Zou ZY - Search Results

1

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.

2

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

3

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

4

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.

5

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.

6

Clinical genetics of Alzheimer's disease.

Zou Z, Liu C, Che C, Huang H. Zou Z, et al. Biomed Res Int. 2014;2014:291862. doi: 10.1155/2014/291862. Epub 2014 May 13. Biomed Res Int. 2014. PMID: 24955352 Free PMC article. Review.

7

Clinical features and genetic characteristics of hereditary diffuse leukoencephalopathy with spheroids due to CSF1R mutation: a case report and literature review.

Zhuang LP, Liu CY, Li YX, Huang HP, Zou ZY. Zhuang LP, et al. Among authors: zou zy. Ann Transl Med. 2020 Jan;8(1):11. doi: 10.21037/atm.2019.12.17. Ann Transl Med. 2020. PMID: 32055602 Free PMC article.

8

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

9

Serum cytokines profile changes in amyotrophic lateral sclerosis.

Xu CZ, Huan X, Luo SS, Zhong HH, Zhao CB, Chen Y, Zou ZY, Chen S. Xu CZ, et al. Among authors: zou zy. Heliyon. 2024 Mar 27;10(7):e28553. doi: 10.1016/j.heliyon.2024.e28553. eCollection 2024 Apr 15. Heliyon. 2024. PMID: 38596011 Free PMC article.

10

Eomesodermin expression in CD4⁺T-cells associated with disease progression in amyotrophic lateral sclerosis.

Chen S, Huan X, Xu CZ, Luo SS, Zhao CB, Zhong HH, Zheng XY, Qiao K, Dong Y, Wang Y, Liu CY, Huang HP, Chen Y, Zou ZY. Chen S, et al. Among authors: zou zy. CNS Neurosci Ther. 2024 Apr;30(4):e14503. doi: 10.1111/cns.14503. Epub 2023 Oct 18. CNS Neurosci Ther. 2024. PMID: 37850654 Free PMC article.

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