Genetics

New genes with mutations for developmental disorders identified

The causes of intelligence impairment or epilepsy remain unexplained in more than 50% of cases. Together with international colleagues, researchers at Leipzig University Hospital have discovered two genes with mutations that ...

Neuroscience

New study reveals how the brain says 'oops!'

Researchers from Cedars-Sinai's Center for Neural Science and Medicine and Department of Neurosurgery have uncovered how signals from a group of neurons in the brain's frontal lobe simultaneously give humans the flexibility ...

Neuroscience

Zeroing in on a new treatment for autism and epilepsy

Children with Dravet syndrome, a severe form of epilepsy that begins in infancy, experience seizures, usually for their entire life. They are at high risk of sudden unexpected death in epilepsy (SUDEP) and can also develop ...

Neuroscience

Team identifies compound with potent antiseizure effects

Researchers studying epileptic seizures of the temporal lobe—the most common type of epilepsy—discovered a compound that reduces seizures in the hippocampus, a brain region where many such seizures originate. The compound, ...

Genetics

Potassium channel dysfunction in genetic epilepsy

Northwestern Medicine scientists have discovered functional links between dozens of potassium channel gene variants and neonatal epilepsy, according to a study published in JCI Insight.

Neuroscience

Harnessing the brain's plasticity to acquire epilepsy resilience

Around 1 percent of the world's population lives with epilepsy; yet only 65 percent of epilepsy patients can manage their symptoms with medication. Currently, surgically removing the lesion in the brain responsible for the ...

Neuroscience

New autism marker discovered in kids

Why do so many children with autism often suffer from epilepsy? Northwestern Medicine scientists have discovered an important brain protein that quiets overactive brain cells and is at abnormally low levels in children with ...

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