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 …

Circulating noncoding RNAs as biomarkers of cardiovascular disease and injury

J Viereck, T Thum - Circulation research, 2017 - Am Heart Assoc
The discovery of thousands of noncoding RNAs (ncRNAs) has expanded our view on
mammalian genomes and transcriptomes, as well as their organization and regulation …

Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): a randomised, double-blind, placebo-controlled, phase 3 trial

I Olivotto, A Oreziak, R Barriales-Villa, TP Abraham… - The Lancet, 2020 - thelancet.com
Background Cardiac muscle hypercontractility is a key pathophysiological abnormality in
hypertrophic cardiomyopathy, and a major determinant of dynamic left ventricular outflow …

Effect of mavacamten on echocardiographic features in symptomatic patients with obstructive hypertrophic cardiomyopathy

SM Hegde, SJ Lester, SD Solomon, M Michels… - Journal of the American …, 2021 - jacc.org
Abstract Background EXPLORER-HCM (Clinical Study to Evaluate Mavacamten [MYK-461]
in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy) demonstrated that …

The feline cardiomyopathies: 2. Hypertrophic cardiomyopathy

MD Kittleson, E Côté - Journal of feline medicine and …, 2021 - journals.sagepub.com
Practical relevance: Hypertrophic cardiomyopathy (HCM) is the most common form of feline
cardiomyopathy observed clinically and may affect up to approximately 15% of the domestic …

Cardiomyopathy: an overview

JAY Brieler, MA Breeden, J Tucker - American family physician, 2017 - aafp.org
The definition and classification of cardiomyopathy have evolved considerably in recent
years. Cardiomyopathy can be separated into primary (genetic, mixed, or acquired) and …

Pharmacological management of hypertrophic cardiomyopathy: from bench to bedside

C Palandri, L Santini, A Argirò, F Margara, R Doste… - Drugs, 2022 - Springer
Hypertrophic cardiomyopathy (HCM), the most common inherited heart disease, is still
orphan of a specific drug treatment. The erroneous consideration of HCM as a rare disease …

Efficacy of ranolazine in patients with symptomatic hypertrophic cardiomyopathy: the RESTYLE-HCM randomized, double-blind, placebo-controlled study

I Olivotto, PG Camici, PA Merlini, C Rapezzi… - Circulation: Heart …, 2018 - Am Heart Assoc
Background The late sodium current inhibitor ranolazine reverses the main
electrophysiological and mechanical abnormalities of human hypertrophic cardiomyopathy …

Update on hypertrophic cardiomyopathy and a guide to the guidelines

S Sen-Chowdhry, D Jacoby, JC Moon… - Nature Reviews …, 2016 - nature.com
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disorder,
affecting 1 in 500 individuals worldwide. Existing epidemiological studies might have …

Temporal trend of age at diagnosis in hypertrophic cardiomyopathy: an analysis of the international sarcomeric human cardiomyopathy registry

M Canepa, C Fumagalli, G Tini… - Circulation: Heart …, 2020 - Am Heart Assoc
Background: Over the last 50 years, the epidemiology of hypertrophic cardiomyopathy
(HCM) has changed because of increased awareness and availability of advanced …