Wang Z - Search Results

1

Autosomal recessive spastic ataxia of Charlevoix-Saguenay caused by novel mutations in SACS gene: A report of two Chinese families.

Wang Z, Song Y, Wang X, Li X, Xu F, Si L, Dong Y, Yao T, Zhu J, Lai H, Li W, Lin F, Huang H, Wang C. Wang Z, et al. Among authors: wang x, wang c. Neurosci Lett. 2021 May 1;752:135831. doi: 10.1016/j.neulet.2021.135831. Epub 2021 Mar 18. Neurosci Lett. 2021. PMID: 33746006 Free article.

2

Mutation Screening of the GLE1 Gene in a Large Chinese Cohort of Amyotrophic Lateral Sclerosis Patients.

Li Y, Sun B, Wang Z, He Z, Yang F, Wang H, Cui F, Chen Z, Ling L, Wang C, Huang X. Li Y, et al. Among authors: wang h, wang z, wang c. Front Neurosci. 2021 May 5;15:595775. doi: 10.3389/fnins.2021.595775. eCollection 2021. Front Neurosci. 2021. PMID: 34025336 Free PMC article.

3

A novel FBXO7-R345P mutation in a Chinese family with autosomal recessive parkinsonian-pyramidal syndrome.

Wang Z, Song Y, Zhu W, Wang X, Li X, Xu F, Si L, Yao T, Zhu J, Lai H, Li W, Lin F, Wang C. Wang Z, et al. Among authors: wang x, wang c. Parkinsonism Relat Disord. 2021 Jul;88:62-67. doi: 10.1016/j.parkreldis.2021.06.005. Epub 2021 Jun 10. Parkinsonism Relat Disord. 2021. PMID: 34144229

4

Genetic, clinical and neuroimaging profiles of sporadic and autosomal recessive hereditary spastic paraplegia cases in Chinese.

Dong Y, Li XY, Wang XL, Xu F, Wang ZJ, Song Y, Li Q, Lin R, Wang C. Dong Y, et al. Neurosci Lett. 2021 Sep 14;761:136108. doi: 10.1016/j.neulet.2021.136108. Epub 2021 Jul 10. Neurosci Lett. 2021. PMID: 34256108

5

Hartnup disease presenting as hereditary spastic paraplegia and severe peripheral neuropathy.

Wang X, Li XY, Piao Y, Yuan G, Lin Y, Chen H, Wang Z, Li C, Wang C. Wang X, et al. Among authors: wang z, wang c. Am J Med Genet A. 2022 Jan;188(1):237-242. doi: 10.1002/ajmg.a.62475. Epub 2021 Aug 30. Am J Med Genet A. 2022. PMID: 34459558

6

Sequencing of neurofilament genes identified NEFH Ser787Arg as a novel risk variant of sporadic amyotrophic lateral sclerosis in Chinese subjects.

Lin F, Lin W, Zhu C, Lin J, Zhu J, Li XY, Wang Z, Wang C, Huang H. Lin F, et al. Among authors: wang z, wang c. BMC Med Genomics. 2021 Sep 11;14(1):222. doi: 10.1186/s12920-021-01073-z. BMC Med Genomics. 2021. PMID: 34511133 Free PMC article.

7

Cervical Cord Hemorrhage in Cerebral Cavernous Malformations.

Wang Z, Wu H, Piao Y, Wang C. Wang Z, et al. Among authors: wang c. J Clin Neurol. 2021 Oct;17(4):576-578. doi: 10.3988/jcn.2021.17.4.576. J Clin Neurol. 2021. PMID: 34595868 Free PMC article. No abstract available.

8

Development and Validation of a Predictive Nomogram for Possible REM Sleep Behavior Disorders.

Lai H, Li XY, Hu J, Li W, Xu F, Zhu J, He R, Weng H, Chen L, Yu J, Li X, Song Y, Wang X, Wang Z, Li W, Kang R, Li Y, Xu J, Deng Y, Ye Q, Wang C. Lai H, et al. Among authors: wang x, wang z, wang c. Front Neurol. 2022 Jun 29;13:903721. doi: 10.3389/fneur.2022.903721. eCollection 2022. Front Neurol. 2022. PMID: 35847229 Free PMC article.

9

Identification of TARDBP Gly298Ser as a founder mutation for amyotrophic lateral sclerosis in Southern China.

Xu F, Huang S, Li XY, Lin J, Feng X, Xie S, Wang Z, Li X, Zhu J, Lai H, Xu Y, Huang X, Yao X, Wang C. Xu F, et al. Among authors: wang z, wang c. BMC Med Genomics. 2022 Aug 5;15(1):173. doi: 10.1186/s12920-022-01327-4. BMC Med Genomics. 2022. PMID: 35932023 Free PMC article.

10

Spatial metabolomics identifies lipid profiles of human carotid atherosclerosis.

Li W, Luo J, Peng F, Liu R, Bai X, Wang T, Zhang X, Zhu J, Li XY, Wang Z, Liu W, Wang J, Zhang L, Chen X, Xue T, Ding C, Wang C, Jiao L. Li W, et al. Among authors: wang z, wang j, wang t, wang c. Atherosclerosis. 2023 Jan;364:20-28. doi: 10.1016/j.atherosclerosis.2022.11.019. Epub 2022 Nov 24. Atherosclerosis. 2023. PMID: 36459728

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