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2020-1-CZ01-KA203-078218

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Severe myoclonic epilepsy of infancy (SMEI) or Dravet syndrome from one point of view may be classified as an idiopathic genetic disorder, since children are healthy and normally developed until onset of the epilepsy, and there is a clear genetic cause (usually a SCN1A defect) in the majority of cases

Glutathione reductase from Escherichia coli : cloning and sequence analysis of the gene and relationship to other flavoprotein disulfide oxidoreductases

Suppression of Alzheimer's disease-like pathology progression by mitochondria-targeted antioxidant SKQ1: a transcriptome profiling study

Mice of desired strains were age-matched and assigned randomly to their treatment groups