Bilaketaren emaitzak - Fatah, Meena

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

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

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Comparison of presentation and disease progression between gene positive and gene negative patients evaluated for arrhythmogenic right ventricular cardiomyopathy nork Chungsomprasong, Paweena, Hamilton, Robert, Fatah, Meena, Etoom, Yousef, Govindapillai, Sindu, Manlhiot, Cedric, Yoo, Shi-Joon, McCrindle, Brian W, Grosse-Wortmann, Lars

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An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis nork 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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Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry nork 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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Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy nork 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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