Springer, 2019. — 176 p. — ISBN: 978-3-030-17719-5 This book provides a comprehensive but concise overview of noncompaction cardiomyopathy. Information on congestive heart failure, thromboembolic events, (potentially lethal) arrhythmias, and sudden cardiac death is presented. Topics covered include the use of modern imaging modalities, such as contrast echocardiography and...
Springer, 2019. — 456 p. — ISBN: 978-3-030-17720-1 This book provides a comprehensive but concise overview of noncompaction cardiomyopathy. Information on congestive heart failure, thromboembolic events, (potentially lethal) arrhythmias, and sudden cardiac death is presented. Topics covered include the use of modern imaging modalities, such as contrast echocardiography and...
Nova Biomedical, 2018. — 187 p. Hypertrophic cardiomyopathy (HCM) is the most common form of genetically inherited cardiovascular disease, with a prevalence of one in 500 individuals. Hypertrophic cardiomyopathy is characterized by both increased ventricular wall thickness in the absence of other causative conditions and potentially fatal arrhythmias. Tunisian authors, together...
Nova Science Publishers, 2016. — 229 p. Takotsubo cardiomyopathy (TC) is a relatively new pathological concept in cardiovascular disease, originally described in the Japanese population at the beginning of the 1990s. It is a left ventricular dysfunction that resembles acute myocardial infarction. This book examines risk factors, discusses management options, and reviews...
Wiley-Blackwell, 2004. — 518 p. Diagnosis and Management of Hypertrophic Cardiomyopathy is a unique, multi-authored compendium of information regarding the complexities of clinical and genetic diagnosis, natural history, and management of hypertrophic cardiomyopathy (HCM)—the most common and important of the genetic cardiovascular diseases — as well as related issues impacting...
3rd ed. — Wiley-Blackwel, 2014. — 150 p. If you are reading this book, you probably fall into three potential groups: (1) you have HCM, (2) a friend or relative has HCM, or (3) you are a healthcare provider. An effort has been made here to inform each of these groups about HCM in language that is only as scientific as necessary yet at the same time comprehensive, up to date,...
ITexLi, 2021. — 456 p. — ISBN: 1789852234 9781789852233 1789859239 9781789859232. This book examines the various cardiomyopathies, including arrhythmogenic cardiomyopathy, hypertrophic cardiomyopathy, and dilated cardiomyopathy, as well as their genetic basis. Cardiomyopathies are diseases of the heart muscle with diverse etiologies ranging from myocarditis to gene mutations....
2nd edition. — Springer, 2019. — 484 p. — ISBN: 978-3-319-92422-9 This extensively updated edition provides a comprehensive review of hypertrophic cardiomyopathy, the most common genetic disorder of the heart characterized by dysfunctional contractility at the sarcomere level. The disease produces abnormal and oftentimes focal hypertrophy on a macroscopic level that further...
Springer basel AG: 2010 - 306 p. , ISBN: 3764383518 Cardiomyopathy is one of the most frequent causes of heart failure. It is often associated with inadequate heart pumping or other heart function abnormalities. There are many different causes of the disease, therefore many different kinds of cardiomyopathies exist. This volume, written by a leading expert, focuses on...
Springer, 2019. — 239 p. — ISBN: 978-3-030-13863-9 This book presents a comprehensive overview of dilated cardiomyopathy, providing readers with practical guidelines for its clinical management. The first part of the book analyzes in detail the disease’s pathophysiology, its diagnostic work up as well as the prognostic stratification, and illustrates the role of genetics and...
Springer, 2018. — 118 p. This book details the advances in cardiac MRI that have enabled quantitative tissue characterization of the myocardium using myocardial and blood T1 measurements, which have enabled reliable detection of diffuse pathological processes in both the cardiomyocytes and the interstitial cells of the myocardium. Evaluation of the native myocardial and...
Springer, 2018. — 368 p. This book details the advances in cardiac MRI that have enabled quantitative tissue characterization of the myocardium using myocardial and blood T1 measurements, which have enabled reliable detection of diffuse pathological processes in both the cardiomyocytes and the interstitial cells of the myocardium. Evaluation of the native myocardial and...
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