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BMC Genetics|June 21, 2013
Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of FallotJulian Palomino Doza, Ana Topf, Jamie Bentham, et al.
European Heart Journal|December 12, 2018
Clinical presentation and survival of childhood hypertrophic cardiomyopathy: a retrospective study in United KingdomGabrielle Norrish, Ella Field, Karen Mcleod, et al.
Archives of Disease in Childhood|October 6, 2021
Friedreich's ataxia-associated childhood hypertrophic cardiomyopathy: a national cohort studyGabrielle Norrish, Thomas Rance, Elena Montanes, et al.
Frontiers in Neurology|July 7, 2022
International Consensus Recommendations for the Assessment and Management of Individuals With CDKL5 Deficiency DisorderSam Amin, Marie Monaghan, Angel Aledo-Serrano, et al.
Lancet (London, England)|December 15, 2019
Irbesartan in Marfan syndrome (AIMS): a double-blind, placebo-controlled randomised trialMichael Mullen, Xu Yu Jin, Anne Child, et al.
International Journal of Cardiology|October 10, 2022
The use of 2-D speckle tracking echocardiography in assessing adolescent athletes with left ventricular hypertrabeculation meeting the criteria for left ventricular non-compaction cardiomyopathyDan M Dorobantu, Cristina R Radulescu, Nathan Riding, et al.
Echo Research and Practice|March 14, 2025
Echocardiography in the cardiac assessment of young athletes: a 2025 guideline from the British Society of Echocardiography (endorsed by Cardiac Risk in the Young)David Oxborough, Keith George, Robert Cooper, et al.
The New England Journal of Medicine|August 9, 2018
Outcomes of Cardiac Screening in Adolescent Soccer PlayersAneil Malhotra, Harshil Dhutia, Gherardo Finocchiaro, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|June 4, 2019
A validation study of the European Society of Cardiology guidelines for risk stratification of sudden cardiac death in childhood hypertrophic cardiomyopathyGabrielle Norrish, Tao Ding, Ella Field, et al.
Circulation. Cardiovascular Genetics|April 17, 2012
A common variant in the PTPN11 gene contributes to the risk of tetralogy of FallotJudith A Goodship, Darroch Hall, Ana Topf, et al.
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