The DOI matches its Crossref record; 149 of the 149 references it cites were found in a registry or an index.
Arrhythmogenic Cardiomyopathy
Open accessAbstract
Arrhythmogenic cardiomyopathy is an inherited heart muscle disorder, predisposing to sudden cardiac death, particularly in young patients and athletes. Pathological features include loss of myocytes and fibrofatty replacement of right ventricular myocardium; biventricular involvement is often observed. It is a cell-to-cell junction cardiomyopathy, typically caused by genetically determined abnormalities of cardiac desmosomes, which leads to detachment of myocytes and alteration of intracellular signal transduction. The diagnosis of arrhythmogenic cardiomyopathy does not rely on a single gold standard test but is achieved using a scoring system, which encompasses familial and genetic factors, ECG abnormalities, arrhythmias, and structural/functional ventricular alterations. The main goal of treatment is the prevention of sudden cardiac death. Implantable cardioverter defibrillator is the only proven lifesaving therapy; however, it is associated with significant morbidity because of device-related complications and inappropriate implantable cardioverter defibrillator interventions. Selection of patients who are the best candidates for implantable cardioverter defibrillator implantation is one of the most challenging issues in the clinical management.
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Self-citationMuscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis
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Right Ventricular Cardiomyopathy and Sudden Death in Young People
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Self-citationRight Ventricular Dysplasia: A Report of 24 Adult Cases
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Self-citationDoes sports activity enhance the risk of sudden death in adolescents and young adults?
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Self-citationMcKoy, G., Protonotarios, N., Crosby, A., Tsatsopoulou, A., Anastasakis, A., Coonar, A., Norman, M., Baboonian, C., Jeffery, S., & McKenna, W. J. (2000) · The Lancet · doi:10.1016/s0140-6736(00)02379-5 · Cited by 1,098
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Cited by
Corrado, D., van Tintelen, P. J., McKenna, W. J., Hauer, R. N. W., Anastastakis, A., Asimaki, A., Basso, C., Bauce, B., Brunckhorst, C., Bucciarelli-Ducci, C., et al. (2020) · European Heart Journal · doi:10.1093/eurheartj/ehz669 · Cited by 366
Self-citationCardiovascular disease models: A game changing paradigm in drug discovery and screening
Savoji, H., Mohammadi, M. H., Rafatian, N., Toroghi, M. K., Wang, E. Y., Zhao, Y., Korolj, A., Ahadian, S., & Radisic, M. (2019) · Biomaterials · doi:10.1016/j.biomaterials.2018.09.036 · Cited by 223
The Role of the Epicardium During Heart Development and Repair
Quijada, P., Trembley, M. A., & Small, E. M. (2020) · Circulation Research · doi:10.1161/circresaha.119.315857 · Cited by 201
Braunwald, E. (2017) · Circulation Research · doi:10.1161/circresaha.117.311812 · Cited by 150
Caforio, A. L. P., Re, F., Avella, A., Marcolongo, R., Baratta, P., Seguso, M., Gallo, N., Plebani, M., Izquierdo-Bajo, A., Cheng, C.-Y., et al. (2020) · Circulation · doi:10.1161/circulationaha.119.043931 · Cited by 104
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Metadata
- Authors
- Corrado, D., Basso, C., & Judge, D. P.
- Venue
- Circulation Research
- Published
- 2017-09-15
- Volume
- 121
- Issue
- 7
- Pages
- 784-802
- ISSN
- 0009-7330 (ISSN-L)
- 1524-4571
- OpenAlex
- W4211192828
- Cited by
- 452
- References
- 149
- FWCI
- 21.02
- Type
- journal article
- Language
- en
- Open access
- bronze
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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