未登录Identifying sex-based differences in heart failure with preserved ejection fraction
Eaton, Deborah; Berretta, Remus; Lynch, Jacqueline; Travers, Joshua; Woulfe, Kathleen; Pfeiffer, Ryan; Hulke, Michelle; Zhao, Huaqing; Hobby, Alexander; Schena, Giana; Johnson, Jaslyn; Wallner, Markus; Lau, Edward; Lam, Maggie; Tucker, Nathan; McKinsey, Timothy; Wolfson, Marla; Houser, Steven .png)
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收藏分享 收藏 Susceptibility to Ventricular Arrhythmias Resulting from Mutations in FKBP1B, PXDNL, and SCN9A Evaluated in hiPSC CardiomyocytesBarajas-Martinez, Hector; Smith, Maya; Hu, Dan; Goodrow, Robert J.; Puleo, Colleen; Hasdemir, Can; Antzelevitch, Charles; Pfeiffer, Ryan; Treat, Jacqueline A.; Cordeiro, Jonathan M. 分享 收藏 Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT SyndromeLahrouchi, Najim; Tadros, Rafik; Crotti, Lia; Mizusawa, Yuka; Postema, Pieter G.; Beekman, Leander; Walsh, Roddy; Hasegawa, Kanae; Barc, Julien; Ernsting, Marko; Turkowski, Kari L.; Mazzanti, Andrea; Beckmann, Britt M.; Shimamoto, Keiko; Diamant, Ulla-Britt; Wijeyeratne, Yanushi D.; Kucho, Yu; Robyns, Tomas; Ishikawa, Taisuke; Arbelo, Elena; Christiansen, Michael; Winbo, Annika; Jabbari, Reza; Lubitz, Steven A.; Steinfurt, Johannes; Rudic, Boris; Loeys, Bart; Shoemaker, M. Ben; Weeke, Peter E.; Pfeiffer, Ryan; Davies, Brianna; Andorin, Antoine; Hofman, Nynke; Dagradi, Federica; Pedrazzini, Matteo; Tester, David J.; Bos, J. Martijn; Sarquella-Brugada, Georgia; Campuzano, Oscar; Platonov, Pyotr G.; Stallmeyer, Birgit; Zumhagen, Sven; Nannenberg, Eline A.; Veldink, Jan H.; van den Berg, Leonard H.; Al-Chalabi, Ammar; Shaw, Christopher E.; Shaw, Pamela J.; Morrison, Karen E.; Andersen, Peter M.; Mueller-Nurasyid, Martina; Cusi, Daniele; Barlassina, Cristina; Galan, Pilar; Lathrop, Mark; Munter, Markus; Werge, Thomas; Ribases, Marta; Aung, Tin; Khor, Chiea C.; Ozaki, Mineo; Lichtner, Peter; Meitinger, Thomas; van Tintelen, J. Peter; Hoedemaekers, Yvonne; Denjoy, Isabelle; Leenhardt, Antoine; Napolitano, Carlo; Shimizu, Wataru; Schott, Jean-Jacques; Gourraud, Jean-Baptiste; Makiyama, Takeru; Ohno, Seiko; Itoh, Hideki; Krahn, Andrew D.; Antzelevitch, Charles; Roden, Dan M.; Saenen, Johan; Borggrefe, Martin; Odening, Katja E.; Ellinor, Patrick T.; Tfelt-Hansen, Jacob; Skinner, Jonathan R.; van den Berg, Maarten P.; Olesen, Morten Salling; Brugada, Josep; Brugada, Ramon; Makita, Naomasa; Breckpot, Jeroen; Yoshinaga, Masao; Behr, Elijah R.; Rydberg, Annika; Aiba, Takeshi; Kaeaeb, Stefan; Priori, Silvia G.; Guicheney, Pascale; Tan, Hanno L.; Newton-Cheh, Christopher; Ackerman, Michael J.; Schwartz, Peter J.; Schulze-Bahr, Eric; Probst, Vincent; Horie, Minoru; Wilde, Arthur A.; Tanck, Michael W. T.; Bezzina, Connie R. 分享 收藏 Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction DefectVeltmann, Christian; Barajas-Martinez, Hector; Wolpert, Christian; Borggrefe, Martin; Schimpf, Rainer; Pfeiffer, Ryan; Caceres, Gabriel; Burashnikov, Elena; Antzelevitch, Charles; Hu, Dan 分享 收藏 High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardiaHasdemir, Can; Payzin, Serdar; Kocabas, Umut; Sahin, Hatice; Yildirim, Nihal; Alp, Alpay; Aydin, Mehmet; Pfeiffer, Ryan; Burashnikov, Elena; Wu, Yuesheng; Antzelevitch, Charles 分享 收藏 ABCC9 is a novel Brugada and early repolarization syndrome susceptibility geneHu, 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 分享 收藏 A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Nav1.5 and Kv4.3 channel currentsHu, 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 分享 收藏 分享 收藏 Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac deathBurashnikov, 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 分享 收藏 分享 收藏 An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testingKapplinger, Jamie D.; Tester, David J.; Alders, Marielle; Benito, Begona; Berthet, Myriam; Brugada, Josep; Brugada, Pedro; Fressart, Veronique; Guerchicoff, Alejandra; Harris-Kerr, Carole; Kamakura, Shiro; Kyndt, Florence; Koopmann, Tamara T.; Miyamoto, Yoshihiro; Pfeiffer, Ryan; Pollevick, Guido D.; Probst, Vincent; Zumhagen, Sven; Vatta, Matteo; Towbin, Jeffrey A.; Shimizu, Wataru; Schulze-Bahr, Eric; Antzelevitch, Charles; Salisbury, Benjamin A.; Guicheney, Pascale; Wilde, Arthur A. M.; Brugada, Ramon; Schott, Jean-Jacques; Ackerman, Michael J. 分享 收藏 分享 收藏 分享 收藏 Dual Variations in SCN5A and CACNB2b Underlie Cardiac Conduction Disease without Brugada SyndromeHu, Dan; Martinez, Hector Barajas; Pfeiffer, Ryan; Guerchicoff, Alejandra; Cordeiro, Jonathan M.; Curtis, Anne B.; Pollevick, Guido D.; Wu, Yuesheng; Burashnikov, Elena; Antzelevitch, Charles 分享 收藏 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 deathAntzelevitch, 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 分享 收藏 Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndromeCordeiro, 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 分享 收藏 
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