Wang N - Search Results

1

Disease Progression and Multiparametric Imaging Characteristics of Spinocerebellar Ataxia Type 3 With Spastic Paraplegia.

Ye ZX, Xu HL, Chen NP, Chen XY, Li MC, Yuan RY, Lin W, Qiu L, Lin M, Chen WJ, Wang N, Hu JP, Fu Y, Gan SR; as OSCCAR Investigators. Ye ZX, et al. Among authors: wang n. Neurol Genet. 2024 Jun 4;10(3):e200162. doi: 10.1212/NXG.0000000000200162. eCollection 2024 Jun. Neurol Genet. 2024. PMID: 38841628 Free PMC article.

2

Biallelic variants in the COQ7 gene cause distal hereditary motor neuropathy in two Chinese families.

Liu XX, Wang N, Chen YK, Lv WQ, Hong JM, Xu GR, Zhou LY, Chen WJ, Fan DS, He J. Liu XX, et al. Among authors: wang n. Brain. 2023 May 2;146(5):e27-e30. doi: 10.1093/brain/awad040. Brain. 2023. PMID: 36758993 No abstract available.

3

An epigenetic basis for genetic anticipation in facioscapulohumeral muscular dystrophy type 1.

Zheng F, Qiu L, Chen L, Zheng Y, He Q, Lin X, Lin M, Lin Y, Fu Y, Wang N, Wang Z. Zheng F, et al. Among authors: wang z, wang n. Brain. 2023 Dec 1;146(12):e107-e110. doi: 10.1093/brain/awad215. Brain. 2023. PMID: 37352893 No abstract available.

4

Alu Retrotransposition Event in SPAST Gene as a Novel Cause of Hereditary Spastic Paraplegia.

Chen YJ, Wang MW, Qiu YS, Yuan RY, Wang N, Lin X, Chen WJ. Chen YJ, et al. Among authors: wang n, wang mw. Mov Disord. 2023 Sep;38(9):1750-1755. doi: 10.1002/mds.29522. Epub 2023 Jul 2. Mov Disord. 2023. PMID: 37394769

5

Lacunes are associated with late-stage multiple sclerosis comorbidities.

Zhang L, Yu X, Zheng Y, Lin A, Zhang Z, Li S, Wang N, Fu Y. Zhang L, et al. Among authors: wang n. Front Neurol. 2023 Aug 8;14:1224748. doi: 10.3389/fneur.2023.1224748. eCollection 2023. Front Neurol. 2023. PMID: 37614972 Free PMC article.

6

Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients.

Lin F, Yang K, Lin X, Jin M, Chen L, Zheng FZ, Qiu LL, Ye ZX, Chen HZ, Lin MT, Wang N, Wang ZQ. Lin F, et al. Among authors: wang n, wang zq. Orphanet J Rare Dis. 2023 Nov 16;18(1):356. doi: 10.1186/s13023-023-02897-x. Orphanet J Rare Dis. 2023. PMID: 37974208 Free PMC article.

7

Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular Characterization.

Lin X, Jiang JY, Hong DJ, Lin KJ, Li JJ, Chen YJ, Qiu YS, Wang Z, Liao YC, Yang K, Shi Y, Wang MW, Hsu SL, Hong S, Zeng YH, Chen XC, Wang N, Lee YC, Chen WJ. Lin X, et al. Among authors: wang z, wang n, wang mw. Mov Disord. 2024 Jan;39(1):152-163. doi: 10.1002/mds.29664. Epub 2023 Nov 28. Mov Disord. 2024. PMID: 38014483

8

enOsCas12f1-mediated exon skipping for Duchenne muscular dystrophy therapy in humanized mouse model.

Jin M, Lin J, Zhang Y, Xiao Q, Kong X, Zhang X, Shao Z, Wang Y, Yu Y, Li J, Chen WJ, Li G, Yang H, Wang N. Jin M, et al. Among authors: wang y, wang n. J Genet Genomics. 2024 Feb;51(2):256-259. doi: 10.1016/j.jgg.2023.12.003. Epub 2023 Dec 14. J Genet Genomics. 2024. PMID: 38103683 No abstract available.

9

CGG repeat expansion in LOC642361/NUTM2B-AS1 typically presents as oculopharyngodistal myopathy.

Shi Y, Cao C, Zeng Y, Ding Y, Chen L, Zheng F, Chen X, Zhou F, Yang X, Li J, Xu L, Xu G, Lin M, Ishiura H, Tsuji S, Wang N, Wang Z, Chen WJ, Yang K. Shi Y, et al. Among authors: wang z, wang n. J Genet Genomics. 2024 Feb;51(2):184-196. doi: 10.1016/j.jgg.2023.12.009. Epub 2023 Dec 29. J Genet Genomics. 2024. PMID: 38159879

10

Effect of Regional Brain Activity Following Repeat Transcranial Magnetic Stimulation in SCA3: A Secondary Analysis of a Randomized Clinical Trial.

Liu X, Zhang L, Xu HL, Liu XH, Sikandar A, Li MC, Xia XY, Huang ZQ, Chen NP, Tu YQ, Hu JP, Gan SR, Chen QL, Chen XY, Wang SZ; Members of the Organization in South-East China for Cerebellar Ataxia Research (OSCCAR). Liu X, et al. Cerebellum. 2024 Oct;23(5):1923-1931. doi: 10.1007/s12311-024-01689-8. Epub 2024 Apr 1. Cerebellum. 2024. PMID: 38558026 Clinical Trial.

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