Results 181 to 190 of about 266,382 (322)

Diagnostic Criteria for the Long QT Syndrome An Update

Circulation, 1993
Peter J. Schwartz, Arthur J. Moss, G. M. Vincent, Richard S. Crampton   +3 more
semanticscholar   +1 more source

LQTS: Gender Differences and Mother-Son vs. Mother-Daughter [PDF]

, 2014
Long QT syndrome is a chronic disorder, and one of the most common genetic arrhythmia syndromes that can cause unexpected cardiac arrest and death in individuals. Treatment options include medications, use of implantable cardioverter defibrillators (ICD)
Gallagher, Thea
core   +1 more source

2025 Japanese Heart Rhythm Society / Japanese Circulation Society Consensus Statement on the Appropriate Use of Ambulatory and Wearable Electrocardiographs

Journal of Arrhythmia, Volume 41, Issue 3, June 2025.
Recently, some clinicians have been diagnosing and treating arrhythmias on the basis of electrocardiogram (ECG) devices with low accuracy. In Europe and the US, several statements on the use of ECGs have already been published by related academic societies.
Takanori Ikeda, Takashi Ashihara, Yu‐ki Iwasaki, Maki Ono, Nobuyuki Kagiyama, Takehiro Kimura, Kengo Kusano, Ritsuko Kohno, Keita Saku, Tetsuo Sasano, Keitaro Senoo, Seiji Takatsuki, Naohiko Takahashi, Mitsuru Takami, Yukiko Nakano, Kenichi Hashimoto, Katsuhito Fujiu, Tadashi Fujino, Atsushi Mizuno, Koichiro Yoshioka, Eiichi Watanabe, Wataru Shimizu, Koichi Node   +22 more
wiley   +1 more source

Arrhythmias in the congenital long QT syndrome: how often is torsade de pointes pause dependent? [PDF]

, 2000
Sami Viskin
openalex   +1 more source

Long‐term of epicardial radiofrequency ablation and benefit for recurrent ventricular arrhythmia in Brugada syndrome: A systematic review and meta‐analysis

Journal of Arrhythmia, Volume 41, Issue 3, June 2025.
Epicardial radiofrequency ablation significantly reduces recurrent ventricular arrhythmias and ICD shocks in Brugada syndrome, with excellent long‐term safety and no reported mortality. Epicardial ablation is an effective strategy for sustained rhythm stabilization. Abstract Background Brugada syndrome (BrS) is a rare cardiac channelopathy linked to an
Arga Setyo Adji, Atiyatum Billah, Juliardi Eka Putra Sit, Bryan Gervais de Liyis, Angga Nugraha, Angela Puspita, Abdillah Maulana Satrioaji, Ragil Nur Rosyadi   +7 more
wiley   +1 more source

A Natural History Study of Timothy Syndrome

Orphanet Journal of Rare Diseases
Background Timothy syndrome (OMIM #601005) is a rare disease caused by variants in the gene CACNA1C. Initially, Timothy syndrome was characterized by a cardiac presentation of long QT syndrome and syndactyly of the fingers and/or toes, all associated ...
Katherine W. Timothy, Rosemary Bauer, Kerry A. Larkin, Edward P. Walsh, Dominic J. Abrams, Cecilia Gonzalez Corcia, Alexandra Valsamakis, Geoffrey S. Pitt, Ivy E. Dick, Andy Golden   +9 more
doaj   +1 more source

Molecular Pharmacology of the Sodium Channel Mutation D1790G Linked to the Long-QT Syndrome [PDF]

, 2000
Hugues Abriel, Xander H.T. Wehrens, Jesaia Benhorin, Batsheva Kerem, Robert S. Kass   +4 more
openalex   +1 more source

Clinical insights into the role of bepridil in recurrence prevention after ablation of persistent atrial fibrillation

Journal of Arrhythmia, Volume 41, Issue 3, June 2025.
This retrospective study included 232 consecutive persistent atrial fibrillation patients according to the inclusion criteria. Despite patients characteristics with more severe atrial substrates in the Bepridil group, Kaplan–Meier curves showed no significant difference in the AF/AT freedom rate and clinical adverse events between the Bepridil and No ...
Moyuru Hirata, Koichi Nagashima, Ryuta Watanabe, Yuji Wakamatsu, Naoto Otsuka, Shu Hirata, Masanaru Sawada, Yuji Saito, Sayaka Kurokawa, Kenta Murotani, Yasuo Okumura   +10 more
wiley   +1 more source

Integration of validated functional evidence to support the pathogenicity of KCNH2 variants

Genetics in Medicine Open
Functional investigation of genetic variants found in long QT syndrome can provide evidence that is needed to confirm the genetic diagnosis and establish the cause of the condition.
Reema W. Aljassar, Qianyi Shen, Buthaina Albash, Jamie I. Vandenberg, Mohammad A. Ebrahim, Chai-Ann Ng   +5 more
doaj  

Microminipig, a Non-rodent Experimental Animal Optimized for Life Science Research: In Vivo Proarrhythmia Models of Drug-Induced Long QT Syndrome: Development of Chronic Atrioventricular Block Model of Microminipig

Journal of Pharmacological Sciences, 2011
A new in vivo proarrhythmia model of drug-induced long QT syndrome was developed using the Microminipig, an incredibly small minipig established by Fuji Micra Inc. (Shizuoka).
Atsushi Sugiyama, Yuji Nakamura, Yasuki Akie, Hiroyuki Saito, Yasukatsu Izumi, Hiroshi Yamazaki, Naoki Kaneko, Katzuhiko Itoh   +7 more
doaj