Pages that link to "Q24299388"
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The following pages link to Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy (Q24299388):
Displaying 50 items.
- Plakophilin 2 (Q22683547) (← links)
- Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations (Q24306468) (← links)
- Cardiovascular Disease Modeling Using Patient-Specific Induced Pluripotent Stem Cells (Q26798131) (← 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)
- Arrhythmogenic ventricular cardiomyopathy: A paradigm shift from right to biventricular disease (Q27024037) (← links)
- Mutations with pathogenic potential in proteins located in or at the composite junctions of the intercalated disk connecting mammalian cardiomyocytes: a reference thesaurus for arrhythmogenic cardiomyopathies and for Naxos and Carvajal diseases (Q27024101) (← links)
- Cardiomyopathies: New test for arrhythmogenic right ventricular cardiomyopathy (Q28249832) (← links)
- Comprehensive desmosome mutation analysis in north americans with arrhythmogenic right ventricular dysplasia/cardiomyopathy (Q28268639) (← links)
- Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy (Q28275501) (← links)
- Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice (Q28279991) (← links)
- Recurrent and founder mutations in the Netherlands : Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia (Q28304979) (← links)
- Exploration of pathomechanisms triggered by a single-nucleotide polymorphism in titin's I-band: the cardiomyopathy-linked mutation T2580I. (Q30393558) (← links)
- Imaging phenotype vs genotype in nonhypertrophic heritable cardiomyopathies: dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy (Q30473247) (← links)
- Arrhythmogenic right ventricular cardiomyopathy: diagnosis and risk stratification (Q33157574) (← links)
- Geographical distribution of plakophilin-2 mutation prevalence in patients with arrhythmogenic cardiomyopathy (Q33161238) (← links)
- Brugada ECG pattern: a physiopathological prospective study based on clinical, electrophysiological, angiographic, and genetic findings (Q33162217) (← links)
- Natural history of arrhythmogenic right ventricular cardiomyopathy in the boxer dog: a prospective study (Q33164451) (← links)
- Phenotypic expression is a prerequisite for malignant arrhythmic events and sudden cardiac death in arrhythmogenic right ventricular cardiomyopathy. (Q33165969) (← links)
- Arrhythmogenic Cardiomyopathy: Electrical and Structural Phenotypes (Q33167672) (← links)
- Stop-gain mutations in PKP2 are associated with a later age of onset of arrhythmogenic right ventricular cardiomyopathy (Q33812341) (← links)
- Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy? (Q34365559) (← links)
- A mutation in the Z-line Cypher/ZASP protein is associated with arrhythmogenic right ventricular cardiomyopathy. (Q34429834) (← links)
- In vitro functional analyses of arrhythmogenic right ventricular cardiomyopathy-associated desmoglein-2-missense variations (Q34447898) (← links)
- Arrhythmogenic right ventricular cardiomyopathy: From genetics to diagnostic and therapeutic challenges (Q34780116) (← links)
- Arrhythmogenic right ventricular cardiomyopathy mutations alter shear response without changes in cell-cell adhesion (Q34974510) (← links)
- Desmoglein 2 mutant mice develop cardiac fibrosis and dilation. (Q35017328) (← links)
- Clinical and genetic issues in dilated cardiomyopathy: A review for genetics professionals (Q35054950) (← links)
- Shared desmosome gene findings in early and late onset arrhythmogenic right ventricular dysplasia/cardiomyopathy (Q35110260) (← links)
- Genetic variation in titin in arrhythmogenic right ventricular cardiomyopathy-overlap syndromes (Q35197101) (← links)
- Long-range silencing and position effects at telomeres and centromeres: parallels and differences (Q35587934) (← links)
- Novel frame-shift mutation in PKP2 associated with arrhythmogenic right ventricular cardiomyopathy: a case report (Q35877751) (← links)
- Diagnostic dilemmas: overlapping features of brugada syndrome and arrhythmogenic right ventricular cardiomyopathy (Q35982138) (← links)
- Electrophysiological abnormalities precede overt structural changes in arrhythmogenic right ventricular cardiomyopathy due to mutations in desmoplakin-A combined murine and human study. (Q36131473) (← links)
- Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy (Q36330386) (← links)
- The Achilles’ Heel of Cardiovascular Genetic Testing: Distinguishing Pathogenic Mutations From Background Genetic Noise (Q36391360) (← links)
- Recurrent and founder mutations in the Netherlands-Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy (Q36868447) (← links)
- A woman with incidental findings of ventricular aneurysms and a desmosomal cardiomyopathy (Q36977770) (← links)
- Plakophilin-2 c.419C>T and risk of heart failure and arrhythmias in the general population (Q37058496) (← links)
- Family history: an essential tool for cardiovascular genetic medicine (Q37078819) (← links)
- Genetic testing and genetic counseling in cardiovascular genetic medicine: overview and preliminary recommendations (Q37133904) (← links)
- The cycle of genome-directed medicine (Q37149250) (← links)
- Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it all (Q37255253) (← links)
- Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a not so rare "disease of the desmosome" with multiple clinical presentations (Q37389311) (← links)
- Prognostic factors in chronic heart failure. A review of serum biomarkers, metabolic changes, symptoms, and scoring systems (Q37445574) (← links)
- Sudden adult death (Q37556149) (← links)
- Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic, and arrhythmogenic right ventricular dysplasia/cardiomyopathy. (Q37609685) (← links)
- The role of genetic testing in paediatric syndromes of sudden death: state of the art and future considerations (Q37621582) (← links)
- The genetics of cardiomyopathy: genotyping and genetic counseling (Q37636605) (← links)
- Incremental value of cardiac magnetic resonance imaging in arrhythmic risk stratification of arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers. (Q37676235) (← links)