Luo YY - Search Results

1

Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Chinese Han patients with hereditary spastic paraplegia.

Du J, Shen L, Zhao GH, Wang YG, Liao SS, Chen C, Zhou ZF, Luo YY, Jiang H, Xia K, Tang BS. Du J, et al. Among authors: luo yy. Chin Med J (Engl). 2009 Sep 5;122(17):2064-6. Chin Med J (Engl). 2009. PMID: 19781397 No abstract available.

2

Six cases of SCA3/MJD patients that mimic hereditary spastic paraplegia in clinic.

Wang YG, Du J, Wang JL, Chen J, Chen C, Luo YY, Xiao ZQ, Jiang H, Yan XX, Xia K, Pan Q, Tang BS, Shen L. Wang YG, et al. Among authors: luo yy. J Neurol Sci. 2009 Oct 15;285(1-2):121-4. doi: 10.1016/j.jns.2009.06.027. Epub 2009 Jul 15. J Neurol Sci. 2009. PMID: 19608203

3

Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1.

Du J, Hu YC, Tang BS, Chen C, Luo YY, Zhan ZX, Zhao GH, Jiang H, Xia K, Shen L. Du J, et al. Among authors: luo yy. Clin Neurol Neurosurg. 2011 Jul;113(6):480-2. doi: 10.1016/j.clineuro.2011.02.011. Epub 2011 Mar 17. Clin Neurol Neurosurg. 2011. PMID: 21419568

4

SUMO-1 modification on K166 of polyQ-expanded ataxin-3 strengthens its stability and increases its cytotoxicity.

Zhou YF, Liao SS, Luo YY, Tang JG, Wang JL, Lei LF, Chi JW, Du J, Jiang H, Xia K, Tang BS, Shen L. Zhou YF, et al. Among authors: luo yy. PLoS One. 2013;8(1):e54214. doi: 10.1371/journal.pone.0054214. Epub 2013 Jan 31. PLoS One. 2013. PMID: 23382880 Free PMC article.

5

Exome sequencing released a case of X-linked adrenoleukodystrophy mimicking recessive hereditary spastic paraplegia.

Zhan ZX, Liao XX, Du J, Luo YY, Hu ZT, Wang JL, Yan XX, Zhang JG, Dai MZ, Zhang P, Xia K, Tang BS, Shen L. Zhan ZX, et al. Among authors: luo yy. Eur J Med Genet. 2013 Jul;56(7):375-8. doi: 10.1016/j.ejmg.2013.04.008. Epub 2013 May 9. Eur J Med Genet. 2013. PMID: 23664929

6

A diagnostic gene chip for hereditary spastic paraplegias.

Luo Y, Du J, Zhan Z, Chen C, Wang J, Hu Y, Hu Z, Xia K, Tang B, Shen L. Luo Y, et al. Brain Res Bull. 2013 Aug;97:112-8. doi: 10.1016/j.brainresbull.2013.07.002. Epub 2013 Jul 10. Brain Res Bull. 2013. PMID: 23850684

7

Association study between SNP rs150689919 in the DNA demethylation gene, TET1, and Parkinson's disease in Chinese Han population.

Liao XX, Zhan ZX, Luo YY, Li K, Wang JL, Guo JF, Yan XX, Xia K, Tang BS, Shen L. Liao XX, et al. Among authors: luo yy. BMC Neurol. 2013 Dec 11;13:196. doi: 10.1186/1471-2377-13-196. BMC Neurol. 2013. PMID: 24325350 Free PMC article.

8

C9orf72 hexanucleotide repeat expansion analysis in Chinese spastic paraplegia patients.

Luo Y, Jiao B, Wang J, Du J, Yan X, Xia K, Tang B, Shen L. Luo Y, et al. J Neurol Sci. 2014 Dec 15;347(1-2):104-6. doi: 10.1016/j.jns.2014.09.028. Epub 2014 Sep 28. J Neurol Sci. 2014. PMID: 25284081

9

Mutation and clinical characteristics of autosomal-dominant hereditary spastic paraplegias in China.

Luo Y, Chen C, Zhan Z, Wang Y, Du J, Hu Z, Liao X, Zhao G, Wang J, Yan X, Jiang H, Pan Q, Xia K, Tang B, Shen L. Luo Y, et al. Neurodegener Dis. 2014;14(4):176-83. doi: 10.1159/000365513. Epub 2014 Oct 22. Neurodegener Dis. 2014. PMID: 25341883

10

SPG46 and SPG56 are rare causes of hereditary spastic paraplegia in China.

Yang YJ, Zhou ZF, Liao XX, Luo YY, Zhan ZX, Huang MF, Zhou L, Tang BS, Shen L, Du J. Yang YJ, et al. Among authors: luo yy. J Neurol. 2016 Oct;263(10):2136-8. doi: 10.1007/s00415-016-8256-3. Epub 2016 Aug 23. J Neurol. 2016. PMID: 27553021 No abstract available.

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