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European heart journal, ISSN 0195-668X, 06/2019, Volume 40, Issue 21, pp. 1678 - 1680
Journal Article
International Journal of Cardiology, ISSN 0167-5273, 01/2018, Volume 251, pp. 71 - 73
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2009, Volume 54, Issue 3, pp. 220 - 228
Journal Article
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2016, Volume 67, Issue 12, pp. 1399 - 1409
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 04/2017, Volume 54, Issue 4, pp. 288 - 296
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2013, Volume 62, Issue 21, pp. 2010 - 2019
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2011, Volume 58, Issue 8, pp. 839 - 848
Objectives The purpose of this study was to assess myocardial blood flow (MBF) using positron emission tomography in patients with hypertrophic cardiomyopathy... 
Cardiovascular | Internal Medicine | microvascular dysfunction | hypertrophic cardiomyopathy | positron emission tomography | genetic testing | BINDING-PROTEIN-C | DIAGNOSIS | CARDIAC & CARDIOVASCULAR SYSTEMS | CARDIOVASCULAR MAGNETIC-RESONANCE | IDENTIFICATION | MYOCARDIAL BLOOD-FLOW | ATRIAL-FIBRILLATION | DISEASE | ENHANCEMENT | DYSFUNCTION | CHAIN GENE | Tropomyosin - genetics | Cardiomyopathy, Hypertrophic, Familial - genetics | Humans | Myosin Heavy Chains - genetics | Male | Positron-Emission Tomography | Young Adult | Microcirculation | Ventricular Remodeling | Sarcomeres - genetics | Adult | Female | Radiopharmaceuticals | Actin Cytoskeleton - genetics | Coronary Circulation | Severity of Illness Index | Troponin T - genetics | Cardiac Myosins - genetics | Dipyridamole | Genotype | Myocardium - pathology | Magnetic Resonance Imaging, Cine | Ammonia | Carrier Proteins - genetics | Regression Analysis | Vasodilator Agents | Adolescent | Mutation | Nitrogen Radioisotopes | Rare earth metals | Cruelty to animals | Care and treatment | Cardiomyopathy, Hypertrophic | Gene mutations | PET imaging | Cytogenetics | Protein C | Genetic aspects | Proteins | Confidence intervals | Medical imaging | Nuclear magnetic resonance--NMR | Cardiomyopathy | Genes | Cardiovascular disease | Family medical history | Cardiology | Age | Acquisitions & mergers
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2014, Volume 64, Issue 24, pp. 2589 - 2600
Abstract Background Mild hypertrophy but increased arrhythmic risk characterizes the stereotypic phenotype proposed for hypertrophic cardiomyopathy (HCM)... 
Cardiovascular | Internal Medicine | end-stage | diastolic function | troponin | triphasic filling | genotype to phenotype correlation | correlation triphasic filling troponin | genotype to phenotype | diastolic function end-stage | CARDIAC & CARDIOVASCULAR SYSTEMS | CARDIOVASCULAR MAGNETIC-RESONANCE | HEARTS BEARING | PREVALENCE | LEFT-VENTRICULAR HYPERTROPHY | TASK-FORCE | CARDIAC TROPONIN-T | DISEASE | DYSFUNCTION | ALPHA-TROPOMYOSIN | DOPPLER-ECHOCARDIOGRAPHY | Follow-Up Studies | Humans | Middle Aged | Male | Cardiomyopathy, Hypertrophic - complications | Death, Sudden, Cardiac - etiology | Ventricular Fibrillation - etiology | Ventricular Outflow Obstruction - etiology | Actins - genetics | Ventricular Dysfunction, Left - genetics | Ventricular Fibrillation - genetics | Adult | Female | Heart Function Tests | Actin Cytoskeleton - genetics | Severity of Illness Index | Troponin T - genetics | Ventricular Outflow Obstruction - genetics | Cardiomyopathy, Hypertrophic - genetics | Genetic Predisposition to Disease | MAP Kinase Kinase Kinases - genetics | Ventricular Dysfunction, Left - etiology | Patient Outcome Assessment | Cardiomyopathy, Hypertrophic - diagnosis | Disease Progression | Cardiomyopathy, Hypertrophic - physiopathology | Italy | Mutation | Sects | Genetic aspects | Cardiomyopathy, Hypertrophic | Gene mutations | Heart | Medical research | Tachycardia | Actin | Genes | Myosin | Medicine, Experimental | Protein binding | Heart attacks | Cardiology | Drug therapy | Clinical outcomes | MYH7, myosin heavy chain | TNNT2, cardiac troponin T gene | HR, hazard ratio | SCD, sudden cardiac death | ICD, implantable cardioverter-defibrillator | TPM1, cardiac α-tropomyosin gene | LVH, left ventricular hypertrophy | MYBPC3, myosin binding protein C | LV, left ventricular | ECG, electrocardiography | LGE, late gadolinium enhancement | AF, atrial fibrillation | NSVT, nonsustained ventricular tachycardia | ACTC, cardiac α-actin gene | Original Investigation | CMR, cardiac magnetic resonance | HCM, hypertrophic cardiomyopathy | TNNI3, cardiac troponin I gene | NYHA, New York Heart Association
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2008, Volume 52, Issue 7, pp. 559 - 566
Journal Article
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