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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
Российский кардиологический журнал, ISSN 1560-4071, 08/2018, Issue 7, pp. 80 - 83
Clinical case demonstrates a cardiovascular phenotype of Fabry disease — rare inherited disorder, linked with female sex. Clinically manifest Fabry disease is... 
Fabry disease | ECG | hypertrophic cardiomyopathy | atrial fribrillation
Journal Article
Journal of Electrocardiology, ISSN 0022-0736, 07/2019, Volume 55, pp. 102 - 106
Brugada syndrome (BrS) is an inherited ion channelopathy that may predispose affected individuals to atrial cardiomyopathy. We tested the hypothesis that BrS... 
Electrocardiography | P-wave | Brugada syndrome | Atrial | FIBRILLATION | TACHYARRHYTHMIAS | CARDIAC & CARDIOVASCULAR SYSTEMS | MANAGEMENT | NEW-ONSET | INTERATRIAL BLOCK | PREVALENCE | INDIVIDUALS | VENTRICULAR-ARRHYTHMIAS | SUDDEN CARDIAC DEATH | TYPE-1 ECG PATTERN | Medical research | Atrial fibrillation | Analysis | Electrocardiogram | Medicine, Experimental | Genetic aspects
Journal Article
Heart Rhythm, ISSN 1547-5271, 2011, Volume 8, Issue 11, pp. 1686 - 1695
Background Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart muscle disease carrying a risk of sudden death. Information about the... 
Cardiovascular | ARVC | late enhancement | LVEF | left ventricular ejection fraction | multiple mutations | right ventricular outflow tract | RVOT | BSA | electrocardiogram | right ventricular end-diastolic volume | RVEDA | PLAX | right ventricular fraction shortening | parasternal long axis | LVEDV | signal-averaged electrocardiogram | PSAX | ventricular fibrillation | left ventricular end diastolic volume | right ventricular | right ventricular end-diastolic area | ECG | CMR | SAECG | parasternal short axis | ventricular tachycardia | RVFS | left ventricular, ventricle | RVEDV | arrhythmogenic right ventricular cardiomyopathy | premature ventricular complex | PVC | cardiac magnetic resonance | body surface area | PLAKOGLOBIN CAUSES | CARDIAC & CARDIOVASCULAR SYSTEMS | NAXOS-DISEASE | FAMILIES | WOOLLY HAIR | DYSPLASIA | DESMOGLEIN-2 | PLAKOPHILIN-2 | DESMOCOLLIN-2 | DYSPLASIA/CARDIOMYOPATHY | FEATURES | Diagnosis, Differential | Echocardiography | Prognosis | Follow-Up Studies | Humans | Male | Arrhythmogenic Right Ventricular Dysplasia - diagnosis | Arrhythmogenic Right Ventricular Dysplasia - genetics | Phenotype | Magnetic Resonance Imaging, Cine - methods | Desmosomes - genetics | DNA - analysis | DNA Mutational Analysis | Pedigree | Adolescent | Electrocardiography | Female | Retrospective Studies | Mutation | Child | Pediatrics | Gene mutations | Cardiomyopathy | Electrocardiogram | Genes | Genetic research | Genetic aspects | Diagnosis | Children | Heart diseases | Health aspects | ARVC, arrhythmogenic right ventricular cardiomyopathy | RVOT, right ventricular outflow tract | MM, multiple mutations | RV, right ventricular | LVEF, left ventricular ejection fraction | PLAX, parasternal long axis | RVFS, right ventricular fraction shortening | Clinical | SAECG, signal-averaged electrocardiogram | VF, ventricular fibrillation | PSAX, parasternal short axis | RVEDV, right ventricular end-diastolic volume | PVC, premature ventricular complex | LVEDV, left ventricular end diastolic volume | BSA, body surface area | VT, ventricular tachycardia | ECG, electrocardiogram | RVEDA, right ventricular end-diastolic area | CMR, cardiac magnetic resonance | LE, late enhancement | LV, left ventricular, ventricle
Journal Article
HeartRhythm Case Reports, ISSN 2214-0271, 07/2016, Volume 2, Issue 4, pp. 280 - 282
Journal Article
Journal of Electrocardiology, ISSN 0022-0736, 11/2018, Volume 51, Issue 6, pp. 1125 - 1130
Increasing evidence doubts the benign nature of metabolically healthy obesity (MHO). An investigation of the association of MHO and other obesity phenotypes... 
Metabolically healthy obesity | NHANES-III | ECG-LVH | CRITERIA | CARDIAC & CARDIOVASCULAR SYSTEMS | ABNORMALITIES | GLUCOSE-INTOLERANCE | ATHEROSCLEROSIS | BLOOD-PRESSURE | DISEASE | OVERWEIGHT | HYPERTENSION | CARDIOVASCULAR RISK | Obesity | Medical colleges | Phenotype | Heart enlargement | Analysis | Electrocardiogram | Electrocardiography | Genetic aspects | Risk factors
Journal Article
Circulation: Cardiovascular Genetics, ISSN 1942-325X, 04/2017, Volume 10, Issue 2, pp. e001482 - e001482
Journal Article
Circulation. Arrhythmia and electrophysiology, ISSN 1941-3149, 2/2009, Volume 2, Issue 1, pp. 24 - 28
Background— Atrial fibrillation (AF) is heterogeneous at the clinical and molecular levels. Association studies have reported that common single-nucleotide... 
ECG | Atrial fibrillation | gene variants | Kardiologi | Clinical Medicine | atrial fibrillation | Cardiac and Cardiovascular Systems | genetics | electrophysiology | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | electrocardiography
Journal Article