New Genetic Variant Found in Rare Ataxia Disorder
This study looked at a rare genetic disorder called spinocerebellar ataxia type 13 (SCAR13) in two families from Pakistan.
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.
This study looked at the levels of a molecule called miR-155 in people with epilepsy compared to healthy individuals.
This study looked at how parents of children and youth with epilepsy (CYE) view their child’s cognitive abilities and how this affects their experiences with moving from pediatric to adult healthcare.
Researchers studied the effects of vitamin E as an additional treatment for epilepsy by reviewing 11 randomized controlled trials that included a total of 824 patients.
This study looked at four children who had mutations in a specific gene called BCKDK.
Researchers studied the effects of a new treatment called repetitive transcranial magnetic stimulation (rTMS) on dogs with drug-resistant epilepsy.