Results 111 to 120 of about 25,737 (250)

Abnormal electrocardiogram changes in body surface limb leads: A sign of poor prognosis for brugada syndrome?

Cardiology Plus, 2017
Background: Simple and effective methods to identify Brugada syndrome patients at high risk have yet to be identified. We aim to explore the methods for evaluation and prediction of Brugada syndrome in patients at high risk of sudden cardiac death ...
Yong-Ming He, Xin Zhao, Xiang-Jun Yang
doaj   +1 more source

Quinidine for Brugada syndrome: Panacea or poison? [PDF]

, 2016
published_or_final_versio
Chan, PHM, Hai, SHJJ, Siu, DCW, Tse, HF, Wong, CK, Yung, TC   +5 more
core   +1 more source

The study on the modifying role of mitochondrial DNA polymorphism in the Brugada syndrome manifestation

Alʹmanah Kliničeskoj Mediciny, 2019
Background: Brugada syndrome is a hereditary disease with genetic and phenotypic variability characterized by a high risk for arrhythmia and sudden cardiac death.
M. V. Golubenko, V. S. Mikhaylov, E. V. Zaklyazminskaya   +2 more
doaj   +1 more source

May Fever Trigger Ventricular Fibrillation? [PDF]

, 2005
The clinical precipitants of ventricular fibrillation (VF) remain poorly understood. Clinical factors such as hypoxemia, acidosis or electrolyte imbalance, drug-related toxicity, autonomic nervous system disorders as well as viral myocarditis have been ...
Pasquié, Jean Luc
core   +1 more source

Age of First Arrhythmic Event in Brugada Syndrome: Data From the SABRUS (Survey on Arrhythmic Events in Brugada Syndrome) in 678 Patients. [PDF]

, 2017
BACKGROUND: Data on the age at first arrhythmic event (AE) in Brugada syndrome are from limited patient cohorts. The aim of this study is 2-fold: (1) to define the age at first AE in a large cohort of patients with Brugada syndrome, and (2) to assess the
Aiba, T, Andorin, A, Arbelo, E, Behr, ER, Belhassen, B, Brugada, J, Brugada, P, Brugada, R, Calo, L, Casado-Arroyo, R, Champagne, J, Conte, G, Corrado, D, Delise, P, Denjoy, I, Gaita, F, Giustetto, C, Gourraud, J-B, Hirao, K, Hochstadt, A, Huang, Z, Juang, JJM, Kamakura, T, Kim, S-H, Kusano, KF, Leenhardt, A, Leshem, E, Mabo, P, Maeda, S, Michowitz, Y, Milman, A, Mizusawa, Y, Nam, G-B, Napolitano, C, Postema, PG, Priori, SG, Probst, V, Rahkovich, M, Sacher, F, Sarquella-Brugada, G, Takagi, M, Takahashi, Y, Tfelt-Hansen, J, Veltmann, C, Wijeyeratne, YD, Wilde, AAM, Yan, G-X   +46 more
core   +2 more sources

Diagnosis Sindrom Brugada

Majalah Kardiologi Indonesia, 2015
Brugada syndrome is an inherited autosomal dominant disease that cause sudden death, which related with mutation of SCN5A gene, ? subunit of sodium channel. The risk Brugada syndrome in male is 8 times more than females.
Edward Faisal
doaj   +1 more source

Malignant ventricular arrhythmias induction by programmed electrical stimulation of the right ventricular outflow tract only during type 1 brugada ECG maximization [PDF]

, 2016
OBJECTIVE: The role of electrophysiology study in Brugada syndrome (BS) sudden cardiac death risk stratification remains controversial and seems to depend on the phenotypic expression of the channelopathy.
ALESSANDRI, Nicola, DE ANGELIS, STEFANO, DEI GIUDICI, ANGELA, NGUYEN, BICH LIEN, SERGIACOMI, ROBERTA, TERSIGNI, FLAVIA, TUFANO, Fabrizio, URCIUOLI, FEDERICA   +7 more
core  

SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome. [PDF]

, 2009
International audienceBACKGROUND: Mutations in SCN5A are identified in approximately 20% to 30% of probands affected by Brugada syndrome (BrS). However, in familial studies, the relationship between SCN5A mutations and BrS remains poorly understood.
Albuisson, Juliette, Babuty, Dominique, Barc, Julien, Gouas, Laetitia, Guicheney, Pascale, Kyndt, Florence, Le Caignec, Cedric, Le Marec, Hervé, Le Scouarnec, Solena, Mabo, Philippe, Mansourati, Jacques, Meregalli, Paola G, Probst, Vincent, Sacher, Frederic, Schott, Jean-Jacques, Tan, Hanno L, Wilde, Arthur A M   +16 more
core   +3 more sources

Ventricular Tachycardia in the Absence of Structural Heart Disease [PDF]

, 2005
In up to 10% of patients who present with ventricular tachycardia (VT), obvious structural heart disease is not identified. In such patients, causes of ventricular arrhythmia include right ventricular outflow tract (RVOT) VT, extrasystoles, idiopathic ...
Appleton, Christopher P, Lester, Steven J, Munger, Thomas M, Scott, Luis R P, Srivathsan, Komandoor   +4 more
core   +1 more source

Detailed Association Between Electrocardiogram Abnormality and Primary Myocardial Fibrosis

Clinical Cardiology, Volume 48, Issue 12, December 2025.
Yu Nomoto, Naoya Kataoka, Teruhiko Imamura   +2 more
wiley   +1 more source