The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Need for an International Registry
Abstract
Abstract —Arrhythmogenic right ventricular (RV) dysplasia/cardiomyopathy (ARVD/C) is a heart muscle disease characterized by peculiar RV involvement and electrical instability that precipitates ventricular arrhythmias and sudden death. The purpose of the present consensus report of the Study Group on ARVD/C of the Working Groups on Myocardial and Pericardial Disease and Arrhythmias of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the World Heart Federation is to review the considerable progress in our understanding of the etiopathogenesis, morbid anatomy, and clinical presentation of ARVD/C since it first was described in 1977. The present article focuses on important but still unanswered issues, mostly regarding risk stratification, clinical outcome, and management of affected patients. Because ARVD/C is relatively uncommon and any one center may have experience with only a few patients, an international registry is being established to accumulate information and enhance the numbers of patients that can be analyzed and thus answer pending questions. The registry also will facilitate pathological, molecular, and genetics research on the causes and pathogenesis of the ARVD/C. Furthermore, availability of an international database will enhance awareness of this largely unrecognized condition among the medical community. Physicians are encouraged to enroll patients in the International Registry of ARVD/C.
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Citations
Cites
Corrado, D., Basso, C., Thiene, G., McKenna, W. J., Davies, M. J., Fontaliran, F., Nava, A., Silvestri, F., Blomstrom-Lundqvist, C., Wlodarska, E. K., et al. (1997) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(97)00332-x · Cited by 978
Self-citationThe arrhythmogenic right ventricle. Dysplasia versus cardiomyopathy
Fontaine, G., Fontaliran, F., Rosas Andrade, F., Velasquez, E., Tonet, J., Jouven, X., Fujioka, Y., & Frank, R. (1995) · Heart and Vessels · doi:10.1007/bf01744901 · Cited by 55
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Cited by
Committee Members, Cheitlin, M. D., Armstrong, W. F., Aurigemma, G. P., Beller, G. A., Bierman, F. Z., Davis, J. L., Douglas, P. S., Faxon, D. P., Gillam, L. D., et al. (2003) · Circulation · doi:10.1161/01.cir.0000073597.57414.a9 · Cited by 745
Corrado, D., Leoni, L., Link, M. S., Bella, P. D., Gaita, F., Curnis, A., Salerno, J. U., Igidbashian, D., Raviele, A., Disertori, M., et al. (2003) · Circulation · doi:10.1161/01.cir.0000103130.33451.d2 · Cited by 587
Self-citationSoejima, K., Stevenson, W. G., Sapp, J. L., Selwyn, A. P., Couper, G., & Epstein, L. M. (2004) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2004.01.029 · Cited by 485
Sudden cardiac death in young people with apparently normal heart
Corrado, D. (2001) · Cardiovascular Research · doi:10.1016/s0008-6363(01)00254-1 · Cited by 378
Self-citationSyrris, P., Ward, D., Evans, A., Asimaki, A., Gandjbakhch, E., Sen-Chowdhry, S., & McKenna, W. J. (2006) · The American Journal of Human Genetics · doi:10.1086/509122 · Cited by 377
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Metadata
- Authors
- Corrado, D., Fontaine, G., Marcus, F. I., McKenna, W. J., Nava, A., Thiene, G., & Wichter, T.
- Venue
- Circulation
- Published
- 2000-03-21
- Volume
- 101
- Issue
- 11
- Pages
- E101-6
- ISSN
- 0009-7322 (ISSN-L)
- 1524-4539
- OpenAlex
- W2913029703
- Cited by
- 337
- References
- 2
- FWCI
- 12.69
- Type
- journal article
- Language
- en
- Open access
- closed
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- Corrado, D., Fontaine, G., Marcus, F. I., McKenna, W. J., Nava, A., Thiene, G., & Wichter, T. (2000). Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Need for an International Registry. Circulation. https://doi.org/10.1161/01.cir.101.11.e101
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
