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Huntington disease.

作者信息

Vonsattel J P, DiFiglia M

机构信息

Massachusetts General Hospital and Harvard Medical School, Boston, USA.

出版信息

J Neuropathol Exp Neurol. 1998 May;57(5):369-84. doi: 10.1097/00005072-199805000-00001.

DOI:10.1097/00005072-199805000-00001
PMID:9596408
Abstract
摘要

相似文献

1
Huntington disease.亨廷顿病
J Neuropathol Exp Neurol. 1998 May;57(5):369-84. doi: 10.1097/00005072-199805000-00001.
2
The current model of basal ganglia organization under scrutiny.目前正在接受审视的基底神经节组织模型。
Mov Disord. 1998 Mar;13(2):199-202. doi: 10.1002/mds.870130202.
3
Huntington disease in a 9-year-old boy: clinical course and neuropathologic examination.一名9岁男孩的亨廷顿病:临床病程及神经病理学检查
J Child Neurol. 2006 Dec;21(12):1068-73. doi: 10.1177/7010.2006.00244.
4
[Basal ganglia disease. Functional neuroanatomy and therapeutic perspectives].[基底神经节疾病。功能性神经解剖学与治疗前景]
Ugeskr Laeger. 2000 Oct 9;162(41):5480-3.
5
Neurotransmitters in Huntington's Chorea--a clinician's view.
Prog Brain Res. 1982;55:445-64. doi: 10.1016/S0079-6123(08)64214-4.
6
[Quantitative studies of human basal ganglia in extrapyramidal motor disorders].
Verh Anat Ges. 1977(71 Pt 1):99-101.
7
Basal ganglia volume is strongly related to P3 event-related potential in premanifest Huntington's disease.基底节体积与前驱期亨廷顿病的 P3 事件相关电位密切相关。
Eur J Neurol. 2011 Aug;18(8):1105-8. doi: 10.1111/j.1468-1331.2010.03309.x. Epub 2011 Jan 25.
8
The relationships of aging changes in the basal ganglia to manifestations of Huntington's chorea.
Ann Neurol. 1980 May;7(5):406-11. doi: 10.1002/ana.410070503.
9
[Huntington's chorea and neurofibromatosis (von Recklinghausen's disease). Concurrence of two generations of a family with inherited Huntington's chorea].[亨廷顿舞蹈病与神经纤维瘤病(冯·雷克林豪森病)。一个家族两代人遗传性亨廷顿舞蹈病并发]
Z Neurol. 1971 Apr 28;199(1):39-45.
10
p75NTR in Huntington's disease: beyond the basal ganglia.亨廷顿舞蹈病中的p75神经营养因子受体:基底神经节之外的情况
Oncotarget. 2016 Jan 5;7(1):1-2. doi: 10.18632/oncotarget.6646.

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Huntingtin preserves mitochondrial genome integrity in neurons, which is impaired in Huntington's disease.亨廷顿蛋白可维持神经元中线粒体基因组的完整性,而在亨廷顿舞蹈症中这种完整性会受到损害。
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Time-restricted eating in early-stage Huntington's disease: A 12-week interventional clinical trial protocol.早期亨廷顿舞蹈症的限时饮食:一项为期12周的干预性临床试验方案。
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Presymptomatic targeted circuit manipulation for ameliorating Huntington's disease pathogenesis.用于改善亨廷顿病发病机制的症状前靶向回路操纵。
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Human striatal progenitor cells that contain inducible safeguards and overexpress BDNF rescue Huntington's disease phenotypes.含有可诱导保护机制并过表达脑源性神经营养因子(BDNF)的人类纹状体祖细胞可挽救亨廷顿病的表型。
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