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Academic Article Translational research on the mitral valve: from developmental mechanisms to new therapies.
Concept Ventricular Flutter
Concept Cytokines
Concept Muscle, Smooth, Vascular
Concept Membrane Proteins
Concept Enzyme-Linked Immunosorbent Assay
Concept Extracellular Matrix
Concept Age Factors
Concept Disease Models, Animal
Concept Maryland
Concept Calcium Channel Blockers
Concept PPAR alpha
Concept Maleimides
Concept Electrocardiography, Ambulatory
Concept Informed Consent
Concept Patient Selection
Concept Endocarditis
Concept DNA-Binding Proteins
Concept Magnetic Resonance Imaging, Cine
Concept Transforming Growth Factor beta
Concept Joint Instability
Concept Serum Amyloid A Protein
Concept Protein Folding
Concept RNA, Small Interfering
Concept Bone Development
Concept Biological Specimen Banks
Concept Blood Pressure
Concept Kaplan-Meier Estimate
Concept Cell Lineage
Concept Ankyrins
Concept Animals, Newborn
Concept Receptor, Angiotensin, Type 2
Concept Mitochondria
Concept Simethicone
Concept Endocardium
Concept Incidence
Concept Heart Block
Concept Proportional Hazards Models
Concept Genes, Tumor Suppressor
Concept Recurrence
Concept Drug Discovery
Concept Postmortem Changes
Concept Morbidity
Concept Ion Channels
Concept Marfan Syndrome
Concept Magnetic Resonance Imaging
Concept Age of Onset
Concept Actins
Concept Gene Expression
Concept Receptors, Transforming Growth Factor beta
Concept Membrane Potentials
Concept Desmosomes
Concept Rare Diseases
Concept Canada
Concept Pyrazoles
Concept Myocarditis
Concept Loeys-Dietz Syndrome
Concept Disease Progression
Concept Desmogleins
Concept Cadherins
Concept Sensitivity and Specificity
Concept Death, Sudden, Cardiac
Concept Aorta, Thoracic
Concept Anthracyclines
Concept Myopathies, Structural, Congenital
Concept Single-Blind Method
Concept Cell Adhesion
Concept Heart Transplantation
Concept Registries
Concept Treatment Outcome
Concept Brugada Syndrome
Concept Genes, Dominant
Concept Genomics
Concept Clinical Trials, Phase III as Topic
Concept Administration, Oral
Concept Child Development
Concept NIH 3T3 Cells
Concept Protein Kinase Inhibitors
Concept Genetic Testing
Concept Confidence Intervals
Concept Genetics
Concept Amino Acid Substitution
Concept Myosin Heavy Chains
Concept Animals
Concept Chi-Square Distribution
Concept Interviews as Topic
Concept Syndrome
Concept Stearic Acids
Concept Feasibility Studies
Concept Mitogen-Activated Protein Kinase 1
Concept Carrier Proteins
Concept Chronic Disease
Concept Adrenergic beta-Antagonists
Concept Electrophysiology
Concept Societies, Medical
Concept Plectin
Concept Magnetic Resonance Angiography
Concept Double-Blind Method
Concept Cell Cycle Proteins
Concept Statistics as Topic
Concept Amino Acid Sequence
Concept Disease-Free Survival
Concept Algorithms
Concept Mice, Knockout
Concept Vasodilator Agents
Concept Cohort Studies
Concept Nuclear Envelope
Concept Antibodies
Concept Boston
Concept Antineoplastic Agents
Concept Natriuretic Peptide, Brain
Concept Coronary Artery Disease
Concept Myocytes, Cardiac
Concept Multilevel Analysis
Concept Desmoplakins
Concept Mortality
Concept Calcium
Concept Nuclear Proteins
Concept Platelet Factor 4
Concept Clinical Trials, Phase II as Topic
Concept Chromosomes, Human, Pair 4
Concept Acute Disease
Concept Propranolol
Concept Coronary Vessels
Concept Recombinant Proteins
Concept Pancreatic Neoplasms
Concept Sarcomeres
Concept Smad2 Protein
Concept Preconception Care
Concept Cardiomyopathies
