Sunday, June 3, 2012

The Brugada Syndrome

The Brugada Syndrome



Author:
Edition: 1
Publisher: Wiley-Blackwell
Binding: Paperback
ISBN: 0879934344



The Brugada Syndrome: From Bench To Bedside (Clinical Approaches to Tachyarrhythmias)


Until recently, the cellular basis for sudden death, the Brugada Syndrome, has largely remained an unknown to modern arrhythmologists and cardiologists, particularly in the absence of any structural heart disease. Medical books The Brugada Syndrome. Detailed observations of age-groups, especially the young, families and populations where sudden death frequently occurs, and improved understanding of its contributory factors and mechanisms are, however, showing the way forward.

This addition to the Clinical Approaches to Tachyarrhythmias (CATA) Series, written by the investigators who discovered and probed the Brugada Syndrome, discusses the history, etiology, pathology and clinical manifestations of sudden death. From diagnosis, prognosis, to therapeutic approaches using the latest in cathater ablation techniques, electrophysiological surgery, and genetic appraisal, the work is a testimony to the author's investigation. Using clinical cases in Thailand and Laos, they further unravel the syndrome's molecular mechanisms, studying related syndromes, such as the long-QT syndrome, infant death, and arryhthmogenic right ventricular cardiomyopathy Medical books The Brugada Syndrome From Bench To Bedside. Until recently the cellular basis for sudden death the Brugada Syndrome has largely remained an unknown to modern arrhythmologists and cardiologists particularly in the absence of any structural heart disease. Detailed observations of age-groups especially the young families and populations where sudden death frequently occurs and improved understanding of its contributory factors and mechanisms are however showing the way forward.This addition to the Clinical Approaches to Tachyarrhythmias CATA Series written by the investigators who discovered and probed the Brugada Syndrome discusses the history etiology pathology and clinical manifestations of sudden death. From diagnosis prognosis to therapeutic approaches using the latest in cathater ablation techniques electrophysiological surgery and genetic appraisal the work is a testimony to the authors investigation. Using clinical cases in Thailand and Laos they further unravel the syndromes molecular mechanisms studying related syndromes such as the long-QT syndrome infant death and arryhthmogenic right ventricular cardiomyopathy.By being informed of the electrophysiological abnormalities that contribute to familial and genetic diseases physicians cardiologists and all those who care for patients with cardiac arrhythmias will be better able to identify and treat patients in whom the Brugada Syndrome may strike next.

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Download link for The Brugada Syndrome: Diagnosis And Treatment By Charles Antzelevitch Hardco

Until recently the cellular basis for sudden death the Brugada Syndrome has largely remained an unknown to modern arrhythmologists and cardiologists particularly in the absence of any structural heart disease. Detailed observations of age-groups especially the young families and populations where sudden death frequently occurs and improved understanding of its contributory factors and mechanisms are however showing the way forward.This addition to the Clinical Approaches to Tachyarrhythmias CATA Series written by the investigators who discovered and probed the Brugada Syndrome discusses the hi

New Hardcover.

Categories: Tachycardia, Ventricular. Contributors: Charles Antzelevitch - Editor. Format: Paperback





Medical Book The Brugada Syndrome



Detailed observations of age-groups, especially the young, families and populations where sudden death frequently occurs, and improved understanding of its contributory factors and mechanisms are, however, showing the way forward.

This addition to the Clinical Approaches to Tachyarrhythmias (CATA) Series, written by the investigators who discovered and probed the Brugada Syndrome, discusses the history, etiology, pathology and clinical manifestations of sudden death. From diagnosis, prognosis, to therapeutic approaches using the latest in cathater ablation techniques, electrophysiological surgery, and genetic appraisal, the work is a testimony to the author's investigation. Using clinical cases in Thailand and Laos, they further unravel the syndrome's molecular mechanisms, studying related syndromes, such as the long-QT syndrome, infant death, and arryhthmogenic right ventricular cardiomyopathy.

By being informed of the electrophysiological abnormalities that contribute to familial and genetic diseases, physicians, cardiologists and all those who care for patients with cardiac arrhythmias will be better able to identify and treat patients in whom the Brugada Syndrome may strike next.

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