Item Type | Name |
Academic Article
|
The learning curve for sentinel node biopsy in breast cancer: practical considerations.
|
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
|
Maleimides
|
Concept
|
Electrocardiography, Ambulatory
|
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
|
Costs and Cost Analysis
|
Concept
|
Simethicone
|
Concept
|
Endocardium
|
Concept
|
Incidence
|
Concept
|
Proportional Hazards Models
|
Concept
|
Genes, Tumor Suppressor
|
Concept
|
Recurrence
|
Concept
|
Drug Discovery
|
Concept
|
Postmortem Changes
|
Concept
|
Morbidity
|
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
|
Single-Blind Method
|
Concept
|
Cell Adhesion
|
Concept
|
Heart Transplantation
|
Concept
|
Registries
|
Concept
|
Treatment Outcome
|
Concept
|
Brugada Syndrome
|
Concept
|
Genes, Dominant
|
Concept
|
Genomics
|
Concept
|
Administration, Oral
|
Concept
|
Child Development
|
Concept
|
NIH 3T3 Cells
|
Concept
|
Protein Kinase Inhibitors
|
Concept
|
Genetic Testing
|
Concept
|
Confidence Intervals
|
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
|
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
|
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
|
Benzoxazoles
|
Concept
|
Disease Management
|
Concept
|
Serotonin Uptake Inhibitors
|
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
|
Chromosomes, Human, Pair 6
|
Concept
|
DNA Primers
|
Concept
|
Immunoglobulin kappa-Chains
|
Concept
|
Emergency Service, Hospital
|
Concept
|
Delayed Diagnosis
|
Concept
|
Ventricular Fibrillation
|
Concept
|
Early Termination of Clinical Trials
|
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
|
Multivariate Analysis
|
Concept
|
Decision Support Techniques
|
Concept
|
Mitral Valve Insufficiency
|
Concept
|
Quality of Life
|
Concept
|
Antigens, CD
|
Concept
|
Epitopes
|
Concept
|
Gastrointestinal Hemorrhage
|
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
|
Transgenes
|
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
|
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
|
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
|
Clinical Competence
|
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
|
Angiotensin-Converting Enzyme Inhibitors
|
Concept
|
Netherlands
|
Concept
|
Genetic Counseling
|
Concept
|
Physical Endurance
|
Concept
|
Cardiomyopathy, Hypertrophic, Familial
|
Concept
|
Ehlers-Danlos Syndrome
|
Concept
|
Graft Rejection
|
Concept
|
Prevalence
|
Concept
|
Case-Control Studies
|
Concept
|
Monoclonal Gammopathy of Undetermined Significance
|
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
|
African Americans
|
Concept
|
Ventricular Dysfunction, Right
|
Concept
|
Mitral Valve
|
Concept
|
Biphenyl Compounds
|
Concept
|
Codon, Nonsense
|
Concept
|
Infant, Newborn
|
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
|
Breast Neoplasms
|
Concept
|
Chromosome Deletion
|
Concept
|
Glucocorticoids
|
Concept
|
Farnesyltranstransferase
|
Concept
|
Heart Ventricles
|
Concept
|
Fluoroscopy
|
Concept
|
Point Mutation
|
Concept
|
Nicotinic Acids
|
Concept
|
Lymphatic Metastasis
|
Concept
|
Desmoglein 2
|
Concept
|
Greece
|
Concept
|
Polymerase Chain Reaction
|
Concept
|
Cardiovascular Abnormalities
|
Concept
|
United States
|
Concept
|
Heart Valve Diseases
|
Concept
|
Polyploidy
|
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
|
Branchio-Oto-Renal Syndrome
|
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-ß 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
|
The learning curve for sentinel node biopsy in breast cancer: practical considerations.
|
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-ß 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
|
Evidence for a critical contribution of haploinsufficiency in the complex pathogenesis of Marfan syndrome.
|
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
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Comparison of Features of Fatal Versus Nonfatal Cardiac Arrest in Patients With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
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Academic Article
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Reader- and instrument-dependent variability in the electrocardiographic assessment of arrhythmogenic right ventricular dysplasia/cardiomyopathy.
