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  1. Pregnancy in women with Fontan physiology poses a significant management challenge and is deemed high risk. The aim of this study is to describe short and long-term pregnancy outcomes in women who have undergo...

    Authors: Sayqa Arif, Aliyah Chaudhary, Paul F. Clift, R. Katie Morris, Tara J. Selman, Sarah E. Bowater, Lucy E. Hudsmith, Peter J. Thompson and Sara A. Thorne
    Citation: Journal of Congenital Cardiology 2017 1:10

    The Correction to this article has been published in Journal of Congenital Cardiology 2019 3:6

  2. Triadin-1, encoded by TRDN, is an important component of the calcium release unit (CRU) in the sarcoplasmic reticulum of cardiac myocytes, interacting both with ryanodine receptors and calsequestrin. This article...

    Authors: Jules C. Hancox, Andrew F. James, Mark A. Walsh and Alan G. Stuart
    Citation: Journal of Congenital Cardiology 2017 1:9
  3. A Fontan circulation is a series of palliative surgical procedures, which result in the diversion of the systemic venous return into pulmonary arterial circulation without passing through a ventricle. It is on...

    Authors: Michael Yeong, Will Loughborough, Mark Hamilton and Nathan Manghat
    Citation: Journal of Congenital Cardiology 2017 1:8
  4. The imaging of pulmonary venous anatomy has traditionally been performed with echocardiography and catheter pulmonary angiography. Magnetic resonance imaging (MRI) and notably multi-detector row computed tomog...

    Authors: Stephen Lyen, Shalini Wijesuriya, Eleanor Ngan-Soo, Helen Mathias, Michael Yeong, Mark Hamilton and Nathan Manghat
    Citation: Journal of Congenital Cardiology 2017 1:7
  5. Atrial arrhythmias (AA) are common in adults with congenital heart disease (ACHD). Although Intra-atrial Reentrant Tachycardia (IART) is well described in ACHD, Atrial Fibrillation (AF) is uncommon, but increa...

    Authors: Darryl Wan, Clara Tsui, Jasmine Grewal, Marla Kiess, Amanda Barlow, Derek Human, Andrew Krahn and Santabhanu Chakrabarti
    Citation: Journal of Congenital Cardiology 2017 1:6
  6. Congenital heart disease (CHD) is one of the most common causes of pulmonary arterial hypertension (PAH), with a prevalence nearing that of idiopathic PAH in registries. Despite similarities in pulmonary vascu...

    Authors: Konstantinos Dimopoulos, Carl Harries and Lisa Parfitt
    Citation: Journal of Congenital Cardiology 2017 1:5
  7. To describe the institutional experience, technical aspects and outcome of stenting of the right ventricular outflow tract (RVOT) in the initial palliation of symptomatic patients with severely limited pulmona...

    Authors: D. Quandt, G. Penford, B. Ramchandani, V. Bhole, C. Mehta and O. Stumper
    Citation: Journal of Congenital Cardiology 2017 1:3
  8. Pulmonary arterial hypertension is a condition associated with raised right heart pressures and subsequent remodelling of the right atrium and ventricle with relative preservation of left heart function. There...

    Authors: Ian Peter Temple
    Citation: Journal of Congenital Cardiology 2017 1:2