Left-dominant arrhythmogenic cardiomyopathy: an under-recognized clinical entity

scientific article published on 01 December 2008

Left-dominant arrhythmogenic cardiomyopathy: an under-recognized clinical entity is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/J.JACC.2008.09.019
P698PubMed publication ID19095136

P50authorDudley PennellQ42778112
P2093author name stringSrijita Sen-Chowdhry
William J McKenna
Sanjay K Prasad
Petros Syrris
Siân E Hughes
Deirdre Ward
Robert Merrifield
P433issue25
P921main subjectcardiomyopathyQ847583
P304page(s)2175-2187
P577publication date2008-12-01
P1433published inJournal of the American College of CardiologyQ2984355
P1476titleLeft-dominant arrhythmogenic cardiomyopathy: an under-recognized clinical entity
P478volume52

Reverse relations

cites work (P2860)
Q90017963A case report of arrhythmogenic ventricular cardiomyopathy presenting with sustained ventricular tachycardia arising from the right and the left ventricles before structural changes are documented
Q28250468A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy
Q38816327A meta-analysis for echocardiographic assessment of right ventricular structure and function in ARVC
Q58128759A novel desmin mutation causing severe left ventricular arrhythmogenic cardiomyopathy/dysplasia
Q82962303A novel variant in plakophilin-2 gene detected in a family with arrhythmogenic right ventricular cardiomyopathy
Q92759012ACTN2 variant associated with a cardiac phenotype suggestive of left-dominant arrhythmogenic cardiomyopathy
Q96233952An unusual cause of ventricular fibrillatory arrest
Q53561111Arrhythmic risk assessment in genotyped families with arrhythmogenic right ventricular cardiomyopathy.
Q33167672Arrhythmogenic Cardiomyopathy: Electrical and Structural Phenotypes
Q88311055Arrhythmogenic Cardiomyopathy: Mechanotransduction Going Wrong
Q92740412Arrhythmogenic Left Ventricular Cardiomyopathy: A Clinical and CMR Study
Q33166353Arrhythmogenic Phenotype in Dilated Cardiomyopathy: Natural History and Predictors of Life-Threatening Arrhythmias.
Q90734431Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: An Updated Review of Diagnosis and Management
Q89958699Arrhythmogenic Right Ventricular Cardiomyopathy: Characterization of Left Ventricular Phenotype and Differential Diagnosis With Dilated Cardiomyopathy
Q36651104Arrhythmogenic Right Ventricular Cardiomyopathy: Electroarchitecture of the Substrate
Q38826183Arrhythmogenic Right Ventricular Cardiomyopathy: Risk Stratification and Indications for Defibrillator Therapy.
Q26753099Arrhythmogenic cardiomyopathy
Q93137622Arrhythmogenic cardiomyopathy with left ventricular involvement versus ischemic heart disease: lessons learned from the family study and the reviewed autopsy of a young male
Q33906065Arrhythmogenic cardiomyopathy: diagnosis, genetic background, and risk management
Q90577852Arrhythmogenic left ventricular cardiomyopathy
Q34465268Arrhythmogenic right ventricular cardiomyopathy (ARVC): cardiovascular magnetic resonance update
Q55186296Arrhythmogenic right ventricular cardiomyopathy in Boxer dogs: the diagnosis as a link to the human disease.
Q84905617Arrhythmogenic right ventricular cardiomyopathy. What is needed for a cure?
Q30489889Arrhythmogenic right ventricular cardiomyopathy/dysplasia clinical presentation and diagnostic evaluation: results from the North American Multidisciplinary Study
Q34780116Arrhythmogenic right ventricular cardiomyopathy: From genetics to diagnostic and therapeutic challenges
Q95729750Arrhythmogenic right ventricular cardiomyopathy: evaluation of the current diagnostic criteria and differential diagnosis
Q37994613Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C): a review of molecular and clinical literature
Q35607769Arrhythmogenic substrate at the interventricular septum as a target site for radiofrequency catheter ablation of recurrent ventricular tachycardia in left dominant arrhythmogenic cardiomyopathy.
Q87493446Arrhythmogenic ventricular cardiomyopathy and sudden cardiac death: Left or right?
Q27024037Arrhythmogenic ventricular cardiomyopathy: A paradigm shift from right to biventricular disease
Q60922442Arrythmogenic Right Ventricular Cardiomiopathy/Dysplasia (ARVC/D) - What We Have Learned after 40 Years of the Diagnosis of This Clinical Entity
Q99619173Athlete's heart and other entities to consider around
Q58716506Cardiac Magnetic Resonance Imaging (MRI) Findings in Arrhythmogenic Right Ventricular Dysplasia (ARVD) Compared with Echocardiography
Q30558233Cardiac imaging techniques for physicians: late enhancement
Q46990439Cardiac magnetic resonance imaging: Which information is useful for the arrhythmologist?
