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Page 1
The mutation spectrum of Parkinson-disease-related genes in early-onset Parkinson's disease in ethnic Chinese.
Chen YP, Yu SH, Zhang GH, Hou YB, Gu XJ, Ou RW, Shen Y, Song W, Chen XP, Zhao B, Cao B, Zhang LY, Sun MM, Liu FF, Wei QQ, Liu KC, Lin JY, Yang TM, Yang J, Wu Y, Jiang Z, Liu J, Cheng YF, Xiao Y, Su WM, Feng F, Cai YY, Li SR, Hu T, Yuan XQ, Zhou QQ, Shao N, Ma S, Shang HF. Chen YP, et al. Eur J Neurol. 2022 Nov;29(11):3218-3228. doi: 10.1111/ene.15509. Epub 2022 Aug 4. Eur J Neurol. 2022. PMID: 35861376
Epigenetic clocks in neurodegenerative diseases: a systematic review.
Yang T, Xiao Y, Cheng Y, Huang J, Wei Q, Li C, Shang H. Yang T, et al. Among authors: cheng y. J Neurol Neurosurg Psychiatry. 2023 Dec;94(12):1064-1070. doi: 10.1136/jnnp-2022-330931. Epub 2023 Mar 24. J Neurol Neurosurg Psychiatry. 2023. PMID: 36963821
Mutation screening of SPTLC1 and SPTLC2 in amyotrophic lateral sclerosis.
Li C, Hou Y, Wei Q, Lin J, Jiang Z, Jiang Q, Yang T, Xiao Y, Huang J, Cheng Y, Ou R, Liu K, Chen X, Song W, Zhao B, Wu Y, Cao B, Chen Y, Shang H. Li C, et al. Among authors: cheng y. Hum Genomics. 2023 Mar 25;17(1):28. doi: 10.1186/s40246-023-00479-3. Hum Genomics. 2023. PMID: 36966328 Free PMC article.
Risk factors of amyotrophic lateral sclerosis: a global meta-summary.
Duan QQ, Jiang Z, Su WM, Gu XJ, Wang H, Cheng YF, Cao B, Gao X, Wang Y, Chen YP. Duan QQ, et al. Front Neurosci. 2023 Apr 24;17:1177431. doi: 10.3389/fnins.2023.1177431. eCollection 2023. Front Neurosci. 2023. PMID: 37168926 Free PMC article.
32 results