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Resting state EEG in young children with Tuberous Sclerosis Complex: associations with medications and seizures

Most Recent Articles: Journal of Neurodevelopmental Disorders

By: Caitlin C. Clements， Anne-Michelle Engelstad， Carol L. Wilkinson， Carly Hyde， Megan Hartney， Alexandra Simmons， Helen Tager-Flusberg， Shafali Jeste and Charles A. Nelson

18 January 2025 at 00:00

Tuberous Sclerosis Complex (TSC) is a rare genetic condition caused by mutation to TSC1 or TSC2 genes, with a population prevalence of 1/7000 births. TSC manifests behaviorally with features of autism, epilepsy, ...

Acute administration of NLX-101, a Serotonin 1A receptor agonist, improves auditory temporal processing during development in a mouse model of Fragile X Syndrome

Most Recent Articles: Journal of Neurodevelopmental Disorders

By: Xin Tao， Katilynne Croom， Adrian Newman-Tancredi， Mark Varney and Khaleel A. Razak

3 January 2025 at 00:00

Fragile X syndrome (FXS) is a leading known genetic cause of intellectual disability and autism spectrum disorders (ASD)-associated behaviors. A consistent and debilitating phenotype of FXS is auditory hyperse...