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1984 1
1989 1
1990 1
1994 1
1995 3
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1999 2
2000 1
2001 1
2002 3
2003 3
2004 3
2005 4
2006 1
2008 4
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75 results

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Page 1
Advances in the Diagnosis and Management of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.
Orgeron GM, Calkins H. Orgeron GM, et al. Curr Cardiol Rep. 2016 Jun;18(6):53. doi: 10.1007/s11886-016-0732-y. Curr Cardiol Rep. 2016. PMID: 27108363 Review.
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an inherited cardiomyopathy characterized by ventricular arrhythmias, right ventricular dysfunction, and sudden cardiac death. ...For instance, the discovery of
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an inherited cardiomyopathy characterized
Arrhythmogenic Right Ventricular Cardiomyopathy Diagnosis.
Sayed A, Pal S, Poplawska M, Aronow WS, Frishman WH, Fuisz A, Jacobson JT. Sayed A, et al. Cardiol Rev. 2020 Nov-Dec;28(6):319-324. doi: 10.1097/CRD.0000000000000292. Cardiol Rev. 2020. PMID: 32032135 Review.
Arrhythmogenic right ventricular cardiomyopathy, formerly called "arrhythmogenic right ventricular dysplasia," is an under-recognized clinical entity characterized by ventricular arrhythmias and a characteristic ventricul
Arrhythmogenic right ventricular cardiomyopathy, formerly called "arrhythmogenic right ventricular
Current Concepts on Diagnosis and Prognosis of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia.
Castaños Gutiérrez SL, Kamel IR, Zimmerman SL. Castaños Gutiérrez SL, et al. J Thorac Imaging. 2016 Nov;31(6):324-335. doi: 10.1097/RTI.0000000000000171. J Thorac Imaging. 2016. PMID: 26429589 Review.
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an uncommon cardiac disease characterized by progressive right ventricular dysfunction due to fibrofatty replacement of myocytes and risk of sudden cardiac death from m
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an uncommon cardiac disease characterized
Arrhythmogenic right ventricular dysplasia: a review.
Dalal P, Fujisic K, Hupart P, Schwietzer P. Dalal P, et al. Cardiology. 1994;85(6):361-9. doi: 10.1159/000176737. Cardiology. 1994. PMID: 7697671 Review.
Arrhythmogenic right ventricular (RV) dysplasia is a predominant disorder of the RV, characterized by progressive replacement of myocardium by fibroadipose tissue and arrhythmic manifestations. ...They may miss cases with less involvement where gated M
Arrhythmogenic right ventricular (RV) dysplasia is a predominant disorder of the RV, characterized by progressiv
Arrhythmogenic right ventricular dysplasia/cardiomyopathy.
El Masry HZ, Yadav AV. El Masry HZ, et al. Expert Rev Cardiovasc Ther. 2008 Feb;6(2):249-60. doi: 10.1586/14779072.6.2.249. Expert Rev Cardiovasc Ther. 2008. PMID: 18248278 Review.
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a cardiac disease characterized by fibrofatty replacement of the cardiac myocytes. Patients with ARVD/C frequently present with ventricular tachycardia and many are thought to
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a cardiac disease characterized by fibrofa
Arrhythmogenic right ventricular dysplasia/cardiomyopathy: a review.
Marcus FI, Fontaine G. Marcus FI, et al. Pacing Clin Electrophysiol. 1995 Jun;18(6):1298-314. doi: 10.1111/j.1540-8159.1995.tb06971.x. Pacing Clin Electrophysiol. 1995. PMID: 7659585 Review.
Right ventricular dysplasia is being recognized with increasing frequency. ...Cinemagnetic resonance imaging demonstrates abnormal fatty infiltration of the right ventricular myocardium and can show increased right ventricular dime
Right ventricular dysplasia is being recognized with increasing frequency. ...Cinemagnetic resonance imaging demonstrat
Arrhythmogenic Right Ventricular Cardiomyopathy: Risk Stratification and Indications for Defibrillator Therapy.
Zorzi A, Rigato I, Bauce B, Pilichou K, Basso C, Thiene G, Iliceto S, Corrado D. Zorzi A, et al. Curr Cardiol Rep. 2016 Jun;18(6):57. doi: 10.1007/s11886-016-0734-9. Curr Cardiol Rep. 2016. PMID: 27147509 Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetically determined disease which predisposes to life-threatening ventricular arrhythmias. ...While there is general agreement that patients with a history of cardiac arrest or hemodynamica
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetically determined disease which predisposes to life-th
Diagnosis and management of arrhythmogenic right ventricular cardiomyopathy.
Alblaihed L, Kositz C, Brady WJ, Al-Salamah T, Mattu A. Alblaihed L, et al. Am J Emerg Med. 2023 Mar;65:146-153. doi: 10.1016/j.ajem.2022.12.010. Epub 2022 Dec 12. Am J Emerg Med. 2023. PMID: 36638611 Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetic disorder of the myocardium that can lead to ventricular arrhythmia and sudden cardiac death. ...
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetic disorder of the myocardium that can lead to vent
Cardiomyopathies in children: An overview.
Tsatsopoulou A, Protonotarios I, Xylouri Z, Papagiannis I, Anastasakis A, Germanakis I, Patrianakos A, Nyktari E, Gavras C, Papadopoulos G, Meditskou S, Lazarou E, Miliou A, Lazaros G. Tsatsopoulou A, et al. Hellenic J Cardiol. 2023 Jul-Aug;72:43-56. doi: 10.1016/j.hjc.2023.02.007. Epub 2023 Mar 3. Hellenic J Cardiol. 2023. PMID: 36870438 Free article. Review.
Dilated and hypertrophic cardiomyopathy phenotypes share an incidence of 60% and 25%, respectively. Arrhythmogenic right ventricular cardiomyopathy (ARVC), restrictive cardiomyopathy, and left ventricular noncompaction are less commonly diagnosed. ...S …
Dilated and hypertrophic cardiomyopathy phenotypes share an incidence of 60% and 25%, respectively. Arrhythmogenic right ve
[Arrhythmogenic right ventricular cardiomyopathy/dysplasia. Literature review and case report].
Camargo-Ariza WA, Galvis-Blanco SJ, Camacho-Enciso TDP, Quiroz-Romero CA, Bermudez-Echeverry JJ. Camargo-Ariza WA, et al. Arch Cardiol Mex. 2018 Jan-Mar;88(1):51-59. doi: 10.1016/j.acmx.2017.05.001. Epub 2017 Jun 13. Arch Cardiol Mex. 2018. PMID: 28623036 Review. Spanish.
Arrhythmogenic right ventricular cardiomyopathy/dysplasia is an inherited autosomal dominant disease, with an estimated prevalence of 1:2,500 to 1:5,000, being higher in males (3:1). ...A comprehensive review of the patient's medical records was perfor
Arrhythmogenic right ventricular cardiomyopathy/dysplasia is an inherited autosomal dominant disease, with an es
75 results