Search Results - "Subbiah, N."
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The diagnostic role of T wave morphology biomarkers in congenital and acquired long QT syndrome: A systematic review
Published in Annals of noninvasive electrocardiology (01-01-2023)“…Introduction QTc prolongation is key in diagnosing long QT syndrome (LQTS), however 25%–50% with congenital LQTS (cLQTS) demonstrate a normal resting QTc. T…”
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Left Atrial Appendage Closure Guided by Personalized 3D-Printed Cardiac Reconstruction
Published in JACC. Cardiovascular interventions (01-06-2015)Get full text
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Human ether-a-go-go related gene (hERG) K+ channels: Function and dysfunction
Published in Progress in biophysics and molecular biology (01-10-2008)“…The human Ether-a-go-go Related Gene (hERG) potassium channel plays a central role in regulating cardiac excitability and maintenance of normal cardiac rhythm…”
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Granulomatous sarcoid aortitis: a serious complication of a well-known multisystem disease
Published in The Lancet (British edition) (16-05-2015)“…In March, 2013, because of the thoracic aortic aneurysm size, presence of active disease, and risk of aneurysmal expansion and rupture, he had aortic…”
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5
Heritability of ECG Biomarkers in the Netherlands Twin Registry Measured from Holter ECGs
Published in Frontiers in physiology (29-04-2016)“…The resting ECG is the most commonly used tool to assess cardiac electrophysiology. Previous studies have estimated heritability of ECG parameters based on…”
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Tryptophan scanning mutagenesis of the HERG K+ channel: the S4 domain is loosely packed and likely to be lipid exposed
Published in The Journal of physiology (01-12-2005)“…Inherited mutations or drug-induced block of voltage-gated ion channels, including the human ether-Ã -go-go- related gene (HERG) K + channel, are significant…”
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Coronary Artery Embolization After Successful Surgical Ablation of Atrial Fibrillation
Published in Circulation (New York, N.Y.) (26-02-2013)Get full text
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8
Pulmonary arteriovenous malformation: an unusual cause of exertional dyspnoea
Published in The Lancet (British edition) (20-04-2013)“…PAVMs are usually congenital in origin, but may be acquired in various conditions, such as cirrhosis, trauma, mitral stenosis, and schistosomiasis.1 Although…”
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Esophageal T-tube: A novel approach to atrioesophageal fistula repair
Published in HeartRhythm case reports (01-10-2017)Get full text
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10
Molecular basis of slow activation of the human ether-á-go-go related gene potassium channel
Published in The Journal of physiology (15-07-2004)“…The human ether-á-go-go related gene ( HERG ) encodes the pore forming α-subunit of the rapid delayed rectifier K + channel which is central to the…”
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Unusual adverse consequence of reverse ventricular remodelling following cardiac resynchronization therapy
Published in Europace (London, England) (01-08-2012)“…Cardiac resynchronization therapy has been shown to produce reverse ventricular remodelling in patients with severe heart failure. We report an unusual case of…”
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Associated factors with cervical pre-malignant lesions among the married fisher women community at Sadras, Tamil Nadu
Published in Asia-Pacific Journal of Oncology Nursing (01-01-2015)“…Objective: To identify the associated factors of cervical pre-malignant lesions among the married fisher women residing in the coastal areas of Sadras, Tamil…”
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13
Andersen‐Tawil Syndrome: Management Challenges During Pregnancy, Labor, and Delivery
Published in Journal of cardiovascular electrophysiology (01-09-2008)“…Andersen‐Tawil syndrome (ATS) is characterized by ventricular arrhythmias, hypokalemic periodic paralysis and developmental anomalies. It is caused by…”
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Torsades de pointes during complete atrioventricular block: Genetic factors and electrocardiogram correlates
Published in Canadian journal of cardiology (01-04-2010)“…Introduction Atrioventricular (AV) block is infrequently associated with QT prolongation and torsades de pointes (TdP). It was hypothesized that patients with…”
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Reduction of complex ventricular ectopy and improvement in exercise capacity with flecainide therapy in Andersen-Tawil syndrome
Published in Europace (London, England) (01-08-2008)“…Andersen-Tawil syndrome (ATS) is a rare inherited autosomal disorder characterized by the clinical triad of ventricular arrhythmias, hypokalaemic periodic…”
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Cardiac sarcoidosis masquerading as arrhythmogenic right ventricular cardiomyopathy
Published in Heart, lung & circulation (01-01-2012)“…We present a case of ventricular tachycardia with clinical features suggestive of arrhythmogenic right ventricular cardiomyopathy. However, endomyocardial…”
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Action Potential Morphology Accurately Predicts Proarrhythmic Risk for Drugs With Potential to Prolong Cardiac Repolarization
Published in Circulation. Arrhythmia and electrophysiology (01-07-2023)“…Drug-induced or acquired long QT syndrome occurs as a result of the unintended disruption of cardiac repolarization due to drugs that block cardiac ion…”
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Expression of a Common LQT1 Mutation in Five Apparently Unrelated Families in a Regional Inherited Arrhythmia Clinic
Published in Journal of cardiovascular electrophysiology (01-03-2010)“…Expression of a Common LQT1 Mutation. Background: The Inherited Arrhythmia Clinic at the University of Western Ontario services a catchment area of 1.5 million…”
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Profound bradycardia and hypotension in a normal heart
Published in Heart rhythm (01-10-2010)Get full text
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Multiscale cardiac modelling reveals the origins of notched T waves in long QT syndrome type 2
Published in Nature communications (25-09-2014)“…The heart rhythm disorder long QT syndrome (LQTS) can result in sudden death in the young or remain asymptomatic into adulthood. The features of the surface…”
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