Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria.

scientific article published on 19 February 2010

Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1161/CIRCULATIONAHA.108.840827
P932PMC publication ID2860804
P698PubMed publication ID20172911

P50authorNikos ProtonotariosQ18281573
Gaetano ThieneQ29840356
Barbara BauceQ29840367
Adalena TsatsopoulouQ29840392
Thomas WichterQ82083870
Jeffrey A TowbinQ87444535
James P DaubertQ87446628
Jonathan S SteinbergQ88011806
Harikrishna TandriQ90794759
Danita M Yoerger SanbornQ108327978
Richard HauerQ108328001
Duane L SherrillQ114418205
Moniek G P J CoxQ117194800
Jeffrey E SaffitzQ117194801
William McKennaQ37375368
Michael H. PicardQ37386535
David A. BluemkeQ39818611
Domenico CorradoQ56529119
Wojciech ZarebaQ63963026
Hugh CalkinsQ67190496
Guy FontaineQ77739534
P2093author name stringAndrea Nava
Frank I Marcus
Cristina Basso
Kathleen Gear
P2860cites workMutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathyQ24306039
Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 geneQ24656100
Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratodermaQ28143046
Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosisQ28256371
Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2Q28267888
Mechanisms of disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathyQ28274829
Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathyQ28280387
Epidermolytic palmoplantar keratoderma with woolly hair and dilated cardiomyopathyQ28282549
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathyQ28288328
Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expressionQ28293747
Arrhythmogenic right ventricular cardiomyopathy/dysplasia clinical presentation and diagnostic evaluation: results from the North American Multidisciplinary StudyQ30489889
Genotype-phenotype assessment in autosomal recessive arrhythmogenic right ventricular cardiomyopathy (Naxos disease) caused by a deletion in plakoglobinQ33147005
Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study.Q33175413
Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease).Q33910305
Arrhythmogenic right ventricular cardiomyopathy. Dysplasia, dystrophy, or myocarditis?Q34395507
Arrhythmogenic right ventricular cardiomyopathy: a 'final common pathway' that defines clinical phenotypeQ79782202
Electrocardiographic features of arrhythmogenic right ventricular dysplasia/cardiomyopathy according to disease severity: a need to broaden diagnostic criteriaQ80593673
Activation delay and VT parameters in arrhythmogenic right ventricular dysplasia/cardiomyopathy: toward improvement of diagnostic ECG criteriaQ80974783
Echocardiographic findings in patients meeting task force criteria for arrhythmogenic right ventricular dysplasia: new insights from the multidisciplinary study of right ventricular dysplasiaQ81520934
Do patients with right ventricular outflow tract ventricular arrhythmias have a normal right ventricular wall motion? A quantitative analysis compared to normal subjectsQ81823758
Quantitative assessment of endomyocardial biopsy in arrhythmogenic right ventricular cardiomyopathy/dysplasia: an in vitro validation of diagnostic criteriaQ82088303
Left-dominant arrhythmogenic cardiomyopathy: an under-recognized clinical entityQ83026674
New ECG criteria in arrhythmogenic right ventricular dysplasia/cardiomyopathyQ84754813
Prevalence of T-wave inversion beyond V1 in young normal individuals and usefulness for the diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasiaQ94437210
DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathyQ34568365
Right ventricular cardiomyopathy and sudden death in young peopleQ34687427
Right ventricular dysplasia: a report of 24 adult casesQ34714742
Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International SQ34727600
MR Imaging of arrhythmogenic right ventricular cardiomyopathy: morphologic findings and interobserver reliability.Q35161701
No detection of enteroviral genome in the myocardium of patients with arrhythmogenic right ventricular cardiomyopathyQ35396351
