K Smirnov, T Stroganova, S Molholm… - International Journal of …, 2021 - mdpi.com
Rett syndrome (RTT) is a rare neurodevelopmental disorder that is usually caused by mutations of the MECP2 gene. Patients with RTT suffer from severe deficits in motor …
MA Robinson‐Agramonte, B Michalski… - Drug development …, 2021 - Wiley Online Library
Aberrant neural connectivity and intra‐cortical inhibitory dysfunction are key features of autism. Non‐invasive brain stimulation (NIBS) protocols have been proposed that modulate …
Mutations in the methyl-CpG binding protein 2 (MECP2) gene cause Rett syndrome (RTT), an X-linked neurodevelopmental disorder predominantly impacting females. MECP2 is an …
B Dönmez, K Erbakan, O Erbaş - Journal of Experimental and Basic …, 2021 - jebms.org
Autism spectrum disorder (ASD) is a heterogeneous neurodevelopmental disorder that is characterized by behavioral disorders including deficits in social conversations and …
The endocannabinoid system plays a complex role in synaptogenesis and the subsequent development of neural circuitry during fetal brain development. The cannabinoid receptor …
Down syndrome (DS) is the leading cause of genetically-defined intellectual disability. Additionally, DS individuals often present with increased susceptibility to epileptic seizures …
Aberrant neural connectivity and intra-cortical inhibitory dysfunction are key features of autism. Non-invasive brain stimulation (NIBS) protocols have been proposed that modulate …