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亨廷顿舞蹈症

Huntington's disease.

作者信息

Haddad M S, Cummings J L

机构信息

Department of Neurology, Hospital das Clínicas, University of São Paulo Medical School, Brazil.

出版信息

Psychiatr Clin North Am. 1997 Dec;20(4):791-807. doi: 10.1016/s0193-953x(05)70345-2.

DOI:10.1016/s0193-953x(05)70345-2
PMID:9443350
Abstract

Huntington's disease is a genetically inherited degenerative neuropsychiatric disorder, characterized by motor alterations, including involuntary movements such as chorea, dementia and psychiatric disturbances. In this article, the authors review the clinical features of the disease. They also analyze some genetic and pathophysiologic aspects, that can help to improve our understanding of this disorder involving the basal ganglia.

摘要

亨廷顿舞蹈症是一种遗传性神经退行性精神疾病,其特征为运动改变,包括舞蹈样不自主运动、痴呆和精神障碍。在本文中,作者回顾了该疾病的临床特征。他们还分析了一些遗传和病理生理学方面的内容,这有助于增进我们对这种累及基底神经节的疾病的理解。

相似文献

1
Huntington's disease.亨廷顿舞蹈症
Psychiatr Clin North Am. 1997 Dec;20(4):791-807. doi: 10.1016/s0193-953x(05)70345-2.
2
Pathophysiology of chorea and bradykinesia in Huntington's disease.亨廷顿舞蹈症中舞蹈样动作和运动迟缓的病理生理学
Mov Disord. 1999 May;14(3):398-403. doi: 10.1002/1531-8257(199905)14:3<398::aid-mds1003>3.0.co;2-f.
3
The pattern of neurodegeneration in Huntington's disease: a comparative study of cannabinoid, dopamine, adenosine and GABA(A) receptor alterations in the human basal ganglia in Huntington's disease.亨廷顿舞蹈病中的神经退行性变模式:亨廷顿舞蹈病患者人类基底神经节中大麻素、多巴胺、腺苷和GABA(A)受体改变的比较研究
Neuroscience. 2000;97(3):505-19. doi: 10.1016/s0306-4522(00)00008-7.
4
[Current perspectives in the treatment of Huntington's chorea].[亨廷顿舞蹈症治疗的当前观点]
Neurol Neurochir Pol. 2002 Jul-Aug;36(4):757-65.
5
Huntington's disease: Neuropsychiatric manifestations of Huntington's disease.亨廷顿舞蹈症:亨廷顿舞蹈症的神经精神表现
Australas Psychiatry. 2018 Aug;26(4):366-375. doi: 10.1177/1039856218791036. Epub 2018 Jul 16.
6
The Neuropsychology of Huntington's Disease.亨廷顿舞蹈症的神经心理学
Arch Clin Neuropsychol. 2017 Nov 1;32(7):876-887. doi: 10.1093/arclin/acx086.
7
[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.
8
Chorea.舞蹈病
Curr Opin Neurol. 1996 Aug;9(4):298-302. doi: 10.1097/00019052-199608000-00010.
9
Neuropsychiatry of Huntington's disease and other basal ganglia disorders.亨廷顿舞蹈症及其他基底神经节疾病的神经精神病学
Psychosomatics. 2000 Jan-Feb;41(1):24-30. doi: 10.1016/S0033-3182(00)71170-4.
10
A clinico-genetic study of psychiatric disorder in Huntington's chorea.亨廷顿舞蹈症精神障碍的临床遗传学研究。
Psychol Med. 1993;Suppl 23:1-46. doi: 10.1017/s0264180100001193.

引用本文的文献

1
Safety of Deutetrabenazine for the Treatment of Tardive Dyskinesia and Chorea Associated with Huntington Disease.氘代丁苯那嗪治疗与亨廷顿病相关的迟发性运动障碍和舞蹈症的安全性
Neurol Ther. 2024 Jun;13(3):655-675. doi: 10.1007/s40120-024-00600-1. Epub 2024 Apr 1.
2
Biological functions and potential therapeutic applications of huntingtin-associated protein 1: progress and prospects.亨廷顿蛋白相关蛋白 1 的生物学功能及潜在治疗应用:进展与展望。
Clin Transl Oncol. 2022 Feb;24(2):203-214. doi: 10.1007/s12094-021-02702-w. Epub 2021 Sep 26.
3
Structural and functional features of medium spiny neurons in the BACHDΔN17 mouse model of Huntington's Disease.
亨廷顿病 BACHDΔN17 小鼠模型中中间棘神经元的结构和功能特征。
PLoS One. 2020 Jun 23;15(6):e0234394. doi: 10.1371/journal.pone.0234394. eCollection 2020.
4
Differential changes to D1 and D2 medium spiny neurons in the 12-month-old Q175+/- mouse model of Huntington's Disease.亨廷顿病 Q175+/- 小鼠 12 月龄模型中 D1 和 D2 中型多棘神经元的差异变化。
PLoS One. 2018 Aug 17;13(8):e0200626. doi: 10.1371/journal.pone.0200626. eCollection 2018.
5
The Tiny for the Biggest Answers in Huntington's Disease.亨廷顿病研究的重大突破:微小的希望。
Int J Mol Sci. 2018 Aug 14;19(8):2398. doi: 10.3390/ijms19082398.
6
ANN and Fuzzy Logic Based Model to Evaluate Huntington Disease Symptoms.基于 ANN 和模糊逻辑的亨廷顿病症状评估模型。
J Healthc Eng. 2018 Mar 11;2018:4581272. doi: 10.1155/2018/4581272. eCollection 2018.
7
Striatal Direct and Indirect Pathway Output Structures Are Differentially Altered in Mouse Models of Huntington's Disease.纹状体直接和间接通路输出结构在亨廷顿病小鼠模型中发生差异改变。
J Neurosci. 2018 May 16;38(20):4678-4694. doi: 10.1523/JNEUROSCI.0434-18.2018. Epub 2018 Apr 24.
8
Altered excitatory and inhibitory inputs to striatal medium-sized spiny neurons and cortical pyramidal neurons in the Q175 mouse model of Huntington's disease.亨廷顿舞蹈病Q175小鼠模型中纹状体中等棘状神经元和皮质锥体神经元的兴奋性和抑制性输入改变。
J Neurophysiol. 2015 Apr 1;113(7):2953-66. doi: 10.1152/jn.01056.2014. Epub 2015 Feb 11.
9
Electroconvulsive shock ameliorates disease processes and extends survival in huntingtin mutant mice.电休克疗法可改善亨廷顿突变小鼠的疾病进程并延长其生存时间。
Hum Mol Genet. 2011 Feb 15;20(4):659-69. doi: 10.1093/hmg/ddq512. Epub 2010 Nov 24.
10
Preclinical Huntington's disease: compensatory brain responses during learning.临床前亨廷顿舞蹈病:学习过程中的大脑代偿反应
Ann Neurol. 2006 Jan;59(1):53-9. doi: 10.1002/ana.20684.