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doi: 10.1158/1078-0432.Ccr-22-2263 192 Beloueche-BabariMCasals GalobartTDelgado-GoniTWantuchSParkesHGTandyDet al

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

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

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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