Concept Heart Failure
Concept Myocardial Infarction
Concept Genetics, Medical
Concept Genetic Predisposition to Disease
Concept Syncope
Concept Muscular Dystrophy, Emery-Dreifuss
Concept Benzoxazoles
Concept Disease Management
Concept Microfibrils
Concept Observer Variation
Concept Biopsy
Concept Myocardium
Concept Pregnancy Complications, Cardiovascular
Concept Head and Neck Neoplasms
Concept Amyloid
Concept Logistic Models
Concept Connexin 43
Concept Leukoencephalopathies
Concept Mice
Concept Contrast Media
Concept Cardiovascular Agents
Concept Arrhythmias, Cardiac
Concept Clinical Trials as Topic
Concept Myristates
Concept Mesoderm
Concept Sodium
Concept DNA Primers
Concept Immunoglobulin kappa-Chains
Concept Diastole
Concept Emergency Service, Hospital
Concept Delayed Diagnosis
Concept Ventricular Fibrillation
Concept Early Termination of Clinical Trials
Concept Barth Syndrome
Concept Linear Models
Concept Mitogen-Activated Protein Kinase 3
Concept Hypertrophy, Left Ventricular
Concept Echocardiography
Concept Microscopy, Confocal
Concept Fat Necrosis
Concept Pacemaker, Artificial
Concept Angiotensin II Type 1 Receptor Blockers
Concept Aortic Aneurysm
Concept Antihypertensive Agents
Concept Live Birth
Concept Melanoma
Concept Mitral Valve Prolapse
Concept Dopamine
Concept Matrix Metalloproteinase 9
Concept Patch-Clamp Techniques
Concept Sodium Channels
Concept Matrix Metalloproteinase 2
Concept Defibrillators, Implantable
Concept Mice, Inbred C57BL
Concept RNA, Transfer, Leu
Concept Bone Morphogenetic Proteins
Concept Polycystic Kidney, Autosomal Dominant
Concept Sarcoidosis
Concept Retrospective Studies
Concept Models, Statistical
Concept Cells, Cultured
Concept Isolated Noncompaction of the Ventricular Myocardium
Concept Mice, Transgenic
Concept Proteins
Concept Aortic Rupture
Concept Zebrafish Proteins
Concept Multivariate Analysis
Concept Mitogen-Activated Protein Kinase 14
Concept Mitral Valve Insufficiency
Concept Quality of Life
Concept Antigens, CD
Concept Gastrointestinal Hemorrhage
Concept Professional-Family Relations
Concept Cicatrix
Concept Mole Rats
Concept Heart Rate
Concept Hospitalization
Concept Ventricular Dysfunction, Left
Concept Hydralazine
Concept Exercise
Concept RNA Splice Sites
Concept Severity of Illness Index
Concept RNA, Messenger
Concept Cell Proliferation
Concept Survival Rate
Concept Expert Testimony
Concept MAP Kinase Signaling System
Concept Humans
Concept Heart
Concept Likelihood Functions
Concept Pericardium
Concept Desmocollins
Concept Cell Movement
Concept Heart Conduction System
Concept Homeodomain Proteins
Concept beta Catenin
Concept Receptor, Angiotensin, Type 1
Concept Cardiomyopathy, Hypertrophic
Concept Europe
Concept Chromosomes, Human, Pair 15
Concept Adaptor Proteins, Signal Transducing
Concept Cardiomegaly
Concept Dystrophin
Concept Longitudinal Studies
Concept TRPP Cation Channels
Concept Calpain
Concept Endomyocardial Fibrosis
Concept Glucuronidase
Concept Heart-Assist Devices
Concept Physical Conditioning, Animal
Concept Protein Modification, Translational
Concept Mitogen-Activated Protein Kinase 8
Concept Fatal Outcome
Concept Inflammation
Concept Cause of Death
Concept American Heart Association
Concept Plakophilins
Concept Genes, Mitochondrial
Concept Diabetic Neuropathies
Concept Protein Multimerization
Concept Ambulatory Care Facilities
Concept Giant Cells
Concept Aorta
Concept Neutralization Tests
Concept Microsatellite Repeats
Concept alpha-Galactosidase
Concept Atrial Fibrillation
Concept Muscular Dystrophy, Duchenne
Concept Health Care Costs
