Recognizing Early Seizures After Stroke Is Crucial
This study looked at how to recognize early seizures that can happen after a stroke, focusing on adults who had either an ischemic stroke or a type of bleeding in the brain.
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Understanding Epilepsy in Dentatorubral-Pallidoluysian Atrophy Patients
This study looked at epilepsy in people with a rare genetic condition called dentatorubral-pallidoluysian atrophy (DRPLA).
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Epilepsy Research Summaries | Genetics | Imaging & EEG | New Studies | Pediatrics | 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.
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Drug-Resistant Epilepsy | Epilepsy Research Summaries | Imaging & EEG | New Studies | Safety & First Aid
SEEG Improves Epilepsy Surgery Outcomes with Expert Care
Researchers studied the use of stereoelectroencephalography (SEEG) in patients with drug-resistant focal epilepsy.
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SEEG and SDE Are Safe Options for Seizure Localization
Researchers studied two methods used to monitor brain activity in people with epilepsy: stereoelectroencephalography (SEEG) and subdural electrodes (SDE).
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AI Models Predict Seizure Control in New Epilepsy Patients
This study focused on how artificial intelligence (AI) can help predict how well people with epilepsy will respond to their first two antiseizure medications (ASMs).
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Glymphatic System Dysfunction Linked to Memory Issues in Epilepsy
This study looked at how the glymphatic system, which helps clear waste from the brain, functions in different types of temporal lobe epilepsy (TLE).
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Devices & Neuromodulation | Epilepsy Research Summaries | Genetics | Imaging & EEG | New Studies | Pediatrics
Understanding Genetic Factors in Pediatric Epilepsy and Movement Disorders
This study looked at children with epilepsy and movement disorders, known as EPIMDs, to better understand their genetic causes and how these conditions present.
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New Genetic Link Found for Developmental Epileptic Encephalopathies
Researchers studied a gene called BAIAP2 to understand its role in developmental and epileptic encephalopathies (DEEs), which are severe forms of epilepsy that can affect a child’s development.
