Search Results - Hamilton, Robert M

Electroanatomical voltage mapping of atrial Mahaim potentials to guide catheter ablation by Asakai, Hiroko, Fenwick, Laura, Hamilton, Robert M.

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Magnetic Resonance Imaging Assessment of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia in Children by Yoo, Shi-Joon, Grosse-Wortmann, Lars, Hamilton, Robert M.

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Antiepileptic rufinamide and QTc interval shortening in a patient with long QT syndrome: case report by Mondal, Tapas, Sullivan, Kristen, Divakaramenon, Syam, Hamilton, Robert M

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Congenital heart disease confounding the diagnosis of arrhythmogenic right ventricular cardiomyopathy by Kiamanesh, Omid, Farhan, Maryam, Sanatani, Shubhayan, Grosse-Wortmann, Lars, Duncan, Walter, Hamilton, Robert M.

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Evaluating the 12-Lead Electrocardiogram for Diagnosing ARVC in Young Populations: Implications for Preparticipation Screening of Athletes by Landry, Cameron H., Fatah, Meena, Connelly, Kim A., Angaran, Paul, Hamilton, Robert M., Dorian, Paul

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Abnormal connexin43 in arrhythmogenic right ventricular cardiomyopathy caused by plakophilin-2 mutations by Fidler, Lee M, Wilson, Gregory J, Liu, Fanfan, Cui, Xuezhi, Scherer, Stephen W, Taylor, Glenn P, Hamilton, Robert M

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Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy by Chaix, Marie-A., Koopmann, Tamara T., Goyette, Philippe, Alikashani, Azadeh, Latour, Frédéric, Fatah, Meena, Hamilton, Robert M., Rioux, John D.

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A Novel Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Biomarker—Anti-DSG2—Is Absent in Athletes With Right Ventricular Enlargement by Dorian, David, Chatterjee, Diptendu, Connelly, Kim A., Goodman, Jack M., Yan, Andrew T., Bentley, Robert F., Banks, Laura, Hamilton, Robert M., Dorian, Paul

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TMEM43 Mutation p.S358L Alters Intercalated Disc Protein Expression and Reduces Conduction Velocity in Arrhythmogenic Right Ventricular Cardiomyopathy by Siragam, Vinayakumar, Cui, Xuezhi, Masse, Stephane, Ackerley, Cameron, Aafaqi, Shabana, Strandberg, Linn, Tropak, Michael, Fridman, Michael D., Nanthakumar, Kumaraswamy, Liu, Jun, Sun, Yu, Su, Bin, Wang, Caroline, Liu, Xiaoru, Yan, Yuqing, Mendlowitz, Ariel, Hamilton, Robert M.

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The Cardiac Myosin Binding Protein C Arg502Trp Mutation: A Common Cause of Hypertrophic Cardiomyopathy by Saltzman, Adam J., Mancini-DiNardo, Debora, Li, Chumei, Chung, Wendy K., Ho, Carolyn Y., Hurst, Stephanie, Wynn, Julia, Care, Melanie, Hamilton, Robert M., Seidman, Gregor W., Gorham, Joshua, McDonough, Barbara, Sparks, Elizabeth, Seidman, Jonathan G., Seidman, Christine E., Rehm, Heidi L.

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Congenital Heart Block Maternal Sera Autoantibodies Target an Extracellular Epitope on the α(1G) T-Type Calcium Channel in Human Fetal Hearts by Strandberg, Linn S., Cui, Xuezhi, Rath, Arianna, Liu, Jie, Silverman, Earl D., Liu, Xiaoru, Siragam, Vinayakumar, Ackerley, Cameron, Su, Brenda Bin, Yan, Jane Yuqing, Capecchi, Marco, Biavati, Luca, Accorroni, Alice, Yuen, William, Quattrone, Filippo, Lung, Kalvin, Jaeggi, Edgar T., Backx, Peter H., Deber, Charles M., Hamilton, Robert M.

