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晚发型脊髓小脑性共济失调3型一例 |
张桂风1,夏章勇2,贾晓东3,陈德哲2,李莉1,张柳英1,王晓婷1点击查看XML格式全文 |
1山东第一医科大学(山东省医学科学院),山东省泰安市 271016; 2山东省聊城市人民医院神经内科 山东省心脑血管病微创治疗工程技术研究中心 252000; 3山东省聊城市人民医院转化医学研究联合实验室 252000 |
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Late onset spinocerebellar ataxia type 3: a case report |
Zhang Guifeng1,Xia Zhangyong2,Jia Xiaodong3, Chen Dezhe2, Li Li1, Zhang Liuying1, Wang Xiaoting1 |
1Shandong First Medical University & Shangdong Academy of Medical Sciences, Taian 271016, China; 2Department of Neurology, Liaocheng People's Hospital, Liaocheng 25200, China; 3Joint Laboratory for Translational Medicine Research of Liaocheng People's Hospital, Liaocheng 252000, China |
引用本文: |
张桂风,夏章勇,贾晓东,陈德哲,李莉,张柳英,王晓婷. 晚发型脊髓小脑性共济失调3型一例[J]. 中华解剖与临床杂志, 2019, 24(2): 188-189.
Zhang Guifeng,Xia Zhangyong,Jia Xiaodong, Chen Dezhe, Li Li, Zhang Liuying, Wang Xiaoting. Late onset spinocerebellar ataxia type 3: a case report. Chinese Journal of Anatomy and Clinics, 2019, 24(2): 188-189.
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链接本文: |
http://www.cjac.com.cn/CN/10.3760/cma.j.issn.2095-7041.2019.02.018 或 http://www.cjac.com.cn/CN/Y2019/V24/I2/188 |
[1] |
Paulson HL, Shakkottai VG, Clark HB, et al. Polyglutamine spinocerebellar ataxias-from genes to potential treatments[J]. Nat Rev Neurosci, 2017, 18(10): 613-626. DOI:10.1038/nrn.2017.92.
|
[2] |
Seidel K, Siswanto S, Brunt ER, et al. Brain pathology of spinocerebellar ataxias[J]. Acta Neuropathol, 2012, 124(1): 1-21. DOI:10.1007/s00401-012-1000-x.
|
[3] |
王俊岭, 徐倩, 雷立芳, 等. 脊髓小脑共济失调患者CAG病理重复次数检测[J]. 中华医学遗传学杂志, 2009, 26(6): 620-625. DOI:10.3760/cma.j.issn.1003-9406.2009.06.005.
|
[4] |
Sun YM, Lu C, Wu ZY. Spinocerebellar ataxia: relationship between phenotype and genotype - a review[J]. Clin Genet, 2016, 90(4): 305-314. DOI:10.1111/cge.12808.
|
[5] |
Ashizawa T,z G, Paulson HL. Author correction: spinocerebellar ataxias: prospects and challenges for therapy development[J]. Nat Rev Neurol, 2018, 14(12): 749. DOI:10.1038/s41582-018-0102-z.
|
[6] |
Velázquez-Pérez L. An insight into the natural history of spinocerebellar ataxias[J]. Lancet Neurol, 2015, 14(11): 1067-1069. DOI:10.1016/S1474-4422(15)00218-5.
|
[7] |
Hsieh J, Liu JW, Harn HJ, et al. Human olfactory ensheathing cell transplantation improves motor function in a mouse model of type 3 spinocerebellar ataxia[J]. Cell Transplant, 2017, 26(10): 1611-1621. DOI:10.1177/0963689717732578.
|
[8] |
Manes M, Alberici A, Di Gregorio E, et al. Docosahexaenoic acid is a beneficial replacement treatment for spinocerebellar ataxia 38[J]. Ann Neurol, 2017, 82(4): 615-621. DOI:10.1002/ana.25059.
|
[9] |
Lo RY, Figueroa KP, Pulst SM, et al. Depression and clinical progression in spinocerebellar ataxias[J]. Parkinsonism Relat Disord, 2016, 22: 87-92. DOI:10.1016/j.parkreldis.2015.11.021.
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