Zobrazeno 1 - 10
of 108
pro vyhledávání: '"Elijah R. Behr"'
Autor:
Andrew D. Krahn, Elijah R. Behr, Robert Hamilton, Vincent Probst, Zachary Laksman, Hui-Chen Han
Publikováno v:
JACC: Clinical Electrophysiology. 8:386-405
Brugada syndrome (BrS) is an "inherited" condition characterized by predisposition to syncope and cardiac arrest, predominantly during sleep. The prevalence is ∼1:2,000, and is more commonly diagnosed in young to middle-aged males, although patient
Autor:
Puck J. Peltenburg, Dania Kallas, Johan M. Bos, Krystien V.V. Lieve, Sonia Franciosi, Thomas M. Roston, Isabelle Denjoy, Katrina B. Sorensen, Seiko Ohno, Ferran Roses-Noguer, Takeshi Aiba, Alice Maltret, Martin J. LaPage, Joseph Atallah, John R. Giudicessi, Sally-Ann B. Clur, Nico A. Blom, Michael Tanck, Fabrice Extramiana, Koichi Kato, Julien Barc, Martin Borggrefe, Elijah R. Behr, Georgia Sarquella-Brugada, Jacob Tfelt-Hansen, Esther Zorio, Heikki Swan, Janneke A.E. Kammeraad, Andrew D. Krahn, Andrew Davis, Frederic Sacher, Peter J. Schwartz, Jason D. Roberts, Jonathan R. Skinner, Maarten P. van den Berg, Prince J. Kannankeril, Fabrizio Drago, Tomas Robyns, Kristina Haugaa, Terezia Tavacova, Christopher Semsarian, Jan Till, Vincent Probst, Ramon Brugada, Wataru Shimizu, Minoru Horie, Antoine Leenhardt, Michael J. Ackerman, Shubhayan Sanatani, Christian van der Werf, Arthur A.M. Wilde
Publikováno v:
Circulation, 145(5), 333-344. Lippincott Williams & Wilkins
Circulation, 145(5), 333-344. Lippincott Williams and Wilkins
Peltenburg, P J, Kallas, D, Bos, J M, Lieve, K V V, Franciosi, S, Roston, T M, Denjoy, I, Sorensen, K B, Ohno, S, Roses-Noguer, F, Aiba, T, Maltret, A, Lapage, M J, Atallah, J, Giudicessi, J R, Clur, S-A B, Blom, N A, Tanck, M, Extramiana, F, Kato, K, Barc, J, Borggrefe, M, Behr, E R, Sarquella-Brugada, G, Tfelt-Hansen, J, Zorio, E, Swan, H, Kammeraad, J A E, Krahn, A D, Davis, A, Sacher, F, Schwartz, P J, Roberts, J D, Skinner, J R, van den Berg, M P, Kannankeril, P J, Drago, F, Robyns, T, Haugaa, K, Tavacova, T, Semsarian, C, Till, J, Probst, V, Brugada, R, Shimizu, W, Horie, M, Leenhardt, A, Ackerman, M J, Sanatani, S, van der Werf, C & Wilde, A A M 2022, ' An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia ', Circulation, vol. 145, no. 5, pp. 333-344 . https://doi.org/10.1161/CIRCULATIONAHA.121.056018
Circulation, 145(5), 333-344. LIPPINCOTT WILLIAMS & WILKINS
Circulation
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Circulation, 145(5), 333-344. Lippincott Williams and Wilkins
Peltenburg, P J, Kallas, D, Bos, J M, Lieve, K V V, Franciosi, S, Roston, T M, Denjoy, I, Sorensen, K B, Ohno, S, Roses-Noguer, F, Aiba, T, Maltret, A, Lapage, M J, Atallah, J, Giudicessi, J R, Clur, S-A B, Blom, N A, Tanck, M, Extramiana, F, Kato, K, Barc, J, Borggrefe, M, Behr, E R, Sarquella-Brugada, G, Tfelt-Hansen, J, Zorio, E, Swan, H, Kammeraad, J A E, Krahn, A D, Davis, A, Sacher, F, Schwartz, P J, Roberts, J D, Skinner, J R, van den Berg, M P, Kannankeril, P J, Drago, F, Robyns, T, Haugaa, K, Tavacova, T, Semsarian, C, Till, J, Probst, V, Brugada, R, Shimizu, W, Horie, M, Leenhardt, A, Ackerman, M J, Sanatani, S, van der Werf, C & Wilde, A A M 2022, ' An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia ', Circulation, vol. 145, no. 5, pp. 333-344 . https://doi.org/10.1161/CIRCULATIONAHA.121.056018
Circulation, 145(5), 333-344. LIPPINCOTT WILLIAMS & WILKINS
Circulation
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Background: Symptomatic children with catecholaminergic polymorphic ventricular tachycardia (CPVT) are at risk for recurrent arrhythmic events. β-Blockers decrease this risk, but studies comparing individual β-blockers in sizeable cohorts are lacki
