• Abstract : The MYBPC3 gene mutations can cause hypertrophic cardiomyopathy (HCM).

    摘要MYBPC3基因突变是家族性肥厚型心肌病原因之一。

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  • Conclusion HRT can not predict clinical prognosis of patients with hypertrophic cardiomyopathy.

    结论肥厚型心肌病患者窦性心率震荡无异常,不能预测其临床预后

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  • Objective:To evaluate the diagnostic value of pre-apical hypertrophic cardiomyopathy (PAHCM) by echocardiography.

    目的探讨早期心尖肥厚心肌病PAHCM超声心动图诊断及鉴别诊断。

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  • Objective: To report and analyze the reasons of misdiagnosis in patients with apical hypertrophic cardiomyopathy (AHCM).

    目的报告分析心尖肥厚性心肌病(AHCM)误诊原因

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  • Another option for some, such as those with hypertrophic cardiomyopathy, is an implantable cardioverter-defibrillator (ICD).

    对于一些人比如说那些肥厚性心肌病的人,个方法则植入一个心律转复除颤器(ICD)。

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  • Purpose: To evaluate left ventriculography and coronary angiography in diagnosing apical hypertrophic cardiomyopathy (AHCM).

    目的探讨心室及冠状动脉造影诊断心尖肥厚型心肌病的价值。

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  • The characteristics of hypertrophic cardiomyopathy (HCM) are hypertrophy of ventricular muscle and increase of cardiac weight.

    肥厚型心肌病(HCM)病变特征心室肥厚心脏重量增加

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  • Objective to conclude some elementary experience in the surgical operation treatment to dilated and hypertrophic cardiomyopathy.

    目的总结心脏外科手术治疗扩张型心肌病肥厚型心肌病初步经验

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  • Objective to evaluate the regional myocardium systolic function in hypertrophic cardiomyopathy (HCM) by MR bright blood techniques.

    目的应用磁共振(MR)白技术评价肥厚心肌病(HCM)局部心肌收缩功能

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  • Hypertrophic cardiomyopathy, or HCM, is a genetic heart disease where the heart muscle is thickened, especially in the left ventricle.

    肥厚性心肌病hcm一种遗传性心肌心脏病尤其多见于心室

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  • Objective To evaluate the value of left ventricular angiography in the diagnosis of special subtypical hypertrophic cardiomyopathy (HCM).

    目的评价心室造影诊断特殊类型肥厚型心肌病临床价值

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  • Conclusions: Relaxation and systolic functions of left ventricle were decreased in patients with non-obstructive hypertrophic cardiomyopathy.

    结论:非梗阻型肥厚型心肌病室长收缩功能及主动松弛功能较正常人减低。

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  • Hypertrophic cardiomyopathy, while usually not fatal in most people, is the most common cause of heart-related sudden death in people under 30.

    虽说肥厚性心肌病对大多数并没有致命危险,它却是30岁以下的人发生心脏猝死主要原因

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  • Objective: The nomenclature and possible cause of hypertrophic cardiomyopathy (HCM) with ventricular dilatation and heart failure were explored.

    目的探讨肥厚型心肌病(HCM)命名伴心室扩张心力衰竭可能原因

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  • Methods and Results - we assessed the relationship between syncope and sudden death in 1511 consecutive patients with hypertrophic cardiomyopathy.

    方法结果我们1511名肥厚性心肌病患者中评价晕厥猝死关系

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  • Objective to evaluate the regional myocardial systolic function in the patients with hypertrophic cardiomyopathy (HCM) by strain imaging technique.

    目的应用应变成像技术对肥厚心肌病患者正常人的心功能进行研究。

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  • The echocardiographic changes associated with an athlete's heart can be similar to those in hypertrophic cardiomyopathy, and can act to mask the latter.

    运动员心脏超声心动图变化肥厚型心肌病相似能够掩饰后者的变化。

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  • Objective To access the diagnostic value of magnetic resonance first pass perfusion imaging in hypertrophic cardiomyopathy (HCM) with myocardial ischemia.

