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Elena Burashnikov

Masonic Medical Research Laboratory

21H指数
64论文数
4.5K被引数
收录论文 20
发表时间
Mutations in Nav1.5 Reveal Calcium-Calmodulin Regulation of Sodium Channel
err2019-06-05
err8
errOAAI
errNof, Eyal; Vysochek, Leonid; Meisel, Eshcar; Burashnikov, Elena; Antzelevitch, Charles; Clatot, Jerome; Beinart, Roy; Luria, David; Glikson, Michael; Oz, Shimrit
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Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect
err2016-07-06
err45
errOAAI
errVeltmann, Christian; Barajas-Martinez, Hector; Wolpert, Christian; Borggrefe, Martin; Schimpf, Rainer; Pfeiffer, Ryan; Caceres, Gabriel; Burashnikov, Elena; Antzelevitch, Charles; Hu, Dan
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High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia
err2015-07-01
err76
PREAI
errHasdemir, Can; Payzin, Serdar; Kocabas, Umut; Sahin, Hatice; Yildirim, Nihal; Alp, Alpay; Aydin, Mehmet; Pfeiffer, Ryan; Burashnikov, Elena; Wu, Yuesheng; Antzelevitch, Charles
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ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene
err2014-02-01
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errOAAI
errHu, Dan; Barajas-Martinez, Hector; Terzic, Andre; Park, Sungjo; Pfeiffer, Ryan; Burashnikov, Elena; Wu, Yuesheng; Borggrefe, Martin; Veltmann, Christian; Schimpf, Rainer; Cai, John J.; Nam, Gi-Byong; Deshmukh, Pramod; Scheinman, Melvin; Preminger, Mark; Steinberg, Jonathan; Lopez-Izquierdo, Angelica; Ponce-Balbuena, Daniela; Wolpert, Christian; Haissaguerre, Michel; Antonio Sanchez-Chapula, Jose; Antzelevitch, Charles
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A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Nav1.5 and Kv4.3 channel currents
err2012-05-01
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errOAAI
errHu, Dan; Barajas-Martinez, 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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Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8
err2012-04-01
err127
errOAAI
errBarajas-Martinez, Hector; Hu, Dan; Ferrer, Tania; Onetti, Carlos G.; Wu, Yuesheng; Burashnikov, Elena; Boyle, Madalene; Surman, Tyler; Urrutia, Janire; Veltmann, Christian; Schimpf, Rainer; Borggrefe, Martin; Wolpert, Christian; Ibrahim, Bassiema B.; Antonio Sanchez-Chapula, Jose; Winters, Stephen; Haissaguerre, Michel; Antzelevitch, Charles
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LQT5 masquerading as LQT2: a dominant negative effect of KCNE1-D85N rare polymorphism on KCNH2 current
err2011-06-28
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errNof, Eyal; Barajas-Martinez, Hector; Eldar, Michael; Urrutia, Janire; Caceres, Gabriel; Rosenfeld, Gail; Bar-Lev, David; Feinberg, Micha; Burashnikov, Elena; Casis, Oscar; Hu, Dan; Glikson, Michael; Antzelevitch, Charles
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Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death
err2010-12-01
err320
errOAAI
errBurashnikov, Elena; Pfeiffer, Ryan; Barajas-Martinez, Hector; Delpon, Eva; Hu, Dan; Desai, Mayurika; Borggrefe, Martin; Haeissaguerre, Michel; Kanter, Ronald; Pollevick, Guido D.; Guerchicoff, Alejandra; Laino, 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
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Overlapping LQT1 and LQT2 Phenotype in a Patient with Long QT Syndrome Associated with Loss-of-Function Variations in KCNQ1 and KCNH2
err2010-01-01
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errCordeiro, Jonathan M.; Perez, Guillermo J.; Pfeiffer, Ryan; Burashnikov, Elena; Borggrefe, Martin; Wolpert, Christian; Schimpf, Rainer; Antzelevitch, Charles
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Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome
err2009-05-01
err86
errOAAI
errCordeiro, Jonathan M.; Marieb, Mark; Pfeiffer, Ryan; Calloe, Kirstine; Burashnikov, Elena; Antzelevitch, Charles
