Channelopathies - Emerging Trends in The Management of Inherited Arrhythmias

Autor: Priya Chockalingam, MBBS, MRCPCH, PhD, Yuka Mizusawa, MD, Arthur A.M. Wilde, MD, PhD

Publikováno v: Indian Pacing and Electrophysiology Journal, Vol 15, Iss 1, Pp 43-54 (2015)

In spite of their relative rarity, inheritable arrhythmias have come to the forefront as a group of potentially fatal but preventable cause of sudden cardiac death in children and (young) adults. Comprehensive management of inherited arrhythmias incl

Externí odkaz: https://doaj.org/article/77b1a46ef7f8442ebb5199e48275903f

Effect of Cigarette Smoking on the Risk of Atrial Fibrillation Recurrence after Pulmonary Vein Isolation

Autor: Seiji Fukamizu, MD, Harumizu Sakurada, MD, Makoto Takano, MD, Rintarou Hojo, MD, Mori Nakai, MD, Takao Yuba, MD, Kota Komiyama, MD, Akiko Tatsumoto, MD, Kenichi Maeno, MD, Yuka Mizusawa, MD, Yasuhiro Tanabe, MD, Makoto Suzuki, MD, Tamotsu Tejima, MD, Mitsuhiro Nishizaki, MD, Youichi Kobayashi, MD, Masayasu Hiraoka, MD

Publikováno v: Journal of Arrhythmia, Vol 26, Iss 1, Pp 21-29 (2010)

Introduction: Previous studies have shown that atrial fibrillation (AF) recurrence after pulmonary vein (PV) isolation depends on various factors; however, the effect of cigarette smoking on AF recurrence after PV isolation has not been investigated.

Externí odkaz: https://doaj.org/article/d6161a40e4554e84b92004dba0529df9

Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events: Insights From the SABRUS in 392 Probands

Autor: Giulio Conte, Kengo Kusano, David C Johnson, P. Delise, Shingo Maeda, Domenico Corrado, Belinda Gray, Leonardo Calò, Gi-Byoung Nam, Ruben Casado-Arroyo, Georgia Sarquella-Brugada, Aviram Hochstadt, Jean-Baptiste Gourraud, Christian Veltmann, Jacob Tfelt-Hansen, Silvia G Priori, Camilla H Jespersen, Ramon Brugada, Kenzo Hirao, Anat Milman, Carla Giustetto, Yuka Mizusawa, Jimmy Jm Juang, Giuseppe Allocca, Vincent Probst, Antoine Leenhardt, Pieter G. Postema, Bernard Belhassen, Andrea Mazzanti, Pedro Brugada, Elijah R. Behr, Elena Arbelo, Josep Brugada, T Kamakura, Antoine Andorin, Masahiko Takagi, Isabelle Denjoy, Yoshihide Takahashi, Fiorenzo Gaita, Zhengrong Huang, Arthur A.M. Wilde, Sung Hwan Kim, Takeshi Aiba, Gan-Xin Yan

Publikováno v: Circulation. Genomic and precision medicine, 14(5). Lippincott Williams and Wilkins Ltd.
Milman, A, Behr, E R, Gray, B, Johnson, D C, Andorin, A, Hochstadt, A, Gourraud, J-B, Maeda, S, Takahashi, Y, Jm Juang, J, Kim, S-H, Kamakura, T, Aiba, T, Postema, P G, Mizusawa, Y, Denjoy, I, Giustetto, C, Conte, G, Huang, Z, Sarquella-Brugada, G, Mazzanti, A, Jespersen, C H, Arbelo, E, Brugada, R, Calo, L, Corrado, D, Casado-Arroyo, R, Allocca, G, Takagi, M, Delise, P, Brugada, J, Tfelt-Hansen, J, Priori, S G, Veltmann, C, Yan, G-X, Brugada, P, Gaita, F, Leenhardt, A, Wilde, A A M, Kusano, K F, Nam, G-B, Hirao, K, Probst, V & Belhassen, B 2021, ' Genotype-Phenotype Correlation of SCN5A Genotype in Patients With Brugada Syndrome and Arrhythmic Events : Insights From the SABRUS in 392 Probands ', Circulation. Genomic and precision medicine, vol. 14, no. 5, e003222 . https://doi.org/10.1161/CIRCGEN.120.003222
Circulation-Genomic and Precision Medicine
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname

Background: Brugada syndrome (BrS) is associated with mutations in the cardiac sodium channel gene, SCN5A. However, genetic studies of patients with BrS with arrhythmic events have been limited. We sought to compare various clinical, ECG, and electro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4996f0a0777debaf7d4e6c5402d63c04
https://pure.amc.nl/en/publications/genotypephenotype-correlation-of-scn5a-genotype-in-patients-with-brugada-syndrome-and-arrhythmic-events(30208168-1225-4d88-9df0-8b320cc73dcd).html

