Results 261 to 270 of about 174,824 (351)
Abstract Objective Developmental and epileptic encephalopathy type 1 (DEE1) is a rare drug‐resistant pediatric epilepsy caused by trinucleotide repeat expansions in the X‐linked ARX gene, leading to elongation of the first polyalanine tract. It presents with early onset tonic seizures or spasms, developmental and cognition delay, and high risk of ...
Lucia Verrillo +9 more
wiley +1 more source
Unveiling the role of local metabolic constraints on the structure and activity of spiking neural networks. [PDF]
Jaras I +3 more
europepmc +1 more source
Abstract Epilepsy affects approximately 1% of the population worldwide, and although medications are effective in the majority of cases, seizures persist in approximately 30% of patients. Despite the effort to develop new antiseizure drugs, the rate of pharmacoresistance in patients has not diminished over the past 3 decades. There is thus a real unmet
Vincent Magloire +9 more
wiley +1 more source
Pain Management with Natural Products: Neurophysiological Insights. [PDF]
Takeda M, Sashide Y.
europepmc +1 more source
Absence seizures and sleep–wake abnormalities in a rat model of GRIN2B neurodevelopmental disorder
Abstract Objective Pathogenic mutations in GRIN2B are an important cause of severe neurodevelopmental disorders resulting in epilepsy, autism, and intellectual disability. GRIN2B encodes the GluN2B subunit of N‐methyl‐d‐aspartate receptors (NMDARs), which are ionotropic glutamate receptors critical for normal development of the nervous system and ...
Katerina Hristova +12 more
wiley +1 more source
A noncanonical parasubthalamic nucleus-to-extended amygdala circuit converts chronic social stress into anxiety. [PDF]
Liu N +7 more
europepmc +1 more source
Deciphering SCN2A: A comprehensive review of rodent models of Scn2a dysfunction
Abstract SCN2A encodes for the alpha subunit of the voltage‐gated sodium channel NaV1.2, which is involved in action potential initiation and backpropagation in excitatory neurons. Currently, it is one of the highest monogenetic risk factors for both epilepsy and autism spectrum disorder.
Katelin E. J. Scott +2 more
wiley +1 more source
The postsynaptic density in excitatory synapses is composed of clustered, heterogeneous nanoblocks. [PDF]
Sun R +8 more
europepmc +1 more source
Abstract Objective Focal cortical dysplasia (FCD) is a developmental malformation of the cerebral cortex and a leading cause of drug‐resistant epilepsy in children and young adults. Disruption of the excitation–inhibition (E–I) balance is a hallmark of neuronal hyperexcitability in FCD, yet the underlying synaptic ultrastructural changes remain poorly ...
Gyu Hyun Kim +6 more
wiley +1 more source
MicroRNA-138-5p suppresses excitatory synaptic strength at the cerebellar input layer. [PDF]
Delvendahl I +6 more
europepmc +1 more source