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Dual Variations in SCN5A and CACNB2b Underlie Cardiac Conduction Disease without Brugada Syndrome
err2009-02-01
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errHu, Dan; Martinez, Hector Barajas; Pfeiffer, Ryan; Guerchicoff, Alejandra; Cordeiro, Jonathan M.; Curtis, Anne B.; Pollevick, Guido D.; Wu, Yuesheng; Burashnikov, Elena; Antzelevitch, Charles
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Biophysical Characterization of a Novel KCNJ2 Mutation Associated with Andersen-Tawil Syndrome and CPVT Mimicry
err2009-02-01
err0
errOAAI
errBarajas-Martinez, Hector; Hu, Dan; Ontiveros, Gustavo; Caceres, Gabriel; Burashnikov, Elena; Scaglione, Jorge; Antzelevitch, Charles
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Gain of function in IKs, secondary to a mutation in KCNE5 associated with atrial fibrillation
err2008-03-01
err105
errOAAI
errRavn, Lasse S.; Aizawa, Yoshiyasu; Pollevick, Guido D.; Hofman-Bang, Jacob; Cordeiro, Jonathan M.; Dixen, Ulrik; Jensen, Gorm; Wu, Yuesheng; Burashnikov, Elena; Haunso, Stig; Guerchicoff, Atejandra; Hu, Dan; Svendsen, Jesper H.; Christiansen, Michaet; Antzelevitch, Charles
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Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction
err2007-08-01
err57
errOAAI
errHu, Dan; Viskin, Sami; Oliva, Antonio; Carrier, Tabitha; Cordeiro, Jonathan M.; Barajas-Martinez, Hector; Wu, Yuesheng; Burashnikov, Etena; Sicouri, Serge; Brugada, Ramon; Rosso, Rafae; Guerchicoff, Alejandra; Pollevick, Guido D.; Antzelevitch, Chares
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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
err2007-01-30
err750
errOAAI
errAntzelevitch, Charles; Pollevick, Guido D.; Cordeiro, Jonathan M.; Casis, Oscar; Sanguinetti, Michael C.; Aizawa, Yoshiyasu; Guerchicoff, Alejandra; Pfeiffer, Ryan; Oliva, Antonio; Wollnik, Bernd; Gelber, Philip; Bonaros, Elias P., Jr.; Burashnikov, Elena; Wu, Yuesheng; Sargent, John D.; Schickel, Stefan; Oberheiden, Ralf; Bhatia, Atul; Hsu, Li-Fern; Haissaguerre, Michel; Schimpf, Rainer; Borggrefe, Martin; Wolpert, Christian
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Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndrome
err2006-11-07
err82
errOAAI
errCordeiro, Jonathan M.; Barajas-Martinez, Hector; Hong, Kui; Burashnikov, Elena; Pfeiffer, Ryan; Orsino, Anne-Marie; Wu, Yue Sheng; Hu, Dan; Brugada, Josep; Brugada, Pedro; Antzelevitch, Charles; Dumaine, Robert; Brugada, Ramon
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Genetic and biophysical basis for bupivacaine-induced ST segment elevation and VT/VF. Anesthesia unmasked Brugada syndrome
err2006-09-01
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errOAAI
errVernooy, 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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De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero
err2005-12-01
err254
PREAI
errHong, K; Piper , DR; Diaz-Valdecantos, A; Brugada, J; Oliva, A; Burashnikov, E; Santos-de-Soto, J; Grueso-Montero, J; Diaz-Enfante, E; Brugada, P; Sachse, F; Sanguinetti, MC; Brugada, R
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Cryptic 5′ splice site activation in SCN5A associated with Brugada syndrome
err2005-04-01
err51
PREAI
errHong, K; Guerchicoff, A; Pollevick, GD; Oliva, A; Dumaine, R; de Zutter, M; Burashnikov, E; Wu, YS; Brugada, J; Brugada, P; Brugada, R
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Sudden death associated with short-QT syndrome linked to mutations in HERG
err2004-01-06
err685
errOAAI
errBrugada, R; Hong, K; Dumaine, R; Cordeiro, J; Gaita, F; Borggrefe, M; Menendez, TM; Brugada, J; Pollevick, GD; Wolpert, C; Burashnikov, E; Matsuo, K; Wu, YS; Guerchicoff, A; Bianchi, F; Giustetto, C; Schimpf, R; Brugada, P; Antzelevitch, C
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