Liao X - Search Results

1

Identification of expanded repeats in NOTCH2NLC in neurodegenerative dementias.

Jiao B, Zhou L, Zhou Y, Weng L, Liao X, Tian Y, Guo L, Liu X, Yuan Z, Xiao X, Jiang Y, Wang X, Yang Q, Li C, Zhu Y, Zhou L, Zhang W, Wang J, Li Y, Gu W, Yang J, Xia J, Huang Q, Yin J, Xue J, Duan R, Tang B, Shen L. Jiao B, et al. Among authors: liao x. Neurobiol Aging. 2020 May;89:142.e1-142.e7. doi: 10.1016/j.neurobiolaging.2020.01.010. Epub 2020 Jan 24. Neurobiol Aging. 2020. PMID: 32081467

2

Cloning, mapping and mutation analysis of human geneGJB5 encoding gap junction protein beta-5.

Xia J, Zheng D, Tang D, Dai H, Pan Q, Long Z, Liao X. Xia J, et al. Among authors: liao x. Sci China C Life Sci. 2001 Feb;44(1):92-8. doi: 10.1007/BF02882077. Sci China C Life Sci. 2001. PMID: 18763093

3

Related factors of ICARS and SARA scores on spinocerebellar ataxia type 3/Machado-Joseph disease.

Zhou J, Lei L, Liao X, Wang J, Jiang H, Tang B, Shen L. Zhou J, et al. Among authors: liao x. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2011 Jun;36(6):498-503. doi: 10.3969/j.issn.1672-7347.2011.06.005. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2011. PMID: 21743140

4

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. 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

5

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. BMC Neurol. 2013 Dec 11;13:196. doi: 10.1186/1471-2377-13-196. BMC Neurol. 2013. PMID: 24325350 Free PMC article.

6

SPG35 contributes to the second common subtype of AR-HSP in China: frequency analysis and functional characterization of FA2H gene mutations.

Liao X, Luo Y, Zhan Z, Du J, Hu Z, Wang J, Guo J, Hu Z, Yan X, Pan Q, Xia K, Tang B, Shen L. Liao X, et al. Clin Genet. 2015;87(1):85-9. doi: 10.1111/cge.12336. Epub 2014 Jan 26. Clin Genet. 2015. PMID: 24359114

7

Spin labeling artery method perfusion MRI study of SPG4 and SCA3/MJD.

Xing W, Wang XY, Liao XX, Liao WH, Shen L. Xing W, et al. Magn Reson Imaging. 2014 Dec;32(10):1330-4. doi: 10.1016/j.mri.2014.08.022. Epub 2014 Aug 28. Magn Reson Imaging. 2014. PMID: 25172988

8

[Diffusion weighted imaging of SCA3/MJD and SPG4].

Xing W, Wang X, Liao X, Shen L, Liao W. Xing W, et al. Among authors: liao w, liao x. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2014 Aug;39(8):825-30. doi: 10.3969/j.issn.1672-7347.2014.08.012. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2014. PMID: 25202952 Chinese.

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. Among authors: liao x. 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. 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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