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Andaleeb Sajid, Yale University, United States Updates Copyright 2020 Nair and Jain

20,77,78 An association between the 11778 mutation in LHON and a demyelinating syndrome that is radiologically and clinically identical to multiple sclerosis was described in 1992 and named Harding syndrome after the reporting author

10.1007/s11064-024-04132-w [DOI] [PMC free article] [PubMed] [Google Scholar] Zhao M, Zhou Y, Sheng R, Zhang H, Xiang J, Wang J, Li P, Ma T, Liu P, Chen Q, Wen W, Xu S (2024b) Gastrodin relieves Parkinsons disease-related motor deficits by facilitating the MEK-dependent VMAT2 to maintain dopamine homeostasis

By decomposing H 2 O 2 , MnO 2 can catalyze the production of O 2 , displaying enhanced CAT-like activity

Response wise Wilcoxon rank sum tests were used as post hoc tests for the Kruskal-Wallis tests