Disease: Dilated cardiomyopathy
- A CASE OF ALSTRÖM SYNDROME WITH A NOVEL VARIANT IN ALMS1 GENE PRESENTING WITH CONE ROD DYSTROPHY AS FIRST FINDING
- A case of myotonic dystrophy type 1 with severe dilated cardiomyopathy: an unusual presenting manifestation of the most common muscular dystrophy in adults
- A Case report of Becker Muscular Dystrophy and Stroke who successfully regained Mobility with Robot Assisted Gait Training
- A Meta-Analysis Approach to Gene Regulatory Network Inference Identifies Key Regulators of Cardiovascular Diseases
- A novel gene-trap line reveals the dynamic patterns and essential roles of cysteine and glycine-rich protein 3 in zebrafish heart development and regeneration
- A Rare Treatable Cause of Cardiomyopathy: Primary Carnitine Deficiency
- A Valuable Genetically Engineered Nonhuman Primate Model of Dilated Cardiomyopathy
- Adipocyte-released adipomes in Chagas cardiomyopathy: Impact on cardiac metabolic and immune regulation
- Alterations in Mitochondrial Oxidative Phosphorylation System: Relationship of Complex V and Cardiac Dysfunction in Human Heart Failure
- Analysis of long-term prognosis and risk factors in patients with dilated cardiomyopathy
- Arrhythmias and cardiac MRI associations in patients with established cardiac dystrophinopathy
- Arrhythmogenic Left Ventricular Cardiomyopathy: From Diagnosis to Risk Management
- Association between dietary selenium and zinc intake and risk of dilated cardiomyopathy in children: a case-control study
- Association of NT-proBNP and sST2 with Left Ventricular Ejection Fraction and Oxidative Stress in Patients with Stable Dilated Cardiomyopathy
- Association of uncertain significance genetic variants with myocardial mechanics and morphometrics in patients with nonischemic dilated cardiomyopathy
- Author Correction: Development and validation of a risk model for intracardiac thrombosis in patients with dilated cardiomyopathy: a retrospective study
- Can a "broken heart" successfully be transplanted? A brief report
- Cardiac manifestations in inherited metabolic diseases
- Cardiac MRI for clinical dilated cardiomyopathy: Improved diagnostic power via combined T1, T2, and ECV
- Causal association of metformin treatment with diverse cardiovascular diseases: a Mendelian randomization analysis
- Causal Relationship Between Immune Cells/Cytokines and Dilated Cardiomyopathy
- Clinical and cardiac MRI characteristics: prognosis in patients with alcoholic cardiomyopathy
- Clinical and genetic analysis of a Chinese patient with Alström syndrome
- CMR Predictors of Favorable Outcome in Myocarditis: A Single-Center Experience
- Conservative Management of a Case of Peripartum Cardiomyopathy in a Young Multigravida
- Correction to: A case of myotonic dystrophy type 1 with severe dilated cardiomyopathy: an unusual presenting manifestation of the most common muscular dystrophy in adults
- Corrigendum: Secretoneurin levels are higher in dilated cardiomyopathy than in ischaemic cardiomyopathy: preliminary results
- Deciphering the role of SMARCA4 in cardiac disorders: Insights from single-cell studies on dilated cardiomyopathy and coronary heart disease
- Dilated cardiomyopathy associated with cardiotoxicity due to consumption of energy drinks
- Dilated cardiomyopathy due to hypocalcaemia: a case report
- Dilated cardiomyopathy-associated skeletal muscle actin (ACTA1) mutation R256H disrupts actin structure and function and causes cardiomyocyte hypocontractility
- Echocardiographic and electrocardiographic findings in Irish Wolfhounds eating high-pulse or low-pulse diets
- Effect of dapagliflozin on left ventricular structure and function in patients with non-ischemic dilated cardiomyopathy: An observational study
- Eosinophilic Myocarditis: From Bench to Bedside
- Evaluating convolutional neural network-enhanced electrocardiography for hypertrophic cardiomyopathy detection in a specialized cardiovascular setting