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Academic Article
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TGF-beta-dependent pathogenesis of mitral valve prolapse in a mouse model of Marfan syndrome.
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Academic Article
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Arrhythmogenic right ventricular dysplasia/cardiomyopathy and cardiac sarcoidosis: distinguishing features when the diagnosis is unclear.
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Academic Article
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Mutations in Alström protein impair terminal differentiation of cardiomyocytes.
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Academic Article
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Heart failure and genomics.
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Academic Article
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The learning curve for sentinel node biopsy in breast cancer: practical considerations.
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Academic Article
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Implantable Cardioverter-Defibrillator Therapy in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Predictors of Appropriate Therapy, Outcomes, and Complications.
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Academic Article
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Cutaneous nerve biomarkers in transthyretin familial amyloid polyneuropathy.
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Academic Article
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Surgical Correction of Tricuspid Regurgitation in Patients with ARVD/C.
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Academic Article
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Giant Ring Mitochondria in a Patient With Heart Failure and Cerebral White Matter Disease Resulting From an MT-TL1 Mitochondrial Gene Mutation.
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Academic Article
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Prospective evaluation of the morbidity and mortality of wild-type and V122I mutant transthyretin amyloid cardiomyopathy: the Transthyretin Amyloidosis Cardiac Study (TRACS).
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Academic Article
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Intracardiac giant cells after left ventricular assist device placement.
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Academic Article
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Morphologic variants of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy a genetics-magnetic resonance imaging correlation study.
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Academic Article
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Long-term safety and efficacy of tafamidis for the treatment of hereditary transthyretin amyloid polyneuropathy: results up to 6 years.
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Academic Article
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Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice.
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Academic Article
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The Clinical Utility of the Heparin Neutralization Assay in the Diagnosis of Heparin-Induced Thrombocytopenia.
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Academic Article
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A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2.
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Academic Article
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A deleterious gene-by-environment interaction imposed by calcium channel blockers in Marfan syndrome.
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Academic Article
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The Role of Genetics in Peripartum Cardiomyopathy.
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Academic Article
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Multi-scale biomechanical remodeling in aging and genetic mutant murine mitral valve leaflets: insights into Marfan syndrome.
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Academic Article
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The learning curve for sentinel node biopsy in breast cancer: practical considerations.
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Academic Article
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Heart Failure Is Common and Under-Recognized in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia.
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Academic Article
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Familial amyloid cardiomyopathy due to TTR mutations: an underdiagnosed cause of restrictive cardiomyopathy [corrected].
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Academic Article
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Novel and highly lethal NKX2.5 missense mutation in a family with sudden death and ventricular arrhythmia.
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Academic Article
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Inheritance Impacts Mitral Valve Insufficiency.
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Academic Article
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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.
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Academic Article
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The change in B-type natriuretic peptide levels over time predicts significant rejection in cardiac transplant recipients.
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Academic Article
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Long-term efficacy of catheter ablation of ventricular tachycardia in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
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Academic Article
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Relationship between monoclonal gammopathy and cardiac amyloid type.
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Academic Article
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Pregnancy course and outcomes in women with arrhythmogenic right ventricular cardiomyopathy.
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Academic Article
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Noncanonical TGFß signaling contributes to aortic aneurysm progression in Marfan syndrome mice.
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Academic Article
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Angiotensin II type 2 receptor signaling attenuates aortic aneurysm in mice through ERK antagonism.
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Academic Article
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Absence of a Primary Role for SCN10A Mutations in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
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Academic Article
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Lack of Relationship Between Serum Cardiac Troponin I Level and Giant Cell Myocarditis Diagnosis and Outcomes.
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Academic Article
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Yield of serial evaluation in at-risk family members of patients with ARVD/C.
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Academic Article
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Therapy of Marfan syndrome.
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Academic Article
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Sildenafil does not improve cardiomyopathy in Duchenne/Becker muscular dystrophy.