    目的评价心肌灌注磁共振成像技术肥厚型心肌病(HCM)心肌缺血诊断作用。

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  • Tears seem appropriate. Enlargement of the heart muscle, or hypertrophic cardiomyopathy, is a serious disease which could lead to congestive heart failure.

    流泪应该心肌扩张或是肥大型心肌病都是重病引起充血性心力衰竭。

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  • Hypertrophic cardiomyopathy (HCM). This is a disease in which the heart muscle (myocardium) becomes abnormally thick, making it harder for the heart to pump blood.

    肥厚心肌病(HCM):患了此病,病人心脏肌肉(心肌)会变得异常肥厚而无法心脏输血

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  • ObjectiveTo assess the left ventricular regional systolic function in patients with hypertrophic cardiomyopathy (HCM) using quantitative tissue velocity imaging (QTVI).

    目的应用定量组织速度成像(QTVI)评价肥厚型心肌病(HCM)患者心室局部收缩功能

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  • Objective To investigate the effects of diltiazem on left ventricular early diastolic flow propagation velocity (VP) in patients with hypertrophic cardiomyopathy (HCM).

    刘丽华 王志斌 聂晶 李艳摘要目的 检测硫氮卓酮肥厚型心肌病(HCM)心室舒张早期血流传播速度VP影响

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  • Objective to study the disease-causing gene mutations in Chinese hypertrophic cardiomyopathy (HCM) and to reveal the relationship between the genotype and the phenotype.

    目的研究中国人家族性肥厚型心肌病(HCM)致病基因突变位点,分析基因临床表型的相互关系

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  • Objective to assess left ventricular systolic and diastolic functions in patients with hypertrophic cardiomyopathy (HCM) using quantitative tissue velocity imaging (QTVI).

    目的应用定量组织速度成像技术(QTVI)评价肥厚型心肌病(HCM)患者心室长轴方向上的收缩舒张功能

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  • Objective To investigate the relationship between hypertrophic cardiomyopathy and serum leptin by measuring the level of serum leptin in patients with hypertrophic cardiomyopathy.

    目的通过测定肥厚心肌病患者血清瘦水平探讨肥厚性心肌病清瘦素浓度之间关系

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  • Objective To study the characteristics of heart structure changes in rat model with hypertrophic cardiomyopathy (HCM) induced by pressure-overload, and the interference of berberine.

    目的研究压力超负荷致心肌肥厚模型心脏结构变化特点小檗碱对此干预作用

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  • Objective: to compare the effects of percutaneous transluminal septal myocardial ablation (PTSMA) with septal myectomy in patients with obstructive hypertrophic cardiomyopathy (OHCM).

    目的对比评价经经腔间隔心肌消融术(消融)室间隔部分切除术(手术)治疗梗阻性肥厚型心肌病(OHCM)的疗效。

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  • Hypertrophic cardiomyopathy is not related to ischemic heart disease but 50% of cases are familial and may be related to genetic mutations in genes encoding for cardiac contractile elements.

    肥厚性心肌病缺血性心脏病无关但是50%病例具有家族性并且基因突变有关。突变基因一般心脏收缩过程先关基因。

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  • Hypertrophic cardiomyopathy patients exhibit myocardial energetic impairment, but a causative role for this energy deficiency in the pathophysiology of hypertrophic cardiomyopathy remains unproven.

    肥厚心肌病患者表现有心肌能量缺乏但是这种肥厚型心肌病能量缺乏病理生理发生机制尚未得到证实

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  • Hypertrophic cardiomyopathy patients exhibit myocardial energetic impairment, but a causative role for this energy deficiency in the pathophysiology of hypertrophic cardiomyopathy remains unproven.

    肥厚心肌病患者表现有心肌能量缺乏但是这种肥厚型心肌病能量缺乏病理生理发生机制尚未得到证实

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