Results 111 to 120 of about 2,212,387 (300)

Matrine Inhibits the Wnt3a/β‐Catenin Signalling to Attenuate Pressure Overload‐Induced Atrial Remodelling and Vulnerability to Atrial Fibrillation

Journal of Cellular and Molecular Medicine, Volume 29, Issue 10, May 2025.
ABSTRACT Atrial fibrillation (AF) is closely associated with atrial electrical and structural remodelling, yet effective drug strategies remain limited. Matrine (MAT), the active compound in Sophora flavescens, has shown anti‐AF effects, but its mechanisms are unclear.
Guoxin Zhang, Xue Dong, Boxuan Sun, Zijun Zhou, Yinli Xu, Yuting Huang, Shan Meng, Zijun Cao, Nana Qin, Yan Zhu, Liming Yu, Huishan Wang   +11 more
wiley   +1 more source

Safety, Efficacy and Evidence Base for Use of the Subcutaneous Implantable Cardioverter Defibrillator [PDF]

, 2018
The trans-venous implantable cardioverter defibrillator (TV-ICD) is effective in treating life-threatening ventricular arrhythmia and reduces mortality in high-risk patients.
Adduci, Carmen, Francia, Pietro, Palano, Francesca   +2 more
core   +2 more sources

Síncope em contexto febril – caso clínico de síndrome de Brugada

Revista Portuguesa de Cardiologia, 2014
Resumo: Em 1992, Brugada et Brugada descreveram pela primeira vez uma entidade, conhecida atualmente por síndrome de Brugada, associada a aumento do risco de arritmias ventriculares e morte súbita cardíaca em indivíduos sem cardiopatia estrutural.
Juliana Martins, Carlos Braga, Carina Arantes, Vítor Ramos, Alberto Salgado, Adília Rebelo, Adelino Correia   +6 more
doaj  

Treatment of Anxiety and Depression in a Patient with Brugada Syndrome

Case Reports in Psychiatry, 2014
Background. Brugada syndrome is rare and has been a clinically diagnosable entity since 1992. Its clinical manifestations are highly variable, and while some patients remain asymptomatic, others endure sudden cardiac death.
Jasper J. Chen, Rajbir S. Sangha
doaj   +1 more source

Electrocardiographic Effects of Propofol versus Etomidate in Patients with Brugada Syndrome

Anesthesiology, 2019
Background: Brugada Syndrome is an inherited arrhythmogenic disease, characterized by the typical coved type ST-segment elevation in the right precordial leads from V1 through V3.
P. Flamée, V. Varnavas, W. Dewals, Hugo Carvalho, W. Cools, J. T. Bhutia, S. Beckers, V. Umbrain, C. Verborgh, P. Forget, G. Chierchia, P. Brugada, J. Poelaert, C. de Asmundis   +13 more
semanticscholar   +1 more source

Acquired Genotype‐Positive Long QT Syndrome After Pediatric Heart Transplantation

Pediatric Transplantation, Volume 29, Issue 3, May 2025.
ABSTRACT Background Congenital long QT syndrome (LQTS) is rare but significant, as it carries a risk for ventricular arrhythmias and sudden cardiac death. Its diagnosis can be made clinically by serial ECGs, ambulatory ECG monitoring, and exercise stress testing; however, genetic testing is confirmatory in the majority of cases.
Nicholas V. Barresi, Jessica Sebastian, Gaurav Arora, Brian Feingold   +3 more
wiley   +1 more source

In a case of female-to-male sex reassignment, testosterone therapy switches on an underlying Brugada

International Journal of Arrhythmia, 2020
Background The Brugada syndrome, diagnosed by a typical electrocardiographic pattern, is a genetic condition characterised by an increased risk of potentially lethal ventricular arrhythmias and sudden cardiac death.
Patrizia Vivona, Federica Dagradi, Michele M. Ciulla   +2 more
doaj   +1 more source

JCS/JHRS 2024 Guideline Focused Update on Management of Cardiac Arrhythmias

Journal of Arrhythmia, Volume 41, Issue 3, June 2025.
Yu‐ki Iwasaki, Takashi Noda, Masaharu Akao, Tadashi Fujino, Teruyuki Hirano, Koichi Inoue, Kengo Kusano, Toshiyuki Nagai, Kazuhiro Satomi, Tetsuji Shinohara, Kyoko Soejima, Yohei Sotomi, Shinya Suzuki, Teiichi Yamane, Tsukasa Kamakura, Hiroyuki Kato, Arimi Katsume, Yusuke Kondo, Kenji Kuroki, Hisaki Makimoto, Hiroshige Murata, Takafumi Oka, Nobuaki Tanaka, Nobuhiko Ueda, Hiro Yamasaki, Seigo Yamashita, Ryobun Yasuoka, Kenji Yodogawa, Kazutaka Aonuma, Takanori Ikeda, Toru Minamino, Hideo Mitamura, Akihiko Nogami, Ken Okumura, Hiroshi Tada, Takashi Kurita, Wataru Shimizu, on behalf of the Japanese Circulation Society and Japanese Heart Rhythm Society Joint Working Group   +37 more
wiley   +1 more source

Mitral Annulus Disjunction Causing Ventricular Tachyarrhythmias in a Young Lady With Palpitations, Cardiac Ablation Terminated the Complaints

Clinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT Mitral annulus disjunction (MAD) is a rare but significant cause of ventricular arrhythmias in young patients. Timely diagnosis using cardiac magnetic resonance imaging and targeted management with catheter ablation can effectively control arrhythmias, improve patient outcomes, and prevent severe complications such as sudden cardiac death.
Mohammad Hosein Nikoo, Reza Heydarzadeh, Alisina Mirzaei, Reza Golchin Vafa   +3 more
wiley   +1 more source

Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia [PDF]

, 2015
Background Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a difficult-to-diagnose cause of sudden cardiac death (SCD). We identified a family of 1400 individuals with multiple cases of CPVT, including 36 SCDs during youth.
Allegue, Catarina, Beltran-Alvarez, Pedro, Berne, Paola, Bosch Calero, Cristina, Brugada, Josep, Brugada, Ramon, Campuzano, Oscar, Iglesias, Anna, Pérez, Carmelo, Pérez, Guillermo J., Ruiz Hernandez, Pablo M., Scornik, Fabiana S., Wangüemert, Fernando   +12 more
core   +2 more sources