Researchers studied a new tool called PredictMed-CDSS, which is designed to help predict the likelihood of developing neuromuscular hip dysplasia (NHD) in children with cerebral palsy (CP).
This study looked at children with a specific genetic condition called SYNGAP1-related developmental and epileptic encephalopathy (DEE), which causes severe developmental issues and epilepsy.
Researchers studied how well antiseizure medications (ASMs) work for people who have recently been diagnosed with focal epilepsy.
Researchers studied the connection between enlarged perivascular spaces (ePVS) in the brain and certain markers of epilepsy in patients undergoing a specific type of brain monitoring called stereo-electroencephalography (SEEG).
This study looked at 37 children who had changes in a specific part of their DNA called the 15q11.2 region.
This study looked at a rare genetic disorder called spinocerebellar ataxia type 13 (SCAR13) in two families from Pakistan.
Researchers studied how often unreported information about genetic changes, known as variants of uncertain significance (VUS), is found in children with epilepsy.
Researchers studied the effects of gamma rhythm stimulation, specifically at 40 Hz, on cognitive function in people with Alzheimer’s disease (AD).
This study looked at children with a condition called acute encephalopathy with biphasic seizures and late reduced diffusion (AESD), which can occur after infections.