Concept Glucagonoma
Concept Survival Analysis
Concept Systole
Concept Angiotensin II
Concept Analysis of Variance
Concept Reverse Transcriptase Polymerase Chain Reaction
Concept Benzoates
Concept Molecular Diagnostic Techniques
Concept Cetrimonium Compounds
Concept Troponin T
Concept Calcium-Binding Proteins
Concept Smad4 Protein
Concept Protein Stability
Concept Amyloidosis
Concept Anti-Arrhythmia Agents
Concept Protein Structure, Quaternary
Concept Diuretics
Concept Action Potentials
Concept Desmoglein 3
Concept Interferon-alpha
Concept Friedreich Ataxia
Concept Angiotensin-Converting Enzyme Inhibitors
Concept Netherlands
Concept Genetic Counseling
Concept Physical Endurance
Concept Mass Screening
Concept Cardiomyopathy, Hypertrophic, Familial
Concept Ehlers-Danlos Syndrome
Concept Graft Rejection
Concept Prevalence
Concept Case-Control Studies
Concept Monoclonal Gammopathy of Undetermined Significance
Concept Body Surface Potential Mapping
Concept Induced Pluripotent Stem Cells
Concept Electrophysiologic Techniques, Cardiac
Concept Microfilament Proteins
Concept Aortic Aneurysm, Thoracic
Concept Predictive Value of Tests
Concept Reproducibility of Results
Concept Baltimore
Concept Prospective Studies
Concept Fabry Disease
Concept Amyloid Neuropathies, Familial
Concept Stem Cell Transplantation
Concept Cross-Sectional Studies
Concept Activin Receptors, Type I
Concept Sequence Homology, Amino Acid
Concept Skull
Concept Collagen
Concept Ventricular Dysfunction, Right
Concept Mitral Valve
Concept Biphenyl Compounds
Concept Codon, Nonsense
Concept Infant, Newborn
Concept Randomized Controlled Trials as Topic
Concept Progeria
Concept Evidence-Based Medicine
Concept Arrhythmogenic Right Ventricular Dysplasia
Concept Genome-Wide Association Study
Concept Arteriovenous Malformations
Concept Cardiomyopathy, Restrictive
Concept Losartan
Concept Proteomics
Concept Creatinine
Concept Cesarean Section
Concept Surveys and Questionnaires
Concept Fibrosis
Concept Enzyme Inhibitors
Concept Rats, Wistar
Concept Cell Line
Concept Myotonic Dystrophy
Concept Glucocorticoids
Concept Farnesyltranstransferase
Concept Heart Ventricles
Concept Fluoroscopy
Concept Point Mutation
Concept Nicotinic Acids
Concept Lymphatic Metastasis
Concept Muscular Dystrophies, Limb-Girdle
Concept Desmoglein 2
Concept Greece
Concept Polymerase Chain Reaction
Concept Indazoles
Concept United States
Concept Heart Valve Diseases
Concept Polyploidy
Concept Ethylenediamines
Concept Exercise Test
Concept Sulfonamides
Concept Myocardial Contraction
Concept Gene Deletion
Concept Epicardial Mapping
Concept Risk Assessment
Concept Skin Neoplasms
Concept In Situ Hybridization, Fluorescence
Concept Exercise Tolerance
Concept Cardiomyopathy, Dilated
Concept Tachycardia, Ventricular
Concept Cardiac Myosins
Concept Mutation, Missense
Concept Risk
Concept Lamin Type A
Concept Risk Factors
Concept Immunoglobulin lambda-Chains
Concept Tachycardia, Sinus
Concept gamma Catenin
Concept Sweden
Concept Base Sequence
Concept Alleles
Concept Follow-Up Studies
Concept Zebrafish
Concept Siblings
Concept Heart Diseases
Concept Immunohistochemistry
Concept Mice, Mutant Strains
Concept Molecular Sequence Data
Concept Tumor Suppressor Proteins
Concept Anthracenes
Concept Rats, Transgenic
Concept RNA-Binding Proteins
Concept Electrocardiography
Concept Mouth Mucosa
Concept Diagnostic Errors
Concept Age Distribution
Concept Troponin I
Academic Article Angiotensin II-dependent TGF-? signaling contributes to Loeys-Dietz syndrome vascular pathogenesis.
