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It was first described in the Journal of Physiology-Paris by Sikiri and colleagues in 1993

[] Additionally, the ESPEN guidelines state that high-dose parenteral glutamine should not be administered to critically ill patients with AKI, especially in the form of alanyl-glutamine because it can be harmful

(2015) conducted a meta-analysis of 6 randomized controlled trials involving Cerebrolysin in Alzheimer's disease, finding statistically significant improvements in global clinical outcomes and cognitive measures at 24 weeks (PMID: 25832905) Cochrane Systematic Review: Cui et al

A., Wilson, M

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