نتائج البحث - Guido D. Pollevick
- يعرض 1 - 15 نتائج من 15
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Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test حسب Jamie D. Kapplinger, David J. Tester, Benjamin A. Salisbury, Janet L. Carr, Carole Harris‐Kerr, Guido D. Pollevick, Arthur A.M. Wilde, Michael J. Ackerman
منشور في 2009Artigo -
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A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype حسب Dan Hu, Hector Barajas‐Martínez, Elena Burashnikov, Michael Springer, Yuesheng Wu, András Varró, Ryan Pfeiffer, Tamara T. Koopmann, Jonathan M. Cordeiro, Alejandra Guerchicoff, Guido D. Pollevick, Charles Antzelevitch
منشور في 2009Artigo -
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Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction حسب Dan Hu, Sami Viskin, Antonio Oliva, Tabitha Carrier, Jonathan M. Cordeiro, Hector Barajas‐Martínez, Yuesheng Wu, Elena Burashnikov, Serge Sicouri, Ramón Brugada, Rafael Rosso, Alejandra Guerchicoff, Guido D. Pollevick, Charles Antzelevitch
منشور في 2007Artigo -
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Functional Effects of <i>KCNE3</i> Mutation and Its Role in the Development of Brugada Syndrome حسب Eva Delpón, Jonathan M. Cordeiro, Lucía Núñez, Poul Erik Bloch Thomsen, Alejandra Guerchicoff, Guido D. Pollevick, Yuesheng Wu, Jørgen K. Kanters, Carsten T. Larsen, Jacob Hofman-Bang, Elena Burashnikov, Michael Christiansen, Charles Antzelevitch
منشور في 2008Artigo -
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Value of Electrocardiographic Parameters and Ajmaline Test in the Diagnosis of Brugada Syndrome Caused by SCN5A Mutations حسب Kui Hong, Josép Brugada, Antonio Oliva, Antonio Berruezo-Sanchez, Domenico Potenza, Guido D. Pollevick, Alejandra Guerchicoff, Kiyotaka Matsuo, Elena Burashnikov, Robert Dumaine, Jeffrey A. Towbin, Vladislav V. Nesterenko, Pedro Brugada, Charles Antzelevitch, Ramón Brugada
منشور في 2004Artigo -
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Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation حسب Lasse Steen Ravn, Yoshiyasu Aizawa, Guido D. Pollevick, Jacob Hofman-Bang, Jonathan M. Cordeiro, Ulrik Dixen, Gorm Boje Jensen, Yuesheng Wu, Elena Burashnikov, Stig Haunsø, Alejandra Guerchicoff, Dan Hu, Jesper Hastrup Svendsen, Michael Christiansen, Charles Antzelevitch
منشور في 2008Carta -
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Sudden Death Associated With Short-QT Syndrome Linked to Mutations in HERG حسب Ramón Brugada, Kui Hong, Robert Dumaine, Jonathan M. Cordeiro, Fiorenzo Gaïta, Martin Borggrefe, Teresa Menéndez, Josép Brugada, Guido D. Pollevick, Christian Wolpert, Elena Burashnikov, Kiyotaka Matsuo, Yue Wu, Alejandra Guerchicoff, Francesca Bianchi, Carla Giustetto, Rainer Schimpf, Pedro Brugada, Charles Antzelevitch
منشور في 2003Artigo -
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Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing حسب Lisa R. Susswein, Megan L. Marshall, Rachel Nusbaum, Kristen J. Vogel Postula, Scott M. Weissman, Lauren Yackowski, Erica Vaccari, Jeffrey Bissonnette, Jessica K. Booker, Mattia Cremona, Federica Gibellini, Patricia D. Murphy, Daniel Pineda‐Alvarez, Guido D. Pollevick, Zhixiong Xu, Gabi Richard, Sherri J. Bale, Rachel T. Klein, Kathleen S. Hruska, Wendy K. Chung