Complementary role of echocardiography and cardiac magnetic resonance in the non-invasive evaluation of suspected arrhythmogenic right ventricular cardiomyopathyQ35845329
Genetics of right ventricular cardiomyopathyQ36230660
Evaluation of the normal values for signal-averaged electrocardiogramQ36752173
Guidelines for autopsy investigation of sudden cardiac deathQ36977658
Quantitative assessment of angiographic right ventricular wall motion in arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C).Q40169874
Arrhythmogenic right ventricular dysplasia, a cell adhesion cardiomyopathy: insights into disease pathogenesis from preliminary genotype--phenotype assessmentQ42829722
Novel mutation in desmoplakin causes arrhythmogenic left ventricular cardiomyopathyQ46630214
Diagnosis of arrhythmogenic right ventricular dysplasia-cardiomyopathy: value of standard ECG revisited.Q47604997
Three-dimensional electroanatomic voltage mapping increases accuracy of diagnosing arrhythmogenic right ventricular cardiomyopathy/dysplasia.Q51442238
Differentiating arrhythmogenic right ventricular cardiomyopathy from right ventricular outflow tract ventricular tachycardia using multilead QRS duration and axis.Q51945069
[Significance of lymphoplasmocytic infiltration in arrhythmogenic right ventricular dysplasia. Apropos of 3 own cases and review of the literature]Q52207617
Evaluation of new software for angiographic determination of right ventricular volumes.Q52935698
Misdiagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy.Q53291585
Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1Q55670706
Feasibility and Variability of Three Dimensional Echocardiography in Arrhythmogenic Right Ventricular Dysplasia/CardiomyopathyQ57736357
Normal Reference Values for the Adult Right Ventricle by Magnetic Resonance ImagingQ57736398
Noninvasive detection of myocardial fibrosis in arrhythmogenic right ventricular cardiomyopathy using delayed-enhancement magnetic resonance imagingQ57736500
MRI of Arrhythmogenic Right Ventricular Cardiomyopathy/DysplasiaQ57736548
Cardiovascular Magnetic Resonance in Arrhythmogenic Right Ventricular Cardiomyopathy RevisitedQ57901962
Remodeling of myocyte gap junctions in arrhythmogenic right ventricular cardiomyopathy due to a deletion in plakoglobin (Naxos disease)Q59218717
Diagnostic Value of Endomyocardial Biopsy Guided by Electroanatomic Voltage Mapping in Arrhythmogenic Right Ventricular Cardiomyopathy/DysplasiaQ59248800
Prospective evaluation of relatives for familial arrhythmogenic right ventricular cardiomyopathy/dysplasia reveals a need to broaden diagnostic criteriaQ59286856
Arrhythmogenic right ventricular cardiomyopathyQ64043862
Cardiac arrhythmias and atrioventricular block in a cohort of asymptomatic individuals without heart diseaseQ79157383
P433issue13
P407language of work or nameEnglishQ1860
P921main subjectdiagnosisQ16644043
arrhythmogenic right ventricular cardiomyopathyQ2555727
P304page(s)1533-1541
P577publication date2010-02-19
P1433published inCirculationQ578091
P1476titleDiagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria.
P478volume121

Reverse relations

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Q64260161Late presentation of arrhythmogenic right ventricular cardiomyopathy in an octogenarian associated with a pathogenic variant in the plakophilin 2 gene: a case report
Q90441553Left Ventricular Involvement in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Predicts Adverse Clinical Outcomes: A Cardiovascular Magnetic Resonance Feature Tracking Study
Q40001914Left bundle branch block morphology ventricular tachycardia in a marathon runner
Q35171347Left ventricular involvement in arrhythmogenic right ventricular cardiomyopathy - a cardiac magnetic resonance imaging study
Q33850323Left ventricular myocardial strain in ventricular arrhythmia without structural heart disease using cardiac magnetic resonance
Q64906938Life-long tailoring of diagnosis and management of patients with idiopathic ventricular fibrillation-future perspectives in research.
