1) dilated-phase hypertrophic cardiomyopathy
扩张期肥厚型心肌病
1.
Purpose To explore the prevalence, predictive factors, clinical and pathologic feature, as well as prognosis of dilated-phase hypertrophic cardiomyopathy (DPHCM), evolved from classic hypertrophic cardiomyopathy (HCM).
目的研究肥厚型心肌病(hypertrophic cardiomyopathy,HCM)演变为呈扩张型低动力状态的扩张期肥厚型心肌病(dilated-phase hypertrophic cardiomyopathy,DPHCM)的发生率、预测因素、临床及病理表现、治疗与预后。
2) Hypertrophic cardiomyopathy
肥厚型心肌病
1.
Evaluation left atrial systolic and diastolic function of hypertrophic cardiomyopathy by tissue velocity imaging;
肥厚型心肌病左房收缩和舒张功能的组织速度成像研究
2.
Clinical significance of coronary artery disease in hypertrophic cardiomyopathy;
肥厚型心肌病合并冠心病的临床意义
3.
Change of 12-lead electrocardiogram in patients with hypertrophic cardiomyopathy after chemical ablation;
肥厚型心肌病化学消融术后心电图改变
3) Cardiomyopathy hypertrophic
心肌病肥厚型
4) HCM
肥厚型心肌病
1.
Objectives To observe the relationship between QT dispersion and the mass of left ventricle in hypertrophic cardiomyopathy, and find whether in HCM paitents the sensitivity to electrical instability of ventricular repolarization is increased and its chief reasons.
目的 观察肥厚型心肌病 (HCM )患者QT离散度 (QTd)与左室重量 (LVM)关系 ,探讨HCM患者心室肌复极电活动稳定性及引起其不稳定的主要原因。
2.
Objective To explore the relationship between hypertrophic cardiomyopathy (HCM)and expression of P53 in peripheral blood lymphocyte.
目的 探讨肥厚型心肌病的心肌肥厚与p5 3蛋白表达之间关系。
3.
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。
5) Dilated cardiomyopathy
扩张型心肌病
1.
Clinical analysis of dilated cardiomyopathy complicating with congestive heart failure treated with CRT pacemaker;
三心腔起搏器治疗扩张型心肌病伴充血性心力衰竭的临床分析
2.
The observation and nursing of Dilated cardiomyopathy arrhythmia;
扩张型心肌病心律失常的观察及护理
3.
The effect of arotinolol on right ventricular function in patients with dilated cardiomyopathy;
阿罗洛尔对扩张型心肌病心力衰竭患者右心室功能的影响
6) DCM
扩张型心肌病
1.
Study on the Role of QTVI and TT in Evaluating the Left Ventricular Function of Contraction in Patients with DCM
QTVI和TT技术对扩张型心肌病患者左室收缩功能的研究
2.
[Objective] To test the effect of oral benazepril on action potetial duration of midmyocardial cel in rabbit models of dilated cariomyopathy (DCM) and find whether this effect plays an important role in suppressing ventricular arrhythmias.
目的探讨贝那普利对扩张型心肌病(DCM)中层心肌细胞动作电位时程的影响及其抑制室性心律失常。
3.
Objective To explore the diagnosis values of quiet dispersion degree(QTd)to the sudden death from dilating cardiomyopathy(DCM).
目的 探讨QT离散度对于扩张型心肌病 (DCM)者猝死的诊断价值。
补充资料：肥厚型心肌病
肥厚型心肌病
hypertrophic cardiomyopathy
原发性心肌病的一型。多见于10岁左右男孩。有人认为本病为常染色体显性遗传。心脏病变主要为室间隔及左室壁心肌肥厚，室间隔更为显著。可分为梗阻型及非梗阻型。早期症状为运动后呼吸困难，心慌、心绞痛、头晕或晕厥。心力衰竭罕见，但可猝死。心脏检查可见心界向左扩大，有抬举性心尖搏动，胸骨左缘下端及近心尖部听到收缩期喷射状杂音等。治疗方面应限制病儿剧烈运动。洋地黄、异丙基肾上腺素等使心脏收缩力加强的药物，可加重流出道梗死，应避免使用。β-肾上腺素能阻滞剂心得安治疗本病，可缓解症状。内科治疗无效者，可外科手术切除肥厚的心肌。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条