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9763d1251c233799ab62ab359429a22b
https://openaccess.sgul.ac.uk/id/eprint/113944/1/CIRCULATIONAHA.121.056018.pdf
https://openaccess.sgul.ac.uk/id/eprint/113944/1/CIRCULATIONAHA.121.056018.pdf
Autor:
Charlotte Glinge, Sára Rossetti, Louise Bruun Oestergaard, Niels Kjær Stampe, Thomas Hadberg Lynge, Regitze Skals, Bo Gregers Winkel, Elisabeth M. Lodder, Connie R. Bezzina, Gunnar Gislason, Jytte Banner, Elijah R. Behr, Christian Torp-Pedersen, Reza Jabbari, Jacob Tfelt-Hansen
Publikováno v:
Glinge, C, Rossetti, S, Oestergaard, L B, Stampe, N K, Lynge, T H, Skals, R, Winkel, B G, Lodder, E M, Bezzina, C R, Gislason, G, Banner, J, Behr, E R, Torp-Pedersen, C, Jabbari, R & Tfelt-Hansen, J 2023, ' Risk of Sudden Infant Death Syndrome among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark ', JAMA network open, vol. 6, no. 1, E2252724 . https://doi.org/10.1001/jamanetworkopen.2022.52724
Glinge, C, Rossetti, S, Oestergaard, L B, Stampe, N K, Lynge, T H, Skals, R, Winkel, B G, Lodder, E M, Bezzina, C R, Gislason, G, Banner, J, Behr, E R, Torp-Pedersen, C, Jabbari, R & Tfelt-Hansen, J 2023, ' Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark ', JAMA Network Open, vol. 6, no. 1, e2252724, pp. E2252724 . https://doi.org/10.1001/jamanetworkopen.2022.52724
JAMA network open, 6(1). American Medical Association
Glinge, C, Rossetti, S, Oestergaard, L B, Stampe, N K, Lynge, T H, Skals, R, Winkel, B G, Lodder, E M, Bezzina, C R, Gislason, G, Banner, J, Behr, E R, Torp-Pedersen, C, Jabbari, R & Tfelt-Hansen, J 2023, ' Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark ', JAMA Network Open, vol. 6, no. 1, e2252724, pp. E2252724 . https://doi.org/10.1001/jamanetworkopen.2022.52724
JAMA network open, 6(1). American Medical Association
ImportanceSudden infant death syndrome (SIDS) remains a leading cause of death during the first year of life. The etiology of SIDS is complex and remains largely unknown.ObjectiveTo evaluate whether siblings of children who died of SIDS have a higher
Autor:
Bernard Belhassen, Vincent Probst, Ruben Casado-Arroyo, Jean-Sylvain Hermida, Guy Zahavi, Laurens P Bosman, Anne Rollin, Giulio Conte, Esther Zorio, Rob W Roudijk, Carla Giustetto, Josef Kautzner, Firat Duru, Xavier Waintraub, Gabriele Paglino, J. Peter van Tintelen, Elijah R. Behr, Jacob Tfelt-Hansen, Philippe Maury, Francisco Bermúdez-Jiménez, Sandro Ninni, Stepan Havranek, Estelle Gandjbakhch, Alessio Gasperetti, Simone Sala, Josep Brugada, Dominique Lacroix, Chris Miles, Frederic Sacher, Laurent Fauchier, Paolo Della Bella, Christian de Chillou, Anneline S.J.M. te Riele, Elena Arbelo, Petr Peichl, Srijita Sen-Chowdhry, Alexandros Protonotarios, Mikael Laredo, Giovanni Peretto, Anat Milman, Richard N.W. Hauer, Leonardo Calò, Guillaume Duthoit, Antoine Andorin, Jean-Marc Sellal, Eyal Nof, Nicolas Badenco, Konstantinos P. Letsas, Roy Beinart, Bertrand Pierre
Publikováno v:
Europace
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
EUROPACE
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
EUROPACE
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
Aims In arrhythmogenic cardiomyopathy (ACM), sustained ventricular tachycardia (VT) typically displays a left bundle branch block (LBBB) morphology while a right bundle branch block (RBBB) morphology is rare. The present study assesses the VT morphol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a568005e23b57a5e7f4c3acf8ccdc8d
https://hdl.handle.net/10668/19774
