Results 81 to 90 of about 3,671 (165)

A1427S missense mutation in scn5a causes type 1 brugada pattern, recurrent ventricular tachyarrhythmias and right ventricular structural abnormalities

open access: yesResearch in Cardiovascular Medicine, 2017
A 66- year-old male presented with recurrent syncope and ventricular fibrillation arrest twenty years ago, for which an implantable cardioverter defibrillator was inserted. Electrocardiography showed a Type 1 Brugada pattern.
Ka Hou Christien Li   +5 more
doaj  

Sudden cardiac death in children and adolescents (excluding Sudden Infant Death Syndrome)

open access: yesAnnals of Pediatric Cardiology, 2010
Sudden death in the young is rare. About 25% of cases occur during sports. Most young people with sudden cardiac death (SCD) have underlying heart disease, with hypertrophic cardiomyopathy and coronary artery anomalies being commonest in most ...
Gajewski Kelly, Saul Philip
doaj  

Case images: Concomitant diagnosis of a large apical right ventricular thrombus in a newly diagnosed case of arrhythmogenic right ventricular dysplasia

open access: yesTürk Kardiyoloji Derneği Arşivi, 2013
Ahmet Taha Alper   +3 more
doaj   +1 more source

Catheter Ablation of Ventricular Tachycardia in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy. [PDF]

open access: yesKorean Circ J, 2018
Chung FP   +10 more
europepmc   +1 more source

Exercise-related sudden cardiac death of an American football player with arrhythmogenic right ventricular dysplasia/cardiomyopathy AND sarcoidosis. [PDF]

open access: yesClin Case Rep, 2019
Müssigbrodt A   +7 more
europepmc   +1 more source

Intracardiac ultrasound to detect aneurysm in arrhythmogenic right ventricular dysplasia/cardiomyopathy. [PDF]

open access: yesOxf Med Case Reports, 2018
Gabriel C   +7 more
europepmc   +1 more source

Epicardial Fat Distribution Assessed with Cardiac CT in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy. [PDF]

open access: yesRadiology, 2018
Aliyari Ghasabeh M   +11 more
europepmc   +1 more source

PKP2 and DSG2 genetic variations in Latvian arrhythmogenic right ventricular dysplasia/cardiomyopathy registry patients. [PDF]

open access: yesAnatol J Cardiol, 2018
Bidina L   +7 more
europepmc   +1 more source

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