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Arch. cardiol. Méx ; 77(supl.2): S2-59-S2-63, abr.-jun. 2007.
Artículo en Español | LILACS | ID: lil-568848

RESUMEN

The convenience to count with a safe and effective pharmacological wealth for atrial fibrillation treatment had conduced, in a way, to a deep depuration of the vast array of antiarrhythmic drugs, keeping only a very restricted number of compounds with a widely proved anti-atrial activity. On the other hand, it had lead to the discovery of the pathophysiological concepts that point to novel therapeutic targets. Within these objectives is that new antiarrhythmic drugs with preferential, even selective, activity on myocardial atrium ion channels had been developed. Among these new antiarrhythmics, dofetilide, and AVE0118, are taken into account. In addition, new possibilities are opened based on the knowledge of the cardioprotective-antiarrhythmic qualities of the opioidergic system.


Asunto(s)
Humanos , Antiarrítmicos , Fibrilación Atrial , Compuestos de Bifenilo , Fenetilaminas , Bloqueadores de los Canales de Potasio , Sulfonamidas , Administración Oral , Antiarrítmicos , Antiarrítmicos/efectos adversos , Antiarrítmicos , Fibrilación Atrial , Compuestos de Bifenilo , Compuestos de Bifenilo , Electrofisiología , Atrios Cardíacos , Canales Iónicos , Fenetilaminas , Fenetilaminas , Bloqueadores de los Canales de Potasio , Bloqueadores de los Canales de Potasio , Ensayos Clínicos Controlados Aleatorios como Asunto , Receptores Opioides , Sulfonamidas , Sulfonamidas , Factores de Tiempo
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