Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Elijah R. Behr"'
Publikováno v:
European heart journal. 42(11):1073-1081
Brugada syndrome (BrS) was first described as a primary electrical disorder predisposing to the risk of sudden cardiac death and characterized by right precordial lead ST elevation. Early description of right ventricular structural abnormalities and
Autor:
Maite Tome, Michael Papadakis, Navin Chandra, Elijah R. Behr, Harshil Dhutia, Raghav Bhatia, Sabiha Gati, Sameer Parpia, Greg Mellor, Gherardo Finocchiaro, Andrew D'Silva, Sanjay Sharma, Rajay Narain, Aneil Malhotra
Publikováno v:
Europace
Aims There is limited information on the role of screening with electrocardiography (ECG) for identifying cardiovascular diseases associated with sudden cardiac death (SCD) in a non-select group of adolescents and young adults in the general populati
Autor:
Stéphane Boulé, Elijah R. Behr, Giulio Conte, Arthur A.M. Wilde, Daniel Scherr, Michael D Spartalis, Estelle Gandjbachkh, Radosław Lenarczyk, Tatjana S. Potpara
Publikováno v:
EP Europace. 22:1904-1910
The spectrum of inherited arrhythmogenic diseases (IADs) includes disorders without overt structural abnormalities (i.e. primary inherited arrhythmia syndromes) and structural heart diseases (i.e. arrhythmogenic ventricular cardiomyopathy, hypertroph
Autor:
Elijah R. Behr, Katie Frampton, Carol Ann Remme, Eloi Marijon, Chiara Scrocco, Eric Schulze-Bahr, Serge Boveda, Konstantinos Iliodromitis, Giulio Conte, Kristine Jubele, Irina Rudaka, Jacob Tfelt-Hansen, Carlo de Asmundis, Arthur A.M. Wilde, Georgia Sarquella Brugada, Jedrzej Kosiuk, Lia Crotti, Nynke Hofman
Publikováno v:
Europace
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
EP Europace, 24(2), 331-339. Oxford University Press
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
EP Europace, 24(2), 331-339. Oxford University Press
The aims of this centre-based survey, promoted and disseminated by the European Heart Rhythm Association (EHRA) was to investigate the current practice for the investigation of Sudden Unexplained Death in the Young (SUDY) amongst European countries.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6dd782933c394fbc1479f192e91ddab
http://hdl.handle.net/10281/392835
http://hdl.handle.net/10281/392835
Autor:
Abhay Bajpai, Manav Sohal, Riyaz Kaba, Mark M Gallagher, Mark Norman, Magdi Saba, Elijah R. Behr, Anthony Li, Ahmed I Elbatran, Zia Zuberi
Publikováno v:
Journal of Interventional Cardiac Electrophysiology
Purpose The effect of adding contact force (CF) sensing to 56-hole tip irrigation in ventricular arrhythmia (VA) ablation has not been previously studied. We aimed to compare outcomes with and without CF sensing in VA ablation using a 56-hole radiofr
Autor:
Wataru Shimizu, Steven A. Lubitz, Marina Cerrone, Michael J. Cutler, Susan P. Etheridge, Mina K. Chung, Michael J. Ackerman, Arthur A.M. Wilde, Raymond W. Sy, M. Benjamin Shoemaker, Eric Schulze-Bahr, Peter F. Aziz, Lee L. Eckhardt, Peter J. Schwartz, Jason D. Roberts, Wojciech Zareba, Elizabeth S. Kaufman, Andrew D. Krahn, Sami Viskin, Dan M. Roden, Silvia G. Priori, Marco V Perez, Jeffrey A. Towbin, Elijah R. Behr
Publikováno v:
Circ Arrhythm Electrophysiol
While published guidelines are useful in the care of patients with long-QT syndrome, it can be difficult to decide how to apply the guidelines to individual patients, particularly those with intermediate risk. We explored the diversity of opinion amo
Autor:
Georgia Brugada-Sarquella, Tatjana S. Potpara, Lia Crotti, Elijah R. Behr, Arthur A.M. Wilde, Giulio Conte, Estelle Gandjbachkh, Radosław Lenarczyk, Daniel Scherr
Publikováno v:
Circulation: Genomic and Precision Medicine, 14(2):003313, 252-254. Lippincott Williams and Wilkins Ltd.