Time-to-first appropriate shock in patients implanted prophylactically with an implantable cardioverter-defibrillator: data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS)

Autor: Antoine Leenhardt, Pietro Delise, Domenico Corrado, Yuka Mizusawa, Shingo Maeda, Carlo Napolitano, Eran Leshem, Christian Veltmann, Anat Milman, Ramon Brugada, Carla Giustetto, Yoav Michowitz, Silvia G. Priori, Elena Arbelo, Jimmy J.M. Juang, Tsukasa Kamakura, Arthur A.M. Wilde, Leonardo Calò, Fiorenzo Gaita, Josep Brugada, Gan-Xin Yan, Elijah R. Behr, Yanushi D. Wijeyeratne, Antoine Andorin, Zhengrong Huang, Kenzo Hirao, Yoshihide Takahashi, Isabelle Denjoy, Michael Rahkovich, Pedro Brugada, Masahiko Takagi, Jean Champagne, Philippe Mabo, Frédéric Sacher, Camilla H Jespersen, Sung Hwan Kim, Bernard Belhassen, Gi-Byoung Nam, Pieter G Postema, Aviram Hochstadt, Vincent Probst, Takeshi Aiba, Giulio Conte, Kengo Kusano, Jacob Tfelt-Hansen, Jean-Baptiste Gourraud

Publikováno v: Milman, A, Hochstadt, A, Andorin, A, Gourraud, J-B, Sacher, F, Mabo, P, Kim, S-H, Conte, G, Arbelo, E, Kamakura, T, Aiba, T, Napolitano, C, Giustetto, C, Denjoy, I, Juang, J J M, Maeda, S, Takahashi, Y, Leshem, E, Michowitz, Y, Rahkovich, M, Jespersen, C H, Wijeyeratne, Y D, Champagne, J, Calo, L, Huang, Z, Mizusawa, Y, Postema, P G, Brugada, R, Wilde, A A M, Yan, G-X, Behr, E R, Tfelt-Hansen, J, Hirao, K, Veltmann, C, Leenhardt, A, Corrado, D, Gaita, F, Priori, S G, Kusano, K F, Takagi, M, Delise, P, Brugada, J, Brugada, P, Nam, G-B, Probst, V & Belhassen, B 2019, ' Time-to-first appropriate shock in patients implanted prophylactically with an implantable cardioverter-defibrillator : data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS) ', Europace, vol. 21, no. 5, pp. 796–802 . https://doi.org/10.1093/europace/euy301
EP Europace, 21(5), 796-802. Oxford University Press

Aims: Data on predictors of time-to-first appropriate implantable cardioverter-defibrillator (ICD) therapy in patients with Brugada Syndrome (BrS) and prophylactically implanted ICD's are scarce.Methods and results: SABRUS (Survey on Arrhythmic Event

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0106949e3073dae2afa1eea6b019e1a
https://doi.org/10.1093/europace/euy301

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

Autor: Yvonne M. Hoedemaekers, M. Ben Shoemaker, Pascale Guicheney, Antoine Leenhardt, Andrea Mazzanti, Minoru Horie, Jan H. Veldink, Isabelle Denjoy, Yu Kucho, Chiea Chuen Khor, Tomas Robyns, Carlo Napolitano, Peter Weeke, J. Martijn Bos, David J. Tester, Hanno L. Tan, Annika Rydberg, Patrick T. Ellinor, Pilar Galan, Taisuke Ishikawa, Seiko Ohno, Peter J. Schwartz, Masao Yoshinaga, Thomas Werge, Marta Ribasés, Bart Loeys, Jean-Jacques Schott, Jacob Tfelt-Hansen, Ulla-Britt Diamant, Marko Ernsting, Georgia Sarquella-Brugada, Yuka Mizusawa, Michael Christiansen, Pyotr G. Platonov, Annika Winbo, Thomas Meitinger, Keiko Shimamoto, Cristina Barlassina, Pieter G. Postema, Takeru Makiyama, Maarten P. van den Berg, Yanushi D. Wijeyeratne, Wataru Shimizu, Charles Antzelevitch, Christopher Newton-Cheh, Martina Müller-Nurasyid, Dan M. Roden, Vincent Probst, Takeshi Aiba, Lia Crotti, Daniele Cusi, Britt M. Beckmann, Johan Saenen, Peter Lichtner, Oscar Campuzano, Tin Aung, Nynke Hofman, Morten S. Olesen, Matteo Pedrazzini, Elijah R. Behr, Karen E. Morrison, Najim Lahrouchi, Katja E. Odening, Andrew D. Krahn, Kari L. Turkowski, J. Peter van Tintelen, Steven A. Lubitz, Federica Dagradi, Josep Brugada, Julien Barc, Birgit Stallmeyer, Stefan Kääb, Sven Zumhagen, Jonathan R. Skinner, Michael W.T. Tanck, Christopher Shaw, Brianna Davies, Eric Schulze-Bahr, Mineo Ozaki, Roddy Walsh, Antoine Andorin, Leonard H. van den Berg, Silvia G. Priori, Johannes Steinfurt, Jean-Baptiste Gourraud, Eline A. Nannenberg, Mark Lathrop, Rafik Tadros, Ramon Brugada, Leander Beekman, Peter M. Andersen, Ryan Pfeiffer, Boris Rudic, Reza Jabbari, Kanae Hasegawa, Jeroen Breckpot, Naomasa Makita, Michael J. Ackerman, Arthur A.M. Wilde, Hideki Itoh, Martin Borggrefe, Elena Arbelo, Connie R. Bezzina, Pamela J. Shaw, Ammar Al-Chalabi, Markus Munter

