High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia von Hasdemir, Can, MD, Payzin, Serdar, MD, Kocabas, Umut, MD, Sahin, Hatice, RN, Yildirim, Nihal, RN, Alp, Alpay, Aydin, Mehmet, MD, Pfeiffer, Ryan, BSc, Burashnikov, Elena, BSc, Wu, Yuesheng, MS, Antzelevitch, Charles, PhD, FHRS

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Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death von ANTZELEVITCH, Charles, POLLEVICK, Guido D, GELBER, Philip, BONAROS, Elias P, BURASHNIKOV, Elena, YUESHENG WU, SARGENT, John D, SCHICKEL, Stefan, OBERHEIDEN, Ralf, BHATIA, Atul, HSU, Li-Fern, HÄÏSSAGUERRE, Michel, CORDEIRO, Jonathan M, SCHIMPF, Rainer, BORGGREFE, Martin, WOLPERT, Christian, CASIS, Oscar, SANGUINETTI, Michael C, AIZAWA, Yoshiyasu, GUERCHICOFF, Alejandra, PFEIFFER, Ryan, OLIVA, Antonio, WOLLNIK, Bernd

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Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death von Burashnikov, Elena, BS, Pfeiffer, Ryan, BS, Barajas-Martinez, Héctor, PhD, Delpón, Eva, PhD, Hu, Dan, MD, PhD, Desai, Mayurika, BS, Borggrefe, Martin, MD, Häissaguerre, Michel, MD, Kanter, Ronald, MD, Pollevick, Guido D., PhD, Guerchicoff, Alejandra, PhD, Laiño, Ruben, MD, Marieb, Mark, MD, Nademanee, Koonlawee, MD, Nam, Gi-Byoung, MD, PhD, Robles, Roberto, MD, Schimpf, Rainer, MD, Stapleton, Dwight D., MD, Viskin, Sami, MD, Winters, Stephen, MD, Wolpert, Christian, MD, Zimmern, Samuel, MD, Veltmann, Christian, MD, Antzelevitch, Charles, PhD, FHRS

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Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8 von Barajas-Martínez, Hector, PhD, Hu, Dan, MD, PhD, Ferrer, Tania, PhD, Onetti, Carlos G., PhD, Wu, Yuesheng, MD, Burashnikov, Elena, BS, Boyle, Madalene, BS, Surman, Tyler, BS, Urrutia, Janire, PhD, Veltmann, Christian, MD, Schimpf, Rainer, MD, Borggrefe, Martin, MD, Wolpert, Christian, MD, Ibrahim, Bassiema B., MD, Sánchez-Chapula, José Antonio, MD, PhD, Winters, Stephen, MD, Haïssaguerre, Michel, MD, Antzelevitch, Charles, PhD, FHRS, AHA

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Long QT, syndactyly, joint contractures, stroke and novel CACNA1C mutation: Expanding the spectrum of Timothy syndrome von Gillis, Jane, Burashnikov, Elena, Antzelevitch, Charles, Blaser, Susan, Gross, Gil, Turner, Lesley, Babul‐Hirji, Riyana, Chitayat, David

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Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome von Cordeiro, Jonathan M, Marieb, Mark, Pfeiffer, Ryan, Calloe, Kirstine, Burashnikov, Elena, Antzelevitch, Charles

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Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect von Veltmann, Christian, Barajas‐Martinez, Hector, Wolpert, Christian, Borggrefe, Martin, Schimpf, Rainer, Pfeiffer, Ryan, Cáceres, Gabriel, Burashnikov, Elena, Antzelevitch, Charles, Hu, Dan

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Mutations in NaV1.5 Reveal Calcium-Calmodulin Regulation of Sodium Channel von Nof, Eyal, Vysochek, Leonid, Meisel, Eshcar, Burashnikov, Elena, Antzelevitch, Charles, Clatot, Jerome, Beinart, Roy, Luria, David, Glikson, Michael, Oz, Shimrit

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Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutations von Hong, Kui, Brugada, Josep, Oliva, Antonio, Berruezo-Sanchez, Antonio, Potenza, Domenico, Pollevick, Guido D, Guerchicoff, Alejandra, Matsuo, Kiyotaka, Burashnikov, Elena, Dumaine, Robert, Towbin, Jeffrey A, Nesterenko, Vladislav, Brugada, Pedro, Antzelevitch, Charles, Brugada, Ramon

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Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation von Ravn, Lasse S., MD, Aizawa, Yoshiyasu, MD, Pollevick, Guido D., PhD, Hofman-Bang, Jacob, PhD, Cordeiro, Jonathan M., PhD, Dixen, Ulrik, PhD, Jensen, Gorm, DMSc, Wu, Yuesheng, MS, Burashnikov, Elena, BS, Haunso, Stig, DMSc, Guerchicoff, Alejandra, PhD, Hu, Dan, MD, PhD, Svendsen, Jesper H., DMSc, Christiansen, Michael, MD, Antzelevitch, Charles, PhD, FHRS

