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   阿尔茨海默病(ad) 的翻译结果: 查询用时:1.177秒
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阿尔茨海默病ad     
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     Results Prevalence rate of senile dementia was 4.19%, among which Alzheimer disease (AD) was 3.60% and vascular dementia (VD) 0.66% and other type of dementia 0.33%.
     结果老年期痴呆的患病率4.19%,其中阿尔茨海默病(AD)患病率3.39%,血管性痴呆0.66%,其他原因所致痴呆0.33%。
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     Objective To explore the relationship between paraoxonase-1 (PON1) gene Gln192Arg polymorphism and sporadic Alzheimer's disease (AD) in Chinese.
     目的探讨对氧磷酶1(paraoxonase-1, PON1)基因Gln192Arg多态性与汉族散发阿尔茨海默病(AD)的关系。
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     Objective To explore the possible association between interleukin-1α-889C/T (IL-1α-889 C/T) polymorphism and Alzheimer's disease(AD) in Chinese Han population.
     目的研究中国汉族人群白介素1α-889C/T(IL-1α-889C/T)多态性与阿尔茨海默病(AD)发病的相关性。
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     Objective To investigate the relationship between serum Aβ_(1-28) level and age in Chinese adults,and lay the foundation for the study of Aβ_(1-28) and Alzheimer's disease.
     目的探讨我国成人血清β淀粉样蛋白(A1β-28)含量与年龄之间的关系,为研究Aβ1-28与阿尔茨海默病(AD)的关系奠定基础。
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     Objective To explore the expressions of HSP70 in hippocampus neurons of Alzheimer's (AD) model rats induced by Aβ_(25~35).
     目的利用β淀粉样蛋白(Aβ25~35)毒性作用诱导大鼠阿尔茨海默病(AD)模型,研究热休克蛋白70(HSP70)在海马神经元损伤中的表达。
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  相似匹配句对
     An investigation of the rehabilitation efficacy in Alzheimer's disease
     阿尔茨海默的康复治疗
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     Amyloid-β immunotherapy for Alzheimer's disease
     阿尔茨海默的免疫治疗
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     Aim:To study the nature of the olfactory dysfunction associated with Alzheimer's disease(AD).
     目的 :研究阿尔茨海默 (AD)患者嗅觉障碍。
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     Objective To investigate the etiology and pathogenesis of Alzheimer's disease(AD).
     目的 探讨阿尔茨海默 (AD)因及发机制。
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     Objective It is known that dementia is a multi-factorial disorder, but the etiological factors other than aging remain to be explored, hence we sought to investigate the risk factors of dementia and Alzheimer' s disease (AD).
     目的探讨老年痴呆和阿尔茨海默(AD)的危险因素。
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  alzheimer ' s disease (ad)
β-Amyloid peptide (Aβ), a normal constituent of neuronal and non-neuronal cells, has been proved to be the major component of extracellular plaque of Alzheimer's disease (AD).
      
A significant proportion of early onset Alzheimer's disease (AD) is caused by mutations in human genes for amyloid precursor protein (APP), presenilins 1 and 2 (PSEN1,2).
      
Missense mutations in human presenilin 1 gene (hPS1) cause an autosomal dominant, early onset form of Alzheimer's disease (AD).
      
Among three isoforms, the apoE4 isoform is associated with increased frequency of atherosclerosis and Alzheimer's disease (AD).
      
Studies of the molecular mechanisms of Alzheimer's disease (AD) have led to two major achievements.
      
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  alzheimer disease (ad)
We describe a patient who was clinically diagnosed with familial early-onset Alzheimer disease (AD) carrying both the E318G substitution in presenilin 1 (PSEN1) and an insertion of 7 octapeptide coding repeats in the prion protein gene (PRNP).
      
A variety of therapeutic modalities have been employed in the treatment of Alzheimer disease (AD).
      
Special emphasis is placed on studies of anticholinergics in patients with Alzheimer disease (AD).
      
Alzheimer disease (AD) is the most common cause of dementia.
      
In order to investigate the pathogenesis of Alzheimer disease (AD) and study the enzymatic progress of amyloid precursor protein (APP), the fluorescent eukaryotic expression plasmid of C99 was constructed containing APP717 mutation.
      
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