The Brugada Syndrome - From Bench To Bedside | Medical Books

Until recently, the cellular groundwork for explosive ending, the Brugada Syndrome, has largely remained an unfamiliar to late arrhythmologists and cardiologists, especially in the epilepsy of any structural bosom disease. Elaborated observations of age-groups, especially the egyptologist, families and populations where unforeseen change oftentimes occurs, and restored inclination of its contributory factors and mechanisms are, notwithstanding, showing the way overfamiliar.


This constituent to the Clinical Approaches to Tachyarrhythmias (CATA) Periodical, holographic by the investigators who unconcealed and probed the Brugada Syndrome, discusses the account, cause, pathology and clinical manifestations of sharp demise. From diagnosis, forecasting, to therapeutic approaches using the fashionable in cathater extirpation techniques, electrophysiological surgery, and heritable categorization, the activity is a testimony to the author's work. Using clinical cases in Siam and Laos, they encourage untangle the syndrome's molecular mechanisms, studying kin syndromes, much as the long-QT syndrome, infant decease, and arryhthmogenic good ventricular myocardiopathy.

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