Pages that link to "Q64043862"
Jump to navigation
Jump to search
The following pages link to Arrhythmogenic right ventricular cardiomyopathy (Q64043862):
Displaying 50 items.
- Desmosomal cadherins are decreased in explanted arrhythmogenic right ventricular dysplasia/cardiomyopathy patient hearts (Q21132519) (← links)
- A Review of the Giant Protein Titin in Clinical Molecular Diagnostics of Cardiomyopathies (Q26738818) (← links)
- Arrhythmogenic cardiomyopathy (Q26753099) (← links)
- Impact of cardiac magnetic resonance imaging in non-ischemic cardiomyopathies (Q26765173) (← links)
- Management of patients with Arrhythmogenic Right Ventricular Cardiomyopathy in the Nordic countries (Q26782057) (← links)
- Treatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: an international task force consensus statement (Q26799094) (← links)
- Treatment of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: An International Task Force Consensus Statement (Q26799143) (← links)
- Significance of deep T-wave inversions in asymptomatic athletes with normal cardiovascular examinations: practical solutions for managing the diagnostic conundrum (Q27005666) (← links)
- Arrhythmogenic ventricular cardiomyopathy: A paradigm shift from right to biventricular disease (Q27024037) (← links)
- The cell biology of disease: cellular mechanisms of cardiomyopathy. (Q27686758) (← links)
- Arrhythmogenic right ventricular dysplasia/cardiomyopathy type 1: a light on molecular mechanisms (Q27690277) (← links)
- Cardiac disease and arrhythmogenesis: Mechanistic insights from mouse models (Q28066019) (← links)
- The Role of Genetic Testing in the Identification of Young Athletes with Inherited Primitive Cardiac Disorders at Risk of Exercise Sudden Death (Q28066330) (← links)
- The genetic background of arrhythmogenic right ventricular cardiomyopathy (Q28074493) (← links)
- Desmosomes and the sodium channel complex: implications for arrhythmogenic cardiomyopathy and Brugada syndrome (Q28236522) (← links)
- Restrictive loss of plakoglobin in cardiomyocytes leads to arrhythmogenic cardiomyopathy (Q28246772) (← links)
- Phenotypic analysis of arrhythmogenic cardiomyopathy in the Hutterite population: role of electrocardiogram in identifying high-risk desmocollin-2 carriers (Q28253770) (← links)
- The ARVD/C genetic variants database: 2014 update (Q28256845) (← links)
- Loss of cadherin-binding proteins β-catenin and plakoglobin in the heart leads to gap junction remodeling and arrhythmogenesis (Q28257671) (← links)
- Cardiac tissue-restricted deletion of plakoglobin results in progressive cardiomyopathy and activation of {beta}-catenin signaling (Q28303564) (← links)
- Recurrent and founder mutations in the Netherlands : Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia (Q28304979) (← links)
- Genetics of sudden cardiac death syndromes (Q28307856) (← links)
- Analysis of ventricular function by CT (Q30394854) (← links)
- Imaging phenotype vs genotype in nonhypertrophic heritable cardiomyopathies: dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy (Q30473247) (← links)
- Arrhythmogenic right ventricular cardiomyopathy mimics: role of cardiovascular magnetic resonance (Q30537711) (← links)
- New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants (Q30585171) (← links)
- The ICD as primary prevention. Rare indications (Q33158796) (← links)
- Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a review and update (Q33159766) (← links)
- Geographical distribution of plakophilin-2 mutation prevalence in patients with arrhythmogenic cardiomyopathy (Q33161238) (← links)
- Update on Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C). (Q33162846) (← links)
- Risk stratification in arrhythmogenic right ventricular cardiomyopathy. (Q33163382) (← links)
- Comparative study of CMR characteristics between arrhythmogenic right ventricular cardiomyopathy patients with/without syncope. (Q33164517) (← links)
- Clinical Presentation and Outcomes by Sex in Arrhythmogenic Right Ventricular Cardiomyopathy: Findings from the North American ARVC Registry (Q33166782) (← links)
- Arrhythmogenic Cardiomyopathy: Electrical and Structural Phenotypes (Q33167672) (← links)
- Proteomic analysis reveals significant elevation of heat shock protein 70 in patients with chronic heart failure due to arrhythmogenic right ventricular cardiomyopathy (Q33471552) (← links)
- Beyond the Electrocardiogram: Mutations in Cardiac Ion Channel Genes Underlie Nonarrhythmic Phenotypes (Q33565907) (← links)
- Congenital heart disease confounding the diagnosis of arrhythmogenic right ventricular cardiomyopathy (Q33643955) (← links)
- Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria (Q33764619) (← links)
- Pitfalls in the diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia (Q33815199) (← links)
- Arrhythmogenic cardiomyopathy: diagnosis, genetic background, and risk management (Q33906065) (← links)
- Effect of the 2010 task force criteria on reclassification of cardiovascular magnetic resonance criteria for arrhythmogenic right ventricular cardiomyopathy (Q33927637) (← links)
- Gap junctions and blood-tissue barriers (Q33941978) (← links)
- Role of genomics in cardiovascular medicine (Q34444807) (← links)
- Circadian rhythms, Wnt/beta-catenin pathway and PPAR alpha/gamma profiles in diseases with primary or secondary cardiac dysfunction (Q34452078) (← links)
- Arrhythmogenic right ventricular cardiomyopathy (ARVC): cardiovascular magnetic resonance update (Q34465268) (← links)
- Right ventricular strain analysis from three-dimensional echocardiography by using temporally diffeomorphic motion estimation. (Q34562400) (← links)
- Cardiac-specific NRAP overexpression causes right ventricular dysfunction in mice (Q34762120) (← links)
- Arrhythmogenic right ventricular cardiomyopathy: From genetics to diagnostic and therapeutic challenges (Q34780116) (← links)
- The causes, consequences, and treatment of left or right heart failure (Q34987168) (← links)
- Desmoglein 2 mutant mice develop cardiac fibrosis and dilation. (Q35017328) (← links)