Academic Article Mitral valve disease--morphology and mechanisms.
Academic Article Right ventricular afterload sensitivity dramatically increases after left ventricular assist device implantation: A multi-center hemodynamic analysis.
Academic Article Targeted Mybpc3 Knock-Out Mice with Cardiac Hypertrophy Exhibit Structural Mitral Valve Abnormalities.
Academic Article Contemporary cardiac issues in Duchenne muscular dystrophy. Working Group of the National Heart, Lung, and Blood Institute in collaboration with Parent Project Muscular Dystrophy.
Academic Article Angiotensin II antagonism is associated with reduced risk for gastrointestinal bleeding caused by arteriovenous malformations in patients with left ventricular assist devices.
Academic Article Exercise has a disproportionate role in the pathogenesis of arrhythmogenic right ventricular dysplasia/cardiomyopathy in patients without desmosomal mutations.
Academic Article Genotype and Phenotype of Transthyretin Cardiac Amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey).
Academic Article Outcomes and ventricular tachycardia recurrence characteristics after epicardial ablation of ventricular tachycardia in arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article Allelic variation in normal human FBN1 expression in a family with Marfan syndrome: a potential modifier of phenotype?
Academic Article Clinical features of arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in plakophilin-2.
Academic Article Mechanisms of disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article Why should cardiologists consider genetic testing for hypertrophic cardiomyopathy?
Academic Article The benefit of upgrading chronically right ventricle-paced heart failure patients to resynchronization therapy demonstrated by strain rate imaging.
Academic Article Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome.
Academic Article Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriers.
Academic Article Exercise testing in asymptomatic gene carriers exposes a latent electrical substrate of arrhythmogenic right ventricular cardiomyopathy.
Academic Article Incremental value of cardiac magnetic resonance imaging in arrhythmic risk stratification of arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers.
Academic Article Malignant arrhythmogenic right ventricular dysplasia/cardiomyopathy with a normal 12-lead electrocardiogram: a rare but underrecognized clinical entity.
Academic Article Transthyretin cardiac amyloidosis: pathogenesis, treatments, and emerging role in heart failure with preserved ejection fraction.
Academic Article Use of a coronary sinus lead and biventricular ICD to correct a sensing abnormality in a patient with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article Untangling Wild-Type Transthyretin?Amyloidosis.
Academic Article Exercise increases age-related penetrance and arrhythmic risk in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers.
Academic Article Mutation-positive arrhythmogenic right ventricular dysplasia/cardiomyopathy: the triangle of dysplasia displaced.
Academic Article Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome.
Academic Article DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article Cardiac findings and events observed in an open-label clinical trial of tafamidis in patients with non-Val30Met and non-Val122Ile hereditary transthyretin amyloidosis.
Academic Article Angiotensin II blockade and aortic-root dilation in Marfan's syndrome.
Academic Article Prevalence of atrial arrhythmias in arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article Cardiac transplantation in arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members.
Academic Article Further evidence of harm from exercise in ARVD/C.
Academic Article A Pkd1-Fbn1 genetic interaction implicates TGF-? signaling in the pathogenesis of vascular complications in autosomal dominant polycystic kidney disease.
Academic Article Tafamidis in transthyretin amyloid cardiomyopathy: effects on transthyretin stabilization and clinical outcomes.
Academic Article Genetic evaluation of familial cardiomyopathy.
Academic Article Plasma BIN1 correlates with heart failure and predicts arrhythmia in patients with arrhythmogenic right ventricular cardiomyopathy.