Q33168780Lifelong arrhythmic risk stratification in arrhythmogenic right ventricular cardiomyopathy: distribution of events and impact of periodical reassessment
Q48726319Long-term follow-up in patients with arrhythmogenic right ventricular cardiomyopathy
Q40357862Long-term follow-up of arrhythmogenic right ventricular cardiomyopathy patients with an implantable cardioverter-defibrillator for prevention of sudden cardiac death
Q35997409Long-term outcomes of catheter ablation of ventricular tachycardia in patients with structural heart disease
Q30358689Longitudinal assessment of right ventricular structure and function by cardiovascular magnetic resonance in breast cancer patients treated with trastuzumab: a prospective observational study.
Q47575418Lower than expected burden of premature ventricular contractions impairs myocardial function
Q34903406MR and CT imaging of Arrhythmogenic Cardiomyopathy
Q33355124MRI for arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C)
Q42431617Magnetic Resonance Imaging Assessment of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia in Children
Q38100155Magnetic resonance imaging in the evaluation of congestive cardiac failure
Q35166584Management of a rare case of arrhythmogenic right ventricular dysplasia in pregnancy: a case report
Q26782057Management of patients with Arrhythmogenic Right Ventricular Cardiomyopathy in the Nordic countries
Q38568707Mechanism, diagnosis, and treatment of outflow tract tachycardia
Q36723709Mechanisms of arrhythmias and conduction disorders in older adults
Q24306468Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations
Q33881246MiR-320a as a Potential Novel Circulating Biomarker of Arrhythmogenic CardioMyopathy.
Q42805646MicroRNA-130a Regulation of Desmocollin 2 in a Novel Model of Arrhythmogenic Cardiomyopathy
Q82662379Microvascular dysfunction in nonfailing arrhythmogenic right ventricular cardiomyopathy
Q34250400Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations
Q30378666Monogenec Arrhythmic Syndromes: From Molecular and Genetic Aspects to Bedside.
Q47827654Multichannel electrocardiogram diagnostics for the diagnosis of arrhythmogenic right ventricular dysplasia.
Q53066001Multiplane two-dimensional strain echocardiography for segmental analysis of right ventricular mechanics: new-RV study.
Q36731937Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathies
Q37676232Mutation-positive arrhythmogenic right ventricular dysplasia/cardiomyopathy: the triangle of dysplasia displaced
Q64012839Mutations in ILK, encoding integrin-linked kinase, are associated with arrhythmogenic cardiomyopathy
Q54332402Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy.
Q82429955Myocardial Fat at Cardiac Imaging: How Can We Differentiate Pathologic from Physiologic Fatty Infiltration?
Q34090483Myocardial edema imaging by cardiovascular magnetic resonance: current status and future potential.
Q38377428Myocardial fat as a part of cardiac visceral adipose tissue: physiological and pathophysiological view
Q57654519Myocardial fat overgrowth in Proteus syndrome
Q90632760Natural History of Arrhythmogenic Cardiomyopathy
Q55101134Naxos disease: from the origin to today.
Q28083928New Imaging Technologies To Characterize Arrhythmic Substrate
Q38850894New approaches to predicting the risk of sudden death.
Q38211723New electrocardiographic features in Brugada syndrome
Q33165264New strategies for ventricular tachycardia and ventricular fibrillation ablation
Q89661633Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy
Q38588152Nomenclature and systems of classification for cardiomyopathy in children
Q90215796Non-sarcomeric causes of heart failure
Q36585526Noninvasive Multimodality Imaging in ARVD/C
Q34646112Noninvasive cardiac screening in young athletes with ventricular arrhythmias.
Q37983728Noninvasive imaging modalities and sudden cardiac arrest in the young: can they help distinguish subjects with a potentially life-threatening abnormality from normals?
Q89913812Normal reference intervals for cardiac dimensions and function for use in echocardiographic practice: a guideline from the British Society of Echocardiography
Q52330345Novel Insights and Treatment Strategies for Right Heart Failure.
