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ataxia相关的网络例句

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与 ataxia 相关的网络例句 [注:此内容来源于网络,仅供参考]

Syndrome of Ophthalmoplegia,Ataxia and Areflexia: A Disease of Peripheral or Central Nervous System?

篇名 眼肌麻庳、运动失调和深部肌腱反射消失症候群:病变位置在周边或是中枢神经系统?

Although most individuals develop spastic paraparesis, mild ataxia, and occasional mild cognitive deficit in their second decade, the course of the disease is relatively stable.

虽然大多数患者下肢轻瘫、轻度共济失调和偶而出现在十几岁时的轻度认知障碍,此病的进程相对稳定。

The neurological abnormalities can be classifi ed as: an akinetic-rigid syndrome similar to Parkinson's disease, pseudosclerosis dominated by tremor, ataxia, and a dystonic syndrome.

神经系统的异常可以分为以下几类:a 类似于帕金森氏病的运动不能-肌强直综合征;b以震颤为主要表现的假性多发性硬化;c共济失调; d 肌张力障碍综合征。

Progressive supranuclear palsy is a degenerative neurological disorder of uncertain etiology characterized by gait ataxia, slowing or inability to generate voluntary saccadic eye movements, and axial rigidity.

译:进行性核上性麻痹是病因不明的神经系统退行性病变,临床表现为共济失调步态、自主眼球扫视运动无法完成或完成缓慢、躯干强直。

The authors describe the case of a 45-year-old man with progressive gait ataxia and sensorimotor deficits of the upper and lower extremities.

作者描述了一例45岁男性渐进性的步态共济失调和手足感觉运动缺陷患者。

Spinocerebellar ataxia type 7 (SCA7) is less variable in clinical presentation than other SCAs.

脊髓小脑性共济失调7型(SCA7)的临床表现形式较其它SCA类型少。

Ataxin-1 is another pathogenic protein which causes a disease called spinocerebellar ataxia, which is also an incurable hereditary nervous disorder.

Ataxin-1是另一种致病蛋白,它能够引起脊髓小脑性共济失调,也是一种不能治愈的遗传性神经系统疾病。

Objective To screen for proteins interacting with ataxin-3 by yeast two-hybrid system 3, and to discuss the function of ataxin-3 and pathogenesis of spinocerebellar ataxia type 3 and Machado-Joseph disease (SCA3/MJD).

目的:利用酵母双杂交系统3筛选与ataxin-3相互作用的蛋白质,探讨ataxin-3的功能和脊髓小脑型共济失调Ⅲ型(SCA3/MJD)的发病机制。

Study on the gene mutation of spinocerebellar ataxia types 1~3 in patients with primary dystonia LI Guibing, WANG Jin.

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Oint mutation of PKCγ gene can induce inherited retinitis pigmentosa,spinocerebellar ataxia and tumors.

KCγ基因点突变可诱发遗传性色素性视网膜炎、脊髓小脑共济失调和肿瘤等。

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