Q90435028Cardiomyopathies
Q37848215Cardiovascular magnetic resonance in heart failure
Q41451219Case reports of two pedigrees with recessive arrhythmogenic right ventricular cardiomyopathy associated with homozygous Thr335Ala variant in DSG2.
Q38662414Cell models of arrhythmogenic cardiomyopathy: advances and opportunities
Q98894474Clinical Presentation, Cardiac Magnetic Resonance Findings, and Prognosis of Patients with Arrhythmogenic Right Ventricular Cardiomyopathy - An Experience from Pakistan
Q35054950Clinical and genetic issues in dilated cardiomyopathy: A review for genetics professionals
Q35488614Clinical phenotype and diagnosis of arrhythmogenic right ventricular cardiomyopathy in pediatric patients carrying desmosomal gene mutations.
Q37349517Clinical usefulness of immunohistochemistry for plakoglobin, N-cadherin, and connexin-43 in the diagnosis of arrhythmogenic right ventricular cardiomyopathy
Q99613010Comparison of different prediction models for the indication of implanted cardioverter defibrillator in patients with arrhythmogenic right ventricular cardiomyopathy
Q62476511Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology
Q39030731Comprehensive multi-modality imaging approach in arrhythmogenic cardiomyopathy-an expert consensus document of the European Association of Cardiovascular Imaging
Q37572134Connexin defects underlie arrhythmogenic right ventricular cardiomyopathy in a novel mouse model
Q90613298Desmoplakin Variant-Associated Arrhythmogenic Cardiomyopathy Presenting as Acute Myocarditis
Q33764619Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria
Q55638651Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria.
Q30463822Diagnostic and prognostic value of cardiovascular magnetic resonance in non-ischaemic cardiomyopathies
Q88454366Diagnostic and therapeutic strategies for arrhythmogenic right ventricular dysplasia/cardiomyopathy patient
Q87396216Dilated cardiomyopathy
Q91899324Dilated cardiomyopathy
Q39283141Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing
Q89441783Epsilon waves: Milestones in the discovery and progress
Q50167027Evolving concepts in dilated cardiomyopathy.
Q94478119Familial screening in case of acute myocarditis reveals inherited arrhythmogenic left ventricular cardiomyopathies
Q92132136Fibrosis in Arrhythmogenic Cardiomyopathy: The Phantom Thread in the Fibro-Adipose Tissue
Q90082106Genetic Risk of Arrhythmic Phenotypes in Patients With Dilated Cardiomyopathy
Q39270856Genetic and epigenetic regulation of arrhythmogenic cardiomyopathy
Q38107893Genetic evaluation of dilated cardiomyopathy
Q38058475Genetic testing in the contemporary diagnosis of cardiomyopathy
Q91799093High risk of heart failure associated with desmoglein-2 mutations compared to plakophilin-2 mutations in arrhythmogenic right ventricular cardiomyopathy/dysplasia
Q38211720How to recognize epicardial origin of ventricular tachycardias?
Q41892305Identification of a new modulator of the intercalated disc in a zebrafish model of arrhythmogenic cardiomyopathy.
Q30473247Imaging phenotype vs genotype in nonhypertrophic heritable cardiomyopathies: dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy
Q58577361Impact of Cardiovascular Magnetic Resonance Imaging on Identifying the Etiology of Cardiomyopathy in Patients Undergoing Cardiac Transplantation
Q41485480Incessant left ventricular tachycardia of unusual etiology
Q48501295Inherited cardiomyopathies and sports participation
Q55317616Isolated, premature ventricular complex-induced right ventricular dysfunction mimicking arrhythmogenic right ventricular cardiomyopathy.
Q35171347Left ventricular involvement in arrhythmogenic right ventricular cardiomyopathy - a cardiac magnetic resonance imaging study
Q42404059Left-dominant Arrhythmogenic Cardiomyopathy: A Case Misdiagnosed as Pseudoaneurysm
Q96768170Left-dominant arrhythmogenic cardiomyopathy with a nonsense mutation in DSP
Q92877503Letter by Pérez-Riera et al Regarding Article, "Left-Dominant Arrhythmogenic Cardiomyopathy With Heterozygous Mutations in DSP and MYBPC3"
Q34903406MR and CT imaging of Arrhythmogenic Cardiomyopathy
Q38887628Management of survivors of cardiac arrest - the importance of genetic investigation
Q42805646MicroRNA-130a Regulation of Desmocollin 2 in a Novel Model of Arrhythmogenic Cardiomyopathy
Q91524160Minimal inflammatory foci of unknown etiology may be a tentative sign of early stage inherited cardiomyopathy
Q83299496Molecular genetics and pathogenesis of arrhythmogenic right ventricular cardiomyopathy: a disease of cardiac stem cells
Q91557750Molecular mechanisms of arrhythmogenic cardiomyopathy
