How Gene Changes Affect SSADH Deficiency Symptoms
Researchers looked at a rare inherited neurometabolic disorder called succinic semialdehyde dehydrogenase deficiency (SSADHD), which is caused by variants in the ALDH5A1 gene.
Researchers looked at a rare inherited neurometabolic disorder called succinic semialdehyde dehydrogenase deficiency (SSADHD), which is caused by variants in the ALDH5A1 gene.
Researchers tested whether a risk-stratified care pathway could be added to routine epilepsy care for adults who also had clinically relevant symptoms of depression or anxiety.
Researchers looked at whether turning vagus nerve stimulation (VNS) on or off changed brain blood flow-related measurements in people with drug-resistant epilepsy.
This paper was a systematic review, which means the authors gathered and summarized earlier studies rather than testing one new group of patients.
This study was a systematic review and meta-analysis.
This study looked at 31 children seen at one tertiary referral center in Kazakhstan for epilepsy or epilepsy-associated neurodevelopmental disorders who were found to have genetic findings considered clinically relevant or potentially relevant.
This study looked at whether epilepsy in children with autism spectrum disorder (ASD) was associated with results from neurologic evaluations, including EEG, brain imaging, genetic testing, and developmental assessments.
This case-control study looked at whether a brain-related immune area near the skull shows signs of activation in children with focal lesional epilepsy.
No abstract was provided, so there is not enough information to say what kind of study this was or who took part.