|
|
|
|
|
|
|
|
|
1. |
Record Nr. |
UNINA9910877204703321 |
|
|
Titolo |
Diagnosis and management of hypertrophic cardiomyopathy / / edited by Barry J. Maron |
|
|
|
|
|
|
|
Pubbl/distr/stampa |
|
|
Malden, Mass., : Blackwell Futura, c2004 |
|
|
|
|
|
|
|
ISBN |
|
1-280-19730-7 |
9786610197309 |
0-470-79903-X |
0-470-98746-4 |
1-4051-4615-X |
|
|
|
|
|
|
|
|
Descrizione fisica |
|
1 online resource (526 p.) |
|
|
|
|
|
|
Altri autori (Persone) |
|
MaronBarry J <1941-> (Barry Joel) |
|
|
|
|
|
|
Disciplina |
|
|
|
|
|
|
|
|
Soggetti |
|
|
|
|
|
|
Lingua di pubblicazione |
|
|
|
|
|
|
Formato |
Materiale a stampa |
|
|
|
|
|
Livello bibliografico |
Monografia |
|
|
|
|
|
Note generali |
|
Description based upon print version of record. |
|
|
|
|
|
|
Nota di bibliografia |
|
Includes bibliographical references and index. |
|
|
|
|
|
|
Nota di contenuto |
|
Diagnosis and Management of Hypertrophic Cardiomyopathy; Contents; Foreword; Dedication and Acknowledgments; List of Contributors; 1 Phenotypic Expression and Clinical Course of Hypertrophic Cardiomyopathy; 2 Genetic Mutations that Remodel the Heart in Hypertrophic Cardiomyopathy; 3 Genetic Basis and Genotype-Phenotype Relationships in Familial Hypertrophic Cardiomyopathy; 4 Historical Perspective, Mechanism, and Clinical Significance of Left Ventricular Outflow Tract Obstruction in Hypertrophic Cardiomyopathy |
5 Hypertrophic Cardiomyopathy with Latent (Provocable) Obstruction: Pathophysiology and Management6 Pathophysiology and Clinical Consequences of Atrial Fibrillation in Hypertrophic Cardiomyopathy; 7 Other Modes of Disability or Death Including Stroke, and Treatment Strategies, in Hypertrophic Cardiomyopathy; 8 Disturbed Vascular Control in Hypertrophic Cardiomyopathy: Mechanisms and Clinical Significance; 9 Clinical Significance of Diastolic Dysfunction and the Effect of Therapeutic Interventions |
10 Value of Exercise Testing in Assessing Clinical State and Prognosis in Hypertrophic Cardiomyopathy11 Pathophysiology and Significance of |
|
|
|
|
|
|
|
|
|
|
|
Myocardial Ischemia in Hypertrophic Cardiomyopathy; 12 Hypertrophic Cardiomyopathy in Japan: Clinical, Morphologic and Genetic Expression; 13 Prevalence, Prevention and Treatment of Infective Endocarditis in Hypertrophic Cardiomyopathy; 14 Pharmacologic Treatment of Symptomatic Hypertrophic Cardiomyopathy; 15 Obstructive Hypertrophic Cardiomyopathy: Results of Septal Myectomy |
16 United States Perspectives on the Role of Dual-Chamber Pacing in Patients with Hypertrophic Cardiomyopathy17 Dual-Chamber Pacing for Hypertrophic Obstructive Cardiomyopathy; 18 Alcohol Septal Ablation; 19 Alcohol Septal Ablation in the Treatment of Hypertrophic Obstructive Cardiomyopathy: A Seven-Year Experience; 20 Role of Septal Ablation in a Surgical Center; 21 Molecular and Clinical Tools for Sudden Death Risk Assessment in Hypertrophic Cardiomyopathy; 22 Risk Stratification for Sudden Death in Hypertrophic Cardiomyopathy: Extreme Left Ventricular Hypertrophy as a New Indicator of Risk |
23 Implantable Defibrillator for Prevention of Sudden Death in Hypertrophic Cardiomyopathy24 Hypertrophic Cardiomyopathy and Other Causes of Sudden Death in the Trained Athlete: An Electrophysiologist Perspective on the Management of Benign and Not So Benign Arrhythmias; 25 The Athlete's Heart, ECG, and Differential Diagnosis with Hypertrophic Cardiomyopathy and Other Cardiomyopathies; 26 Importance of Congenital Coronary Artery Anomalies |
27 Arrhythmogenic Right Ventricular Cardiomyopathy and Hypertrophic Cardiomyopathy: Identification with the Italian Preparticipation Athlete Screening Program |
|
|
|
|
|
|
Sommario/riassunto |
|
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 the health of trained athletes. Edited by Dr. Barry J. Maron, a world authority on HCM, and with major contributions from all of the international experts in this field, this book provides a single comprehensive source of information conce |
|
|
|
|
|
|
|
| |