Liao XX - Search Results

1

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. Among authors: liao wh, liao xx. 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

2

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. 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

3

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: liao xx. 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

4

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.

5

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

6

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

Xing W, Wang X, Liao X, Shen L, Liao W. Xing W, et al. 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.

7

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

8

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: liao xx. 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.

9

[Value of 1H-MRS on SCA3/MJD diagnosis and clinical course].

Xing W, Liao X, Guan T, Xie F, Shen L, Liao W, Wang X. Xing W, et al. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2017 Mar 28;42(3):291-297. doi: 10.11817/j.issn.1672-7347.2017.03.009. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2017. PMID: 28364102 Free article. Chinese.

10

Resting state fMRI studies in SPG4-linked hereditary spastic paraplegia.

Liao X, Huang M, Xing W, Wu X, Liao W, Wang X, Tang B, Shen L. Liao X, et al. J Neurol Sci. 2018 Jan 15;384:1-6. doi: 10.1016/j.jns.2017.10.048. Epub 2017 Oct 28. J Neurol Sci. 2018. PMID: 29249364

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