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Co-occurrence of Wilson's Disease and Spinocerebellar Ataxia Type 3 in a Chinese Patient.

作者信息

Xu Lei, Hou Zhi-Feng, Wang Yan-Xin, Ni Ming-Zhu, Zhang Chuan-Feng

机构信息

Department of Neurology, The First Affiliated Hospital, Anhui University of Chinese Medicine, Hefei, Anhui, China.

Department of Radiology, The First Affiliated Hospital, Anhui University of Chinese Medicine, Hefei, Anhui, China.

出版信息

Acta Neurol Belg. 2025 Aug 4. doi: 10.1007/s13760-025-02852-6.

DOI:10.1007/s13760-025-02852-6
PMID:40758170
Abstract
摘要

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本文引用的文献

1
Spinocerebellar Ataxia Type 3 Pathophysiology-Implications for Translational Research and Clinical Studies.脊髓小脑性共济失调 3 型的病理生理学——对转化研究和临床研究的启示。
Int J Mol Sci. 2024 Apr 3;25(7):3984. doi: 10.3390/ijms25073984.
2
A multidisciplinary approach to the diagnosis and management of Wilson disease: Executive summary of the 2022 Practice Guidance on Wilson disease from the American Association for the Study of Liver Diseases.威尔逊病诊断与管理的多学科方法：美国肝病研究协会2022年威尔逊病实践指南执行摘要
Hepatology. 2023 Apr 1;77(4):1428-1455. doi: 10.1002/hep.32805. Epub 2022 Dec 7.
3
Profiling of mitochondrial genomes in SCA3/MJD patients from mainland China.
中国内地 SCA3/MJD 患者的线粒体基因组分析。
Gene. 2020 May 15;738:144487. doi: 10.1016/j.gene.2020.144487. Epub 2020 Feb 19.
4
A randomized controlled pilot trial of game-based training in individuals with spinocerebellar ataxia type 3.基于游戏的训练对脊髓小脑共济失调 3 型个体的随机对照初步试验。
Sci Rep. 2018 May 18;8(1):7816. doi: 10.1038/s41598-018-26109-w.
5
Families with Wilson's disease in subsequent generations: clinical and genetic analysis.威尔逊氏病后代家庭：临床与遗传学分析。
Mov Disord. 2014 Dec;29(14):1828-32. doi: 10.1002/mds.26057. Epub 2014 Oct 18.