Academic Article Current treatment of adult Duchenne muscular dystrophy.
Academic Article Effects of tafamidis on transthyretin stabilization and clinical outcomes in patients with non-Val30Met transthyretin amyloidosis.
Academic Article GLA-Ring Opportunities and Challenges for Fabry Disease.
Academic Article Optimization of Serum Immunoglobulin Free Light Chain Analysis for Subclassification of Cardiac Amyloidosis.
Academic Article The diagnosis of hypertrophic cardiomyopathy by cardiovascular magnetic resonance.
Academic Article Baseline Characteristics Predict the Presence of Amyloid on Endomyocardial Biopsy.
Academic Article Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis.
Academic Article Neonatal Transplantation Confers Maturation of PSC-Derived Cardiomyocytes Conducive to Modeling Cardiomyopathy.
Academic Article Penetrance of mutations in plakophilin-2 among families with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article Association of common variations on chromosome 4q25 and left atrial volume in patients with atrial fibrillation.
Academic Article Evaluation of Structural Progression in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
Academic Article Characterization of microsatellite markers flanking FBN1: utility in the diagnostic evaluation for Marfan syndrome.
Academic Article Fluctuating creatinine in the cardiac unit.
Academic Article Reversible dilated cardiomyopathy associated with glucagonoma.
Academic Article Genetic testing for dilated cardiomyopathy in clinical practice.
Academic Article Recessive arrhythmogenic right ventricular dysplasia due to novel cryptic splice mutation in PKP2.
Academic Article Outcomes of catheter ablation of ventricular tachycardia in arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article Shared desmosome gene findings in early and late onset arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype.
Academic Article Use of genetics in the clinical evaluation and management of heart failure.
Academic Article Approach to family screening in arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article Safety of American Heart Association-recommended minimum exercise for desmosomal mutation carriers.
Academic Article Genetic testing improves identification of transthyretin amyloid (ATTR) subtype in cardiac amyloidosis.
Academic Article Comparison of Features of Fatal Versus Nonfatal Cardiac Arrest in Patients With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
Academic Article Reader- and instrument-dependent variability in the electrocardiographic assessment of arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article TGF-beta-dependent pathogenesis of mitral valve prolapse in a mouse model of Marfan syndrome.
Academic Article Short-term effects of right-left heart sequential cardiac resynchronization in patients with heart failure, chronic atrial fibrillation, and atrioventricular nodal block.
Academic Article Arrhythmogenic right ventricular dysplasia/cardiomyopathy and cardiac sarcoidosis: distinguishing features when the diagnosis is unclear.
Academic Article Mutations in Alstr?m protein impair terminal differentiation of cardiomyocytes.
Academic Article Heart failure and genomics.
Academic Article The complex genetics of atrial fibrillation.
Academic Article Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy.
Academic Article Implantable Cardioverter-Defibrillator Therapy in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Predictors of Appropriate Therapy, Outcomes, and Complications.
Academic Article Cutaneous nerve biomarkers in transthyretin familial amyloid polyneuropathy.
Academic Article Surgical Correction of Tricuspid Regurgitation in Patients with ARVD/C.
Academic Article Giant Ring Mitochondria in a Patient With Heart Failure and Cerebral White Matter Disease Resulting From an MT-TL1 Mitochondrial Gene Mutation.
Academic Article Prospective evaluation of the morbidity and mortality of wild-type and V122I mutant transthyretin amyloid cardiomyopathy: the Transthyretin Amyloidosis Cardiac Study (TRACS).
Academic Article Intracardiac giant cells after left ventricular assist device placement.
Academic Article Morphologic variants of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy a genetics-magnetic resonance imaging correlation study.
Academic Article Long-term safety and efficacy of tafamidis for the treatment of hereditary transthyretin amyloid polyneuropathy: results up to 6 years.
Academic Article Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice.
Academic Article The Clinical Utility of the Heparin Neutralization Assay in the Diagnosis of Heparin-Induced Thrombocytopenia.
Academic Article A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2.