Circ Genom Precis Med
Circ Genom Precis Med
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc7f88c276f116839de41677b53293e2
https://pure.amc.nl/en/publications/importance-of-dedicated-units-for-the-management-of-patients-with-inherited-arrhythmia-syndromes(9d9f0527-deb5-4dd5-8f82-85f91bcc2bcc).html
https://pure.amc.nl/en/publications/importance-of-dedicated-units-for-the-management-of-patients-with-inherited-arrhythmia-syndromes(9d9f0527-deb5-4dd5-8f82-85f91bcc2bcc).html
Autor:
Abbas Zaidi, Efstathios Papatheodorou, Elena Fabi, Chiara Cappelletto, Joe Brook, Chris Miles, Rajan Sharma, Aneil Malhotra, Virginia Attard, Gianfranco Sinagra, Maite Tome, Elijah R. Behr, Gherardo Finocchiaro, Gerald Carr-White, Tessa Homfray, Sanjay Sharma, Bode Ensam, Michael Papadakis, Harshil Dhutia, Rachel Bastiaenen, Marco Merlo
Publikováno v:
Finocchiaro, G, Papadakis, M, Dhutia, H, Zaidi, A, Malhotra, A, Fabi, E, Cappelletto, C, Brook, J, Papatheodorou, E, Ensam, B, Miles, C J, Bastiaenen, R, Attard, V, Homfray, T, Sharma, R, Tome, M, Carr-White, G, Merlo, M, Behr, E R, Sinagra, G & Sharma, S 2019, ' Electrocardiographic differentiation between 'benign T-wave inversion' and arrhythmogenic right ventricular cardiomyopathy ', Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology, vol. 21, no. 2, pp. 332-338 . https://doi.org/10.1093/europace/euy179
Aims: To characterize the most common electrocardiographic (ECG) abnormalities in patients with arrhythmogenic right ventricular cardiomyopathy (ARVC), including anterior T-wave inversion (TWI) and to compare the characteristics of TWI in patients wi
Autor:
Michael Papadakis, Maite Tome-Esteban, Elijah R. Behr, B. Devine, Chiara Scrocco, Sanjay Sharma, Yael Ben-Haim, Peter W. Macfarlane
Publikováno v:
Heart rhythm. 19(1)
Background Experience with implantable loop recorders (ILRs) in Brugada syndrome (BrS) is limited. Objective The purpose of this study was to evaluate the indications and yield of ILR monitoring in a single-center BrS registry. Methods Demographic, c
Autor:
Charles Antzelevitch, Ahmad S. Amin, Bo Gregers Winkel, Dan M. Roden, Stefan Kääb, Jonathan R. Skinner, Seiko Ohno, Julien Barc, Birgit Stallmeyer, Carla Giustetto, Connie R. Bezzina, Francesco Mazzarotto, Tomas Robyns, Carlo Napolitano, Stellan Mörner, Doris Škorić-Milosavljević, Sven Dittmann, Kenichiro Yamagata, Sonia Van Dooren, Anniek Corveleyn, Carlo de Asmundis, Ramon Brugada, K Usuda, Yuji Tanaka, Sven Zumhagen, Tadashi Nakajima, Johan Saenen, Elijah R. Behr, Hector Barajas-Martinez, Stéphane Bézieau, Masao Yoshinaga, Georgia Sarquella-Brugada, Paul G.A. Volders, Juan R. Gimeno, Lia Crotti, Charlotte Glinge, Andrea Mazzanti, Ingrid P.C. Krapels, Nicola Whiffin, Sebastian Clauss, Yoshiaki Kaneko, James S. Ware, Minoru Horie, Keiko Shimamoto, Isabelle Denjoy, Pieter G. Postema, Christian Krijger, Takeshi Aiba, Masahiko Kurabayashi, Pyotr G. Platonov, Regina Sebastiano, Cristina Gil Ortuño, Annika Rydberg, Roddy Walsh, Michael J. Ackerman, Hideki Itoh, M. Benjamin Shoemaker, Can Hasdemir, Pascale Guicheney, J. Martijn Bos, Frederic Sacher, Takeru Makiyama, Julieta Lazarte, Maarten P. van den Berg, Dominique Babuty, David J. Tester, Silvia Castelletti, Jacques Mansourati, Antoine Leenhardt, Paul A. van der