Q40334492Novel electrocardiographic criteria for the diagnosis of arrhythmogenic right ventricular cardiomyopathy
Q35877751Novel frame-shift mutation in PKP2 associated with arrhythmogenic right ventricular cardiomyopathy: a case report
Q52585976Number of pregnancies and subsequent phenotype in a cross-sectional cohort of women with arrhythmogenic cardiomyopathy.
Q38846518Outcomes of Catheter Ablation of Ventricular Tachycardia in the Setting of Structural Heart Disease
Q37980342Overview of sudden cardiac death in young athletes.
Q38310158Passive ventricular remodeling in cardiac disease: focus on heterogeneity.
Q28085550Pathogenesis of Arrhythmogenic Cardiomyopathy
Q38859214Pectus excavatum: echocardiographic, pathophysiologic, and surgical insights
Q64965420Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies.
Q46269501Pharmacological and non-pharmacological therapy for arrhythmias in the pediatric population: EHRA and AEPC-Arrhythmia Working Group joint consensus statement
Q28253770Phenotypic analysis of arrhythmogenic cardiomyopathy in the Hutterite population: role of electrocardiogram in identifying high-risk desmocollin-2 carriers
Q33165969Phenotypic expression is a prerequisite for malignant arrhythmic events and sudden cardiac death in arrhythmogenic right ventricular cardiomyopathy.
Q38813888Physical Activity, Endurance Exercise, and Excess-Can One Overdose?
Q33815199Pitfalls in the diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia
Q41107820Plakophilin-2 is required for transcription of genes that control calcium cycling and cardiac rhythm.
Q35949057Plasma BIN1 correlates with heart failure and predicts arrhythmia in patients with arrhythmogenic right ventricular cardiomyopathy
Q38074319Postmortem imaging of sudden cardiac death
Q51834996Predictors and Therapy of Cardiomyopathy Caused by Frequent Ventricular Ectopy.
Q33161842Predictors of appropriate ICD therapy in patients with arrhythmogenic right ventricular cardiomyopathy: long term experience of a tertiary care center
Q36577311Pregnancy course and outcomes in women with arrhythmogenic right ventricular cardiomyopathy.
Q37238663Prevalence and prognostic significance of exercise-induced nonsustained ventricular tachycardia in asymptomatic volunteers: BLSA (Baltimore Longitudinal Study of Aging).
Q58580209Profile of patients presenting with sustained ventricular tachycardia in a tertiary care center
Q37010626Profiling of differentially expressed microRNAs in arrhythmogenic right ventricular cardiomyopathy
Q35068177Prognostic value of cardiovascular magnetic resonance derived right ventricular function in patients with interstitial lung disease
Q52355584Pulmonary arterial hypertension: pathogenesis and clinical management.
Q64104540QRS alternans due to localized intraventricular block during ventricular tachycardia in Uhl's anomaly: a case report
Q89805299Quantitative Approach to Fragmented QRS in Arrhythmogenic Cardiomyopathy: From Disease towards Asymptomatic Carriers of Pathogenic Variants
Q47913364Quantitative analysis of PKP2 and neighbouring genes in a patient with arrhythmogenic right ventricular cardiomyopathy caused by heterozygous PKP2 deletion.
Q36816108Quantitative analysis of myocardial tissue with digital autofluorescence microscopy.
Q38639575Radiofrequency Ablation in Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC).
Q53077201Reader- and instrument-dependent variability in the electrocardiographic assessment of arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Q34644575Reappraisal of cardiac magnetic resonance imaging in idiopathic outflow tract arrhythmias.
Q28304979Recurrent and founder mutations in the Netherlands : Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia
Q91911427Reflections on the early invasive clinical cardiac electrophysiology era through fifty manuscripts: 1967-1992
Q57822608Regional Strain by Cardiac Magnetic Resonance Imaging Improves Detection of Right Ventricular Scar Compared With Late Gadolinium Enhancement on a Multimodality Scar Evaluation in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy
Q55365268Relations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome.
