Search Results - "Subbiah, N."

Refine Results
  1. 1

    The diagnostic role of T wave morphology biomarkers in congenital and acquired long QT syndrome: A systematic review by Tardo, Daniel T., Peck, Matthew, Subbiah, Rajesh N., Vandenberg, Jamie I., Hill, Adam. P.

    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…”
    Get full text
    Journal Article
  2. 2
  3. 3

    Human ether-a-go-go related gene (hERG) K+ channels: Function and dysfunction by Perrin, Mark J., Subbiah, Rajesh N., Vandenberg, Jamie I., Hill, Adam P.

    “…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…”
    Get full text
    Journal Article
  4. 4

    Granulomatous sarcoid aortitis: a serious complication of a well-known multisystem disease by Wang, Louis W, Dr, Omari, Abdullah, Prof, Emmett, Louise, MD, Jansz, Paul C, PhD, Huilgol, Ravi, MBBS, Rainer, Stephen, MBChB, Subbiah, Rajesh N, PhD

    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…”
    Get full text
    Journal Article
  5. 5

    Heritability of ECG Biomarkers in the Netherlands Twin Registry Measured from Holter ECGs by Hodkinson, Emily C, Neijts, Melanie, Sadrieh, Arash, Imtiaz, Mohammad S, Baumert, Mathias, Subbiah, Rajesh N, Hayward, Christopher S, Boomsma, Dorret, Willemsen, Gonneke, Vandenberg, Jamie I, Hill, Adam P, De Geus, Eco

    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…”
    Get full text
    Journal Article
  6. 6

    Tryptophan scanning mutagenesis of the HERG K+ channel: the S4 domain is loosely packed and likely to be lipid exposed by Subbiah, Rajesh N., Kondo, Mari, Campbell, Terence J., Vandenberg, Jamie I.

    Published in The Journal of physiology (01-12-2005)
    “…Inherited mutations or drug-induced block of voltage-gated ion channels, including the human ether-à-go-go- related gene (HERG) K + channel, are significant…”
    Get full text
    Journal Article
  7. 7
  8. 8

    Pulmonary arteriovenous malformation: an unusual cause of exertional dyspnoea by Wang, Louis W, Dr, Kotlyar, Eugene, MD, Bester, Lourens, MMed, Feneley, Michael P, Prof, Omari, Abdullah, Prof, Subbiah, Rajesh N, PhD

    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…”
    Get full text
    Journal Article
  9. 9
  10. 10

    Molecular basis of slow activation of the human ether-á-go-go related gene potassium channel by Subbiah, Rajesh N., Clarke, Catherine E., Smith, David J., Zhao, JingTing, Campbell, Terence J., Vandenberg, Jamie I.

    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…”
    Get full text
    Journal Article
  11. 11

    Unusual adverse consequence of reverse ventricular remodelling following cardiac resynchronization therapy by Chia, Pow-Li, Subbiah, Rajesh N, Kuchar, Dennis, Walker, Bruce

    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…”
    Get full text
    Journal Article
  12. 12

    Associated factors with cervical pre-malignant lesions among the married fisher women community at Sadras, Tamil Nadu by Ganesan, Sornam, Subbiah, Vasantha N., Michael, Jothi Clara J.

    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…”
    Get full text
    Journal Article
  13. 13

    Andersen‐Tawil Syndrome: Management Challenges During Pregnancy, Labor, and Delivery by SUBBIAH, RAJESH N., GULA, LORNE J., SKANES, ALLAN C., KRAHN, ANDREW D.

    “…Andersen‐Tawil syndrome (ATS) is characterized by ventricular arrhythmias, hypokalemic periodic paralysis and developmental anomalies. It is caused by…”
    Get full text
    Journal Article
  14. 14
  15. 15

    Reduction of complex ventricular ectopy and improvement in exercise capacity with flecainide therapy in Andersen-Tawil syndrome by Fox, David J., Klein, George J., Hahn, Angelika, Skanes, Allan C., Gula, Lorne J., Yee, Raymond K., Subbiah, Rajesh N., Krahn, Andrew D.

    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…”
    Get full text
    Journal Article
  16. 16

    Cardiac sarcoidosis masquerading as arrhythmogenic right ventricular cardiomyopathy by Chia, Pow-Li, M.Med(Int Med), Subbiah, Rajesh N., PhD, Kuchar, Dennis, MD, Walker, Bruce, PhD

    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…”
    Get full text
    Journal Article
  17. 17

    Action Potential Morphology Accurately Predicts Proarrhythmic Risk for Drugs With Potential to Prolong Cardiac Repolarization by Lee, William, Ng, Ben, Mangala, Melissa M., Perry, Matthew D., Subbiah, Rajesh N., Vandenberg, Jamie I., Hill, Adam P.

    “…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…”
    Get full text
    Journal Article
  18. 18

    Expression of a Common LQT1 Mutation in Five Apparently Unrelated Families in a Regional Inherited Arrhythmia Clinic by GRAY, CHRISTOPHER, GULA, LORNE J., KLEIN, GEORGE J., SKANES, ALLAN C., YEE, RAYMOND, SY, RAYMOND, SALISBURY, BENJAMIN A., WONG, JORGE, CHATTHA, ISHVINDER, SUBBIAH, RAJESH N., KRAHN, ANDREW D.

    “…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…”
    Get full text
    Journal Article
  19. 19
  20. 20

    Multiscale cardiac modelling reveals the origins of notched T waves in long QT syndrome type 2 by Sadrieh, Arash, Domanski, Luke, Pitt-Francis, Joe, Mann, Stefan A, Hodkinson, Emily C, Ng, Chai-Ann, Perry, Matthew D, Taylor, John A, Gavaghan, David, Subbiah, Rajesh N, Vandenberg, Jamie I, Hill, Adam P

    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…”
    Get full text
    Journal Article