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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
Luo, H.C. ; Dimaano, V.L. ; Kembro, J.M. ; Hilser, A. ; Hurtado-De-Mendoza, D. ; Pozios, I. ; Tomas, M.S. ; Yalcin, H. ; Dolores-Cerna, K. ; Mormontoy, W. ; Aon, M.A. ; Cameron, D. ; Bluemke, D.A. ; Stewart, K.J. ; Russell, S.D. ; Cordova, J.G. ; Abraham, T.P. ; Abraham, M.R. | Elsevier | 2019-04-24T18:23:49ZThe exercise heart rate (HR) profile and its relation to cardiac function and arrhythmias were investigated in patients with hypertrophic cardiomyopathy (HC). Chronotropic response (CR) and heart rate recovery (HRR) were computed during and afte[...]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[...]texto impreso
Sivalokanathan, S. ; Zghaib, T. ; Greenland, G.V. ; Vasquez, N. ; Kudchadkar, S.M. ; Kontari, E. ; Lu, D.-Y. ; Dolores-Cerna, K. ; van der Geest, R.J. ; Kamel, I.R. ; Olgin, J.E. ; Abraham, T.P. ; Nazarian, S. ; Zimmerman, S.L. ; Abraham, M.R. | Elsevier | 2019-07-04T17:00:16ZObjectives: This study hypothesized that paroxysmal atrial fibrillation (PAF) reflects the presence of a more severe cardiac hypertrophic cardiomyopathy (HCM) phenotype. Background: HCM is characterized by myocyte hypertrophy, fibrosis, and a hi[...]
