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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 2
2009 1
2010 1
2011 1
2013 1
2014 2
2015 4
2016 5
2017 4
2018 1
2019 3
2020 4
2021 4
2022 6
2023 2
2024 4

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Page 1
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.
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: ouyang z. Mov Disord. 2020 Apr;35(4):679-686. doi: 10.1002/mds.27973. Epub 2020 Jan 17. Mov Disord. 2020. PMID: 31951047
Familial recurrent Bell's palsy.
Qin D, Ouyang Z, Luo W. Qin D, et al. Among authors: ouyang z. Neurol India. 2009 Nov-Dec;57(6):783-4. doi: 10.4103/0028-3886.59478. Neurol India. 2009. PMID: 20139511 Free article.
37 results