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Judge, Daniel
One or more keywords matched the following items that are connected to Judge, Daniel
Item TypeName
Concept Cytokines
Concept Piperazines
Concept Enzyme-Linked Immunosorbent Assay
Concept Extracellular Matrix
Concept Age Factors
Concept Disease Models, Animal
Concept Fibroblasts
Concept Drug Administration Schedule
Concept Sequence Analysis, DNA
Concept Maleimides
Concept Elastin
Concept Electrocardiography, Ambulatory
Concept Informed Consent
Concept Magnetic Resonance Imaging, Cine
Concept Transforming Growth Factor beta
Concept Bone Development
Concept Diagnostic Techniques, Cardiovascular
Concept Blood Pressure
Concept Kaplan-Meier Estimate
Concept Genetic Association Studies
Concept Cell Lineage
Concept Equipment Failure
Concept False Negative Reactions
Concept Incidence
Concept Proportional Hazards Models
Concept Genes, Tumor Suppressor
Concept Electric Countershock
Concept Heterozygote
Concept Morbidity
Concept Marfan Syndrome
Concept Epistasis, Genetic
Concept Magnetic Resonance Imaging
Concept Age of Onset
Concept Drug Therapy, Combination
Concept Practice Guidelines as Topic
Concept Pyrazoles
Concept Loeys-Dietz Syndrome
Concept Desmogleins
Concept Cadherins
Concept Sensitivity and Specificity
Concept Death, Sudden, Cardiac
Concept Aorta, Thoracic
Concept Single-Blind Method
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 Thrombocytopenia
Concept Amino Acid Substitution
Concept Chi-Square Distribution
Concept Interviews as Topic
Concept Apoptosis Inducing Factor
Concept Feasibility Studies
Concept Heparin
Concept Mitogen-Activated Protein Kinase 1
Concept Electrophysiology
Concept Magnetic Resonance Angiography
Concept Double-Blind Method
Concept Statistics as Topic
Concept Disease-Free Survival
Concept Algorithms
Concept Mice, Knockout
Concept Cohort Studies
Concept Antibodies
Concept Coronary Artery Disease
Concept Mortality
Concept Platelet Factor 4
Concept Clinical Trials, Phase II as Topic
Concept Chromosomes, Human, Pair 4
Concept Propranolol
Concept Pancreatic Neoplasms
Concept Smad2 Protein
Concept Ventricular Remodeling
Concept Genetics, Medical
Concept Genetic Predisposition to Disease
Concept Syncope
Concept Muscular Dystrophy, Emery-Dreifuss
Concept Microfibrils
Concept Observer Variation
Concept Biopsy
Concept Cardiac Output
Concept Up-Regulation
Concept Early Diagnosis
Concept Stroke Volume
Concept Logistic Models
Concept Prealbumin
Concept Mice
Concept Clinical Trials as Topic
Concept Aging
Concept Equipment Failure Analysis
Concept Immunoglobulin kappa-Chains
Concept Diastole
Concept Genetic Variation
Concept Emergency Service, Hospital
Concept Early Termination of Clinical Trials
Concept Tensile Strength
Concept Barth Syndrome
Concept Linear Models
Concept Lung Diseases
Concept Mitogen-Activated Protein Kinase 3
Concept Hypertrophy, Left Ventricular
Concept Echocardiography
Concept Microscopy, Confocal
Concept Fat Necrosis
Concept Pacemaker, Artificial
Concept Scleroderma, Systemic
Concept Cardiac Catheterization
Concept Haplotypes
Concept Dopamine
Concept Matrix Metalloproteinase 9
Concept Matrix Metalloproteinase 2
Concept Defibrillators, Implantable
Concept Mice, Inbred C57BL
Concept Polycystic Kidney, Autosomal Dominant
Concept Retrospective Studies
Concept Gene Expression Regulation
Concept Enzyme Activation
Concept Models, Statistical
Concept Isolated Noncompaction of the Ventricular Myocardium
Concept Mice, Transgenic
Concept Zebrafish Proteins
Concept Multivariate Analysis
Concept Mitogen-Activated Protein Kinase 14
Concept Biomechanical Phenomena
Concept Diphenylamine
Concept Antigens, CD
Concept Cicatrix
Concept Mole Rats
Concept Heart Rate
Concept DNA Mutational Analysis
Concept Hydralazine
Concept Exercise
Concept RNA Splice Sites
Concept Severity of Illness Index
Concept Cell Proliferation
Concept Survival Rate
Concept Pedigree
Concept Humans
Concept Sequence Analysis, RNA
Concept Likelihood Functions
Concept Desmocollins
Concept Mutation
Concept Radionuclide Imaging
Concept Chromosomes, Human, Pair 15
Concept Adaptor Proteins, Signal Transducing
Concept Cardiomegaly
Concept Electrophoresis
Concept Longitudinal Studies
Concept Candida glabrata
Concept Calpain
Concept Heredity
Concept Heart-Assist Devices
Concept Ventricular Function, Left
Concept Protein Modification, Translational
Concept Mitogen-Activated Protein Kinase 8
Concept Fatal Outcome
Concept Health Services Needs and Demand
Concept Cause of Death
Concept Genes, Mitochondrial
Concept Diabetic Neuropathies
Concept Neutralization Tests
Concept Microsatellite Repeats
Concept Muscular Dystrophy, Duchenne
Concept Positron-Emission Tomography
Concept Health Care Costs
Concept Glucagonoma
Concept Survival Analysis
Concept Systole
Concept Sex Factors
Concept Respiration, Artificial
Concept Analysis of Variance
Concept Reverse Transcriptase Polymerase Chain Reaction
Concept Atherosclerosis
