Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Elijah R. Behr"'
Autor:
Elijah R. Behr
Publikováno v:
Journal of the American College of Cardiology. 78:1618-1620
Autor:
Antonios Pantazis, Daniel Jacoby, Chris Miles, William J. McKenna, Annina S. Vischer, Kris Denhaerynck, Petros Syrris, Elijah R. Behr, Ardan M. Saguner, Andrew D. Krahn, Deniz Akdis, Rachel Bastiaenen, Silvia Castelletti
Publikováno v:
International Journal of Cardiology. 290:100-105
Aims Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetically determined heart muscle disorder associated with an increased risk of life-threatening arrhythmias in some patients. Risk stratification remains challenging. Therefore, we s
Autor:
Gaia Tanzarella, Gherardo Finocchiaro, Igor Diemberger, Chris Miles, Mary N. Sheppard, Michael Papadakis, Harshil Dhutia, Sanjay Sharma, Elijah R. Behr, Aneil Malhotra
Publikováno v:
JACC: Clinical Electrophysiology. 5:516-522
Objectives This study sought to describe the clinical and pathological features of anomalous origin of a coronary artery (AOCA) in sudden cardiac death (SCD) victims. Background AOCA from the inappropriate sinus of Valsalva or from the pulmonary arte
Autor:
Elijah R. Behr, Peter J. Fleming, Alban-Elouen Baruteau, Marta C. Cohen, Amie Jaye, Leonie C.H. Wong, Pritha Chanana, Michael A. Simpson, Belinda Gray, David J. Tester, Jacob Tfelt-Hansen, Michael J. Ackerman, Iona Jeffrey, Jared M. Evans, Margaret J. Evans
Publikováno v:
Gray, B, Tester, D J, Wong, L C, Chanana, P, Jaye, A, Evans, J M, Baruteau, A E, Evans, M, Fleming, P, Jeffrey, I, Cohen, M, Tfelt-Hansen, J, Simpson, M A, Ackerman, M J & Behr, E R 2019, ' Noncardiac genetic predisposition in sudden infant death syndrome ', Genetics in Medicine, vol. 21, no. 3, pp. 641–649 . https://doi.org/10.1038/s41436-018-0131-4
Gray, B, Tester, D J, Wong, L C, Chanana, P, Jaye, A, Evans, J M, Baruteau, A-E, Evans, M, Fleming, P, Jeffrey, I, Cohen, M, Tfelt-Hansen, J, Simpson, M A, Ackerman, M J & Behr, E R 2018, ' Noncardiac genetic predisposition in sudden infant death syndrome ', Genetics in Medicine . https://doi.org/10.1038/s41436-018-0131-4
Gray, B, Tester, D J, Wong, L C, Chanana, P, Jaye, A, Evans, J M, Baruteau, A-E, Evans, M, Fleming, P, Jeffrey, I, Cohen, M, Tfelt-Hansen, J, Simpson, M A, Ackerman, M J & Behr, E R 2018, ' Noncardiac genetic predisposition in sudden infant death syndrome ', Genetics in Medicine . https://doi.org/10.1038/s41436-018-0131-4
PURPOSE: Sudden infant death syndrome (SIDS) is the commonest cause of sudden death of an infant; however, the genetic basis remains poorly understood. We aimed to identify noncardiac genes underpinning SIDS and determine their prevalence compared wi
Autor:
Raquel Neves, Michael A. Simpson, Elijah R. Behr, Michael J. Ackerman, David J. Tester, John R. Giudicessi
Publikováno v:
Heart Rhythm. 18:S382-S383
Autor:
Dania Kallas, Prince J. Kannankeril, Vincent Probst, Jonathan R. Skinner, Michael W.T. Tanck, Andrew D. Krahn, Guillermo J. Pérez, Jacob Tfelt-Hansen, Habib Khan, Vibeke M. Almaas, Kristina H. Haugaa, Sing-Chien Yap, Georgia Sarquella Brugada, Andrew M. Davis, Wataru Shimizu, Ferran Rosés I. Noguer, Martin J. LaPage, Arthur A.M. Wilde, Boris Rudic, Elijah R. Behr, Janneke A.E. Kammeraad, Thomas M. Roston, Esther Zorio Grima, Ramon Brugada, Maarten P. van den Berg, Michael J. Ackerman, Frederic Sacher, Heikki Swan, Minoru Horie, Christopher Semsarian, Christian van der Werf, Shubhayan Sanatani, Peter J. Schwartz, Antoine Leenhardt, Nico A. Blom, Alice Maltret, Jason D. Roberts, Puck Peltenburg, Krystien V.V. Lieve, John R. Giudicessi, Jan Till, Sonia Franciosi, Anwar Baban, Katrina B. Sorensen, Isabelle Denjoy, Yuko Wada, Johan M Bos, Terezia Tavacova, Sally-Ann B. Clur, Tomas Robyns