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Academic Article
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Characterizing the Molecular Pathology of Arrhythmogenic Cardiomyopathy in Patient Buccal Mucosa Cells.
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Academic Article
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The variable natural history of idiopathic dilated cardiomyopathy.
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Academic Article
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A clinical approach to a family history of sudden death.
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Academic Article
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Mechanism of Action and Clinical Application of Tafamidis in Hereditary Transthyretin Amyloidosis.
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Academic Article
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Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise.
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Academic Article
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A family with a complex clinical presentation characterized by arrhythmogenic right ventricular dysplasia/cardiomyopathy and features of branchio-oculo-facial syndrome.
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Academic Article
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Comprehensive Versus Targeted Genetic Testing in Children with Hypertrophic Cardiomyopathy.
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Academic Article
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Arrhythmogenic right ventricular dysplasia/cardiomyopathy: a family affair.
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Academic Article
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Performance of the 2015 International Task Force Consensus Statement Risk Stratification Algorithm for Implantable Cardioverter-Defibrillator Placement in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
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Academic Article
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Extensive cardiac allograft vasculitis and concurrent fat necrosis 6 years after orthotopic heart transplantation.
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Academic Article
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Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline.
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Academic Article
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Reversible cardiomyopathy caused by administration of interferon alpha.
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Academic Article
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Familial hypertrophic cardiomyopathy associated with cardiac beta-myosin heavy chain and troponin I mutations.
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Academic Article
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Pathophysiology and therapy of cardiac dysfunction in Duchenne muscular dystrophy.
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Academic Article
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KLOTHO allele status and the risk of early-onset occult coronary artery disease.
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Academic Article
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Marfan's syndrome.
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Academic Article
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Arrhythmogenic right ventricular dysplasia: a United States experience.
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Academic Article
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Use of genetics in the clinical evaluation of cardiomyopathy.
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Academic Article
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Mitral valve disease in Marfan syndrome and related disorders.
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Academic Article
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Central role for GSK3ß in the pathogenesis of arrhythmogenic cardiomyopathy.
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Academic Article
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Comprehensive desmosome mutation analysis in north americans with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
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Academic Article
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The mitral valve in hypertrophic cardiomyopathy: old versus new concepts.
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Academic Article
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Incidence and predictors of implantable cardioverter-defibrillator therapy in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy undergoing implantable cardioverter-defibrillator implantation for primary prevention.
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Academic Article
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LMNA-associated cardiocutaneous progeria: an inherited autosomal dominant premature aging syndrome with late onset.
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Academic Article
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Risk stratification in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers.
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Academic Article
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Cardiac phenotype and long-term prognosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia patients with late presentation.
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Academic Article
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Protein molecular modeling techniques investigating novel TAB2 variant R347X causing cardiomyopathy and congenital heart defects in multigenerational family.
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Academic Article
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Identification of sarcomeric variants in probands with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC).
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Academic Article
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Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy in the Pediatric Population: Clinical Characterization and Comparison With Adult-Onset Disease.
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Academic Article
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Bringing Autopsies Into the Molecular Genetic Era.
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Academic Article
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Managing Secondary Genomic Findings Associated With Arrhythmogenic Right Ventricular Cardiomyopathy: Case Studies and Proposal for Clinical Surveillance.
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Academic Article
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Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy.
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Academic Article
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No major role for rare plectin variants in arrhythmogenic right ventricular cardiomyopathy.
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Academic Article
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Seven factors predict a delayed diagnosis of cardiac amyloidosis.
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Academic Article
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Cardiac Management of the Patient With Duchenne Muscular Dystrophy.
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Academic Article
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Four-Chamber Intracardiac Thrombi Complicating Wild-Type TTR Amyloidosis.
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Academic Article
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Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy.
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Academic Article
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Transthyretin Stabilization by AG10 in Symptomatic Transthyretin Amyloid Cardiomyopathy.
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Academic Article
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A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy.
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Academic Article
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Genetic aetiologies should be considered in paediatric cases of acute heart failure presumed to be myocarditis.
