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Fruit Fly Muscles With A Hypertrophic Cardiomyopathy Mutation Don’t Relax Properly（图）
Fruit Fly Muscles Hypertrophic Cardiomyopathy Mutation Don’t Relax Properly
2017/10/25
Using fruit flies, Johns Hopkins researchers have figured out why a particular inherited human heart condition that is almost always due to genetic mutations causes the heart to enlarge, thicken and f...
Role of Implantable Cardioverter Defibrillators in the Treatment of Hypertrophic Cardiomyopathy
Hypertrophic cardiomyopathy implantable defibrillator sudden cardiac death
2015/8/3
Hypertrophic cardiomyopathy (HCM) is an important cardiovascular disease with sudden cardiac death as the most devastating presentation. Implantable cardioverter defibrillators (ICD) are the optimal t...
Risk Stratification for Sudden Cardiac Death In Patients With Non-ischemic Dilated Cardiomyopathy
Non Ischemic Dilated Cardiomyopathy Ischemic Dilated Cardiomyopathy Risk Stratification Implantable cardioverter defibrillator Sudden Cardiac Death
2015/8/3
Non ischemic dilated cardiomyopathy (NIDCM) is a disorder of myocardium. It has varying etiologies. Albeit the varying etiologies of this heart muscle disorder, it presents with symptoms of heart fail...
Identification and characterization of altered mitochondrial protein acetylation in Friedreich's ataxia cardiomyopathy
Identification and characterization mitochondrial protein acetylation
2015/5/21
Friedreich’s Ataxia (FRDA) is a rare and poorly understood autosomal recessive disease caused by a pathological deficiency of the mitochondrial protein frataxin. Patients suffer neurodegeneration, ata...
The role of echocardiography in the differential diagnosis between training induced myocardial hypertrophy versus cardiomyopathy
Left ventricle physical exercises
2015/4/1
Increased myocardial mass due to regular high-volume
intense exercise training (so-called athlete’s heart) is not
uncommon. Although directly correlated with the extent
of training loads, myocar...
Aortic Dissection and Postpartum Cardiomyopathy in a Postpartum Young Woman:A Case Report Study
Aortic Aneurysm Familial Thoracic 1 Cardiomyopathies Peripartum Period Women
2015/10/12
Introduction:: Aortic dissection is a rare condition in young women and usually related with congenital anomalies of aorta and connective tissue disorders. We reported a 34-year-old postpartum woman w...
西安交通大学医学院循环系统疾病课件 Cardiomyopathy。
A new diagnostic feasibility for cardiomyopathy utilizing acoustic microscopy
Cardiomyopathy Acoustic Microscopy Heart Failure Myocytes Sound Speed Diagnosis
2013/2/19
Aims: Dilated cardiomyopathy often shows left ventricular systolic dysfunction, although histologically it always exhibits non-specific abnormality. We hypothesized that myocyte sound speed might be a...
Variant of takotsubo cardiomyopathy associated with sepsis and respiratory failure in an elderly female
Takotsubo Cardiomyopathy Inverted Cardiomyopathy Stress Induced Cardiomyopathy
2013/2/19
Stress induced cardiomyopathy/Takotsubo cardiomyopathy (TSO CMO) has been widely reported. It is characterized by apical hypokinesis or akinesis. Variants of this called as inverted/reverse cardiomyop...
Detraining-Related Changes in Left Ventricular Wall Thickness and Longitudinal Strain in a Young Athlete Likely to Have Hypertrophic Cardiomyopathy
Athlete’s heart detraining echocardiography hypertrophic cardiomyopathy left ventricular hypertrophy myocardial function strain echocardiography
2015/5/12
One of the diagnostic criteria in order to differentiate between physiological and pathological left ventricular hypertrophy is the wall thickness reduction after at least 3-month detraining period, w...
Left Ventricular Non-compaction with Associated Anomalies:A Rare Congenital Cardiomyopathy
Left Ventricular Non-compaction Congenital Cardiomyopathy
2015/9/21
A 22-year-old man was admitted with chief complaint of dyspnea on exertion. The patient had a history of operation 10 years ago for coarctation of the aorta. Transthoracic echocardiography showed bicu...
The Efficacy of L-Carnitine Treatment in Dilated Cardiomyopathy
L-Carnitine Dilated Cardiomypopathy Doppler Echocardiography
2009/7/2
This study was carried out to investigate clinical effects of treatment with the supplementation of L-carnitine in cases with dilated cardiomyopathy. B Mode, M-Mode, and continuous Doppler echocardiog...
中国人扩张型心肌病与受磷蛋白基因关系的研究 Association between Mutation of Phospholamban Gene and Dilated Cardiomyopathy
扩张型心肌病 受磷蛋白基因 突变
2008/1/8
摘要
受磷蛋白（phospholamban）是心肌收缩的一个重要调节因子，可抑制心肌肌浆网钙ATPase的活性、降低其对钙的亲和力。正常情况下，受磷蛋白可被不同的蛋白激酶磷酸化从而解除其肌浆网钙ATPase的抑制作用。国外两个DCM家系研究发现受磷蛋白基因突变与DCM的发生有关，研究目的旨在探讨中国人群心肌特异性受磷蛋白基因突变与特发性扩张型心肌病发病的关系。收集60例确诊的特发性扩张型心肌病...