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An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis by Chatterjee, Diptendu, Fatah, Meena, Akdis, Deniz, Spears, Danna A, Koopmann, Tamara T, Mittal, Kirti, Rafiq, Muhammad A, Cattanach, Bruce M, Zhao, Qili, Healey, Jeff S, Ackerman, Michael J, Bos, Johan Martijn, Sun, Yu, Maynes, Jason T, Brunckhorst, Corinna, Medeiros-Domingo, Argelia, Duru, Firat, Saguner, Ardan M, Hamilton, Robert M

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Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features by Ghidoni, Alice, Elliott, Perry M., Syrris, Petros, Calkins, Hugh, James, Cynthia A., Judge, Daniel P., Murray, Brittney, Barc, Julien, Probst, Vincent, Schott, Jean Jacques, Song, Jiang-Ping, Hauer, Richard N.W., Hoorntje, Edgar T., van Tintelen, J. Peter, Schulze-Bahr, Eric, Hamilton, Robert M., Mittal, Kirti, Semsarian, Christopher, Behr, Elijah R., Ackerman, Michael J., Basso, Cristina, Parati, Gianfranco, Gentilini, Davide, Kotta, Maria-Christina, Mayosi, Bongani M., Schwartz, Peter J., Crotti, Lia

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Catecholaminergic Polymorphic Ventricular Tachycardia in Children: An Analysis of Therapeutic Strategies and Outcomes from an International Multicenter Registry by Roston, Thomas M., Vinocur, Jeffrey M., Maginot, Kathleen R., Mohammed, Saira, Salerno, Jack C., Etheridge, Susan P., Cohen, Mitchell, Hamilton, Robert M., Pflaumer, Andreas, Kanter, Ronald J., Potts, James E., LaPage, Martin J., Collins, Kathryn K., Gebauer, Roman A., Temple, Joel D., Batra, Anjan S., Erickson, Christopher, Miszczak-Knecht, Maria, Kubuš, Peter, Bar-Cohen, Yaniv, Kantoch, Michal, Thomas, Vincent C., Hessling, Gabriele, Anderson, Chris, Young, Ming-Lon, Ortega, Michel Cabrera, Lau, Yung R., Johnsrude, Christopher L., Fournier, Anne, Kannankeril, Prince J., Sanatani, Shubhayan

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The Canadian Rare Diseases Models and Mechanisms (RDMM) Network: Connecting Understudied Genes to Model Organisms by Boycott, Kym M., Campeau, Philippe M., Howley, Heather E., Pavlidis, Paul, Rogic, Sanja, Oriel, Christine, Berman, Jason N., Hamilton, Robert M., Hicks, Geoffrey G., Lipshitz, Howard D., Masson, Jean-Yves, Shoubridge, Eric. A., Junker, Anne, Leroux, Michel R., McMaster, Christopher R., Michaud, Jaques L., Turvey, Stuart E., Dyment, David, Innes, A. Micheil, van Karnebeek, Clara D., Lehman, Anna, Cohn, Ronald D., MacDonald, Ian M., Rachubinski, Richard A., Frosk, Patrick, Vandersteen, Anthony, Wozniak, Richard W., Pena, Izabella A., Wen, Xiao-Yan, Lacaze-Masmonteil, Thierry, Rankin, Catharine, Hieter, Philip

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The clinical and genetic spectrum of catecholaminergic polymorphic ventricular tachycardia: findings from an international multicentre registry by Roston, Thomas M, Yuchi, Zhiguang, Kannankeril, Prince J, Hathaway, Julie, Vinocur, Jeffrey M, Etheridge, Susan P, Potts, James E, Maginot, Kathleen R, Salerno, Jack C, Cohen, Mitchell I, Hamilton, Robert M, Pflaumer, Andreas, Mohammed, Saira, Kimlicka, Lynn, Kanter, Ronald J, LaPage, Martin J, Collins, Kathryn K, Gebauer, Roman A, Temple, Joel D, Batra, Anjan S, Erickson, Christopher, Miszczak-Knecht, Maria, Kubuš, Peter, Bar-Cohen, Yaniv, Kantoch, Michal, Thomas, Vincent C, Hessling, Gabriele, Anderson, Chris, Young, Ming-Lon, Choi, Sally H J, Cabrera Ortega, Michel, Lau, Yung R, Johnsrude, Christopher L, Fournier, Anne, Van Petegem, Filip, Sanatani, Shubhayan

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Arrhythmogenic right ventricular cardiomyopathy: evaluation of the current diagnostic criteria and differential diagnosis by Corrado, Domenico, van Tintelen, Peter J, McKenna, William J, Hauer, Richard N W, Anastastakis, Aris, Asimaki, Angeliki, Basso, Cristina, Bauce, Barbara, Brunckhorst, Corinna, Bucciarelli-Ducci, Chiara, Duru, Firat, Elliott, Perry, Hamilton, Robert M, Haugaa, Kristina H, James, Cynthia A, Judge, Daniel, Link, Mark S, Marchlinski, Francis E, Mazzanti, Andrea, Mestroni, Luisa, Pantazis, Antonis, Pelliccia, Antonio, Marra, Martina Perazzolo, Pilichou, Kalliopi, Platonov, Pyotr G A, Protonotarios, Alexandros, Rampazzo, Alessandra, Saffitz, Jeffry E, Saguner, Ardan M, Schmied, Christian, Sharma, Sanjay, Tandri, Hari, Te Riele, Anneline S J M, Thiene, Gaetano, Tsatsopoulou, Adalena, Zareba, Wojciech, Zorzi, Alessandro, Wichter, Thomas, Marcus, Frank I, Calkins, Hugh

