SCA10 Patients Show Brain Connectivity Changes and Atrophy
This study looked at people with spinocerebellar ataxia type 10 (SCA10), a rare genetic condition that affects movement and can cause seizures.
This study looked at people with spinocerebellar ataxia type 10 (SCA10), a rare genetic condition that affects movement and can cause seizures.
Researchers studied how certain genetic mutations in two proteins, KCNH1 and KCNH5, are linked to epilepsy and developmental disorders.
Researchers studied how children with movement disorders, specifically those with severe muscle stiffness (known as hypertonia), are evaluated before undergoing neurosurgery.
Researchers studied the use of a specific type of brain monitoring called thalamic stereoEEG in people with epilepsy.
Researchers studied the characteristics and risk factors for developing epilepsy in people who had autoimmune or infectious encephalitis.
The I-ACQUIRE Phase 3 trial studied infants and toddlers aged 8 to 36 months who had experienced perinatal arterial ischemic stroke, which can lead to movement difficulties and other disabilities.
Researchers studied 47 patients with drug-resistant temporal lobe epilepsy and hippocampal sclerosis who were undergoing surgery to help control their seizures.
Researchers studied the stigma faced by people living with epilepsy in Nigeria.
This study looked at the effects of a medication called cenobamate on young adults with tuberous sclerosis complex (TSC) who have epilepsy that does not respond to other treatments.