Disease: Obstructive asymmetric septal hypertrophy
- A bibliometric and visual analysis of research trends and hotspots of familial hypertrophic cardiomyopathy: A review
- A Cadaveric Evaluation of Hypertrophic Obstructive Cardiomyopathy
- A MYH7 variant in a five-generation-family with hypertrophic cardiomyopathy
- A New Leu714Arg Variant in the Converter Domain of MYH7 is Associated with a Severe Form of Familial Hypertrophic Cardiomyopathy
- A Novel <em>TPM1</em> Mutation Causes Familial Hypertrophic Cardiomyopathy in an Indian Family: Genetic and Clinical Correlation
- A Novel TPM1 Mutation Causes Familial Hypertrophic Cardiomyopathy in an Indian Family: Genetic and Clinical Correlation
- A novel αB-crystallin R123W variant drives hypertrophic cardiomyopathy by promoting maladaptive calcium-dependent signal transduction
- A perspective on Notch signalling in progression and arrhythmogenesis in familial hypertrophic and dilated cardiomyopathies
- A Pharmacologic Update: New Treatments for Patients with Cardiovascular Disease
- A Review of Pediatric Cardiomyopathy
- Allele-Specific Suppression of Variant MHC With High-Precision RNA Nuclease CRISPR-Cas13d Prevents Hypertrophic Cardiomyopathy
- Altered myocardial lipid regulation in junctophilin-2-associated familial cardiomyopathies
- An Unbiased Screen Identified the Hsp70-BAG3 Complex as a Regulator of Myosin-Binding Protein C3
- Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy
- Biochemical characterization of cardiac alpha-actin mutations A21V and D26N implicated in hypertrophic cardiomyopathy
- Biomarkers and Proteomics in Sarcomeric Hypertrophic Cardiomyopathy in the Young-FGF-21 Highly Associated with Overt Disease
- Cardiomyopathies in children and adolescents: aetiology, management, and outcomes in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis Registry
- Case Report: Four cases of cardiac sarcoidosis in patients with inherited cardiomyopathy-a phenotypic overlap, co-existence of two rare cardiomyopathies or a second-hit disease
- Clinical and Genetic Screening for Hypertrophic Cardiomyopathy in Paediatric Relatives: Changing Paradigms in Clinical Practice
- Clinical and genetic yield of familial screening after a sudden unexplained death at a young age
- Clinical phenotypic characteristics in patients carrying MYH7-R143Q mutation with hypertrophic cardiomyopathy
- Clinical to Population Prevalence of Hypertrophic Cardiomyopathy Phenotype: Insights From the National Echo Database Australia
- Concealed Inherited Cardiomyopathies Detected in Cardio-Oncology Screening
- Cytoskeletal disarray increases arrhythmogenic vulnerability during sympathetic stimulation in a model of hypertrophic cardiomyopathy
- Diagnostic yield from cardiac gene testing for inherited cardiac conditions and re-evaluation of pre-ACMG variants of uncertain significance
- Emerging Themes in Genetics of Hypertrophic Cardiomyopathy: Current Status and Clinical Application
- Emerging Themes in Genetics of Hypertrophic Cardiomyopathy. Current status and clinical application
- Eosinophilic infiltration as the initial trace of acute mixed cellular and antibody mediated rejection in a heart transplant patient with concomitant immense epitope-associated HLA-antibody production: a case report
- Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy
- Evolution of genetic testing and gene therapy in hypertrophic cardiomyopathy
- Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying MYBPC3 nonsense mutations
- Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying the MYBPC3 missense c.1484G>A mutation
- Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying the MYBPC3 missense c.1484G>A mutation
- Genetic heterogeneity of cardiomyopathy and its correlation with patient care
- Genotype-Phenotype Taxonomy of Hypertrophic Cardiomyopathy
- High prevalence of ALPK3 premature terminating variants in Korean hypertrophic cardiomyopathy patients
- Identification of variants in genes associated with hypertrophic cardiomyopathy in Mexican patients
- Innovative Animal Models Of Cardiac Remodeling: Development And Evaluation
- Investigation of mutation spectrum amongst patients with familial primary cardiomyopathy using targeted NGS in Indian population
- Is Hypertrophic Cardiomyopathy Always a Familial and Inherited Disease?
- Left ventricular hypertrophy: do not forget Fabry disease. Diagnostic work-up and differential diagnosis
- Mavacamten in hypertrophic obstructive cardiomyopathy: Prospects for AI integration and mitigating healthcare disparities
- Mechanisms of ischaemia-induced arrhythmias in hypertrophic cardiomyopathy: a large-scale computational study
- Mechanisms of Pathogenicity of Hypertrophic Cardiomyopathy-Associated Troponin T (TNNT2) Variant R278C <sup>+/-</sup> During Development
- Medical Treatment Strategies for Hypertrophic Cardiomyopathy
- Modeling cardiomyocyte signaling and metabolism predicts genotype-to-phenotype mechanisms in hypertrophic cardiomyopathy
- Molecular autopsy in Chinese sudden cardiac death in the young
- Novel electrocardiographic criteria may render possible the more accurate recognition of cardiac amyloidosis
- Obstructive hypertrophic cardiomyopathy: a review of new therapies
- Patients With Hypertrophic Cardiomyopathy and Normal Genetic Investigations Have Few Affected Relatives
- Preserving mitochondria to treat hypertrophic cardiomyopathy: From rare mitochondrial DNA mutation to heart failure therapy?
- Prognosis of patients with familial hypertrophic cardiomyopathy: A single-center cohort study with ten-year follow-up by propensity score matching analysis
- Promising therapies for adults with symptomatic obstructive hypertrophic cardiomyopathy: 2023 and beyond
- Real-world utilization of guideline-directed genetic testing in inherited cardiovascular diseases
- Recommendations for the Management of Cardiomyopathy Mutation Carriers: Evidence, Doubts, and Intentions
- Results of comprehensive genetic testing in patients presenting to a multidisciplinary inherited heart disease clinic in India
- Role of Genetics in Diagnosis and Management of Hypertrophic Cardiomyopathy: A Glimpse into the Future
- Role of non-coding variants in cardiovascular disease
- Sarcomeric gene variants among Indians with hypertrophic cardiomyopathy: A scoping review
- Scar architecture affects the electrophysiological characteristics of induced ventricular arrhythmias in hypertrophic cardiomyopathy
- Sengers syndrome and AGK-related disorders - Minireview of phenotypic variability and clinical outcomes in molecularly confirmed cases
- Structure of the native myosin filament in the relaxed cardiac sarcomere
- Tale of two hearts: a TNNT2 hypertrophic cardiomyopathy case report
- The Impact of Integration of a Genetic Clinic Into a Pediatric Cardiac Unit
- Three-dimensional spatial quantitative analysis of cardiac lymphatics in the mouse heart
- Titin: The Missing Link in Cardiac Physiology
- Transapical beating-heart septal myectomy for recurrent left ventricular outflow tract obstruction after septal reduction therapy in hypertrophic obstructive cardiomyopathy
- Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency