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Hurtado-De-Mendoza, D. ; Corona-Villalobos, C. P. ; Pozios, I. ; Gonzales, J. ; Soleimanifard, Y. ; Sivalokanathan, S. ; Montoya-Cerrillo, D. ; Vakrou, S. ; Kamel, I. ; Mormontoy-Laurel, W. ; Dolores-Cerna, K. ; Suárez, J. ; Perez-Melo, S. ; Bluemke, D. A. ; Abraham, T. P. ; Zimmerman, S. L. ; Abraham, M. R. | Wiley | 2019-01-25T16:36:28ZBackground: Hypertrophic cardiomyopathy (HCM) is characterized by myocyte hypertrophy, disarray, fibrosis, and increased risk for ventricular arrhythmias. Increased QT dispersion has been reported in patients with HCM, but the underlying mechani[...]texto impreso
Corona-Villalobos, C. P. ; Saha, S. ; Pozios, I. ; Paz, D. H. D. ; Sorensen, L. ; Cordoba, J. G. ; Dolores-Cerna, K. ; Kamel, I. R. ; Laurel, W. M. ; Bluemke, D. A. ; Abraham, T. P. ; Zimmerman, S. L. ; Abraham, M. R. | Elsevier | 2019-01-25T16:36:28ZHypertrophic cardiomyopathy (HCM) is frequently associated with exercise-related sudden death. One possible contributor to arrhythmias is pathologic hypertrophy, which can lead to QTc prolongation. Since beta-adrenergic stimulation increases inw[...]
