A Prospective Study of Sudden Cardiac Death among Children and Young Adults.
By R. Bagnall, R. Weintraub, J. Ingles, Johan Duflou, L. Yeates, L. Lam, A. Davis, T. Thompson, V. Connell, J. Wallace and 18 more. New England Journal of Medicine, 2016
739 citations recorded by the source corpus.
Subfields: Cardiology and Cardiovascular Medicine, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/1a9abab4c5a2e2a2c8e0107bed90d1432c080670
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In Cardiology and Cardiovascular Medicine
In Molecular Biology
Citations in the corpus
- 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy. (2019, background): “ACM-associated genes can also be evaluated in autopsy-negative SCD cases because ventricular arrhythmias leading to SCD may precede structural abnormalities.(138)”
- Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy. (2017, background): “Prognosis HCM is the most common cause of SCD in adolescents and young adults, particularly in competitive athletes.(202,203,212,213,219) The risk factors for SCD are shown in Table 3 and discussed below.”