Wang S - Search Results

1

Variants in LAMC3 Causes Occipital Cortical Malformation.

Qian X, Liu X, Zhu Z, Wang S, Song X, Chen G, Wu J, Cao Y, Luan X, Tang H, Cao L. Qian X, et al. Among authors: wang s. Front Genet. 2021 Jul 20;12:616761. doi: 10.3389/fgene.2021.616761. eCollection 2021. Front Genet. 2021. PMID: 34354730 Free PMC article.

2

Teaching Video NeuroImages: Cautious walking gait in siblings with hereditary hyperekplexia.

Zhang C, Wang SG, Wang Y, Liu XL, Cao L. Zhang C, et al. Neurology. 2019 Apr 23;92(17):e2068-e2069. doi: 10.1212/WNL.0000000000007375. Neurology. 2019. PMID: 31010918 No abstract available.

3

Primary familial brain calcification presenting as paroxysmal kinesigenic dyskinesia: Genetic and functional analyses.

Zhan FX, Tian WT, Zhang C, Zhu ZY, Wang SG, Huang XJ, Cao L. Zhan FX, et al. Neurosci Lett. 2020 Jan 1;714:134543. doi: 10.1016/j.neulet.2019.134543. Epub 2019 Oct 13. Neurosci Lett. 2020. PMID: 31618668

4

Excessive Startle with Novel GLRA1 Mutations in 4 Chinese Patients and a Literature Review of GLRA1-Related Hyperekplexia.

Zhan F, Zhang C, Wang S, Zhu Z, Chen G, Zhao M, Cao L. Zhan F, et al. Among authors: wang s. J Clin Neurol. 2020 Apr;16(2):230-236. doi: 10.3988/jcn.2020.16.2.230. J Clin Neurol. 2020. PMID: 32319239 Free PMC article.

5

Novel mutation of the PRRT2 gene in two cases of paroxysmal kinesigenic dyskinesia: Two case reports.

Fang J, Wang S, Zhao G, Cao L. Fang J, et al. Among authors: wang s. Biomed Rep. 2020 Jun;12(6):309-312. doi: 10.3892/br.2020.1293. Epub 2020 Mar 17. Biomed Rep. 2020. PMID: 32346475 Free PMC article.

6

The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China.

Huang XJ, Wang SG, Guo XN, Tian WT, Zhan FX, Zhu ZY, Yin XM, Liu Q, Yin KL, Liu XR, Zhang Y, Liu ZG, Liu XL, Zheng L, Wang T, Wu L, Rong TY, Wang Y, Zhang M, Bi GH, Tang WG, Zhang C, Zhong P, Wang CY, Tang JG, Lu W, Zhang RX, Zhao GH, Li XH, Li H, Chen T, Li HY, Luo XG, Song YY, Tang HD, Luan XH, Zhou HY, Tang BS, Chen SD, Cao L. Huang XJ, et al. Mov Disord. 2020 Aug;35(8):1428-1437. doi: 10.1002/mds.28061. Epub 2020 May 11. Mov Disord. 2020. PMID: 32392383

7

Altered structural and functional connectivity in CSF1R-related leukoencephalopathy.

Zhan FX, Zhu ZY, Liu Q, Zhou HY, Luan XH, Huang XJ, Liu XL, Tian WT, Wang SG, Song XX, Chen G, Zhao ML, Wang Y, Tang HD, Hu J, Chen SD, Li BY, Cao L. Zhan FX, et al. Brain Imaging Behav. 2021 Jun;15(3):1655-1666. doi: 10.1007/s11682-020-00360-0. Brain Imaging Behav. 2021. PMID: 32705467

8

c.1263+1G>A Is a Latent Hotspot for CYP27A1 Mutations in Chinese Patients With Cerebrotendinous Xanthomatosis.

Jiang J, Chen G, Wu J, Luan X, Zhou H, Liu X, Zhu Z, Song X, Wang S, Qian X, Du J, Huang X, Zhang M, Xu W, Cao L. Jiang J, et al. Among authors: wang s. Front Genet. 2020 Jul 1;11:682. doi: 10.3389/fgene.2020.00682. eCollection 2020. Front Genet. 2020. PMID: 32714376 Free PMC article.

9

Neurodevelopmental disorder caused by a truncating de novo variant of IRF2BPL.

Qian XH, Liu XY, Zhu ZY, Wang SG, Song XX, Chen G, Wu JY, Tang HD, Cao L. Qian XH, et al. Seizure. 2021 Jan;84:47-52. doi: 10.1016/j.seizure.2020.11.006. Epub 2020 Nov 19. Seizure. 2021. PMID: 33278788 Free article.

10

Expanding the clinical spectrum of adult-onset neuronal intranuclear inclusion disease.

Cao Y, Wu J, Yue Y, Zhang C, Liu S, Zhong P, Wang S, Huang X, Deng W, Pan J, Zheng L, Liu Q, Shang L, Zhang B, Yang J, Chen G, Chen S, Cao L, Luan X. Cao Y, et al. Among authors: wang s. Acta Neurol Belg. 2022 Jun;122(3):647-658. doi: 10.1007/s13760-021-01622-4. Epub 2021 Feb 24. Acta Neurol Belg. 2022. PMID: 33625684

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