- Evaluation of cardiac arrhythmia in pediatric patients with Left Ventricular Assist Device (L-VAD)
- Exploring the Role of Platelets in Virus-Induced Inflammatory Demyelinating Disease and Myocarditis
- Expression and Potential Significance of miR-499 and IL-1beta in Serum of Dilated Cardiomyopathy Patients with Atrial Fibrillation
- Familial dilated cardiomyopathy in a child: a case report
- Fenofibrate Induces a Resolving Profile in Heart Macrophage Subsets and Attenuates Acute Chagas Myocarditis
- Ferroptosis in Cardiovascular Disease and Cardiomyopathies: Therapeutic Implications of Glutathione and Iron Chelating Agents
- Generation of a pluripotent stem cell line (UMGi270-A) and a corresponding CRISPR/Cas9 modified isogenic control (UMGi270-A-1) from a patient with sudden onset dilated cardiomyopathy harboring a FLNC p.R2187P mutation
- Genetic dilated cardiomyopathy with inflammation in an infant that responded to immunosuppressive therapy evaluated using cardiovascular magnetic resonance
- Harnessing molecular mechanism for precision medicine in dilated cardiomyopathy caused by a mutation in troponin T
- Heart in Disguise: Unmasking a Novel Gene Deletion in Dilated Cardiomyopathy
- HOIL-1L deficiency induces cell cycle alteration which causes immaturity of skeletal muscle and cardiomyocytes
- Implementing a clinical scientist-led screening clinic for hypertrophic and dilated cardiomyopathies
- Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy
- Integrated machine learning and multimodal data fusion for patho-phenotypic feature recognition in iPSC models of dilated cardiomyopathy
- Investigation of mutation spectrum amongst patients with familial primary cardiomyopathy using targeted NGS in Indian population
- KDM8 epigenetically controls cardiac metabolism to prevent initiation of dilated cardiomyopathy
- Left bundle branch block-induced dilated cardiomyopathy: Definitions, pathophysiology, and therapy
- Left Ventricular Longitudinal Strain Abnormalities in Childhood Exposure to Anthracycline Chemotherapy
- Left Ventricular Segmentation, Warping, and Myocardial Registration for Automated Strain Measurement
- LMNA p.Arg624His Variant Reduces Lamin Expression at mRNA Level: Elucidating Molecular Pathways toward Cardiac Involvement in Laminopathies
- Loss of ADAM15 in female mice does not worsen pressure overload cardiomyopathy, independent of ovarian hormones
- Low-Salt Diet Regulates the Metabolic and Signal Transduction Genomic Fabrics, and Remodels the Cardiac Normal and Chronic Pathological Pathways
- Management of incessant ventricular arrhythmias in a patient with left ventricular assist device: a case report
- Metabolomic insights in advanced cardiomyopathy of chronic chagasic and idiopathic patients that underwent heart transplant
- Minimally-Invasive Approach in the Setting of a Malignant Primary Cardiac Tumor
- Mitigation of Stress-induced Structural Remodeling and Functional Deficiency in iPSC-CMs with PLN R9C Mutation by Promoting Autophagy
- Mitochondrial extracellular vesicles, autoimmunity and myocarditis
- Mst4, a novel cardiac STRIPAK complex associated kinase, regulates cardiomyocyte growth and survival and is upregulated in human cardiomyopathy
- mTOR Inhibition Prolongs Survival and Has Beneficial Effects on Heart Function After Onset of Lamin A/C Gene Mutation Cardiomyopathy in Mice
- Myocardial injury in dogs: a retrospective analysis on etiological, echocardiographic, electrocardiographic, therapeutic, and outcome findings in 102 cases
- Nesprin proteins: bridging nuclear envelope dynamics to muscular dysfunction
- Nesprin-2 is a novel scaffold protein for telethonin and FHL-2 in the cardiomyocyte sarcomere
- New Guidelines of Pediatric Cardiac Implantable Electronic Devices: What Is Changing in Clinical Practice?
