• [[en]]Pregnancy in women with genetic variants of dilated cardiomyopathy
• A case report of Danon's disease with dilated phenotype
• An unusual cause of inappropriate shocks delivered by an implantable cardioverter defibrillator
• Analysis of pediatric heart transplantation supported by extracorporeal membrane oxygenation
• Anesthesia management for percutaneous mitral valve repair in a patient with mitochondrial cardiomyopathy and low cardiac function: a case report
• Anesthetic management and anesthesia-related complications in dogs with a dilated cardiomyopathy phenotype: a retrospective study of 30 dogs (2010-2024)
• Arrhythmias and conduction disorders in patients with viral heart disease
• Atrial fibrillation at the Principal Hospital of Dakar, Senegal: outcomes and limits of management
• CaMK II in Cardiovascular Diseases, Especially CaMK II-δ: Friends or Enemies
• Cardiac Amyloidosis Mimicking Non-ST-Segment Myocardial Infarction: A Case Report
• Cardiac disease discrimination from 3D-convolutional kinematic patterns on cine-MRI sequences
• Cardiac Involvement in LAMA2-Related Muscular Dystrophy and SELENON-Related Congenital Myopathy: A Case Series
• Cardiac resynchronization therapy-defibrillator implantation with shock lead placement in the left bundle branch area: a case report
• Cardiac Sarcoidosis: A Comprehensive Clinical Review
• Cardiomyopathy and Sudden Cardiac Death: Bridging Clinical Practice with Cutting-Edge Research
• Cardiomyopathy discovered during pregnancy: Insights from speckle tracking echocardiography in a cohort of pregnant patients
• Cardiovascular magnetic resonance parametric mapping in the risk stratification of patients affected by chronic myocarditis
• Characterization and Long-Term Prognosis of Patients with Different Phenotypes of Dilated Cardiomyopathy
• Characterization and natural history of patients with LMNA-related dilated cardiomyopathy in the phase 3 REALM-DCM trial
• Characterizing left ventricular systolic dysfunction in sickle cell disease: three contrasting case reports
• Coexistence of dilated cardiomyopathy with preexisting testicular cancer in a young man. Interdisciplinary cooperation: success in treatment
• Combining Bulk and Single Cell RNA-Sequencing Data to Identify Hub Genes of Fibroblasts in Dilated Cardiomyopathy
• Comparative Analysis of Mitochondria Surrounding the Intercalated Discs in Heart Diseases-An Ultrastructural Pilot Study
• Compliance with Guideline-Directed Medical Therapy and Early Implantable Cardioverter-Defibrillator Activation in Heart Failure: A Retrospective Study
• Comprehensive analysis of aberrantly methylated differentially expressed genes and validation of CDC6 in melanoma
• Conduction time from left bundle branch pacing to the left ventricular lateral wall in two patients in whom cardiac resynchronization therapy pacemaker was implanted
• Coupling of β-adrenergic and Hippo pathway signaling: Implications for heart failure pathophysiology and metabolic therapy
• CRT for Dilated Cardiomyopathy: Time for a Personalized Approach
• Cypher/ZASP drives cardiomyocyte maturation via actin-mediated MRTFA-SRF signalling
• Dapagliflozin-induced abnormal uterine bleeding in a patient with dilated cardiomyopathy and chronic heart failure: a case report
• Description and Prognosis of Patients with Recovered Dilated Cardiomyopathy: A Retrospective Cohort Study
• Diagnosis and management of arrhythmogenic cardiomyopathy: a case report
• Differences in T cell-associated serum markers between ischemic cardiomyopathy and dilated cardiomyopathy
• Dilated cardiomyopathy caused by mutation of the PNPLA2 gene: a case report and literature review
• Dilated cardiomyopathy due to a novel combination of TTN and BAG3 genetic variants: From acute heart failure to subclinical phenotypes
• Dilated cardiomyopathy mutation in beta-cardiac myosin enhances actin activation of the power stroke and phosphate release
