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Six-Year Follow-Up of Dysphagia in Patients with Parkinson's Disease.
Wang P, Wang B, Chen X, Xiong B, Xie F, Wu S, Tang Y, Chen S, Ding X, Liu P, Luo W. Wang P, et al. Among authors: chen s, chen x. Dysphagia. 2022 Oct;37(5):1271-1278. doi: 10.1007/s00455-021-10387-0. Epub 2021 Nov 26. Dysphagia. 2022. PMID: 34826007
LRP10 in autosomal-dominant Parkinson's disease.
Chen Y, Cen Z, Zheng X, Pan Q, Chen X, Zhu L, Chen S, Wu H, Xie F, Wang H, Yang D, Wang L, Zhang B, Luo W. Chen Y, et al. Among authors: chen s, chen x. Mov Disord. 2019 Jun;34(6):912-916. doi: 10.1002/mds.27693. Epub 2019 Apr 9. Mov Disord. 2019. PMID: 30964957
Underestimated disease prevalence and severe phenotypes in patients with biallelic variants: A cohort study of primary familial brain calcification from China.
Chen S, Cen Z, Fu F, Chen Y, Chen X, Yang D, Wang H, Wu H, Zheng X, Xie F, Ouyang Z, Tang W, Zhang S, Yin L, Zhang Y, Meng P, Zhu X, Zhang H, Jiang F, Zhang K, He J, Zhang D, Ming H, Song D, Zhou Z, Luo Y, Gu Q, Su Y, Wu X, Tang H, Wu C, Chen W, Liu JY, Luo W; Chinese PFBC Study Group. Chen S, et al. Among authors: chen w, chen x, chen y. Parkinsonism Relat Disord. 2019 Jul;64:211-219. doi: 10.1016/j.parkreldis.2019.04.009. Epub 2019 Apr 11. Parkinsonism Relat Disord. 2019. PMID: 31003906
Intronic (TTTGA)n insertion in SAMD12 also causes familial cortical myoclonic tremor with epilepsy.
Cen Z, Chen Y, Yang D, Zhu Q, Chen S, Chen X, Wang B, Xie F, Ouyang Z, Jiang Z, Fu A, Hu B, Yin H, Qiu X, Yu F, Du X, Hao W, Liu Y, Wang H, Wang L, Yu X, Xiao Y, Liu C, Xiao J, Zhou Y, Yang W, Zhang B, Luo W. Cen Z, et al. Among authors: chen s, chen x, chen y. Mov Disord. 2019 Oct;34(10):1571-1576. doi: 10.1002/mds.27832. Epub 2019 Sep 4. Mov Disord. 2019. PMID: 31483537
Biallelic loss-of-function mutations in JAM2 cause primary familial brain calcification.
Cen Z, Chen Y, Chen S, Wang H, Yang D, Zhang H, Wu H, Wang L, Tang S, Ye J, Shen J, Wang H, Fu F, Chen X, Xie F, Liu P, Xu X, Cao J, Cai P, Pan Q, Li J, Yang W, Shan PF, Li Y, Liu JY, Zhang B, Luo W. Cen Z, et al. Among authors: chen s, chen x, chen y. Brain. 2020 Feb 1;143(2):491-502. doi: 10.1093/brain/awz392. Brain. 2020. PMID: 31851307
MYORG Mutation Heterozygosity Is Associated With Brain Calcification.
Chen Y, Cen Z, Chen X, Wang H, Chen S, Yang D, Fu F, Wang L, Liu P, Wu H, Zheng X, Xie F, Ouyang Z, Zhang Y, Zhou Y, Huang X, Wang F, Huang G, An H, Liang Y, Hong W, Wang A, Huang S, Chen W, Yin L, Yang Y, Huang H, Zeng R, Zhao N, Jiang B, Zhang B, Luo W; Chinese PFBC Study Group. Chen Y, et al. Among authors: chen s, chen w, chen x. Mov Disord. 2020 Apr;35(4):679-686. doi: 10.1002/mds.27973. Epub 2020 Jan 17. Mov Disord. 2020. PMID: 31951047
Altered Cerebello-Motor Network in Familial Cortical Myoclonic Tremor With Epilepsy Type 1.
Wang B, Wang J, Cen Z, Wei W, Xie F, Chen Y, Sun H, Hu Y, Yang D, Lou Y, Chen X, Ouyang Z, Chen S, Wang H, Wang L, Wang S, Qiu X, Ding Y, Yin H, Wu S, Zhang B, Zang YF, Luo W. Wang B, et al. Among authors: chen s, chen x, chen y. Mov Disord. 2020 Jun;35(6):1012-1020. doi: 10.1002/mds.28014. Epub 2020 Mar 4. Mov Disord. 2020. PMID: 32129927
Genetic profile of Chinese patients with Charcot-Marie-Tooth disease.
Ouyang ZY, Chen Y, Qin DQ, Cen ZD, Zheng XS, Xie F, Chen S, Wang HT, Yang DH, Chen XH, Wang LB, Zhang BR, Luo W. Ouyang ZY, et al. Chin Med J (Engl). 2020 Nov 5;133(21):2633-2634. doi: 10.1097/CM9.0000000000001095. Chin Med J (Engl). 2020. PMID: 32941234 Free PMC article. No abstract available.
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