High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia
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
Published in Heart rhythm (01.07.2015)
Published in Heart rhythm (01.07.2015)
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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
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
Published in Circulation (New York, N.Y.) (30.01.2007)
Published in Circulation (New York, N.Y.) (30.01.2007)
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Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death
Burashnikov, Elena, Pfeiffer, Ryan, Barajas-Martinez, Héctor, Delpón, Eva, Hu, Dan, Desai, Mayurika, Borggrefe, Martin, Häissaguerre, Michel, Kanter, Ronald, Pollevick, Guido D, Guerchicoff, Alejandra, Laiño, Ruben, Marieb, Mark, Nademanee, Koonlawee, Nam, Gi-Byoung, Robles, Roberto, Schimpf, Rainer, Stapleton, Dwight D, Viskin, Sami, Winters, Stephen, Wolpert, Christian, Zimmern, Samuel, Veltmann, Christian, Antzelevitch, Charles
Published in Heart rhythm (01.12.2010)
Published in Heart rhythm (01.12.2010)
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Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8
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
Published in Heart rhythm (01.04.2012)
Published in Heart rhythm (01.04.2012)
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Long QT, syndactyly, joint contractures, stroke and novel CACNA1C mutation: Expanding the spectrum of Timothy syndrome
Gillis, Jane, Burashnikov, Elena, Antzelevitch, Charles, Blaser, Susan, Gross, Gil, Turner, Lesley, Babul‐Hirji, Riyana, Chitayat, David
Published in American journal of medical genetics. Part A (01.01.2012)
Published in American journal of medical genetics. Part A (01.01.2012)
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Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome
Cordeiro, Jonathan M, Marieb, Mark, Pfeiffer, Ryan, Calloe, Kirstine, Burashnikov, Elena, Antzelevitch, Charles
Published in Journal of molecular and cellular cardiology (01.05.2009)
Published in Journal of molecular and cellular cardiology (01.05.2009)
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Mutations in NaV1.5 Reveal Calcium-Calmodulin Regulation of Sodium Channel
Nof, Eyal, Vysochek, Leonid, Meisel, Eshcar, Burashnikov, Elena, Antzelevitch, Charles, Clatot, Jerome, Beinart, Roy, Luria, David, Glikson, Michael, Oz, Shimrit
Published in Frontiers in physiology (05.06.2019)
Published in Frontiers in physiology (05.06.2019)
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Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect
Veltmann, Christian, Barajas‐Martinez, Hector, Wolpert, Christian, Borggrefe, Martin, Schimpf, Rainer, Pfeiffer, Ryan, Cáceres, Gabriel, Burashnikov, Elena, Antzelevitch, Charles, Hu, Dan
Published in Journal of the American Heart Association (05.07.2016)
Published in Journal of the American Heart Association (05.07.2016)
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Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation
Ravn, Lasse S, Aizawa, Yoshiyasu, Pollevick, Guido D, Hofman-Bang, Jacob, Cordeiro, Jonathan M, Dixen, Ulrik, Jensen, Gorm, Wu, Yuesheng, Burashnikov, Elena, Haunso, Stig, Guerchicoff, Alejandra, Hu, Dan, Svendsen, Jesper H, Christiansen, Michael, Antzelevitch, Charles
Published in Heart rhythm (01.03.2008)
Published in Heart rhythm (01.03.2008)
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Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutations
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
Published in Circulation (New York, N.Y.) (09.11.2004)
Published in Circulation (New York, N.Y.) (09.11.2004)
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Lidocaine-Induced Brugada Syndrome Phenotype Linked to a Novel Double Mutation in the Cardiac Sodium Channel
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
Published in Circulation research (15.08.2008)
Published in Circulation research (15.08.2008)
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A Common Single Nucleotide Polymorphism Can Exacerbate Long-QT Type 2 Syndrome Leading to Sudden Infant Death
Nof, Eyal, Cordeiro, Jonathan M, Pérez, Guillermo J, Scornik, Fabiana S, Calloe, Kirstine, Love, Barry, Burashnikov, Elena, Caceres, Gabriel, Gunsburg, Moshe, Antzelevitch, Charles
Published in Circulation. Cardiovascular genetics (01.04.2010)
Published in Circulation. Cardiovascular genetics (01.04.2010)
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Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction
Hu, Dan, Viskin, Sami, Oliva, Antonio, Carrier, Tabitha, Cordeiro, Jonathan M, Barajas-Martinez, Hector, Wu, Yuesheng, Burashnikov, Elena, Sicouri, Serge, Brugada, Ramon, Rosso, Rafael, Guerchicoff, Alejandra, Pollevick, Guido D, Antzelevitch, Charles
Published in Heart rhythm (01.08.2007)
Published in Heart rhythm (01.08.2007)
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Genetic and biophysical basis for bupivacaine-induced ST segment elevation and VT/VF. Anesthesia unmasked Brugada syndrome
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
Published in Heart rhythm (01.09.2006)
Published in Heart rhythm (01.09.2006)
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Journal Article
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
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
Published in Heart rhythm (01.05.2012)
Published in Heart rhythm (01.05.2012)
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SCN5A Mutation associated with acute myocardial infarction
Oliva, Antonio, Hu, Dan, Viskin, Sami, Carrier, Tabitha, Cordeiro, Jonathan M, Barajas-Martinez, Hector, Wu, Yusheng, Burashnikov, Elena, Brugada, Ramon, Rosso, Rafael, Guerchicoff, Alexandra, Pollevick, Guido, Pascali, Vincenzo L, Antzelevitch, Charlie
Published in Legal medicine (Tokyo, Japan) (01.04.2009)
Published in Legal medicine (Tokyo, Japan) (01.04.2009)
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A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype
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
Published in Circulation. Cardiovascular genetics (01.06.2009)
Published in Circulation. Cardiovascular genetics (01.06.2009)
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Journal Article
Functional Effects of KCNE3 Mutation and Its Role in the Development of Brugada Syndrome
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
Published in Circulation. Arrhythmia and electrophysiology (01.08.2008)
Published in Circulation. Arrhythmia and electrophysiology (01.08.2008)
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Journal Article
A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype
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
Published in Circulation. Cardiovascular genetics (01.06.2009)
Published in Circulation. Cardiovascular genetics (01.06.2009)
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Journal Article
A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Nav1.5 and Kv4.3 channel currents
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
Published in Heart rhythm (01.05.2012)
Published in Heart rhythm (01.05.2012)
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