• Dynamic LVEF Decline and Serum NT-proBNP and Uric Acid Levels before Heart Transplantation are Independent Predictors of Adverse Outcomes in Young Adult Patients with Dilated Cardiomyopathy
• Effect and mechanism of T lymphocytes on human induced pluripotent stem cell-derived cardiomyocytes via Proteomics
• Effect of Atrial Septostomy on Left Ventricular Function in Pediatric Dilated Cardiomyopathy Requiring ECMO
• Efficacy of mesenchymal stem cell transplantation on major adverse cardiovascular events and cardiac function indices in patients with chronic heart failure: a meta-analysis of randomized controlled trials
• Emerging role of sphingolipids and extracellular vesicles in development and therapeutics of cardiovascular diseases
• Generation of four distinct isogenic cell lines with truncating variants in I-band or A-band titin
• Generation of human induced pluripotent stem cell (hiPSC) lines derived from three patients carrying the pathogenic CRYAB (A527G) mutation and one non-carrier family member
• Generation of two iPSC lines from dilated cardiomyopathy patients with pathogenic variants in the SCN5A gene
• Genetic analysis and family screening for dilated cardiomyopathy: a retrospective analysis of the stepwise pedigree approach
• Genotype is associated with left ventricular reverse remodelling and early events in recent-onset dilated cardiomyopathy
• Homozygosity for a Rare FASTKD2 Variant Resulting in an Adult Onset Autosomal Recessive Mitochondrial Podocytopathy
• How can we use stem cell-derived cardiomyocytes to understand the involvement of energetic metabolism in alterations of cardiac function?
• How Normal Is Low-Normal Left Ventricular Ejection Fraction in Familial Dilated Cardiomyopathy?
• Identification of a SCN5A Genetic Variant Associated With Type 1 Brugada Syndrome (BrS) in a Family
• Identification of novel TTN gene variant in a patient exhibiting severe dilated cardiomyopathy co-occurring with acute fibrinoid organizing pneumonia
• Identification of senescence related hub genes and potential therapeutic compounds for dilated cardiomyopathy via comprehensive transcriptome analysis
• Impact of Concurrent Ischaemic Stroke on Unfavourable Outcomes in Men and Women with Dilated Cardiomyopathy
• Impact of Heart Failure Etiology on Waitlist Mortality in Heart Transplant Candidates Supported With Extracorporeal Membrane Oxygenation
• Impella-assisted ventricular tachycardia ablation in a patient with dilated cardiomyopathy and electrical storm
• Increased expression of human endogenous retrovirus K in endomyocardial biopsies from patients with cardiomyopathy - a transcriptomics meta-analysis
• Lamin A/C deficiency-mediated ROS elevation contributes to pathogenic phenotypes of dilated cardiomyopathy in iPSC model
• Left ventricular apical pacing-induced heart failure in a child after congenital heart surgery: a case report
• Left Ventricular Non-compaction Cardiomyopathy: A Report of a Rare Case From Saudi Arabia
• LncRNA MAAMT facilitates macrophage recruitment and proinflammatory activation and exacerbates autoimmune myocarditis through the SRSF1/NF-κB axis
• Long-term risk of heart failure in adult cancer survivors: a systematic review and meta-analysis
• Luminescence "Turn-On" Sensing of Brain Natriuretic Peptide (BNP) - Dilated Cardiomyopathy Biomarker Based on the MoS(2) Nanosheet Quenched Terbium Citrate Complex
• Magnetic resonance mapping for the assessment of cardiomyopathies and myocardial disease
• Metabolic cycles: A unifying concept for energy transfer in the heart
• Mexican Registry of Cardiomyopathies: baseline data, diagnostic strategies, and treatment approaches in Mexico
• Multimodal Mapping of Electrical and Mechanical Latency of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocyte Layers