Academic Article A deleterious gene-by-environment interaction imposed by calcium channel blockers in Marfan syndrome.
Academic Article The Role of Genetics in Peripartum Cardiomyopathy.
Academic Article Role of Genetic Testing in Inherited Cardiovascular Disease: A Review.
Academic Article Multi-scale biomechanical remodeling in aging and genetic mutant murine mitral valve leaflets: insights into Marfan syndrome.
Academic Article Prolonged RV endocardial activation duration: a novel marker of arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article Management of Cardiac Involvement Associated With Neuromuscular Diseases: A Scientific Statement From the American Heart Association.
Academic Article Heart Failure Is Common and Under-Recognized in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia.
Academic Article Familial amyloid cardiomyopathy due to TTR mutations: an underdiagnosed cause of restrictive cardiomyopathy [corrected].
Academic Article Novel and highly lethal NKX2.5 missense mutation in a family with sudden death and ventricular arrhythmia.
Academic Article Inheritance Impacts Mitral Valve Insufficiency.
Academic Article Identification of a new modulator of the intercalated disc in a zebrafish model of arrhythmogenic cardiomyopathy.
Academic Article Loss of elastic fiber integrity and reduction of vascular smooth muscle contraction resulting from the upregulated activities of matrix metalloproteinase-2 and -9 in the thoracic aortic aneurysm in Marfan syndrome.
Academic Article The change in B-type natriuretic peptide levels over time predicts significant rejection in cardiac transplant recipients.
Academic Article Long-term efficacy of catheter ablation of ventricular tachycardia in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article Relationship between monoclonal gammopathy and cardiac amyloid type.
Academic Article Pregnancy course and outcomes in women with arrhythmogenic right ventricular cardiomyopathy.
Academic Article Noncanonical TGF? signaling contributes to aortic aneurysm progression in Marfan syndrome mice.
Academic Article Angiotensin II type 2 receptor signaling attenuates aortic aneurysm in mice through ERK antagonism.
Academic Article Absence of a Primary Role for SCN10A Mutations in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
Academic Article Lack of Relationship Between Serum Cardiac Troponin I Level and Giant Cell Myocarditis Diagnosis and Outcomes.
Academic Article Yield of serial evaluation in at-risk family members of patients with ARVD/C.
Academic Article Therapy of Marfan syndrome.
Academic Article Sildenafil does not improve cardiomyopathy in Duchenne/Becker muscular dystrophy.
Academic Article Characterizing the Molecular Pathology of Arrhythmogenic Cardiomyopathy in Patient Buccal Mucosa Cells.
Academic Article The variable natural history of idiopathic dilated cardiomyopathy.
Academic Article A clinical approach to a family history of sudden death.
Academic Article Mechanism of Action and Clinical Application of Tafamidis in Hereditary Transthyretin Amyloidosis.
Academic Article Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise.
Academic Article Comprehensive Versus Targeted Genetic Testing in Children with Hypertrophic Cardiomyopathy.
Academic Article Arrhythmogenic right ventricular dysplasia/cardiomyopathy: a family affair.
Academic Article Performance of the 2015 International Task Force Consensus Statement Risk Stratification Algorithm for Implantable Cardioverter-Defibrillator Placement in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
Academic Article Extensive cardiac allograft vasculitis and concurrent fat necrosis 6 years after orthotopic heart transplantation.
Academic Article Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline.
Academic Article Reversible cardiomyopathy caused by administration of interferon alpha.
Academic Article Familial hypertrophic cardiomyopathy associated with cardiac beta-myosin heavy chain and troponin I mutations.
Academic Article Pathophysiology and therapy of cardiac dysfunction in Duchenne muscular dystrophy.
Academic Article KLOTHO allele status and the risk of early-onset occult coronary artery disease.
Academic Article Marfan's syndrome.
Academic Article Arrhythmogenic right ventricular dysplasia: a United States experience.
Academic Article Use of genetics in the clinical evaluation of cardiomyopathy.
Academic Article Mitral valve disease in Marfan syndrome and related disorders.
