Wilson disease的例句大全

Objective To develop a rapid, exact and effective technique of gene diagnosis for the early diagnosis of patients with Wilson's disease ( WD) and detection of WD heterozygotes.

目的建立快速、准确、有效的Wilson病（Wilson disease，WD）患者早期诊断及杂合子检测的基因诊断技术。

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Treatment of Wilson disease by piggy-back orthotopic liver transplantation

同种原位背驮式肝移植治疗Wilson病

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Clinical diagnosis: hepatolenticular degeneration ( also called Wilson disease) complicated with osteopathy.

临床诊断为肝豆状核变性（亦称Wilson病）并骨质病。

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Hot point mutations of Wilson disease gene in Chinese with DNA sequencing

经DNA测序证实的肝豆状核变性基因突变热区的研究

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Conclusion The most common CT findings in hepatolenticular degeneration patients are mainly brain atrophy and low density of the basal ganglia, especially the symmetrical low density of the lentiform nuclei is characteristic of Wilson disease on CT.

结论肝豆状核变性颅脑CT最多见征象是脑萎缩与基底节低密度灶，特别是双侧豆状核区对称性低密度灶最具有特征性。

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

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

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erythrocyte metabolism and antioxidant status of patients with wilson disease with hemolytic anemia

Wilson病合并溶血性贫血患者的红细胞代谢及抗氧化物水平

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Conclusion Wilson disease complicated with renal impairment in children was easy to be neglected due to the insidious onset. The therapy included of reducing copper intake and absorption, increasing copper excretion and maintaining negative balance of copper metabolism for treatment, and the prognosis is relatively better.

结论儿童肝豆状核变性并肾损害起病隐袭易被临床忽视，治疗上以减少铜摄入和吸收，增加铜排泄、维持铜代谢的负平衡及对症治疗为主，预后较好。

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long-term misdiagnosis analysis on wilson disease characterized by first mental symptom in children

儿童期以精神症状首发的肝豆状核变性长期误诊分析

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Objective: To detect the reasons of misdiagnosis of Wilson disease.

目的了解肝豆状核变性误诊的原因.

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Objective To study the prevalence of mutations of Wilson disease ( WD ) gene in Chinese.

目的研究我国肝豆状核变性 ( WD ) 基因突变的特征.

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Objective To find out the relationship between mutations and pathogenesis of Wilson's disease ( WD) by detecting and analyzing the sequence, checking out the mutations of promoter region of WD gene ( ATP7B).

目的检测肝豆状核变性（Wilson disease，WD）ATP7B基因启动子区的DNA序列，分析其结构，发现存在的突变，通过报告基因瞬时表达研究突变对启动子功能的影响。

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A study on presymptomatic diagnosis of Wilson disease with DNA polymorphic analysis

DNA多态性在肝豆状核变性症状前诊断中的应用

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Cerebral CT Appearance and Clinic in Wilson Disease ( Analysis of 45 cases )

Wilson病的脑CT表现与临床 ( 附45例分析 )

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Clinical study on Wilson's Disease with manifestations of neurologic system as the initial symptoms

Takayasu氏动脉炎的神经系统并发症首发表现神经系统症状的肝豆状核变性的临床研究

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the clinical study of six antidotes against heavy metal poisoning in wilson's disease

六种金属中毒解毒药治疗肝豆状核变性的临床研究

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Methods Chinese agraphia battery ( CAB), and the Xn and AgQ scores were used to identify agraphia in35 patients with Wilson's disease.

方法采用汉语失写检查法对35例脑型肝豆状核变性患者进行中文书写检查。

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Avoid this product if you have Wilson's disease or are allergic to yeast.

患有威尔逊病或对酵母过敏,请不要服用.

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objective to discuss mri manifestation of wilson ′ s disease accompanied with central pontine myelinolysis ( cpm), and to especially detect the value of diffusion-weighted mri ( dwi) in this disease.

目的探讨肝豆状核变性合并中央桥脑髓鞘溶解症（CPM）的MRI表现及弥散加权成像（DWI）的应用价值。

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Micronodular cirrhosis may also be seen with Wilson's disease, primary biliary cirrhosis, and hemochromatosis.

小结节型肝硬化也可见于Wilson病 、 原发性胆汁硬化和血色素沉着症.

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