DEVELOPMENT OF A HYBRID RECOMMENDATION SYSTEM FOR NFTS USING DEEP LEARNING TECHNIQUES


Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant Dravet Syndrome model during development

Dravet syndrome (DS) is characterized by severe infant-onset myoclonic epilepsy Accent Cabinet along with delayed psychomotor development and heightened premature mortality.A primary monogenic cause is mutation of the SCN1A gene, which encodes the voltage-gated sodium channel subunit Nav1.1.The nature and timing of changes caused by SCN1A mutation

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Nationwide safety surveillance of COVID-19 mRNA vaccines following primary series and first booster vaccination in Singapore

Background: The real-world safety profile of COVID-19 mRNA vaccines remains incompletely elucidated.Methods: We performed a nationwide post-market safety surveillance analysis in Singapore, on vacinees aged 5 years and older, through mid-September 2022.Observed-over-expected (O/E) analyses were performed to identify potential safety signals among e

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