Academic Article Central role for GSK3? in the pathogenesis of arrhythmogenic cardiomyopathy.
Academic Article Comprehensive desmosome mutation analysis in north americans with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article The mitral valve in hypertrophic cardiomyopathy: old versus new concepts.
Academic Article Incidence and predictors of implantable cardioverter-defibrillator therapy in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy undergoing implantable cardioverter-defibrillator implantation for primary prevention.
Academic Article LMNA-associated cardiocutaneous progeria: an inherited autosomal dominant premature aging syndrome with late onset.
Academic Article Risk stratification in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers.
Academic Article Cardiac phenotype and long-term prognosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia patients with late presentation.
Academic Article Protein molecular modeling techniques investigating novel TAB2 variant R347X causing cardiomyopathy and congenital heart defects in multigenerational family.
Academic Article Identification of sarcomeric variants in probands with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC).
Academic Article Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy in the Pediatric?Population: Clinical Characterization and Comparison With?Adult-Onset?Disease.
Academic Article Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Academic Article Bringing Autopsies Into the Molecular Genetic Era.
Academic Article Managing Secondary Genomic Findings Associated With Arrhythmogenic Right Ventricular Cardiomyopathy: Case Studies and Proposal for Clinical Surveillance.
Academic Article Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy.
Academic Article No major role for rare plectin variants in arrhythmogenic right ventricular cardiomyopathy.
Academic Article Seven factors predict a delayed diagnosis of cardiac amyloidosis.
Academic Article Cardiac Management of the Patient With Duchenne Muscular Dystrophy.
Academic Article Four-Chamber Intracardiac Thrombi Complicating Wild-Type TTR Amyloidosis.
Academic Article Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy.
Academic Article Transthyretin Stabilization by AG10 in Symptomatic Transthyretin Amyloid?Cardiomyopathy.
Academic Article A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy.
Academic Article Correction: Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Academic Article 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy.
Academic Article Genetic aetiologies should be considered in paediatric cases of acute heart failure presumed to be myocarditis.
Academic Article Definition and treatment of arrhythmogenic cardiomyopathy: an updated expert panel report.
Academic Article Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy.
Academic Article Positive family history decreases diagnosis time by over 200.
Academic Article Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De Novo.
Academic Article Therapeutic Modulation of the Immune Response in Arrhythmogenic Cardiomyopathy.
Academic Article Tnni3k alleles influence ventricular mononuclear diploid cardiomyocyte frequency.
Academic Article SSRI/SNRI Therapy is Associated With a Higher Risk of Gastrointestinal Bleeding in LVAD Patients.
Academic Article 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summary.
Academic Article FLNC truncations cause arrhythmogenic right ventricular cardiomyopathy.
Academic Article Safety and Utility of Cardiopulmonary Exercise Testing in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia.
Academic Article Genetic Dilated Cardiomyopathy Due to TTN Variants Without Known Familial Disease.
Academic Article Sudden Cardiac Death Prediction in Arrhythmogenic Right Ventricular Cardiomyopathy: A Multinational Collaboration.
Academic Article Multivalvular Pulsus Alternans.
Academic Article Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features.
Academic Article Exercise triggers CAPN1-mediated AIF truncation, inducing myocyte cell death in arrhythmogenic cardiomyopathy.
Academic Article Influence of Panel Selection on Yield of Clinically Useful Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Families.
Academic Article Efficacy and safety of tafamidis doses in the Tafamidis in Transthyretin Cardiomyopathy Clinical Trial (ATTR-ACT) and long-term extension study.
Academic Article The prevalent I686T human variant and loss-of-function mutations in the cardiomyocyte-specific kinase gene TNNI3K cause adverse contractility and concentric remodeling in mice.
Academic Article Management of heart failure in cardiac amyloidosis using an ambulatory diuresis clinic.
Academic Article Genetic and Phenotypic Landscape of Peripartum Cardiomyopathy.
Academic Article Drug Discovery and Development in Rare Diseases: Taking a Closer Look at the Tafamidis Story.
