Neuronal hyperexcitability: A key to unraveling hippocampal synaptic dysfunction in Lafora disease
Abstract Background and Objective: Lafora disease (LD) is a rare progressive disorder caused by mutations in the EPM2A or EPM2B…
Paolo Prontera
CDKL5 deficiency-related neurodevelopmental disorders: a multi-center cohort study in Italy
Abstract CDKL5 deficiency disorder (CDD) is a complex clinical condition resulting from non-functional or absent CDKL5 protein, a serine–threonine kinase…