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Lidocaine-Induced Brugada Syndrome Phenotype Linked to a Novel Double Mutation in the Cardiac Sodium Channel von Barajas-Martínez, Hector M, Hu, Dan, Cordeiro, Jonathan M, Wu, Yuesheng, Kovacs, Richard J, Meltser, Henry, Kui, Hong, Elena, Burashnikov, Brugada, Ramon, Antzelevitch, Charles, Dumaine, Robert

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Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction von Hu, Dan, MD, PhD, Viskin, Sami, MD, Oliva, Antonio, MD, PhD, Carrier, Tabitha, BS, Cordeiro, Jonathan M., PhD, Barajas-Martinez, Hector, PhD, Wu, Yuesheng, MS, Burashnikov, Elena, MS, Sicouri, Serge, MD, Brugada, Ramon, MD, Rosso, Rafael, MD, Guerchicoff, Alejandra, PhD, Pollevick, Guido D., PhD, Antzelevitch, Charles, PhD

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A Common Single Nucleotide Polymorphism Can Exacerbate Long-QT Type 2 Syndrome Leading to Sudden Infant Death von Nof, Eyal, Cordeiro, Jonathan M, Pérez, Guillermo J, Scornik, Fabiana S, Calloe, Kirstine, Love, Barry, Burashnikov, Elena, Caceres, Gabriel, Gunsburg, Moshe, Antzelevitch, Charles

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Genetic and biophysical basis for bupivacaine-induced ST segment elevation and VT/VF. Anesthesia unmasked Brugada syndrome von Vernooy, Kevin, Sicouri, Serge, Dumaine, Robert, Hong, Kui, Oliva, Antonio, Burashnikov, Elena, Timmermans, Carl, Delhaas, Tammo, Crijns, Harry J.G.M., Antzelevitch, Charles, Rodriguez, Luz-Maria, Brugada, Ramon

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A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents von Hu, Dan, Barajas-Martínez, Hector, Medeiros-Domingo, Argelia, Crotti, Lia, Veltmann, Christian, Schimpf, Rainer, Urrutia, Janire, Alday, Aintzane, Casis, Oscar, Pfeiffer, Ryan, Burashnikov, Elena, Caceres, Gabriel, Tester, David J, Wolpert, Christian, Borggrefe, Martin, Schwartz, Peter, Ackerman, Michael J, Antzelevitch, Charles

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Sudden death associated with short-QT syndrome linked to mutations in HERG von BRUGADA, Ramon, HONG, Kui, BURASHNIKOV, Elena, MATSUO, Kiyotaka, YUE SHENG WU, GUERCHICOFF, Alejandra, BIANCHI, Francesca, GIUSTETTO, Carla, SCHIMPF, Rainer, BRUGADA, Pedro, ANTZELEVITCH, Charles, DUMAINE, Robert, CORDEIRO, Jonathan, GAITA, Fiorenzo, BORGGREFE, Martin, MENENDEZ, Teresa M, BRUGADA, Josep, POLLEVICK, Guido D, WOLPERT, Christian

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A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype von Hu, Dan, Barajas-Martinez, Hector, Burashnikov, Elena, Springer, Michael, Wu, Yuesheng, Varro, Andras, Pfeiffer, Ryan, Koopmann, Tamara T, Cordeiro, Jonathan M, Guerchicoff, Alejandra, Pollevick, Guido D, Antzelevitch, Charles

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De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero von Hong, Kui, Piper, David R, Diaz-Valdecantos, Aurora, Brugada, Josep, Oliva, Antonio, Burashnikov, Elena, Santos-de-Soto, José, Grueso-Montero, Josefina, Diaz-Enfante, Ernesto, Brugada, Pedro, Sachse, Frank, Sanguinetti, Michael C, Brugada, Ramon

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Functional Effects of KCNE3 Mutation and Its Role in the Development of Brugada Syndrome von Delpón, Eva, Cordeiro, Jonathan M, Núñez, Lucía, Thomsen, Poul Erik Bloch, Guerchicoff, Alejandra, Pollevick, Guido D, Wu, Yuesheng, Kanters, Jørgen K, Larsen, Carsten Toftager, Hofman-Bang, Jacob, Burashnikov, Elena, Christiansen, Michael, Antzelevitch, Charles

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A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype von Hu, Dan, Barajas-Martinez, Hector, Burashnikov, Elena, Springer, Michael, Wu, Yuesheng, Varro, Andras, Pfeiffer, Ryan, Koopmann, Tamara T, Cordeiro, Jonathan M, Guerchicoff, Alejandra, Pollevick, Guido D, Antzelevitch, Charles

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