? GO BACK TO SATURDAY, OCTOBER 17, 2015
08.30-10.30
Oral Communications
HEREDITARY ARRHYTHMOGENIC SYNDROME
Chairmen: P.G. Postema / Amsterdam, The Netherlands – R. Rosso / Tel Aviv, Israel
A novel de novo mutation in lamin a7c gene in emery dreifuss muscular dystrophy patient with atrial standstill: a case report
M. Affani, C. Achmad, A. Zada, A. Hidayatullah, M. Iqbal, E. Martanto, A. Purnomowati, T.M. Aprami / Bandung, Indonesia
Whole-exome sequencing identifies a potentially pathogenic variant in a high proportion of idiopathic ventricular fibrillation probands from the casper registry
R. Tadros, A.D. Krahn, K.S. Lo, N. Chami, J.S. Healey, V.S. Chauhan, D.H. Birnie, J. Champagne, S. Sanatani, P. Angaran, R.M. Gow, S. Chakrabarti, B. Gerull, L. Sterns, R. Yee, L.J. Gula, G.J. Klein, M.H. Gollob, M. Gardner, C.S. Simpson, M. Talajic, G. Lettre / Montreal, Canada
Idiopathic ventricular tachycardia in 21 year old man with short QT interval and early repolarization syndrome
S. Dolginina, S. Garkina, I. Tyurina, O. Rubanenko, S. Khokhlunov, D. Dulpyakov / Samara, Russia
Patient specific induced pluripotent stem cell-derived cardiomyocytes for drug development and screening for catecholaminergic polymorphic ventricular tachycardia
L. Barad, A. Novak, A. Lorber, L. Eldor, J. Itskovitz-Eldor, M. Eldar, M. Arad, O. Binah / Haifa, Israel
A three-dimensional electrophysiological computed model of ST segment abnormalities in type 1 Brugada pattern: the key role of right ventricular outflow tract orientation in the thorax
G. Picciolo, P. Crea, F. Luzza, G. Oreto / Messina, Italy
Challenges of LQTS at Very Young Age
Shkolnikova M., Ildarova R., Polyakova A. / Moscow, Russia