Publikováno v: Circulation, 142(4), 324-338. Lippincott Williams and Wilkins
Circulation
Circulation, American Heart Association, 2020, 142 (4), pp.324-338. ⟨10.1161/CIRCULATIONAHA.120.045956⟩
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Circulation, 142, 4, pp. 324-38
Lahrouchi, N, Tadros, R, Crotti, L, Mizusawa, Y, Postema, P G, Beekman, L, Walsh, R, Hasegawa, K, Barc, J, Ernsting, M, Turkowski, K L, Mazzanti, A, Beckmann, B M, Shimamoto, K, Diamant, U-B, Wijeyeratne, Y D, Kucho, Y, Robyns, T, Ishikawa, T, Arbelo, E, Christiansen, M, Winbo, A, Jabbari, R, Lubitz, S A, Steinfurt, J, Rudic, B, Loeys, B, Shoemaker, M B, Weeke, P E, Pfeiffer, R, Davies, B, Andorin, A, Hofman, N, Dagradi, F, Pedrazzini, M, Tester, D J, Bos, J M, Sarquella-Brugada, G, Campuzano, Ó, Platonov, P G, Stallmeyer, B, Zumhagen, S, Nannenberg, E A, Veldink, J H, van den Berg, L H, Al-Chalabi, A, Shaw, C E, Shaw, P J, Morrison, K E, Andersen, P M, Müller-Nurasyid, M, Cusi, D, Barlassina, C, Galan, P, Lathrop, M, Munter, M, Werge, T, Ribasés, M, Aung, T, Khor, C C, Ozaki, M, Lichtner, P, Meitinger, T, van Tintelen, J P, Hoedemaekers, Y, Denjoy, I, Leenhardt, A, Napolitano, C, Shimizu, W, Schott, J-J, Gourraud, J-B, Makiyama, T, Ohno, S, Itoh, H, Krahn, A D, Antzelevitch, C, Roden, D M, Saenen, J, Borggrefe, M, Odening, K E, Ellinor, P T, Tfelt-Hansen, J, Skinner, J R, van den Berg, M P, Olesen, M S, Brugada, J, Brugada, R, Makita, N, Breckpot, J, Yoshinaga, M, Behr, E R, Rydberg, A, Aiba, T, Kääb, S, Priori, S G, Guicheney, P, Tan, H L, Newton-Cheh, C, Ackerman, M J, Schwartz, P J, Schulze-Bahr, E, Probst, V, Horie, M, Wilde, A A, Tanck, M W T & Bezzina, C R 2020, ' Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome ', Circulation, vol. 142, no. 4, pp. 324-338 . https://doi.org/10.1161/CIRCULATIONAHA.120.045956
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Circulation 142, 324-338 (2020)
Circulation, 142(4), 324-338. LIPPINCOTT WILLIAMS & WILKINS
Lahrouchi, 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; ... (2020). Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. Circulation, 142(4), pp. 324-338. American Heart Association 10.1161/CIRCULATIONAHA.120.045956
Circulation, 142, 324-38

Background: Long QT syndrome (LQTS) is a rare genetic disorder and a major preventable cause of sudden cardiac death in the young. A causal rare genetic variant with large effect size is identified in up to 80% of probands (genotype positive) and cas

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a06b61364655bada7ed23840f1c05d61
https://pure.amc.nl/en/publications/transethnic-genomewide-association-study-provides-insights-in-the-genetic-architecture-and-heritability-of-long-qt-syndrome(4064416e-020f-4f3a-baab-fe41d1af246c).html