Q36709335Relationship Between Arrhythmogenic Right Ventricular Cardiomyopathy and Brugada Syndrome: New Insights From Molecular Biology and Clinical Implications.
Q90668307Relationship Between Electrocardiographic Findings and Cardiac Magnetic Resonance Phenotypes in Arrhythmogenic Cardiomyopathy
Q30562548Relationship between MDCT-imaged myocardial fat and ventricular tachycardia substrate in arrhythmogenic right ventricular cardiomyopathy
Q33552944Relationship between right and left ventricular function in candidates for implantable cardioverter defibrillator with low left ventricular ejection fraction
Q38181533Remodeling of cell-cell junctions in arrhythmogenic cardiomyopathy
Q36716425Remodeling of the cardiac sodium channel, connexin43, and plakoglobin at the intercalated disk in patients with arrhythmogenic cardiomyopathy
Q42733827Response to Letter Regarding Article, "Treatment of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: An International Task Force Consensus Statement".
Q43546020Resting ECG findings in elite football players
Q90382961Reversible methamphetamine-induced cardiomyopathy mimicking arrhythmogenic right ventricular cardiomyopathy with ventricular tachycardia
Q37984850Review of novel clinical applications of advanced, real-time, 3-dimensional echocardiography
Q53704446Revisiting Athlete's Heart Versus Pathologic Hypertrophy: ARVC and the Right Ventricle.
Q47653121Right Ventricular Arrhythmogenic Dysplasia in Cardiac Arrest. An Echocardiographic Pattern Not to Forget
Q37468972Right Ventricular Outflow Tract Arrhythmias: Benign Or Early Stage Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia?
Q41901149Right Ventricular Outflow Tract Tachycardia with Structural Abnormalities of the Right Ventricle and Left Ventricular Diverticulum
Q88873897Right bundle branch block and conduction disturbances in Brugada syndrome and arrhythmogenic right ventricular cardiomyopathy
Q38911015Right heart imaging in patients with heart failure: a tale of two ventricles.
Q38253119Right heart structural and functional remodeling in athletes
Q42377424Right precordial-directed electrocardiographical markers identify arrhythmogenic right ventricular cardiomyopathy in the absence of conventional depolarization or repolarization abnormalities.
Q38811546Right ventricular assessment at cardiac MRI: initial clinical experience utilizing an IS-SENSE reconstruction
Q38252394Right ventricular cardiomyopathies: a multidisciplinary approach to diagnosis.
Q35620014Right ventricular cardiomyopathy meeting the arrhythmogenic right ventricular dysplasia revised criteria? Don't forget sarcoidosis!
Q30456010Right ventricular cardiovascular magnetic resonance imaging: normal anatomy and spectrum of pathological findings.
Q35261875Right ventricular obstructive hypertrophic cardiomyopathy in primary myo-adenylate deaminase deficiency.
Q40818100Right ventricular remodelling induced by exercise training in competitive athletes.
Q47936384Right ventricular scar-related ventricular tachycardia in nonischemic cardiomyopathy: Electrophysiological characteristics, mapping, and ablation of underlying heart disease.
Q36813646Right ventricular strain by MR quantitatively identifies regional dysfunction in patients with arrhythmogenic right ventricular cardiomyopathy
Q48049808Right ventricular systolic function and mechanical dispersion identify patients with arrhythmogenic right ventricular cardiomyopathy.
Q36369424Right ventricular volume analysis by angiography in right ventricular cardiomyopathy
Q41552188Risk Stratification in Arrhythmic Right Ventricular Cardiomyopathy Without Implantable Cardioverter-Defibrillators.
Q52776792Risk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy.
Q83014367Risk stratification for prevention of sudden cardiac death
Q33163382Risk stratification in arrhythmogenic right ventricular cardiomyopathy.
