Zou ZY - Search Results

1

A Novel TTBK2 Mutation in a Chinese Pedigree with Spinocerebellar Ataxia 11.

Lu YQ, Chen JM, Huang YL, Zou ZY. Lu YQ, et al. Among authors: zou zy. Cerebellum. 2024 Jun;23(3):1221-1225. doi: 10.1007/s12311-023-01616-3. Epub 2023 Oct 17. Cerebellum. 2024. PMID: 37848700

2

Novel Intronic Mutations of TBK1 Promote Aberrant Splicing Modes in Amyotrophic Lateral Sclerosis.

Lu YQ, Chen JM, Lin H, Feng SY, Che CH, Liu CY, Huang HP, Zou ZY. Lu YQ, et al. Among authors: zou zy. Front Mol Neurosci. 2022 Feb 24;15:691534. doi: 10.3389/fnmol.2022.691534. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35283724 Free PMC article.

3

Clinical and functional characterization of a novel STUB1 mutation in a Chinese spinocerebellar ataxia 48 pedigree.

Li J, Xie W, Chen JM, Xu CZ, Huang YL, Chen S, Liu CY, Lu YQ, Zou ZY. Li J, et al. Among authors: zou zy. Orphanet J Rare Dis. 2024 Dec 20;19(1):471. doi: 10.1186/s13023-024-03456-8. Orphanet J Rare Dis. 2024. PMID: 39707479 Free PMC article.

4

Novel mutation in optineurin causing aggressive ALS+/-frontotemporal dementia.

Feng SM, Che CH, Feng SY, Liu CY, Li LY, Li YX, Huang HP, Zou ZY. Feng SM, et al. Among authors: zou zy. Ann Clin Transl Neurol. 2019 Dec;6(12):2377-2383. doi: 10.1002/acn3.50928. Epub 2019 Dec 15. Ann Clin Transl Neurol. 2019. PMID: 31838784 Free PMC article.

5

Novel FUS mutation Y526F causing rapidly progressive familial amyotrophic lateral sclerosis.

Zou ZY, Che CH, Feng SY, Fang XY, Huang HP, Liu CY. Zou ZY, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2021 Feb;22(1-2):73-79. doi: 10.1080/21678421.2020.1797815. Epub 2020 Jul 28. Amyotroph Lateral Scler Frontotemporal Degener. 2021. PMID: 32720527

6

Novel TARDBP missense mutation caused familial amyotrophic lateral sclerosis with frontotemporal dementia and parkinsonism.

Chen S, Zhou RL, Zhang W, Che CH, Feng SY, Huang HP, Liu CY, Zou ZY. Chen S, et al. Among authors: zou zy. Neurobiol Aging. 2021 Nov;107:168-173. doi: 10.1016/j.neurobiolaging.2021.05.017. Epub 2021 Jun 1. Neurobiol Aging. 2021. PMID: 34175147

7

Novel Variants in the FIG4 Gene Associated With Chinese Sporadic Amyotrophic Lateral Sclerosis With Slow Progression.

Liu CY, Lin JL, Feng SY, Che CH, Huang HP, Zou ZY. Liu CY, et al. Among authors: zou zy. J Clin Neurol. 2022 Jan;18(1):41-47. doi: 10.3988/jcn.2022.18.1.41. J Clin Neurol. 2022. PMID: 35021275 Free PMC article.

8

Phenotype of VCP Mutations in Chinese Amyotrophic Lateral Sclerosis Patients.

Feng SY, Lin H, Che CH, Huang HP, Liu CY, Zou ZY. Feng SY, et al. Among authors: zou zy. Front Neurol. 2022 Feb 7;13:790082. doi: 10.3389/fneur.2022.790082. eCollection 2022. Front Neurol. 2022. PMID: 35197922 Free PMC article.

9

Novel mutations in the ABCD1 gene caused adrenomyeloneuropathy in the Chinese population.

He R, Zhang J, Huang T, Cai G, Zou Z, Ye Q. He R, et al. Front Neurol. 2023 Feb 28;14:1126729. doi: 10.3389/fneur.2023.1126729. eCollection 2023. Front Neurol. 2023. PMID: 36925939 Free PMC article.

10

Identification of a novel missense mutation in angiogenin in a Chinese amyotrophic lateral sclerosis cohort.

Zou ZY, Wang XN, Liu MS, Sun Q, Li XG, Cui LY, Kong J. Zou ZY, et al. Amyotroph Lateral Scler. 2012 May;13(3):270-5. doi: 10.3109/17482968.2011.643900. Epub 2012 Jan 31. Amyotroph Lateral Scler. 2012. PMID: 22292798

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