2022 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: Developed by the task force for the …

K Zeppenfeld, J Tfelt-Hansen, M De Riva… - European heart …, 2022 - academic.oup.com
4004 ESC Guidelines label use of medication should be limited to situations where it is in
the patient's interest to do so, with regard to the quality, safety, and efficacy of care, and only …

2023 ESC Guidelines for the management of cardiomyopathies: Developed by the task force on the management of cardiomyopathies of the European Society of …

E Arbelo, A Protonotarios, JR Gimeno… - European heart …, 2023 - academic.oup.com
• The specific situation of the patient. Unless otherwise provided for by national regulations,
off-label use of medication should be limited to situations where it is in the patient's interest …

Penetrance of hypertrophic cardiomyopathy in sarcomere protein mutation carriers

M Lorenzini, G Norrish, E Field, JP Ochoa… - Journal of the American …, 2020 - jacc.org
Background Predictive genetic screening of relatives of patients with hypertrophic
cardiomyopathy (HCM) caused by sarcomere protein (SP) gene mutations is current …

Management of Hypertrophic Cardiomyopathy: JACC State-of-the-Art Review

BJ Maron, MY Desai, RA Nishimura, P Spirito… - Journal of the American …, 2022 - jacc.org
Hypertrophic cardiomyopathy (HCM), a relatively common, globally distributed, and often
inherited primary cardiac disease, has now transformed into a contemporary highly treatable …

[HTML][HTML] Evolution of risk stratification and sudden death prevention in hypertrophic cardiomyopathy: twenty years with the implantable cardioverter-defibrillator

BJ Maron, EJ Rowin, MS Maron - Heart Rhythm, 2021 - Elsevier
Hypertrophic cardiomyopathy (HCM) is a relatively common inherited myocardial disorder,
once regarded as largely untreatable with ominous prognosis and most visibly as a common …

Sex‐Related Differences in Genetic Cardiomyopathies

A Argirò, C Ho, SM Day, J van der Velden… - Journal of the …, 2022 - Am Heart Assoc
Cardiomyopathies are a heterogeneous collection of diseases that have in common primary
functional and structural abnormalities of the heart muscle, often genetically determined. The …

Associations between female sex, sarcomere variants, and clinical outcomes in hypertrophic cardiomyopathy

NK Lakdawala, I Olivotto, SM Day, L Han… - Circulation: Genomic …, 2021 - Am Heart Assoc
Background: The impact of sex on phenotypic expression in hypertrophic cardiomyopathy
(HCM) has not been well characterized in genotyped cohorts. Methods: Retrospective cohort …

Sex differences in hypertrophic cardiomyopathy: interaction with genetics and environment

A Butters, NK Lakdawala, J Ingles - Current heart failure reports, 2021 - Springer
Abstract Purpose of Review We explore the sex-specific interaction of genetics and the
environment on the clinical course and outcomes of hypertrophic cardiomyopathy (HCM) …

Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis

A Lopez-Sainz, F Dominguez, LR Lopes… - Journal of the American …, 2020 - jacc.org
Background PRKAG2 gene variants cause a syndrome characterized by cardiomyopathy,
conduction disease, and ventricular pre-excitation. Only a small number of cases have been …

Prevalence and disease expression of pathogenic and likely pathogenic variants associated with inherited cardiomyopathies in the general population

M Bourfiss, M Van Vugt, AI Alasiri… - Circulation: Genomic …, 2022 - Am Heart Assoc
Background: Pathogenic and likely pathogenic variants associated with arrhythmogenic
right ventricular cardiomyopathy (ARVC), dilated cardiomyopathy (DCM), and hypertrophic …