Wang X - Search Results

1

Sporadic Cases with Novel Mutations and Pedigree in Hereditary Leukoencephalopathy with Axonal Spheroids.

Wu L, Liu J, Sha L, Wang X, Li J, Dong J, Jia J. Wu L, et al. Among authors: wang x. J Alzheimers Dis. 2017;56(3):893-898. doi: 10.3233/JAD-161193. J Alzheimers Dis. 2017. PMID: 28059798

2

A clinical and gene analysis of late-onset combined methylmalonic aciduria and homocystinuria, cblC type, in China.

Wang X, Sun W, Yang Y, Jia J, Li C. Wang X, et al. J Neurol Sci. 2012 Jul 15;318(1-2):155-9. doi: 10.1016/j.jns.2012.04.012. Epub 2012 May 4. J Neurol Sci. 2012. PMID: 22560872

3

A novel KIAA0196 (SPG8) mutation in a Chinese family with spastic paraplegia.

Wang X, Yang Y, Wang X, Li C, Jia J. Wang X, et al. Chin Med J (Engl). 2014;127(10):1987-9. Chin Med J (Engl). 2014. PMID: 24824269 No abstract available.

4

Clinical Features and Sleep Analysis of Chinese Patients with Fatal Familial Insomnia.

Wu L, Lu H, Wang X, Liu J, Huang C, Ye J, Li C, Lu J, Wang Y, Jia J, Zhan S. Wu L, et al. Among authors: wang x, wang y. Sci Rep. 2017 Jun 15;7(1):3625. doi: 10.1038/s41598-017-03817-3. Sci Rep. 2017. PMID: 28620158 Free PMC article.

5

Distinct clinical, neuroimaging and genetic profiles of late-onset cobalamin C defects (cb1C): a report of 16 Chinese cases.

Wang X, Yang Y, Li X, Li C, Wang C. Wang X, et al. Among authors: wang c. Orphanet J Rare Dis. 2019 May 15;14(1):109. doi: 10.1186/s13023-019-1058-9. Orphanet J Rare Dis. 2019. PMID: 31092259 Free PMC article.

6

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

7

[The clinical and imaging study of thalamic venous infarction].

Wang X, Yang Y, Wang X, Li C. Wang X, et al. Zhonghua Nei Ke Za Zhi. 2014 Aug;53(8):635-8. Zhonghua Nei Ke Za Zhi. 2014. PMID: 25376827 Chinese.

8

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.

9

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

10

Novel mutations and molecular pathways identified in patients with brain iron accumulation disorders.

Si L, Wang Z, Li XY, Song Y, Yao T, Xu E, Wang X, Wang C. Si L, et al. Among authors: wang x, wang z, wang c. Neurogenetics. 2023 Oct;24(4):231-241. doi: 10.1007/s10048-023-00725-9. Epub 2023 Jul 15. Neurogenetics. 2023. PMID: 37453004

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