منشور في 2015Artigo -
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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 حسب Charles Antzelevitch, Guido D. Pollevick, Jonathan M. Cordeiro, Óscar Casis, Michael C. Sanguinetti, Yoshiyasu Aizawa, Alejandra Guerchicoff, Ryan Pfeiffer, Antonio Oliva, Bernd Wollnik, Philip M. Gelber, Elias P. Bonaros, Elena Burashnikov, Yuesheng Wu, John D. Sargent, STEFAN SCHICKEL, Ralf Oberheiden, Atul Bhatia, LI‐FERN HSU, Michel Haı̈ssaguerre, Rainer Schimpf, Martin Borggrefe, Christian Wolpert
منشور في 2007Artigo -
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Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death حسب Elena Burashnikov, Ryan Pfeiffer, Hector Barajas‐Martínez, Eva Delpón, Dan Hu, Mayurika Desai, Martin Borggrefe, Michel Haı̈ssaguerre, Ronald J. Kanter, Guido D. Pollevick, Alejandra Guerchicoff, R. Laino, Mark Marieb, Koonlawee Nademanee, Gi‐Byoung Nam, Roberto Monreal‐Robles, Rainer Schimpf, Dwight Stapleton, Sami Viskin, Stephen L. Winters, Christian Wolpert, Samuel H. Zimmern, Christian Veltmann, Charles Antzelevitch
منشور في 2010Artigo -
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The Homeodomain Transcription Factor Irx5 Establishes the Mouse Cardiac Ventricular Repolarization Gradient حسب Danny L. Costantini, Eric P. Arruda, Pooja Agarwal, Kyoung-Han Kim, Yonghong Zhu, Wei Zhu, Mélanie Lebel, Chi Cheng, Chong Y. Park, Stephanie A. Pierce, Alejandra Guerchicoff, Guido D. Pollevick, Toby Y.B. Chan, M. Golam Kabir, Shuk Han Cheng, Mansoor Husain, Charles Antzelevitch, Deepak Srivastava, Gil J. Gross, Chi‐chung Hui, Peter H. Backx, Benoit G. Bruneau
منشور في 2005Artigo -
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Distinguishing Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia–Associated Mutations From Background Genetic Noise حسب Jamie D. Kapplinger, Andrew P. Landstrom, Benjamin A. Salisbury, Thomas E. Callis, Guido D. Pollevick, David J. Tester, Moniek G.P.J. Cox, Zahir A. Bhuiyan, Hennie Bikker, Ans C.P. Wiesfeld, Richard N.W. Hauer, J. Peter van Tintelen, Jan D.H. Jongbloed, Hugh Calkins, Daniel P. Judge, Arthur A.M. Wilde, Michael J. Ackerman
منشور في 2011Artigo -
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An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing حسب Jamie D. Kapplinger, David J. Tester, Mariëlle Alders, Begoña Benito, Myriam Berthet, Josép Brugada, Pedro Brugada, Véronique Fressart, Alejandra Guerchicoff, Carole Harris‐Kerr, Shiro Kamakura, Florence Kyndt, Tamara T. Koopmann, Yoshihiro Miyamoto, Ryan Pfeiffer, Guido D. Pollevick, Vincent Probst, Sven Zumhagen, Matteo Vatta, Jeffrey A. Towbin, Wataru Shimizu, Eric Schulze‐Bahr, Charles Antzelevitch, Benjamin A. Salisbury, Pascale Guicheney, Arthur A.M. Wilde, Ramón Brugada, Jean‐Jacques Schott, Michael J. Ackerman
منشور في 2009Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Internal medicine
Medicine
Mutation
Cardiology
Brugada syndrome
Missense mutation
Genetic testing
Long QT syndrome
QT interval
Electrophysiology
Proband
Repolarization
Sudden cardiac death
Sudden death
Calcium
Calcium channel
Electrocardiography
Endocrinology
Heart failure
Molecular biology
Pediatrics
Potassium channel
Short QT syndrome
Ajmaline
Antibody
Arrhythmogenic right ventricular dysplasia
Atrial fibrillation