients with epilepsy about reproductive health.
-
Epilepsy Research Summaries | Genetics | Imaging & EEG | Pediatrics | Recent Research | Status Epilepticus
Understanding Pyridoxine-Dependent Epilepsy in Newborns
Researchers studied a rare condition called Pyridoxine-Dependent Epilepsy (PDE), which is caused by changes in a gene known as ALDH7A1.
