1·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的原因之一。
2·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。
3·Objective:To evaluate the diagnostic value of pre-apical hypertrophic cardiomyopathy (PAHCM) by echocardiography.
目的：探讨早期心尖肥厚型心肌病（PAHCM）超声心动图的诊断及鉴别诊断。
4·Objective: To report and analyze the reasons of misdiagnosis in patients with apical hypertrophic cardiomyopathy (AHCM).
目的：报告并分析心尖肥厚性心肌病(AHCM)误诊的原因。
5·Another option for some, such as those with hypertrophic cardiomyopathy, is an implantable cardioverter-defibrillator (ICD).
对于一些人，比如说那些患肥厚性心肌病的人，另一个方法则是植入一个心律转复除颤器(ICD)。
6·Purpose: To evaluate left ventriculography and coronary angiography in diagnosing apical hypertrophic cardiomyopathy (AHCM).
目的：探讨左心室及冠状动脉造影诊断心尖肥厚型心肌病的价值。
7·The characteristics of hypertrophic cardiomyopathy (HCM) are hypertrophy of ventricular muscle and increase of cardiac weight.
肥厚型心肌病(HCM)病变特征为心室肌肥厚，心脏重量增加。
8·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和肥厚型心肌病初步经验。
9·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)白血技术评价肥厚型心肌病(HCM)局部心肌收缩功能。
10·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，或hcm，是一种遗传性心肌增厚的心脏病，尤其多见于左心室。