Left Ventricular Noncompaction
What's New
Last Posted: Oct 27, 2022
- Genetic Basis of Childhood Cardiomyopathy.
Bagnall Richard D et al. Circulation. Genomic and precision medicine 2022 e003686 - Establishment of a Dedicated Inherited Cardiomyopathy Clinic: From Challenges to Improved Patients' Outcome.
Smith Emily et al. Journal of the American Heart Association 2022 e024501 - Ventricular arrhythmia management in patients with genetic cardiomyopathies.
Sharif Zain I et al. Heart rhythm O2 2022 2(6Part B) 819-831 - Reduced Systolic Function and Not Genetic Variants Determine Outcome in Pediatric and Adult Left Ventricular Noncompaction Cardiomyopathy.
Schultze-Berndt Alina et al. Frontiers in pediatrics 2021 9722926 - [Clinical pathway for cardiomyopathies: a genetic testing strategy proposed by ANMCO in Tuscany].
Girolami Francesca et al. Giornale italiano di cardiologia (2006) 2020 Dec 21(12) 926-934 - Screening for Fabry disease in patients with left ventricular noncompaction.
Azevedo Olga et al. Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology 2020 Jan - Left ventricular noncompaction - Risk stratification and genetic consideration.
Ichida Fukiko et al. Journal of cardiology 2019 Oct - 2019 HRS Expert Consensus Statement on Evaluation, Risk Stratification, and Management of Arrhythmogenic Cardiomyopathy.
Towbin Jeffrey A et al. Heart rhythm 2019 May - Prevalence of pathogenic and likely pathogenic variants in the RASopathy genes in patients who have had panel testing for cardiomyopathy.
Aljeaid Deema et al. American journal of medical genetics. Part A 2019 Feb - Genotype-Positive Status Is Associated With Poor Prognoses in Patients With Left Ventricular Noncompaction Cardiomyopathy.
Li Shijie et al. Journal of the American Heart Association 2018 Oct 7(20) e009910
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- Page last reviewed:Feb 1, 2024
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