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Ram Kannan asserted that GSH passes through the BBB via Na-dependent GSH transporter in human cerebrovascular endothelial cells (HCBC) and Na-dependent GSH transporter exists in the luminal plasma membrane of HCEC (2000, Brain

Pyruvate kinase (PK) deficiency is a common autosomal recessive condition caused by a mutation of PKLR in combination with another mutation or PKLR polymorphism (Fig

These findings indicate that prasinezumab may possess disease-modifying potential in rapidly progressing PD, but its confirmatory efficacy and applicability to broader populations await validation in further clinical trials

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