Concept Benzoates
Concept Molecular Diagnostic Techniques
Concept Smad4 Protein
Concept Sequence Alignment
Concept Genome, Human
Concept Desmoglein 3
Concept Interferon-alpha
Concept Friedreich Ataxia
Concept Angiotensin-Converting Enzyme Inhibitors
Concept Genetic Counseling
Concept Mass Screening
Concept Genotype
Concept Cardiomyopathy, Hypertrophic, Familial
Concept Polymorphism, Genetic
Concept Ehlers-Danlos Syndrome
Concept Medical History Taking
Concept Graft Rejection
Concept Prevalence
Concept Case-Control Studies
Concept Monoclonal Gammopathy of Undetermined Significance
Concept Hemodynamics
Concept Body Surface Potential Mapping
Concept Electrophysiologic Techniques, Cardiac
Concept Predictive Value of Tests
Concept Reproducibility of Results
Concept Sweat Glands
Concept Prospective Studies
Concept Fabry Disease
Concept Amyloid Neuropathies, Familial
Concept Cross-Sectional Studies
Concept Collagen
Concept Biphenyl Compounds
Concept Codon, Nonsense
Concept Randomized Controlled Trials as Topic
Concept Progeria
Concept Genome-Wide Association Study
Concept Losartan
Concept Proteomics
Concept Consensus
Concept Creatinine
Concept RNA Splicing
Concept Surveys and Questionnaires
Concept Enzyme Inhibitors
Concept Tomography, X-Ray Computed
Concept Rats, Wistar
Concept Myotonic Dystrophy
Concept Glucocorticoids
Concept Fluoroscopy
Concept Transfection
Concept Point Mutation
Concept Nicotinic Acids
Concept Gene Frequency
Concept Muscular Dystrophies, Limb-Girdle
Concept Desmoglein 2
Concept Cardiac Pacing, Artificial
Concept Polymerase Chain Reaction
Concept Indazoles
Concept Polyploidy
Concept Ethylenediamines
Concept Exercise Test
Concept Myocardial Contraction
Concept Ultrasonography
Concept Gene Deletion
Concept Cell Shape
Concept Epicardial Mapping
Concept Risk Assessment
Concept In Situ Hybridization, Fluorescence
Concept Mutation, Missense
Concept Enalapril
Concept Risk
Concept Risk Factors
Concept Immunoglobulin lambda-Chains
Concept Base Sequence
Concept Alleles
Concept Follow-Up Studies
Concept Autopsy
Concept Immunohistochemistry
Concept Drug Combinations
Concept Mice, Mutant Strains
Concept Rats, Transgenic
Concept Electrocardiography
Concept Diagnostic Errors
Concept Ventricular Function, Right
Concept Tetrazoles
Academic Article Right ventricular afterload sensitivity dramatically increases after left ventricular assist device implantation: A multi-center hemodynamic analysis.
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 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 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 Angiotensin II blockade and aortic-root dilation in Marfan's syndrome.
Academic Article Current treatment of adult Duchenne muscular dystrophy.
Academic Article Baseline Characteristics Predict the Presence of Amyloid on Endomyocardial Biopsy.
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 Genetic testing for dilated cardiomyopathy in clinical practice.
Academic Article Approach to family screening in arrhythmogenic right ventricular dysplasia/cardiomyopathy.
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 Mutations in Alstr?m protein impair terminal differentiation of cardiomyocytes.
Academic Article Surgical Correction of Tricuspid Regurgitation in Patients with ARVD/C.
Academic Article A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2.
Academic Article Novel and highly lethal NKX2.5 missense mutation in a family with sudden death and ventricular arrhythmia.
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 Long-term efficacy of catheter ablation of ventricular tachycardia in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
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 Yield of serial evaluation in at-risk family members of patients with ARVD/C.
Academic Article Comprehensive Versus Targeted Genetic Testing in Children with Hypertrophic Cardiomyopathy.
Academic Article Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline.
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 Comprehensive desmosome mutation analysis in north americans with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Academic Article LMNA-associated cardiocutaneous progeria: an inherited autosomal dominant premature aging syndrome with late onset.
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 Molecular Targeted Therapy
Concept High-Throughput Nucleotide Sequencing
Concept Exome
Concept Cardiac Resynchronization Therapy
Concept Walk Test
Concept Laser Capture Microdissection
Concept CRISPR-Cas Systems
Concept Connectin
Concept Filamins
Concept Vascular Remodeling
Concept Gene Editing
Concept RNAi Therapeutics
Concept Sildenafil Citrate
Concept Loss of Function Mutation
Concept Fibrillins
Concept Fibrillin-1
Concept Homeobox Protein Nkx-2.5
Concept Mice, 129 Strain
Concept Haploinsufficiency
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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