Shen L - Search Results

1

Sensitivity of Sniffer Dogs for a Diagnosis of Parkinson's Disease: A Diagnostic Accuracy Study.

Gao CQ, Wang SN, Wang MM, Li JJ, Qiao JJ, Huang JJ, Zhang XX, Xiang YQ, Xu Q, Wang JL, Liu ZH, Wang JG, Chen ZH, Hu PA, Song Z, Gu SJ, Zhang RX, Lei LF, Zhan KB, Long YT, Zhang Y, Ye M, Zhong Z, Liu YB, Zhang C, He ZM, Fang X, Peng JG, Wang CY, Xu H, Xia BH, Shen L, Tang BS, Zheng CW, Li YA, Guo JF. Gao CQ, et al. Among authors: shen l. Mov Disord. 2022 Sep;37(9):1807-1816. doi: 10.1002/mds.29180. Epub 2022 Aug 25. Mov Disord. 2022. PMID: 36054272

2

[Analysis of the parkin gene deletion mutations in Chinese patients with Parkinson's disease].

Tang B, Liu S, Yan X, Shen L, Jiang H, Yang Q, Ouyang S. Tang B, et al. Among authors: shen l. Zhonghua Nei Ke Za Zhi. 2001 Dec;40(12):799-801. Zhonghua Nei Ke Za Zhi. 2001. PMID: 16206665 Chinese.

3

Mutation analysis of the TATA box-binding protein (TBP) gene in Chinese Han patients with spinocerebellar ataxia.

Xu Q, Li XH, Wang JL, Jiang H, Zhang S, Lei LF, Shen L, Xia K, Pan Q, Long ZG, Tang BS. Xu Q, et al. Among authors: shen l. J Clin Neurosci. 2009 Oct;16(10):1374-5. doi: 10.1016/j.jocn.2009.05.004. Epub 2009 Jul 5. J Clin Neurosci. 2009. PMID: 19581089

4

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. Among authors: shen l. Clin Genet. 2015;87(1):85-9. doi: 10.1111/cge.12336. Epub 2014 Jan 26. Clin Genet. 2015. PMID: 24359114

5

Genetic and clinical analysis of spinocerebellar ataxia type 36 in Mainland China.

Zeng S, Zeng J, He M, Zeng X, Zhou Y, Liu Z, Xia K, Pan Q, Jiang H, Shen L, Yan X, Tang B, Wang J. Zeng S, et al. Among authors: shen l. Clin Genet. 2016 Aug;90(2):141-8. doi: 10.1111/cge.12706. Epub 2016 Jan 20. Clin Genet. 2016. PMID: 26661328

6

Association of rare variants in neurodegenerative genes with familial Alzheimer's disease.

Zhang W, Jiao B, Xiao T, Liu X, Liao X, Xiao X, Guo L, Yuan Z, Yan X, Tang B, Shen L. Zhang W, et al. Among authors: shen l. Ann Clin Transl Neurol. 2020 Oct;7(10):1985-1995. doi: 10.1002/acn3.51197. Epub 2020 Sep 17. Ann Clin Transl Neurol. 2020. PMID: 32941707 Free PMC article.

7

The role of NOTCH3 variants in Alzheimer's disease and subcortical vascular dementia in the Chinese population.

Guo L, Jiao B, Liao X, Xiao X, Zhang W, Yuan Z, Liu X, Zhou L, Wang X, Zhu Y, Yang Q, Wang J, Tang B, Shen L. Guo L, et al. Among authors: shen l. CNS Neurosci Ther. 2021 Aug;27(8):930-940. doi: 10.1111/cns.13647. Epub 2021 May 4. CNS Neurosci Ther. 2021. PMID: 33942994 Free PMC article.

8

The role of vascular dementia associated genes in patients with Alzheimer's disease: A large case-control study in the Chinese population.

Xiao X, Guo L, Liao X, Zhou Y, Zhang W, Zhou L, Wang X, Liu X, Liu H, Xu T, Zhu Y, Yang Q, Hao X, Liu Y, Wang J, Li J, Jiao B, Shen L. Xiao X, et al. Among authors: shen l. CNS Neurosci Ther. 2021 Dec;27(12):1531-1539. doi: 10.1111/cns.13730. Epub 2021 Sep 22. CNS Neurosci Ther. 2021. PMID: 34551193 Free PMC article.

9

The macular inner plexiform layer thickness as an early diagnostic indicator for Parkinson's disease.

Wang X, Jiao B, Jia X, Wang Y, Liu H, Zhu X, Hao X, Zhu Y, Xu B, Zhang S, Xu Q, Wang J, Guo J, Yan X, Tang B, Zhao R, Shen L. Wang X, et al. Among authors: shen l. NPJ Parkinsons Dis. 2022 May 25;8(1):63. doi: 10.1038/s41531-022-00325-8. NPJ Parkinsons Dis. 2022. PMID: 35614125 Free PMC article.

10

CYLD variants identified in Alzheimer's disease and frontotemporal dementia patients.

Xiao X, Xu T, Liu H, Liu X, Liao X, Zhou Y, Zhou L, Wang X, Zhu Y, Yang Q, Hao X, Liu Y, Jiang H, Guo J, Wang J, Tang B, Li J, Shen L, Jiao B. Xiao X, et al. Among authors: shen l. Ann Clin Transl Neurol. 2022 Oct;9(10):1596-1601. doi: 10.1002/acn3.51655. Epub 2022 Aug 24. Ann Clin Transl Neurol. 2022. PMID: 36000313 Free PMC article.

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