CLINICAL CONCEPT RECOGNITION: EVALUATION OF EXISTING SYSTEMS ON EHRS


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 along with delayed psychomotor development and heightened premature mortality.A primary monogenic cause is mutation of the SCN1A gene, which encodes the voltage-gated 8X LAUNDRY DETERGENT sodium channel subunit Nav1.1.The nature and timing of changes caused by SCN1A mut

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Recovery of iron after Fenton-like secondary treatment of olive mill wastewater by nano-filtration and low-pressure reverse osmosis membranes

In this work, the Horse Leads performances of novel nano-filtration (NF) and low-pressure reverse osmosis (RO) polymeric membranes were examined with the aim of recovering the iron used as catalyst in former secondary treatment based on the Fenton-like advanced oxidation of olive mill wastewater (OMW).Results highlight that both membranes exhibit a

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