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Cardiomyopathies - From Basic Research to Clinical Management
Edited by Josef Veselka, ISBN 978-953-307-834-2, Hard cover, 800 pages, Publisher: InTech, Published: February 15, 2012 under CC BY 3.0 license, in subject Cardiology and Cardiovascular Medicine
DOI: 10.5772/1457
Cardiomyopathy means "heart (cardio) muscle (myo) disease (pathy)". Currently, cardiomyopathies are defined as myocardial disorders in which the heart muscle is structurally and/or functionally abnormal in the absence of a coronary artery disease, hypertension, valvular heart disease or congenital heart disease sufficient to cause the observed myocardial abnormalities. This book provides a comprehensive, state-of-the-art review of the current knowledge of cardiomyopathies. Instead of following the classic interdisciplinary division, the entire cardiovascular system is presented as a functional unity, and the contributors explore pathophysiological mechanisms from different perspectives, including genetics, molecular biology, electrophysiology, invasive and non-invasive cardiology, imaging methods and surgery. In order to provide a balanced medical view, this book was edited by a clinical cardiologist.
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Book contents
- Chapter 1Classification and Definitions of Cardiomyopathies
- Chapter 2Management of Hypertrophic Obstructive Cardiomyopathy with a Focus on Alcohol Septal Ablation
- Chapter 3Hypertrophic Cardiomyopathy in Infants and Children
- Chapter 4Quality of Life in Dilated Cardiomyopathy with Refractory Chronic Heart Failure Undergoing Devices Implantation
- Chapter 5Peripartum Cardiomyopathy: A Systematic Review
- Chapter 6Cardiomyopathy Detection from Electrocardiogram Features
- Chapter 7Prevention of Sudden Cardiac Death in Patients with Cardiomyopathy
- Chapter 8Biomarker for Cardiomyopathy-B-Type Natriuretic Peptide
- Chapter 9Heart Muscle and Apoptosis
- Chapter 10Cardiac Myocytes and Mechanosensation
- Chapter 11Dobutamine-Induced Mechanical Alternans
- Chapter 12MicroRNAs Telltale Effects on Signaling Networks in Cardiomyopathy
- Chapter 13Intercellular Connections in the Heart: The Intercalated Disc
- Chapter 14Familial Hypertrophic Cardiomyopathy-Related Troponin Mutations and Sudden Cardiac Death
- Chapter 15Consequences of Mutations in Genes Encoding Cardiac Troponin C, T and I – Molecular Insights
- Chapter 16Cardiomyopathies Associated with Myofibrillar Myopathies
- Chapter 17Functional Consequences of Mutations in the Myosin Regulatory Light Chain Associated with Hypertrophic Cardiomyopathy
- Chapter 18Role of Genetic Factors in Dilated Cardiomyopathy
- Chapter 19Role of Advanced Cardiac Magnetic Resonance Imaging in Atypical Cardiomyopathies such as Stress-Induced Cardiomyopathie and Left-Ventricular Non-Compaction Cardiomyopathy
- Chapter 20The Use of Contrast-Enhancement Cardiovascular Magnetic Resonance Imaging in Cardiomyopathies
- Chapter 21The Evolving Face of Heart Failure Associated with Elevated Cardio-Metabolic Risk Factors
- Chapter 22Diabetic Cardiomyopathy: Cardiac Changes, Pathophysiological Mechanisms, Biologic Markers, and the Available Therapeutic Armamentarium
- Chapter 23Insulin Resistance and Cardiomyopathy
- Chapter 24Taurine Depletion-Related Cardiomyopathy in Animals
- Chapter 25Thyrotoxic Cardiomyopathy
- Chapter 26Drug-Induced Cardiomyopathies
- Chapter 27Anthracycline Cardiotoxicity
- Chapter 28Cardiotonic Steroids and Cardiac Fibrosis
- Chapter 29Stress-Induced Cardiomyopathy: Clinical Observations
- Chapter 30Takotsubo Cardiomyopathy
- Chapter 31Pathology of Takotsubo (Ampulla) Cardiomyopathy
- Chapter 32Torsades de Pointes in Takotsubo Cardiomyopathy with QT Prolongation
- Chapter 33Torsades de Pointes Associated with Takotsubo Cardiomyopathy: Is It Preventable?
- Chapter 34Chagas Heart Disease
- Chapter 35Chagasic Cardiomyopathy
