亨廷顿病

与亨廷顿病严重程度相关的小胶质细胞激活：一项临床及PET研究

Microglial activation correlates with severity in Huntington disease : A clinical and PET study

亨廷顿病潜伏期局部皮质变薄及其与认知功能的关系

Regional cortical thinning in preclinical Huntington disease and its relationship to cognition

中国人亨廷顿病CAG三核苷酸重复的分子分析

Molecular analysis of huntington 's disease with expanded CAG trinucleotide repeat in Chinese

咪唑啉I2受体与抑郁症、帕金森病、亨廷顿病、阿片成瘾及阿尔茨海默病等疾病的发生有关。

I 2 receptor is related to some diseases , such as depression , Parkinson ′ s disease , Huntington ′ s disease , opioid addiction and Alzheimer ′ s disease .

亨廷顿病的临床前期：学习期间大脑的代偿性反应

Preclinical Huntington 's disease : Compensatory brain responses during learning

肝豆状核变性、亨廷顿病和遗传性共济失调的分子诊断方法研究

Molecular Diagnostic Methods for Wilson Disease , Huntington Disease and Spinocerebellar Ataxia

亨廷顿病的基因诊断及家系分析

Molecular Diagnosis of Huntington 's Disease : an analysis of two large families

临床前期及早期亨廷顿病的眼球震颤

Saccades in presymptomatic and early stages of Huntington disease

运动功能减退和运动徐缓在亨廷顿病患者步态障碍中的作用：一项生物力学研究

Role of hypokinesia and bradykinesia in gait disturbances in Huntington 's disease : A biomechanical study

中药复方参乌胶囊对亨廷顿病大鼠模型运动功能及脑内单胺类神经递质含量的影响

Effects of Shen-wu Capsule on motor function and content of dopamine in striatum in Huntington model rats

亨廷顿病使用肌酸安全、可耐受、具有脑内生物效用并可降低血清中8OH2'dG水平

Creatine in Huntington disease is safe , tolerable , bioavailable in brain and reduces serum 8OH2 ′ dG

R6/2型亨廷顿病转基因小鼠胰岛β细胞功能损伤

Impaired function of pancreatic β cells in the R6 / 2 transgenic mouse model of Huntington 's disease

纹状体在语法应用中的作用：亨廷顿病早期模型

The role of the striatum in rule application : The model of Huntington 's disease at early stage

单眼分离性眼颤和眼部追踪运动病例临床前期及早期亨廷顿病的眼球震颤

Clinically evidenced unilateral dissociation of saccades and pursuit eye movements Saccades in presymptomatic and early stages of Huntington disease

西班牙亨廷顿病的发病率和突变率：一项基于9年直接基因检测的结果

Incidence and mutation rates of Huntington 's disease in Spain : Experience of 9 years of direct genetic testing

亨廷顿病是一种大量的脑细胞内蛋白变质为特征的一大类疾病中的一种。

Huntington 's disease is one of a number of degenerative diseases marked by clumps of malformed protein in brain cells .

本文就近年有关成功减轻帕金森病和亨廷顿病中的神经退行性病的神经保护策略进行综述如下。

This paper attempts to review the strategies to protect the neurodegeneration that occurs in both Parkinson 's and Huntington 's diseases .

她拒绝接受亨廷顿病的遗传学检查，主要是由于担心会带来有就业及保险方面的困难。

She declined genetic testing for HD , principally out of concern fora relative who might have difficulty with employment or insurance .

早期亨廷顿病患者的执行能力障碍与纹状体和岛叶萎缩相关：一项神经心理学和基于体素的形态测量学研究

Executive dysfunction in early stages of Huntington 's disease is associated with striatal and insular atrophy : A neuropsychological and voxel-based morphometric study

该疾病主要包括阿尔茨海默氏病、帕金森病、亨廷顿病等。研究发现，神经退行性疾病都有一个共同的特征，即发生神经元的退行性病变和凋亡。

They mainly include Alzheimer disease , Parkinson disease , Huntington disease etc. and they have the common features : neuronal degeneration and apoptosis .

亨廷顿病（舞蹈病）是一种家族遗传病，缘于大脑中的神经元衰弱或退化造成的失调紊乱。

Huntington 's disease : is a disorder passed down through families in which nerve cells in the brain waste away , or degenerate .

在此之后，她才开始显示出亨廷顿病的症状，这是一种会导致恐怖错觉和行动失控的遗传性脑疾。

Only later did she begin to display the symptoms of Huntington 's Disease , an inherited brain disorder that produces horrific delusions and uncontrolled movements .

因为没有人知道亨廷顿病如何累患或传播，所以这个新的重要结果为进一步研究探索提供了一条清晰的思路。

Because no one knows how the disease is incurred or spreads , this new information is critical and establishes a clear path for investigations to move forward .

本文对锥体外系疾病中帕金森病（PD）、Wilson病（WD）、肌张力障碍、亨廷顿舞蹈病（HD）的诊疗进展作一简要介绍。

The progress in the diagnosis and treatment of several extrapyramidal diseases , including Parkinson disease ( PD ), Wilson disease ( WD ), dystonia and Huntington disease ( HD ) was reviewed .

与亨廷顿氏病患者相比，AD患者大脑灰质非水溶性级分三种NF亚基的含量均升高，且升高的NF-H和NF-M主要表现为异常过度磷酸化形式。

Compared with Huntington 's disease ( HD ), the content of NF subunits was increased in AD brain gray matter and the increased level of NF-H and NF-M were mainly in abnormal hyperphosphorylated form .

“如部分红斑狼疮、代谢紊乱、亨廷顿舞蹈病会出现在一些非常年青的孩子中，”Kelley在路透社健康报中说。

" Some of the important causes , such as lupus , metabolic disorders , Huntington chorea , among others , can occur in very young children ," Kelley told Reuters Health .

亨廷顿舞蹈病的分子病理研究进展

Research progress in molecular pathology of Huntington 's disease

早期发病的亨廷顿舞蹈病：一种神经元退行性改变综合征

Early onset Huntington disease : A neuronal degeneration syndrome

这些影像摄自一位70岁女性，临床诊断有亨廷顿舞蹈病。

These images are from an70 year old woman who has a clinical diagnosis of Huntington 's disease .

现代分子遗传学研究发现，亨廷顿氏病是由编码亨廷顿蛋白质的基因突变引起的。

Modern molecular genetics revealed that Huntington 's disease is caused by a mutation in the gene coding for the protein Huntingtin .