Inherited Cardiac Diseases Predisposing to Sudden Death, An Issue of Cardiac Electrophysiology Clinics, 1st Edition
Key Features
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Contains 16 relevant, practice-oriented topics including novelties in Brugada syndrome: complex genetics, risk stratification and catheter ablation; novel approaches to treatment of catecholaminergic polymorphic ventricular tachycardia; investigation of unexplained cardiac arrest: phenotyping and genetic testing; impact of imaging to arrhythmic risk stratification in non-ischemic cardiomyopathy; and more.
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Provides in-depth clinical reviews on inherited cardiac diseases predisposing to sudden death, offering actionable insights for clinical practice.
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Presents the latest information on this timely, focused topic under the leadership of experienced editors in the field. Authors synthesize and distill the latest research and practice guidelines to create clinically significant, topic-based reviews.
Author Information
| ISBN Number | 9780443183348 |
|---|---|
| Description Author List | Edited by Rafik Tadros, MD PhD, Montreal Heart Institute and Université de Montréal; Julia Cadrin-Tourigny, MD MSc, Montreal Heart Institute and Université de Montréal and Jason Roberts |
| Copyright Year | 2023 |
| Edition Number | 1 |
| Format | Book |
| Trim | 178w x 254h (7.00" x 10.00") |
| Imprint | Elsevier |
| Page Count | 240 |
| Publication Date | 11 Aug 2023 |
| Stock Status | Please allow 10-14 working days for delivery |
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A Practical Guide to Genetic Testing in Inherited Heart Disease
Implantable Devices in Genetic Heart Disease: Disease-Specific Device Selection and Programming
Emerging Targeted Therapies for Inherited Cardiomyopathies and Arrhythmias
Novelties in Brugada Syndrome: Complex Genetics, Risk Stratification, and Catheter Ablation
Personalized Care in Long QT Syndrome: Better Management, More Sports, and Fewer Devices
Catecholaminergic Polymorphic Ventricular Tachycardia: A Review of Therapeutic Strategies
Investigation of Unexplained Cardiac Arrest: Phenotyping and Genetic Testing
Calcium Release Deficiency Syndrome: A New Inherited Arrhythmia Syndrome
Short-Coupled Ventricular Fibrillation
The Novel Familial ST-Depression Syndrome – Current Knowledge and Perspectives
Prevention of Sudden Death and Management of Ventricular Arrhythmias in Arrhythmogenic Cardiomyopathy
Sudden Death Risk Assessment in Hypertrophic Cardiomyopathy Across the Lifespan: Reconciling the American and European Approaches
Impact of Cardiac Magnetic Resonance to Arrhythmic Risk Stratification in Nonischemic Cardiomyopathy
Genetic Risk Stratification in Arrhythmogenic Left Ventricular Cardiomyopathy
