| 11.2 Utility and role of a teaching program for physicians to identify brugada syndrome: Experience of the Quebec heart institute with a French Canadian population J Champagne, F Molin, G O'Hara, F Philippon, M Gilbert, L Charbonneau, ... Europace, A18, 2003 | | 2003 |
| 11.8 Utility of the IV procainamide test to unmask a concealed form of brugada syndrome J Champagne, G O'Hara, F Molin, F Philippon, M Chahine, P Poirier, ... Europace, A19-A20, 2003 | | 2003 |
| 134a Sunday, February 3, 2013 O Theriault, M Chahine | | |
| A channel without pore? The primary structure of a proton permeable channel is finally revealed M Chahine, J Blanchet, A El Chemaly, P Bois Medecine Sciences: M/S 22 (11), 930-931, 2006 | | 2006 |
| A COMMON PHENOTYPE FOR DIVERSE NA-CHANNEL MUTATIONS IN PARAMYOTONIA-CONGENITA N Yang, S Ji, M Zhou, M Chahine, RL Barchi, R Horn, AL George BIOPHYSICAL JOURNAL 66 (2), A103-A103, 1994 | 1 | 1994 |
| A distinct de novo expression of Nav1.5 sodium channels in human atrial fibroblasts differentiated into myofibroblasts A Chatelier, A Mercier, B Tremblier, O Thériault, M Moubarak, N Benamer, ... The Journal of Physiology 590 (17), 4307-4319, 2012 | 93 | 2012 |
| A generic non-stationary MIMO channel model for different high-speed train scenarios A Ghazal, CX Wang, Y Liu, P Fan, MK Chahine 2015 IEEE/CIC International Conference on Communications in China (ICCC), 1-6, 2015 | 21 | 2015 |
| A leaky voltage sensor domain of cardiac sodium channels causes arrhythmias associated with dilated cardiomyopathy A Moreau, P Gosselin-Badaroudine, A Mercier, B Burger, DI Keller, ... Scientific reports 8 (1), 13804, 2018 | 37 | 2018 |
| A new C-terminal hERG mutation A915fs+ 47X associated with symptomatic LQT2 and auditory-trigger syncope G Christé, O Thériault, M Chahine, G Millat, C Rodriguez-Lafrasse, ... Heart Rhythm 5 (11), 1577-1586, 2008 | 18 | 2008 |
| A New Cardiac Channelopathy: From Clinical Phenotypes to Molecular Mechanisms Associated With Nav1.5 Gating Pores A Moreau, M Chahine Frontiers in cardiovascular medicine 5, 139, 2018 | 23 | 2018 |
| A Newly Characterized SCN5A Mutation Underlying Brugada Syndrome Unmasked by Hyperthermia NS MOK, SG Priori, C Napolitano, NYIN CHAN, M Chahine, G Baroudi Journal of cardiovascular electrophysiology 14 (4), 407-411, 2003 | 136 | 2003 |
| A non-stationary geometry-based stochastic model for MIMO high-speed train channels A Ghazal, CX Wang, H Haas, M Beach, R Mesleh, D Yuan, X Ge, ... 2012 12th International Conference on ITS Telecommunications, 7-11, 2012 | 18 | 2012 |
| A novel heterozygous HERG/M645R mutation results in long QT syndrome in a patient with tetralogy of fallot O Theriault, M Wu, M Chahine CANADIAN JOURNAL OF CARDIOLOGY 23, 237C-237C, 2007 | | 2007 |
| A novel missense mutation L564P in HERG potassium channel in a French Canadian long QT syndrome family J St-Pierre, L Blier, E Plante, JM Cote, M Gilbert, M Chahine CIRCULATION 98 (17), 57-57, 1998 | | 1998 |
| A Novel Missense Mutation L564P in Hero Potassium Channel in a French Canadian Long Qt Syndrome Family J St-Pierre, L Blier, JM Cote, M Gilbert, M Chahine CANADIAN JOURNAL OF CARDIOLOGY 14, 88-88, 1998 | | 1998 |
| A novel molecular mechanism for the Brugada syndrome: mutation that affects SCN5A protein trafficking M Chahine, G Baroudi, V Pouliot, I Denjoy, P Guicheney, A Shrier EUROPEAN HEART JOURNAL 22, 606-606, 2001 | | 2001 |
| A novel mutation in SCN5A, delQKP 1507–1509, causing long QT syndrome:: Role of Q1507 residue in sodium channel inactivation DI Keller, S Acharfi, E Delacrétaz, N Benammar, M Rotter, JP Pfammatter, ... Journal of molecular and cellular cardiology 35 (12), 1513-1521, 2003 | 57 | 2003 |
| A novel mutation in SCN5A, F1344S, leads to fever-triggered Brugada syndrome D Keller, H Huang, J Zhao, N Schwick, V Suarez, M Brink, S Osswald, ... EUROPEAN HEART JOURNAL 26, 595-595, 2005 | | 2005 |
| A novel mutation in the SCN5A gene is associated with Brugada syndrome DJ Shin, E Kim, SB Park, WC Jang, Y Bae, J Han, Y Jang, B Joung, ... Life sciences 80 (8), 716-724, 2007 | 26 | 2007 |
| A novel PITX2c gain-of-function mutation, p. Met207Val, in patients with familial atrial fibrillation A Mechakra, T Footz, M Walter, A Aránega, F Hernández-Torres, E Morel, ... The American Journal of Cardiology 123 (5), 787-793, 2019 | 13 | 2019 |
Ammar GhazalSenior Lecturer in Wireless Communications在 dmu.ac.uk 的电子邮件经过验证