- Non-dilated left ventricular non-compaction cardiomyopathy with systolic dysfunction is reclassified as non-dilated left ventricular cardiomyopathy with hypertrabeculation
- Pathogenic mutations of human phosphorylation sites affect protein-protein interactions
- Penetrance of Dilated Cardiomyopathy in Genotype-Positive Relatives
- Potential Underestimation of Left Ventricular Mechanical Dyssynchrony in Dyssynchrony and Outcomes Assessment
- Precision therapy in dilated cardiomyopathy: Pipedream or paradigm shift?
- Predicting the Development of Dilated Cardiomyopathy in Kindred With Genetic Risk: Family Matters
- Pregnancy in women with dilated cardiomyopathy genetic variants
- Prevalence of Pathogenic Variants in Cardiomyopathy-Associated Genes in Acute Myocarditis: A Systematic Review and Meta-Analysis
- Primate Model Carrying LMNA Mutation Develops Dilated Cardiomyopathy
- Prognosis value of galectin-3 in patients with dilated cardiomyopathy: a meta-analysis
- Protein phosphatase 2A anchoring disruptor gene therapy for familial dilated cardiomyopathy
- Research trends and hotspots of circular RNA in cardiovascular disease: A bibliometric analysis
- Restrictive annuloplasty or replacement on reverse remodeling for nonischemic dilated cardiomyopathy
- Resveratrol Delays Diabetic Cardiomyopathy Fibrosis by Regulating Mitochondrial Autophagy
- Retracted: Multiomics Analysis of Transcriptome, Epigenome, and Genome Uncovers Putative Mechanisms for Dilated Cardiomyopathy
- Risk Factors Associated with <em>Toxoplasma gondii</em> in Patients with Cardiovascular Diseases from Western Romania
- RNA-Binding Proteins in Cardiomyopathies
- Role of Treg cell subsets in cardiovascular disease pathogenesis and potential therapeutic targets
- Screening for immune-related biomarkers associated with myasthenia gravis and dilated cardiomyopathy based on bioinformatics analysis and machine learning
- Second-Order Motion-Compensated Echo-Planar Cardiac Diffusion-Weighted MRI: Usefulness of Compressed Sensitivity Encoding
- Serum brain natriuretic peptide levels may be a useful marker for early diagnosis of cardiomyopathy secondary to neuroblastoma: A case report
- Short-term efficacy and safety of cardiac contractility modulation in patients with heart failure
- Subclinical systolic dysfunction in genotype-positive phenotype-negative relatives of dilated cardiomyopathy patients: A systematic review and meta-analysis
- Tachycardia Therapy Outcomes of Ischemic Versus Nonischemic Cardiomyopathy on Cardiac Resynchronization Therapy: A Propensity Score-matched Analysis
- Temporal progression of replacement and interstitial fibrosis in optimally managed dilated cardiomyopathy patients: A prospective study
- The Added Value of Advanced Echocardiography for the Morpho-Functional and Prognostic Evaluation of the Right Heart in Dilated Cardiomyopathy: Do Not Forget about the Right Atrium
- The first case report of de novo Crohn's disease after heart transplantation successfully treated with ustekinumab
- The importance of variant reinterpretation in inherited cardiovascular diseases: Establishing the optimal timeframe
- Titin: roles in cardiac function and diseases
- Unlocking the potential of sacubitril/valsartan therapy in improving ECG and echocardiographic parameters in heart failure patients with reduced ejection fraction (HErEF)
- Unraveling the Unsolved Mysteries of the Athletic Heart
- Variants in structural cardiac genes in patients with cancer therapy-related cardiac dysfunction after anthracycline chemotherapy: a case control study