Wang J - Search Results

1

Correction to: Genetic analysis in Chinese patients with familial or young‑onset amyotrophic lateral sclerosis.

Ma J, Pang X, Huang S, Zhang J, Wang J, Zhao R, Chang X, Guo J, Zhang W. Ma J, et al. Among authors: wang j. Neurol Sci. 2022 Apr;43(4):2913. doi: 10.1007/s10072-022-05911-5. Neurol Sci. 2022. PMID: 35064862 No abstract available.

2

A novel thymidine phosphorylase mutation in a Chinese MNGIE patient.

Wang HF, Wang J, Wang YL, Fan JJ, Mo GL, Gong FY, Chai ZM, Zhang J, Meng HX, Li CX, Guo JH, Pu CQ. Wang HF, et al. Among authors: wang j, wang yl. Acta Neurol Belg. 2017 Mar;117(1):259-267. doi: 10.1007/s13760-016-0701-7. Epub 2016 Oct 5. Acta Neurol Belg. 2017. PMID: 27709505

3

Morphological parameters of middle cerebral arteries associated with aneurysm formation.

Zhang W, Wang J, Li T, Mei M. Zhang W, et al. Among authors: wang j. Neuroradiology. 2021 Feb;63(2):179-188. doi: 10.1007/s00234-020-02521-w. Epub 2020 Aug 19. Neuroradiology. 2021. PMID: 32814989 Free PMC article.

4

Whole-exome sequencing identifies a heterozygous mutation in SLC12A6 associated with hereditary sensory and motor neuropathy.

Shi J, Zhao F, Pang X, Huang S, Wang J, Chang X, Zhang J, Liu Y, Guo J, Zhang W. Shi J, et al. Among authors: wang j. Neuromuscul Disord. 2021 Feb;31(2):149-157. doi: 10.1016/j.nmd.2020.11.002. Epub 2020 Nov 18. Neuromuscul Disord. 2021. PMID: 33323309

5

A novel Q93H missense mutation in DCTN1 caused distal hereditary motor neuropathy type 7B and Perry syndrome from a Chinese family.

Zhang J, Wang H, Liu W, Wang J, Zhang J, Chang X, Huang S, Pang X, Guo J, Wang Q, Zhang W. Zhang J, et al. Among authors: wang h, wang j, wang q. Neurol Sci. 2021 Sep;42(9):3695-3705. doi: 10.1007/s10072-020-04962-w. Epub 2021 Jan 14. Neurol Sci. 2021. PMID: 33443672

6

Fasciculation score: a sensitive biomarker in amyotrophic lateral sclerosis.

Ma J, Wen Q, Pang X, Huang S, Zhang J, Wang J, Chang X, Guo J, Zhang W. Ma J, et al. Among authors: wang j. Neurol Sci. 2021 Nov;42(11):4657-4666. doi: 10.1007/s10072-021-05166-6. Epub 2021 Mar 11. Neurol Sci. 2021. PMID: 33704599

7

Pain in acute motor axonal neuropathy.

Zhao F, Wang J, Zhang J, Pang X, Huang S, Chang X, Guo J, Zhang W. Zhao F, et al. Among authors: wang j. Muscle Nerve. 2021 Dec;64(6):739-743. doi: 10.1002/mus.27414. Epub 2021 Sep 24. Muscle Nerve. 2021. PMID: 34506042

8

Genetic analysis in Chinese patients with familial or young-onset amyotrophic lateral sclerosis.

Ma J, Pang X, Huang S, Zhang J, Wang J, Zhao R, Chang X, Guo J, Zhang W. Ma J, et al. Among authors: wang j. Neurol Sci. 2022 Apr;43(4):2579-2587. doi: 10.1007/s10072-021-05634-z. Epub 2021 Sep 26. Neurol Sci. 2022. PMID: 34564799

9

GGC repeat expansions in NOTCH2NLC causing a phenotype of lower motor neuron syndrome.

Zhang W, Ma J, Shi J, Huang S, Zhao R, Pang X, Wang J, Guo J, Chang X. Zhang W, et al. Among authors: wang j. J Neurol. 2022 Aug;269(8):4469-4477. doi: 10.1007/s00415-022-11092-0. Epub 2022 Apr 2. J Neurol. 2022. PMID: 35366689

10

The relationship between amyloid-beta and brain capillary endothelial cells in Alzheimer's disease.

Zhang YL, Wang J, Zhang ZN, Su Q, Guo JH. Zhang YL, et al. Among authors: wang j. Neural Regen Res. 2022 Nov;17(11):2355-2363. doi: 10.4103/1673-5374.335829. Neural Regen Res. 2022. PMID: 35535871 Free PMC article. Review.

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