Electrophysiological mechanisms underlying T wave pseudonormalisation on stress ECGs in hypertrophic cardiomyopathy by Coleman, J, Doste, R, Beltrami, M, Olivotto, I, Raman, B, Bueno-Orovio, A

Effects of ranolazine on the arrhythmic substrate in hypertrophic cardiomyopathy by Coleman, JA, Doste, R, Beltrami, M, Argirò, A, Coppini, R, Olivotto, I, Raman, B, Bueno Orovio, A

Pharmacological management of hypertrophic cardiomyopathy: From bench to bedside by Palandri, C, Santini, L, Argirò, A, Margara, F, Doste, R, Bueno-Orovio, A, Olivotto, I, Coppini, R

Paradoxical prolongation of QT interval during exercise in patients with HCM: Cellular mechanisms and implications for diastolic function by Coppini, R, Beltrami, M, Doste, R, Bueno Orovio, A, Ferrantini, C, Vitale, G, Manuel Pioner, J, Santini, L, Argirò, A, Berteotti, M, Mori, F, Marchionni, N, Stefàno, P, Cerbai, E, Poggesi, C, Olivotto, I

Electrophysiological and Contractile Effects of Disopyramide in Patients With Obstructive Hypertrophic Cardiomyopathy: a Translational Study by Coppini, R, Ferrantini, C, Pioner, J, Santini, L, Wang, Z, Palandri, C, Scardigli, M, Vitale, G, Sacconi, L, Stefàno, P, Flink, L, Riedy, K, Pavone, F, Cerbai, E, Poggesi, C, Mugelli, A, Bueno Orovio, A, Olivotto, I, Sherrid, M

Slower calcium handling balances faster cross-bridge cycling in human MYBPC3 HCM by Pioner, JM, Vitale, G, Steczina, S, Langione, M, Margara, F, Santini, L, Giardini, F, Lazzeri, E, Piroddi, N, Scellini, B, Palandri, C, Schuldt, M, Spinelli, V, Girolami, F, Mazzarotto, F, van der Velden, J, Cerbai, E, Tesi, C, Olivotto, I, Bueno-Orovio, A, Sacconi, L, Coppini, R, Ferrantini, C, Regnier, M, Poggesi, C

Myosin sequestration regulates sarcomere function, cardiomyocyte energetics, and metabolism, informing the pathogenesis of hypertrophic cardiomyopathy by Toepfer, CN, Garfinkel, AC, Venturini, G, Wakimoto, H, Repetti, G, Alamo, L, Sharma, A, Agarwal, R, Ewoldt, JF, Cloonan, P, Letendre, J, Lun, M, Olivotto, I, Colan, S, Ashley, E, Jacoby, D, Michels, M, Redwood, CS, Watkins, HC, Day, SM, Staples, JF, Padrón, R, Chopra, A, Ho, CY, Chen, CS, Pereira, AC, Seidman, JG, Seidman, CE

Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy by Walsh, R, Mazzarotto, F, Whiffin, N, Buchan, R, Midwinter, W, Wilk, A, Li, N, Felkin, L, Ingold, N, Govind, R, Ahmad, M, Mazaika, E, Allouba, M, Zhang, X, De Marvao, A, Day, SM, Ashley, E, Colan, SD, Michels, M, Pereira, AC, Jacoby, D, Ho, CY, Thomson, KL, Watkins, H, Barton, PJR, Olivotto, I, Cook, SA, Ware, JS

Reevaluating the genetic contribution of monogenic dilated cardiomyopathy by Mazzarotto, F, Tayal, U, Buchan, RJ, Midwinter, W, Wilk, A, Whiffin, N, Govind, R, Mazaika, E, de Marvao, A, Dawes, TJW, Felkin, LE, Ahmad, M, Theotokis, PI, Edwards, E, Ing, AY, Thomson, KL, Chan, LHL, Sim, D, Baksi, AJ, Pantazis, A, Roberts, AM, Watkins, H, Funke, B, O'Regan, DP, Olivotto, I, Barton, PJR, Prasad, SK, Cook, SA, Ware, JS, Walsh, R