Academic Article International Evidence Based Reappraisal of Genes Associated With Arrhythmogenic Right Ventricular Cardiomyopathy Using the Clinical Genome Resource Framework.
Academic Article Evidence-Based Assessment of Genes in Dilated Cardiomyopathy.
Academic Article Phase 3 Multicenter Study of Revusiran in Patients with Hereditary Transthyretin-Mediated (hATTR) Amyloidosis with Cardiomyopathy (ENDEAVOUR).
Academic Article Correction to: Phase 3 Multicenter Study of Revusiran in Patients with Hereditary Transthyretin-Mediated (hATTR) Amyloidosis with Cardiomyopathy (ENDEAVOUR).
Academic Article Hypermobile Ehlers-Danlos syndromes: Complex phenotypes, challenging diagnoses, and poorly understood causes.
Academic Article Endomyocardial Biopsy Characterization of Heart?Failure With Preserved Ejection?Fraction and Prevalence of Cardiac Amyloidosis.
Concept Single-Cell Analysis
Concept Amyloidogenic Proteins
Concept Cardiac Resynchronization Therapy
Concept Walk Test
Concept Laser Capture Microdissection
Concept NAV1.5 Voltage-Gated Sodium Channel
Concept NAV1.8 Voltage-Gated Sodium Channel
Concept CRISPR-Cas Systems
Concept Connectin
Concept Filamins
Concept Protein Kinase C beta
Concept Vascular Remodeling
Concept Mouse Embryonic Stem Cells
Concept Clinical Decision-Making
Concept Gene Editing
Concept RNAi Therapeutics
Concept Sildenafil Citrate
Concept Serotonin and Noradrenaline Reuptake Inhibitors
Concept Loss of Function Mutation
Concept Fibrillin-1
Concept Protein Domains
Concept Homeobox Protein Nkx-2.5
Concept Mice, 129 Strain
Concept HEK293 Cells
Concept Haploinsufficiency
Concept Angiotensin Receptor Antagonists
Academic Article Natural history and progression of transthyretin amyloid cardiomyopathy: insights from ATTR-ACT.
Academic Article Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants.
Academic Article Wild-Type Transthyretin Cardiac Amyloidosis Is Associated with Increased Antecedent Physical Activity.
Academic Article Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy.
Academic Article The response to cardiac resynchronization therapy in LMNA cardiomyopathy.
Academic Article A pragmatic implementation research study for In Our DNA SC: a protocol to identify multi-level factors that support the implementation of a population-wide genomic screening initiative in diverse populations.
Academic Article How did transthyretin amyloid cardiomyopathy progress in patients who took placebo in the study ATTR-ACT? A plain language summary.
Academic Article ATTR Epidemiology, Genetics, and Prognostic Factors.
Academic Article A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy.
Academic Article PLEKHM2 Loss-of-Function Is Associated With Dilated Cardiomyopathy.
Academic Article Counseling Family Members and Monitoring for Evidence of Disease in Asymptomatic Carriers of Amyloid Transthyretin Cardiac Amyloidosis.
Academic Article Knowledge of Genome Sequencing and Trust in Medical Researchers Among Patients of Different Racial and Ethnic Groups With Idiopathic Dilated Cardiomyopathy.
Academic Article Efficacy and Safety of ARRY-371797 in LMNA-Related Dilated Cardiomyopathy: A Phase 2 Study.
Academic Article Lessons Learned from the Pilot Phase of a Population-Wide Genomic Screening Program: Building the Base to Reach a Diverse Cohort of 100,000 Participants.
Academic Article Long-Term Efficacy and Safety of ARRY-371797 (PF-07265803) in Patients With Lamin A/C-Related Dilated Cardiomyopathy.
Academic Article Efficacy and Safety of Angiotensin Receptor Blockers in a Pre-Clinical Model of Arrhythmogenic Cardiomyopathy.
Academic Article Plain Language Summary of Publication of the safety and efficacy of ARRY-371797 in people with dilated cardiomyopathy and a faulty LMNA gene.
Academic Article Effectiveness of the Family Heart Talk Communication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized Trial.
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