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Academic Article
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Definition and treatment of arrhythmogenic cardiomyopathy: an updated expert panel report.
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Academic Article
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Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy.
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Academic Article
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Positive family history decreases diagnosis time by over 200.
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Academic Article
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Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De Novo.
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Academic Article
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Therapeutic Modulation of the Immune Response in Arrhythmogenic Cardiomyopathy.
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Academic Article
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Tnni3k alleles influence ventricular mononuclear diploid cardiomyocyte frequency.
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Academic Article
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SSRI/SNRI Therapy is Associated With a Higher Risk of Gastrointestinal Bleeding in LVAD Patients.
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Academic Article
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FLNC truncations cause arrhythmogenic right ventricular cardiomyopathy.
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Academic Article
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Safety and Utility of Cardiopulmonary Exercise Testing in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia.
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Academic Article
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Genetic Dilated Cardiomyopathy Due to TTN Variants Without Known Familial Disease.
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Academic Article
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Sudden Cardiac Death Prediction in Arrhythmogenic Right Ventricular Cardiomyopathy: A Multinational Collaboration.
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Academic Article
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Multivalvular Pulsus Alternans.
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Academic Article
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Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features.
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Academic Article
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Influence of Panel Selection on Yield of Clinically Useful Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Families.
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Academic Article
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Efficacy and safety of tafamidis doses in the Tafamidis in Transthyretin Cardiomyopathy Clinical Trial (ATTR-ACT) and long-term extension study.
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Academic Article
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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.
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Academic Article
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Management of heart failure in cardiac amyloidosis using an ambulatory diuresis clinic.
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Academic Article
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Genetic and Phenotypic Landscape of Peripartum Cardiomyopathy.
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Academic Article
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Drug Discovery and Development in Rare Diseases: Taking a Closer Look at the Tafamidis Story.
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Academic Article
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International Evidence Based Reappraisal of Genes Associated With Arrhythmogenic Right Ventricular Cardiomyopathy Using the Clinical Genome Resource Framework.
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Academic Article
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Evidence-Based Assessment of Genes in Dilated Cardiomyopathy.
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Academic Article
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Phase 3 Multicenter Study of Revusiran in Patients with Hereditary Transthyretin-Mediated (hATTR) Amyloidosis with Cardiomyopathy (ENDEAVOUR).
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Academic Article
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Correction to: Phase 3 Multicenter Study of Revusiran in Patients with Hereditary Transthyretin-Mediated (hATTR) Amyloidosis with Cardiomyopathy (ENDEAVOUR).
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Academic Article
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Hypermobile Ehlers-Danlos syndromes: Complex phenotypes, challenging diagnoses, and poorly understood causes.
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Academic Article
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Endomyocardial Biopsy Characterization of Heart Failure With Preserved Ejection Fraction and Prevalence of Cardiac Amyloidosis.
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Concept
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Single-Cell Analysis
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Concept
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Amyloidogenic Proteins
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Concept
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Cardiac Resynchronization Therapy
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Concept
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Walk Test
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Concept
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Laser Capture Microdissection
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Concept
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NAV1.5 Voltage-Gated Sodium Channel
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Concept
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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
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Academic Article
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Natural history and progression of transthyretin amyloid cardiomyopathy: insights from ATTR-ACT.
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Academic Article
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Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants.
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Academic Article
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Wild-Type Transthyretin Cardiac Amyloidosis Is Associated with Increased Antecedent Physical Activity.
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Academic Article
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Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy.
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Academic Article
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The response to cardiac resynchronization therapy in LMNA cardiomyopathy.
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Academic Article
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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.
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Academic Article
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How did transthyretin amyloid cardiomyopathy progress in patients who took placebo in the study ATTR-ACT? A plain language summary.
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Academic Article
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ATTR Epidemiology, Genetics, and Prognostic Factors.
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Academic Article
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A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy.
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Academic Article
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PLEKHM2 Loss-of-Function Is Associated With Dilated Cardiomyopathy.
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