Xu Y - Search Results

1

CHCHD10 is involved in the development of Parkinson's disease caused by CHCHD2 loss-of-function mutation p.T61I.

Mao C, Wang H, Luo H, Zhang S, Xu H, Zhang S, Rosenblum J, Wang Z, Zhang Q, Tang M, Shepard MJ, Wang X, Wang Y, Zhuang Z, Shi C, Xu Y. Mao C, et al. Among authors: xu h, xu y. Neurobiol Aging. 2019 Mar;75:38-41. doi: 10.1016/j.neurobiolaging.2018.10.020. Epub 2018 Oct 23. Neurobiol Aging. 2019. PMID: 30530185 Free PMC article.

2

Reliability and validity of the Chinese version of the Scale for Assessment and Rating of Ataxia.

Tan S, Niu HX, Zhao L, Gao Y, Lu JM, Shi CH, Avinash C, Wang RH, Xu YM. Tan S, et al. Among authors: xu ym. Chin Med J (Engl). 2013;126(11):2045-8. Chin Med J (Engl). 2013. PMID: 23769555

3

Functional recovery after transplantation of induced pluripotent stem cells in a rat hemorrhagic stroke model.

Qin J, Gong G, Sun S, Qi J, Zhang H, Wang Y, Wang N, Wang QM, Ji Y, Gao Y, Shi C, Yang B, Zhang Y, Song B, Xu Y. Qin J, et al. Among authors: xu y. Neurosci Lett. 2013 Oct 25;554:70-5. doi: 10.1016/j.neulet.2013.08.047. Epub 2013 Sep 1. Neurosci Lett. 2013. PMID: 24005132

4

Vitamin B supplementation, homocysteine levels, and the risk of cerebrovascular disease: a meta-analysis.

Ji Y, Tan S, Xu Y, Chandra A, Shi C, Song B, Qin J, Gao Y. Ji Y, et al. Among authors: xu y. Neurology. 2013 Oct 8;81(15):1298-307. doi: 10.1212/WNL.0b013e3182a823cc. Epub 2013 Sep 18. Neurology. 2013. PMID: 24049135

5

Ataxia and hypogonadism caused by the loss of ubiquitin ligase activity of the U box protein CHIP.

Shi CH, Schisler JC, Rubel CE, Tan S, Song B, McDonough H, Xu L, Portbury AL, Mao CY, True C, Wang RH, Wang QZ, Sun SL, Seminara SB, Patterson C, Xu YM. Shi CH, et al. Hum Mol Genet. 2014 Feb 15;23(4):1013-24. doi: 10.1093/hmg/ddt497. Epub 2013 Oct 9. Hum Mol Genet. 2014. PMID: 24113144 Free PMC article.

6

Genotype-phenotype correlation in a cohort of paroxysmal kinesigenic dyskinesia cases.

Mao CY, Shi CH, Song B, Wu J, Ji Y, Qin J, Li YS, Wang JJ, Shang DD, Sun SL, Xu YM. Mao CY, et al. Among authors: xu ym. J Neurol Sci. 2014 May 15;340(1-2):91-3. doi: 10.1016/j.jns.2014.02.034. Epub 2014 Mar 3. J Neurol Sci. 2014. PMID: 24661410

7

Nerve growth factor for the treatment of spinocerebellar ataxia type 3: an open-label study.

Tan S, Wang RH, Niu HX, Shi CH, Mao CY, Zhang R, Song B, Sun SL, Liu XJ, Hou HM, Liu YT, Gao Y, Fang H, Kong XD, Xu YM. Tan S, et al. Among authors: xu ym. Chin Med J (Engl). 2015 Feb 5;128(3):291-4. doi: 10.4103/0366-6999.150087. Chin Med J (Engl). 2015. PMID: 25635421 Free PMC article.

8

A novel compound WISP3 mutation in a Chinese family with progressive pseudorheumatoid dysplasia.

Luo H, Shi C, Mao C, Jiang C, Bao D, Guo J, Du P, Wang Y, Liu Y, Liu X, Song B, Xu Y. Luo H, et al. Among authors: xu y. Gene. 2015 Jun 10;564(1):35-8. doi: 10.1016/j.gene.2015.03.029. Epub 2015 Mar 17. Gene. 2015. PMID: 25794430

9

Stem cell-based therapies for intracerebral hemorrhage in animal model: a meta-analysis.

Ma X, Qin J, Song B, Shi C, Zhang R, Liu X, Ji Y, Ji W, Gong G, Xu Y. Ma X, et al. Among authors: xu y. Neurol Sci. 2015 Aug;36(8):1311-7. doi: 10.1007/s10072-015-2238-6. Epub 2015 May 14. Neurol Sci. 2015. PMID: 25972140

10

Exome sequencing reveals novel SPG11 mutation in hereditary spastic paraplegia with complicated phenotypes.

Li YS, Mao CY, Shi CH, Song B, Wu J, Qin J, Ji Y, Niu HX, Luo HY, Shang DD, Sun SL, Xu YM. Li YS, et al. Among authors: xu ym. J Clin Neurosci. 2015 Jul;22(7):1150-4. doi: 10.1016/j.jocn.2015.01.014. Epub 2015 May 21. J Clin Neurosci. 2015. PMID: 26003865

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