• Niacin supplementation in a child with novel MTTN variant m.5670A>G causing early onset mitochondrial myopathy and NAD⁺ deficiency
• Non-alcoholic fatty liver disease and heart failure: A comprehensive bioinformatics and Mendelian randomization analysis
• Nuclear envelope lamin-related dilated cardiomyopathy: a case series including histopathology
• Overcoming Double Jeopardy: Successful Orthotopic Heart Transplant in a Recipient With Bacterial and Fungal Infections
• Papillary Muscle Delayed Hyperenhancement: Prevalence and Clinical Implications in a Large Population With Dilated Cardiomyopathy
• Phospholamban Cardiomyopathy Leading to Advanced Heart Failure in an Active Duty Service Member
• Plasma Olink Proteomics Reveals Novel Biomarkers for Prediction and Diagnosis in Dilated Cardiomyopathy with Heart Failure
• Precision prediction of heart failure events in patients with dilated cardiomyopathy and mildly reduced ejection fraction using multi-parametric cardiovascular magnetic resonance
• Prediction of Positive Genetic Testing for Arrhythmogenic Left Ventricular Cardiomyopathy
• Pregnancy in women with genetic variants of dilated cardiomyopathy
• Prognostic implications of genotype findings in non-ischaemic dilated cardiomyopathy: A network meta-analysis
• Prognostic Significance of Biventricular and Biatrial Strain in Dilated Cardiomyopathy: Strain Analysis Derived from Cardiovascular Magnetic Resonance
• Prognostic Value of QRS Duration in Patients with Dilated Cardiomyopathy According to Left Ventricular Ejection Fraction
• Proteomic signatures improve risk prediction for common and rare diseases
• Pulmonary artery banding for cardiomyopathy in young children: First trial in China
• Pulsus alternans under left ventricular assist device in a patient with dilated cardiomyopathy and LMNA mutation
• Rationale, Design, and Interim Observations of the Steady Movement With Innovating Leadership for Heart Failure (SMILE HF) Registry: A Multicenter Prospective Cohort Registry for Patients With Acute Heart Failure
• Research landscape of genetics in dilated cardiomyopathy: insight from a bibliometric analysis
• RNA Helicase DDX5 Maintains Cardiac Function by Regulating <em>CamkIIδ</em> Alternative Splicing
• Ruxolitinib as a CaMKII Inhibitor for the Treatment of Cardiac Arrhythmias: Applications and Prospects
• Serum microRNA-125b-5p expression in patients with dilated cardiomyopathy combined with heart failure and its effect on myocardial fibrosis
• Sex-specific cardiovascular risk factors in the UK Biobank
• Sex-Specific Response to A1BG Loss Results in Female Dilated Cardiomyopathy
• Structural Cardiac Interventions in Patients With Heart Failure: JACC Scientific Statement
• Targeting SOCS2 alleviates myocardial fibrosis by reducing nuclear translocation of β-catenin
• The heart of celiac disease: understanding dilated cardiomyopathy, pathophysiology, and care-a systematic review
• Time Trends of Etiology, Treatment, and Long-Term Outcomes Among Patients with Left Ventricular Thrombus
• Titin Cardiomyopathy Associated With Refractory Ventricular Tachycardia: A Case Report
• Unraveling cardiomyocyte responses and intercellular communication alterations in primary carnitine deficiency cardiomyopathy via single-nucleus RNA sequencing
• Unraveling Nonketotic Hyperglycemia Hemichorea-Hemiballismus Syndrome: A Case Report of Diagnosis and Management
• Uric acid elevation in pediatric patients with dilated cardiomyopathy and prediction of mortality
• Ventricular assist device support in paediatric patients with restrictive cardiomyopathy - Clinical outcomes and haemodynamics
• Ventricular assist device support in paediatric patients with restrictive cardiomyopathy-clinical outcomes and haemodynamics
• Viral Myocarditis as a Factor Leading to the Development of Heart Failure Symptoms, Including the Role of Parvovirus B19 Infection-Systematic Review