Publikováno v:
Heart Rhythm. 18:S289-S290
Autor:
Sandro Ninni, Bernard Belhassen, Mikael Laredo, Esther Zorio, Guy Zahavi, Rob W Roudijk, Dominique Lacroix, Alessio Gasperetti, Laurent Fauchier, Laurens P Bosman, Petr Peichl, Anat Milman, Richard N.W. Hauer, Estelle Gandjbakhch, Chris Miles, J. Peter van Tintelen, Srijita Sen-Chowdhry, Guillaume Duthoit, Giovanni Peretto, Antoine Andorin, Anneline S.J.M. te Riele, Leonardo Calo Stepan Havranek, Firat Duru, Anne Rollin, Carla Giustetto, Philippe Maury, Jean-Sylvain Hermida, Elena Arbelo, Frederic Sacher, Jean-Marc Sellal, Francisco José Bermúdez Jiménez, Giulio Conte, Alexandros Protonarios, Eyal Nof, Nicolas Badenco, Josef Kautzner, Elijah R. Behr, Ruben Casado, Josep Brugada, Jacob Tflet-Hansen, Simone Sala, Vincent Probst, Xavier Waintraub, Christian de Chillou, Paolo Della Bella, Konstantinos P. Letsas, Roy Beinart
Publikováno v:
Heart Rhythm. 18:S347-S348
Autor:
Peter J. Fleming, David R. FitzPatrick, Amie Jaye, Michael A. Simpson, Michael J. Ackerman, David J. Tester, Leonie C.H. Wong, Jared M. Evans, Jacob Tfelt-Hansen, Margaret J. Evans, Elijah R. Behr, Pritha Chanana, Marta C. Cohen, Iona Jeffrey
Publikováno v:
Tester, D J, Wong, L C H, Chanana, P, Jaye, A, Evans, J M, FitzPatrick, D R, Evans, M J, Fleming, P, Jeffrey, I, Cohen, M C, Tfelt-Hansen, J, Simpson, M A, Behr, E R & Ackerman, M J 2018, ' Cardiac Genetic Predisposition in Sudden Infant Death Syndrome ', Journal of the American College of Cardiology, vol. 71, no. 11, pp. 1217-1227 . https://doi.org/10.1016/j.jacc.2018.01.030
Background: Sudden infant death syndrome (SIDS) is a leading cause of postneonatal mortality. Genetic heart diseases (GHDs) underlie some cases of SIDS. Objectives: This study aimed to determine the spectrum and prevalence of GHD-associated mutations
Autor:
Efstathios Papatheodorou, Gherardo Finocchiaro, Mary N. Sheppard, Nina Edwards, Sara Wasim, Maria Tome-Esteban, Sanjay Sharma, Virginia Attard, Hariharan Raju, Bode Ensam, Tessa Homfray, Rachel Bastiaenen, Yanushi D. Wijeyeratne, Michael Papadakis, Andrew D'Silva, Aneil Malhotra, Elijah R. Behr, Velislav N. Batchvarov, Belinda Gray, Greg Mellor, Della Cole
Publikováno v:
Papadakis, M, Papatheodorou, E, Mellor, G, Raju, H, Bastiaenen, R, Wijeyeratne, Y, Wasim, S, Ensam, B, Finocchiaro, G, Gray, B, Malhotra, A, D'Silva, A, Edwards, N, Cole, D, Attard, V, Batchvarov, V N, Tome-Esteban, M, Homfray, T, Sheppard, M N, Sharma, S & Behr, E R 2018, ' The Diagnostic Yield of Brugada Syndrome After Sudden Death With Normal Autopsy ', Journal of the American College of Cardiology, vol. 71, no. 11, pp. 1204-1214 . https://doi.org/10.1016/j.jacc.2018.01.031
BACKGROUND: Familial evaluation after a sudden death with negative autopsy (sudden arrhythmic death syndrome; SADS) may identify relatives at risk of fatal arrhythmias.OBJECTIVES: This study aimed to assess the impact of systematic ajmaline provocati
Autor:
Chiara Scrocco, Elijah R. Behr
Publikováno v:
JACC: Clinical Electrophysiology. 6:1862-1863