Abstractt Purpose of Review This article aims to review the accurate classification of non-
ischemic cardiomyopathy, including the methods, basis, subtype characteristics, and …

Aims Arrhythmogenic right ventricular cardiomyopathy (ARVC) is characterized by right
ventricular myocardial replacement and life-threatening ventricular arrhythmias …

Background Idiopathic dilated cardiomyopathy (DCM) is recognised to be a heritable
disorder, yet clinical genetic testing does not produce a diagnosis in> 50% of paediatric …

Left ventricular non-compaction cardiomyopathy (LVNC) is a rare heart disease, with or
without left ventricular dysfunction, which is characterized by a two-layer structure of the …

The development of the normal human heart, ranging from gestational age to the mature
adult heart, relies on a very delicate and timely orchestrated order of processes. One of the …

Sudden cardiac death (SCD) is referred to as sudden and unexpected death caused by
cardiovascular diseases, in which a person preexisted heart disease or not. Compelling …

I would like to thank the following persons for their help and guidance throughout my work;
Professor Elisabeth Ehler for sharing her enthusiasm and knowledge of the cardiac …

В статье представлены результаты исследований 104 больных с кардиомиопатиями,
госпитализированных в кардиоревматологические отделения Республиканского …

Background The cardiovascular system is significantly agitated by loss of gravity. In
microgravity, the body fluids shift toward the thoracic cavity, induced the heart becomes …

Background Idiopathic dilated cardiomyopathy (DCM) is recognized to be a heritable
disorder, yet clinical genetic testing does not produce a diagnosis in> 50% of paediatric …