Results 11 to 20 of about 2,471,143 (310)

Brugada Syndrome.

JACC: Clinical Electrophysiology, 2022
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 sex ...
A. D. Krahn, Elijah R Behr, R. Hamilton, Vincent Probst, Zachary Laksman, Hui-Chen Han   +5 more
semanticscholar   +3 more sources

The Genetics of Brugada Syndrome.

Annual Review of Genomics and Human Genetics, 2022
Brugada syndrome is a heritable channelopathy characterized by a peculiar electrocardiogram (ECG) pattern and increased risk of cardiac arrhythmias and sudden death.
M. Cerrone, S. Costa, M. Delmar
semanticscholar   +3 more sources

Brugada syndrome and p.E61X_RANGRF

Cardiology Journal, 2014
Background: Brugada syndrome is an inherited cardiac condition transmitted with an autosomal dominant pattern which can lead to sudden cardiac death from malignant ventricular arrhythmias.
Iglesias, Anna, Berne, Paola, Brugada, Ramon, Campuzano Larrea, Oscar, Brugada Terradellas, Josep, Selga Coma, Elisabet, Allegue Toscano, Catarina   +6 more
core   +5 more sources

Genome-wide association analyses identify novel Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

Nature Genetics, 2022
Brugada syndrome (BrS) is a cardiac arrhythmia disorder associated with sudden death in young adults. With the exception of SCN5A, encoding the cardiac sodium channel NaV1.5, susceptibility genes remain largely unknown.
J. Barc, R. Tadros, C. Glinge, David Y. Chiang, Mariam Jouni, F. Simonet, S. Jurgens, M. Baudic, Michele Nicastro, F. Potet, J. Offerhaus, R. Walsh, S. Choi, A. Verkerk, Y. Mizusawa, S. Anys, Damien Minois, M. Arnaud, J. Duchâteau, Y. Wijeyeratne, A. Muir, M. Papadakis, S. Castelletti, M. Torchio, Cristina Gil Ortuño, J. Lacunza, D. Giachino, N. Cerrato, R. Martins, Ó. Campuzano, S. Van Dooren, A. Thollet, F. Kyndt, A. Mazzanti, N. Clementy, A. Bisson, A. Corveleyn, B. Stallmeyer, S. Dittmann, J. Saenen, Antoine Noël, Shohreh Honarbakhsh, B. Rudic, H. Marzak, M. Rowe, C. Federspiel, S. Le Page, L. Placide, A. Milhem, H. Barajas-Martinez, B. Beckmann, I. Krapels, J. Steinfurt, B. Winkel, R. Jabbari, M. Shoemaker, B. Boukens, Doris Škorić-Milosavljević, H. Bikker, Federico Manevy, P. Lichtner, M. Ribasés, T. Meitinger, M. Müller-Nurasyid, Konstantin Annette Holger Lars Reiner Margit Strauch Peters Schulz Schwettmann Leidl Heier, K. Strauch, Annette Peters, H. Schulz, L. Schwettmann, R. Leidl, M. Heier, J. Veldink, L. H. van den Berg, P. van Damme, D. Cusi, C. Lanzani, S. Rigade, Eric Charpentier, E. Baron, S. Bonnaud, S. Lecointe, Audrey Donnart, H. Le Marec, S. Chatel, Matilde Karakachoff, S. Bézieau, B. London, J. Tfelt‐Hansen, D. Roden, K. Odening, M. Cerrone, L. Chinitz, P. Volders, Maarten P. van de Berg, G. Laurent, L. Faivre, C. Antzelevitch, S. Kääb, A. A. Arnaout, J. Dupuis, J. Pasquié, O. Billon, Jason D. Roberts, L. Jesel, M. Borggrefe, P. Lambiase, J. Mansourati, B. Loeys, A. Leenhardt, P. Guicheney, P. Maury, E. Schulze-Bahr, T. Robyns, J. Breckpot, D. Babuty, S. Priori, C. Napolitano, Pascal Frédéric Jean Philippe François Defaye Anselme Darmon Wiart, P. Defaye, F. Anselme, J. Darmon, F. Wiart, C. de Asmundis, P. Brugada, R. Brugada, E. Arbelo, J. Brugada, P. Mabo, N. Béhar, C. Giustetto, M. S. Molina, J. Gimeno, C. Hasdemir, P. Schwartz, L. Crotti, P. McKeown, Sanjay Sharma, E. Behr, M. Haissaguerre, F. Sacher, C. Rooryck, H. Tan, C. Remme, P. Postema, M. Delmar, P. Ellinor, S. Lubitz, J. Gourraud, M. Tanck, Alfred L. George, C. Macrae, P. Burridge, C. Dina, V. Probst, A. Wilde, J. Schott, R. Redon, C. Bezzina   +157 more
semanticscholar   +1 more source

Suspected hyponatremia-induced Brugada phenocopy

International Medical Case Reports Journal, 2019
Koomatie Ramsaroop,1 Rajeev Seecheran,1 Valmiki Seecheran,1 Sangeeta Persad,1 Stanley Giddings,2 Boris Mohammed,1 Naveen Anand Seecheran2 1Department of Medicine, North Central Regional Health Authority, Mt Hope, Trinidad and Tobago; 2Department of ...
Ramsaroop K, Seecheran R, Seecheran V, Persad S, Giddings S, Mohammed B, Seecheran NA   +6 more
doaj   +1 more source

Brugada syndrome and reduced right ventricular outflow tract conduction reserve: a final common pathway?

European Heart Journal, 2021
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.
E. Behr, Y. Ben-Haim, M. Ackerman, A. Krahn, A. Wilde   +4 more
semanticscholar   +1 more source

Clinical presentation and electrocardiographic features of Brugada syndrome in Iraq [PDF]

The Medical Journal of Basrah University, 2021
Background: Brugada syndrome is a clinical entity composed of twelve leads electrocardiographic changes of coved or saddle shaped ST-segment elevation in V1 and V2 with serious ventricular arrhythmias which may cause sudden cardiac death. Objectives: The
AMAR AL-HAMDI
doaj   +1 more source

Brugada Syndrome as a Major Cause of Sudden Cardiac Death in Asians

JACC: Asia, 2022
Brugada syndrome (BrS) is one of the main inherited arrhythmia syndromes causing ventricular fibrillation (VF) and sudden cardiac death in young to middle-aged men, especially in Asians.
Yukiko Nakano, W. Shimizu
semanticscholar   +1 more source

Brugada pattern in adolescent with acute myocarditis due to SARS‐CoV‐2

Journal of the American College of Emergency Physicians Open, 2022
Brugada syndrome is a genetic disorder characterized by abnormal findings on electrocardiogram (ECG) that can precipitate ventricular tachyarrhythmias and sudden cardiac death.
David Bergamo, Courtney Nelson
doaj   +1 more source

Biventricular Myocardial Fibrosis and Sudden Death in Patients With Brugada Syndrome

Journal of the American College of Cardiology, 2021
Background Electrophysiological, imaging, and pathological studies have reported the presence of subtle structural abnormalities in hearts from patients with Brugada syndrome (BrS).
C. Miles, A. Asimaki, I. Ster, M. Papadakis, B. Gray, J. Westaby, G. Finocchiaro, C. Bueno-Betí, Bode Ensam, J. Basu, G. Parry-Williams, H. MacLachlan, Khari A. Edwards, David H. Johnson, M. Tome, Sanjay Sharma, M. Sheppard, E. Behr   +17 more
semanticscholar   +1 more source