Q92010580Monozygotic twins with myocarditis and a novel likely pathogenic desmoplakin gene variant
Q37433690Mutation analysis of the candidate genes SCN1B-4B, FHL1, and LMNA in patients with arrhythmogenic right ventricular cardiomyopathy
Q82429955Myocardial Fat at Cardiac Imaging: How Can We Differentiate Pathologic from Physiologic Fatty Infiltration?
Q57654519Myocardial fat overgrowth in Proteus syndrome
Q37292752Myocyte necrosis underlies progressive myocardial dystrophy in mouse dsg2-related arrhythmogenic right ventricular cardiomyopathy
Q90632760Natural History of Arrhythmogenic Cardiomyopathy
Q41776920Nature and Nurture in Arrhythmogenic Right Ventricular Cardiomyopathy - A Clinical Perspective
Q36706648Next generation sequencing-based copy number analysis reveals low prevalence of deletions and duplications in 46 genes associated with genetic cardiomyopathies
Q63729245Next-generation sequencing of 100 candidate genes in young victims of suspected sudden cardiac death with structural abnormalities of the heart
Q37116397Nonischemic Left Ventricular Scar as a Substrate of Life-Threatening Ventricular Arrhythmias and Sudden Cardiac Death in Competitive Athletes
Q64056904Novel compound mutations in the mitochondrial translation elongation factor (TSFM) gene cause severe cardiomyopathy with myocardial fibro-adipose replacement
Q47131063Novel gene mutation identified in a patient with arrhythmogenic ventricular cardiomyopathy
Q64115173Optimizing RV lead position in RV cardiomyopathy: Are we there yet?
Q38846518Outcomes of Catheter Ablation of Ventricular Tachycardia in the Setting of Structural Heart Disease
Q37962327Pathophysiology of arrhythmogenic cardiomyopathy
Q92718026Patient mutations linked to arrhythmogenic cardiomyopathy enhance calpain-mediated desmoplakin degradation
Q28253770Phenotypic analysis of arrhythmogenic cardiomyopathy in the Hutterite population: role of electrocardiogram in identifying high-risk desmocollin-2 carriers
Q36330386Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy
Q37058496Plakophilin-2 c.419C>T and risk of heart failure and arrhythmias in the general population
Q92612178Position Statement on Indications of Echocardiography in Adults - 2019
Q37721775Post-mortem study of the association between cardiac iron and fibrosis in transfusion dependent anaemia.
Q90082110Predicting Arrhythmia Risk in Dilated Cardiomyopathy Using Genetic Mutation Status
Q34562331Prevalence of left ventricular regional dysfunction in arrhythmogenic right ventricular dysplasia: a tagged MRI study
Q90668307Relationship Between Electrocardiographic Findings and Cardiac Magnetic Resonance Phenotypes in Arrhythmogenic Cardiomyopathy
Q36716425Remodeling of the cardiac sodium channel, connexin43, and plakoglobin at the intercalated disk in patients with arrhythmogenic cardiomyopathy
Q28246772Restrictive loss of plakoglobin in cardiomyocytes leads to arrhythmogenic cardiomyopathy
Q88873897Right bundle branch block and conduction disturbances in Brugada syndrome and arrhythmogenic right ventricular cardiomyopathy
Q38201068Science and practice of arrhythmogenic cardiomyopathy: A paradigm shift
Q91609934Screening young athletes for diseases at risk of sudden cardiac death: role of stress testing for ventricular arrhythmias
Q64230001Sudden Death and Left Ventricular Involvement in Arrhythmogenic Cardiomyopathy
Q38191069Sudden cardiac death in patients with nonischemic cardiomyopathy
Q43095707Sustained ventricular tachycardia in an apparently healthy heart: a very localized left dominant arrhythmogenic cardiomyopathy
Q28256845The ARVD/C genetic variants database: 2014 update
Q37809077The Pathobiology of Arrhythmogenic Cardiomyopathy
Q43962585The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing
Q40954073The phospholamban p.Arg14del founder mutation in Dutch patients with arrhythmogenic cardiomyopathy
Q27692617The pre-participation examination for leisure time physical activity: general medical and cardiological issues
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.
Q42957210Tissue-resident Sca1+ PDGFRα+ mesenchymal progenitors are the cellular source of fibrofatty infiltration in arrhythmogenic cardiomyopathy
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
Q41446453Unique Association of Rare Cardiovascular Disease in an Athlete With Ventricular Arrhythmias
Q39398133Using genetic testing to guide therapeutic decisions in cardiomyopathy
Q89052557Ventricular Arrhythmias in Young Competitive Athletes: Prevalence, Determinants, and Underlying Substrate
Q53303061[Update on cardiac imaging techniques: echocardiography, cardiac magnetic resonance and computed tomography].

Search more.