Q30279246Role of Cardiac MR Imaging in Cardiomyopathies
Q26800070Role of Imaging in the Evaluation of Patients at Risk for Sudden Cardiac Death: Genotype-Phenotype Intersection
Q26744429Role of cardiac MRI in nonischemic cardiomyopathies
Q37980258Role of cardiac magnetic resonance imaging in assessing ischemic and nonischemic cardiomyopathies
Q56761537Role of genetic heart disease in sentinel sudden cardiac arrest survivors across the age spectrum
Q38338232Role of non-invasive imaging in the work-up of cardiomyopathies
Q30433243Role of strain imaging in right heart disease: a comprehensive review
Q33163606SCN5A mutation in Chinese patients with arrhythmogenic right ventricular dysplasia
Q37387146ST segment elevations: always a marker of acute myocardial infarction?
Q53341820Safety, long-term outcomes and predictors of recurrence after first-line combined endoepicardial ventricular tachycardia substrate ablation in arrhythmogenic cardiomyopathy. Impact of arrhythmic substrate distribution pattern. A prospective multicen
Q51821757Screening athletes for cardiovascular disease in Africa: a challenging experience.
Q57083780Sequenom MassARRAY approach in the arrhythmogenic right ventricular cardiomyopathy post-mortem setting: clinical and forensic implications
Q90367424Severe Cardiac Dysfunction and Death Caused by Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Are Improved by Inhibition of Glycogen Synthase Kinase-3β
Q35110260Shared desmosome gene findings in early and late onset arrhythmogenic right ventricular dysplasia/cardiomyopathy
Q55359580Signal-averaged electrocardiography: Past, present, and future.
Q47896111Soluble ST2 is associated with disease severity in arrhythmogenic right ventricular cardiomyopathy
Q87287849Sports in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy and desmosomal mutations
Q40010538Statistical evaluation of reproducibility of automated ECG measurements: an example from arrhythmogenic right ventricular dysplasia/cardiomyopathy clinic
Q38769217Strenuous Exercise and Cardiovascular Disease Outcomes
Q57450981Sudden Arrhythmic Death Syndrome: Diagnostic Yield of Comprehensive Clinical Evaluation of Pediatric First-Degree Relatives
Q64230001Sudden Death and Left Ventricular Involvement in Arrhythmogenic Cardiomyopathy
Q36458885Sudden Unexplained Death - Treating the Family
Q38823957Sudden cardiac death from structural heart diseases in adults: imaging findings with cardiovascular computed tomography and magnetic resonance.
Q48355408Sudden cardiac death in isolated right ventricular hypertrabeculation/noncompaction cardiomyopathy.
Q38191069Sudden cardiac death in patients with nonischemic cardiomyopathy
Q38085134Sudden cardiac death in young athletes: preparticipation screening for underlying cardiovascular abnormalities and approaches to prevention
Q40344851Sudden unexplained death in the young: epidemiology, aetiology and value of the clinically guided genetic screening.
Q38657463Targeted next-generation sequencing detects novel gene-phenotype associations and expands the mutational spectrum in cardiomyopathies
Q28256845The ARVD/C genetic variants database: 2014 update
Q35816007The Different Substrate Characteristics of Arrhythmogenic Triggers in Idiopathic Right Ventricular Outflow Tract Tachycardia and Arrhythmogenic Right Ventricular Dysplasia: New Insight from Noncontact Mapping
Q42735967The ECG in arrhythmogenic right ventricular cardiomyopathy: ε-waves and anterior T-wave inversion
Q58613919The Female Athlete's Heart: Facts and Fallacies
Q33158796The ICD as primary prevention. Rare indications
Q37809077The Pathobiology of Arrhythmogenic Cardiomyopathy
Q57166458The Role of Cardiovascular Magnetic Resonance in Sports Cardiology; Current Utility and Future Perspectives
Q42749505The Value of Cardiac Magnetic Resonance Imaging in Evaluation of Pediatric Patients for Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
Q91703824The chameleon of cardiology: cardiac sarcoidosis before and after heart transplantation
Q38000066The changing spectrum of arrhythmogenic (right ventricular) cardiomyopathy
Q37846095The diagnosis and management of ventricular arrhythmias
Q51133570The diagnostic performance of imaging methods in ARVC using the 2010 Task Force criteria.