https://hdl.handle.net/10668/19774
Autor:
Keerthi Jaliparthy, Aiswarya Rajendran, R. Ross Reichard, Erik K. St. Louis, Mariha Khan, Michael J. Ackerman, Ahmed U. Fayyaz, Aradhana Sahoo, Elson L. So, David J. Tester, Virend K. Somers, William D. Edwards, Elijah R. Behr, Jennifer A. Knight, Michael A. Simpson, Nadeem Khan, C. Anwar A. Chahal, Dongmei Lu
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 23 (2021)
Background Sudden cardiac arrest is the leading mode of death in the United States. Epilepsy affects 1% of Americans; yet epidemiological data show a prevalence of 4% in cases of sudden cardiac arrest. Sudden unexpected death in epilepsy (SUDEP) may
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfda18e6378a499946f6129983441d1f
https://openaccess.sgul.ac.uk/id/eprint/113892/1/JAHA.121.021170.pdf
https://openaccess.sgul.ac.uk/id/eprint/113892/1/JAHA.121.021170.pdf
Autor:
Michael Papadakis, Joe Westaby, Elijah R. Behr, Mary N. Sheppard, Aneil Malhotra, Gherardo Finocchiaro, Sanjay Sharma, Raghav Bhatia
Publikováno v:
Circulation. 144(22)
Autor:
Adam A. Witney, Tessa Homfray, Maite Tome, Elijah R. Behr, Nicholas Bunce, Belinda Gray, Michael Papadakis, Chris Miles, Paulo Bulleros, James S. Ware, Harshil Dhutia, Aneil Malhotra, Rajan Sharma, Bode Ensam, Zeph Fanton, Lisa J. Anderson, Stathis Papatheodorou, Mary N. Sheppard, Sanjay Sharma, Gherardo Finocchiaro
Publikováno v:
Europace
Aims Idiopathic left ventricular hypertrophy (LVH) is defined as LVH in the absence of myocyte disarray or secondary causes. It is unclear whether idiopathic LVH represents the phenotypic spectrum of hypertrophic cardiomyopathy (HCM) or whether it is
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:
Angeliki Asimaki, Joseph Westaby, David C Johnson, Maite Tome, Hamish MacLachlan, Elijah R. Behr, Gherardo Finocchiaro, Mary N. Sheppard, Joyee Basu, Carlos Bueno-Beti, Irina Chis Ster, Bode Ensam, Michael Papadakis, Khari A. Edwards, Sanjay Sharma, Chris Miles, Gemma Parry-Williams, Belinda Gray
BACKGROUND: Electrophysiological, imaging, and pathological studies have reported the presence of subtle structural abnormalities in hearts from patients with Brugada syndrome (BrS). However, data concerning disease involvement outside of the right v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7062080bfc02c761105b40bc2df77234
https://openaccess.sgul.ac.uk/id/eprint/113763/1/j.jacc.2021.08.010.pdf
https://openaccess.sgul.ac.uk/id/eprint/113763/1/j.jacc.2021.08.010.pdf
Autor:
Anat, Milman, Elijah R, Behr, Belinda, Gray, David C, Johnson, Antoine, Andorin, Aviram, Hochstadt, Jean-Baptiste, Gourraud, Shingo, Maeda, Yoshihide, Takahashi, Jimmy, Jm Juang, Sung-Hwan, Kim, Tsukasa, Kamakura, Takeshi, Aiba, Pieter G, Postema, Yuka, Mizusawa, Isabelle, Denjoy, Carla, Giustetto, Giulio, Conte, Zhengrong, Huang, Georgia, Sarquella-Brugada, Andrea, Mazzanti, Camilla H, Jespersen, Elena, Arbelo, Ramon, Brugada, Leonardo, Calo, Domenico, Corrado, Ruben, Casado-Arroyo, Giuseppe, Allocca, Masahiko, Takagi, Pietro, Delise, Josep, Brugada, Jacob, Tfelt-Hansen, Silvia G, Priori, Christian, Veltmann, Gan-Xin, Yan, Pedro, Brugada, Fiorenzo, Gaita, Antoine, Leenhardt, Arthur A M, Wilde, Kengo F, Kusano, Gi-Byoung, Nam, Kenzo, Hirao, Vincent, Probst, Bernard, Belhassen
Publikováno v:
Circulation. Genomic and precision medicine. 14(5)
Brugada syndrome (BrS) is associated with mutations in the cardiac sodium channel gene,Survey on Arrhythmic Events in Brugada Syndrome is a survey of 10 Western and 4 Asian countries, gathering 678 patients with BrS with first arrhythmic event. Only