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Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry by Crotti, Lia, Spazzolini, Carla, Tester, David J, Ghidoni, Alice, Baruteau, Alban-Elouen, Beckmann, Britt-Maria, Behr, Elijah R, Bennett, Jeffrey S, Bezzina, Connie R, Bhuiyan, Zahurul A, Celiker, Alpay, Cerrone, Marina, Dagradi, Federica, De Ferrari, Gaetano M, Etheridge, Susan P, Fatah, Meena, Garcia-Pavia, Pablo, Al-Ghamdi, Saleh, Hamilton, Robert M, Al-Hassnan, Zuhair N, Horie, Minoru, Jimenez-Jaimez, Juan, Kanter, Ronald J, Kaski, Juan P, Kotta, Maria-Christina, Lahrouchi, Najim, Makita, Naomasa, Norrish, Gabrielle, Odland, Hans H, Ohno, Seiko, Papagiannis, John, Parati, Gianfranco, Sekarski, Nicole, Tveten, Kristian, Vatta, Matteo, Webster, Gregory, Wilde, Arthur A M, Wojciak, Julianne, George, Alfred L, Ackerman, Michael J, Schwartz, Peter J

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An International Multi-Center Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2- Catecholaminergic Polymorphic Ventricular Tachycardia by Ng, Kevin, Titus, Erron W., Lieve, Krystien V., Roston, Thomas M., Mazzanti, Andrea, Deiter, Frederick H., Denjoy, Isabelle, Ingles, Jodie, Till, Jan, Robyns, Tomas, Connors, Sean P., Steinberg, Christian, Abrams, Dominic J., Pang, Benjamin, Scheinman, Melvin M., Bos, J. Martijn, Duffett, Stephen A., van der Werf, Christian, Maltret, Alice, Green, Martin S., Rutberg, Julie, Balaji, Seshadri, Cadrin-Tourigny, Julia, Orland, Kate M., Knight, Linda M., Brateng, Caitlin, Wu, Jeremy, Tang, Anthony S., Skanes, Allan C., Manlucu, Jaimie, Healey, Jeff S., January, Craig T., Krahn, Andrew D., Collins, Kathryn K., Maginot, Kathleen R., Fischbach, Peter, Etheridge, Susan P., Eckhardt, Lee L., Hamilton, Robert M., Ackerman, Michael J., Noguer, Ferran Rosés I, Semsarian, Christopher, Jura, Natalia, Leenhardt, Antoine, Gollob, Michael H., Priori, Silvia G., Sanatani, Shubhayan, Wilde, Arthur A. M., Deo, Rahul C., Roberts, Jason D.

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Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy by Roberts, Jason D., Murphy, Nathaniel P., Hamilton, Robert M., Lubbers, Ellen R., James, Cynthia A., Kline, Crystal F., Gollob, Michael H., Krahn, Andrew D., Sturm, Amy C., Musa, Hassan, El-Refaey, Mona, Koenig, Sara, Aneq, Meriam Åström, Hoorntje, Edgar T., Graw, Sharon L., Davies, Robert W., Rafiq, Muhammad Arshad, Koopmann, Tamara T., Aafaqi, Shabana, Fatah, Meena, Chiasson, David A., Taylor, Matthew R.G., Simmons, Samantha L., Han, Mei, van Opbergen, Chantal J.M., Wold, Loren E., Sinagra, Gianfranco, Mittal, Kirti, Tichnell, Crystal, Murray, Brittney, Codima, Alberto, Nazer, Babak, Nguyen, Duy T., Marcus, Frank I., Sobriera, Nara, Lodder, Elisabeth M., van den Berg, Maarten P., Spears, Danna A., Robinson, John F., Ursell, Philip C., Green, Anna K., Skanes, Allan C., Tang, Anthony S., Gardner, Martin J., Hegele, Robert A., van Veen, Toon A.B., Wilde, Arthur A.M., Healey, Jeff S., Janssen, Paul M.L., Mestroni, Luisa, van Tintelen, J. Peter, Calkins, Hugh, Judge, Daniel P., Hund, Thomas J., Scheinman, Melvin M., Mohler, Peter J.

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