Q28074493The genetic background of arrhythmogenic right ventricular cardiomyopathy
Q53026278The multi-modality cardiac imaging approach to the Athlete's heart: an expert consensus of the European Association of Cardiovascular Imaging.
Q33161556The presence of giant epsilon waves in a patient with arrhythmogenic right ventricular cardiomyopathy.
Q38068352The prognostic value of late gadolinium enhancement CMR in nonischemic cardiomyopathies
Q37822294The role of cardiac magnetic resonance imaging in the assessment of non-ischemic cardiomyopathy
Q34439332The role of cardiac magnetic resonance imaging in the evaluation of arrhythmogenic right ventricular dysplasia
Q34679867The role of endomyocardial biopsy in ARVC: looking beyond histology in search of new diagnostic markers.
Q38542918The role of genetic testing in unexplained sudden death
Q37057557The spectrum of epidemiology underlying sudden cardiac death
Q38005780The year of 2010 in electrocardiology.
Q44483582Thermogenic supplement use does not alter characteristics of sudden death in the young
Q28246696Titin and desmosomal genes in the natural history of arrhythmogenic right ventricular cardiomyopathy
Q38255380Transcatheter closure of atrial septal defect associated with arrhythmogenic right ventricular cardiomyopathy: a case report and literature review
Q26799143Treatment of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: An International Task Force Consensus Statement
Q26799094Treatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: an international task force consensus statement
Q35125245Ultrastructural changes in cardiac myocytes from Boxer dogs with arrhythmogenic right ventricular cardiomyopathy
Q48246243Unipolar peak-negative voltage as an endocardial electrographic characteristic to predict overlying abnormal epicardial substrates in patients with right epicardial ventricular tachycardia
Q47155677Unique genetic background and outcome of non-Caucasian Japanese probands with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Q38177854Unveiling nonischemic cardiomyopathies with cardiac magnetic resonance
Q33600733Usefulness of precordial T-wave inversion to distinguish arrhythmogenic right ventricular cardiomyopathy from idiopathic ventricular tachycardia arising from the right ventricular outflow tract
Q92568756Utility of genetic testing in athletes
Q38683303Utility of late gadolinium enhancement in pediatric cardiac MRI.
Q34796656Value of the signal-averaged electrocardiogram in arrhythmogenic right ventricular cardiomyopathy/dysplasia
Q34308404Ventricular arrhythmias and sudden cardiac death
Q38819031Ventricular fibrillation: triggers, mechanisms and therapies
Q38256157Ventricular tachycardia mapping and ablation in arrhythmogenic right ventricular cardiomyopathy/dysplasia: Lessons Learned
Q34782131Vigorous physical activity impairs myocardial function in patients with arrhythmogenic right ventricular cardiomyopathy and in mutation positive family members.
Q38181532When rare illuminates common: how cardiocutaneous syndromes transformed our perspective on arrhythmogenic cardiomyopathy
Q38888147Whole exome sequencing with genomic triangulation implicates CDH2-encoded N-cadherin as a novel pathogenic substrate for arrhythmogenic cardiomyopathy
Q41694294Wnt/β-catenin pathway in arrhythmogenic cardiomyopathy
Q35234588Yield of serial evaluation in at-risk family members of patients with ARVD/C.
Q85508713[Cardiovascular diseases in childhood]
Q33165762[Primary and secondary prophylactic ICD therapy in congenital electrical and structural cardiomyopathies].
Q86485517[Ventricular tachycardia under stress : Characteristic symptom or prognostic relevance?]

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