Shi Y - Search Results

1

New Model for Estimation of the Age at Onset in Spinocerebellar Ataxia Type 3.

Peng L, Chen Z, Long Z, Liu M, Lei L, Wang C, Peng H, Shi Y, Peng Y, Deng Q, Wang S, Zou G, Wan L, Yuan H, He L, Xie Y, Tang Z, Wan N, Gong Y, Hou X, Shen L, Xia K, Li J, Chen C, Qiu R, Klockgether T, Tang B, Jiang H. Peng L, et al. Among authors: shi y. Neurology. 2021 Jun 8;96(23):e2885-e2895. doi: 10.1212/WNL.0000000000012068. Epub 2021 Apr 23. Neurology. 2021. PMID: 33893204

2

[Research progress in roles of microRNA in polyglutamine diseases].

Shi YT, Jiang H, Tang BS. Shi YT, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Aug;27(4):406-9. doi: 10.3760/cma.j.issn.1003-9406.2010.04.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20677146 Chinese.

3

A rare Von Hippel-Lindau disease that mimics acute myelitis: case report and review of the literature.

Jiang H, Shi YT, Wang JL, Tang BS, Wang JY, Peng ZF, Xiao DS. Jiang H, et al. Neurol Sci. 2011 Apr;32(2):305-7. doi: 10.1007/s10072-010-0413-3. Epub 2010 Oct 7. Neurol Sci. 2011. PMID: 20927563 Free PMC article. Review.

4

Serum concentrations of NSE and S100B in spinocerebellar ataxia type 3/Machado-Joseph disease.

Zhou J, Lei L, Shi Y, Wang J, Jiang H, Shen L, Tang B. Zhou J, et al. Among authors: shi y. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2011 Jun;36(6):504-10. doi: 10.3969/j.issn.1672-7347.2011.06.006. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2011. PMID: 21743141

5

Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias.

Wang JL, Cao L, Li XH, Hu ZM, Li JD, Zhang JG, Liang Y, San-A, Li N, Chen SQ, Guo JF, Jiang H, Shen L, Zheng L, Mao X, Yan WQ, Zhou Y, Shi YT, Ai SX, Dai MZ, Zhang P, Xia K, Chen SD, Tang BS. Wang JL, et al. Among authors: shi yt. Brain. 2011 Dec;134(Pt 12):3493-3501. doi: 10.1093/brain/awr289. Epub 2011 Nov 26. Brain. 2011. PMID: 22120146 Free PMC article.

6

Spinocerebellar ataxia type 28 (SCA28) is an uncommon cause of dominant ataxia among Chinese kindreds.

Jia D, Tang B, Chen Z, Shi Y, Sun Z, Zhang L, Wang J, Xia K, Jiang H. Jia D, et al. Among authors: shi y. Int J Neurosci. 2012 Oct;122(10):560-2. doi: 10.3109/00207454.2012.690796. Epub 2012 Jun 22. Int J Neurosci. 2012. PMID: 22563911

7

Spinocerebellar ataxia type 27 (SCA27) is an uncommon cause of dominant ataxia among Chinese Han population.

Chen Z, Li X, Tang B, Wang J, Shi Y, Sun Z, Zhang L, Pan Q, Xia K, Jiang H. Chen Z, et al. Among authors: shi y. Neurosci Lett. 2012 Jun 27;520(1):16-9. doi: 10.1016/j.neulet.2012.05.008. Epub 2012 May 11. Neurosci Lett. 2012. PMID: 22579694

8

Spinocerebellar ataxia type 23 is an uncommon SCA subtype in the Chinese Han population.

Liu YT, Tang BS, Wang JL, Guan WJ, Shen L, Shi YT, Zhou Y, Yan XX, Xia K, Jiang H. Liu YT, et al. Among authors: shi yt. Neurosci Lett. 2012 Oct 18;528(1):51-4. doi: 10.1016/j.neulet.2012.08.062. Epub 2012 Sep 7. Neurosci Lett. 2012. PMID: 22985506

9

A deletion mutation of the VHL gene associated with a patient with sporadic von Hippel-Lindau disease.

Jia D, Tang B, Shi Y, Wang J, Sun Z, Chen Z, Zhang L, Xia K, Jiang H. Jia D, et al. Among authors: shi y. J Clin Neurosci. 2013 Jun;20(6):842-7. doi: 10.1016/j.jocn.2012.06.013. Epub 2013 Apr 28. J Clin Neurosci. 2013. PMID: 23632291

10

Kleine-Levin syndrome with brain atrophy.

Shi YT, Tang BS, Jiang H. Shi YT, et al. J Clin Neurosci. 2013 Jul;20(7):1027-8. doi: 10.1016/j.jocn.2012.07.019. Epub 2013 May 7. J Clin Neurosci. 2013. PMID: 23664128

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