Zwaag, Sanjay Sharma, Elena Arbelo, Candan Celen, Pier D. Lambiase, Maria Christina Kotta, Johannes Steinfurt, Jean-Baptiste Gourraud, Pedro Brugada, Wataru Shimizu, Josep Brugada, Jørgen K. Kanters, Eline A. Nannenberg, Silvia G. Priori, Mary N. Sheppard, Richard Redon, Morten S. Olesen, Jeroen Breckpot, Britt M. Beckmann, Naomasa Makita, Martin Borggrefe, Rafik Tadros, Jean-Jacques Schott, Jacob Tfelt-Hansen, Steven A. Lubitz, Hatice Şahin, Najim Lahrouchi, Michael Papadakis, Daisuke Hazeki, Kenshi Hayashi, Oscar Campuzano, Katja E. Odening, Federica Dagradi, Eric Schulze-Bahr, Boris Rudic, Hiroki Kimoto, Vincent Probst, Jason D. Roberts, Raphaël P. Martins, Bart Loeys, Daniela F. Giachino, F. Kyndt, Kimie Ohkubo, Taisuke Ishikawa, Catarina Lundin, Lut Van Laer, Patrick T. Ellinor, Maria Sabater Molina, Peter J. Schwartz, Annika Winbo
Publikováno v:
Nantes Referral Center for inherited cardiac arrhythmia 2021, ' Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls ', Genetics In Medicine, vol. 23, pp. 47–58 . https://doi.org/10.1038/s41436-020-00946-5
Genetics in Medicine
Genetics in Medicine, Nature Publishing Group, 2020, ⟨10.1038/s41436-020-⟩
Genetics in Medicine, 47-58. Nature Publishing Group
ISSUE=1;STARTPAGE=47;ENDPAGE=58;ISSN=1098-3600;TITLE=Genetics in Medicine
Genetics in medicine
Walsh, Roddy; Lahrouchi, Najim; Tadros, Rafik; Kyndt, Florence; Glinge, Charlotte; Postema, Pieter G; Amin, Ahmad S; Nannenberg, Eline A; Ware, James S; Whiffin, Nicola; Mazzarotto, Francesco; Škorić-Milosavljević, Doris; Krijger, Christian; Arbelo, Elena; Babuty, Dominique; Barajas-Martinez, Hector; Beckmann, Britt M; Bézieau, Stéphane; Bos, J Martijn; Breckpot, Jeroen; ... (2021). Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls. Genetics in medicine, 23(1), pp. 47-58. Springer Nature 10.1038/s41436-020-00946-5
Genetics in medicine, 23(1), 47-58. Lippincott Williams and Wilkins
Genetics in Medicine, 23(1), 47-58. Nature Publishing Group
Genetics in Medicine
Genetics in Medicine, Nature Publishing Group, 2020, ⟨10.1038/s41436-020-⟩
Genetics in Medicine, 47-58. Nature Publishing Group
ISSUE=1;STARTPAGE=47;ENDPAGE=58;ISSN=1098-3600;TITLE=Genetics in Medicine
Genetics in medicine
Walsh, Roddy; Lahrouchi, Najim; Tadros, Rafik; Kyndt, Florence; Glinge, Charlotte; Postema, Pieter G; Amin, Ahmad S; Nannenberg, Eline A; Ware, James S; Whiffin, Nicola; Mazzarotto, Francesco; Škorić-Milosavljević, Doris; Krijger, Christian; Arbelo, Elena; Babuty, Dominique; Barajas-Martinez, Hector; Beckmann, Britt M; Bézieau, Stéphane; Bos, J Martijn; Breckpot, Jeroen; ... (2021). Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls. Genetics in medicine, 23(1), pp. 47-58. Springer Nature 10.1038/s41436-020-00946-5
Genetics in medicine, 23(1), 47-58. Lippincott Williams and Wilkins
Genetics in Medicine, 23(1), 47-58. Nature Publishing Group
Purpose: Stringent variant interpretation guidelines can lead to high rates of variants of uncertain significance (VUS) for genetically heterogeneous disease like long QT syndrome (LQTS) and Brugada syndrome (BrS). Quantitative and disease-specific c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::193437f5ba4e2e30da09bd570e67f778
http://hdl.handle.net/10044/1/82315
http://hdl.handle.net/10044/1/82315