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Quoted phrase not found in phrase index: "Familial isolated arrhythmogenic right ventricular dysplasia"
Page 1
Atrial fibrillation in patients with inherited cardiomyopathies.
Yeung C, Enriquez A, Suarez-Fuster L, Baranchuk A. Yeung C, et al. Europace. 2019 Jan 1;21(1):22-32. doi: 10.1093/europace/euy064. Europace. 2019. PMID: 29684120 Review.
Atrial fibrillation (AF) often complicates the course of inherited cardiomyopathies and, in some cases, may be the presenting feature. ...In this article, we review the current information on the prevalence, pathophysiology, risk factors, and treatment of AF in three diffe …
Atrial fibrillation (AF) often complicates the course of inherited cardiomyopathies and, in some cases, may be the presenting feature …
Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Sen-Chowdhry S, Syrris P, McKenna WJ. Sen-Chowdhry S, et al. J Am Coll Cardiol. 2007 Nov 6;50(19):1813-21. doi: 10.1016/j.jacc.2007.08.008. Epub 2007 Oct 24. J Am Coll Cardiol. 2007. PMID: 17980246 Free article. Review.
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a recognized cause of sudden cardiac death, which may be prevented by timely detection and intervention. ...A role for genetic analysis in prognostication is more tenuous at present, but increas …
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a recognized cause of sudden cardiac death, which may be prev …
Isolated JUP plakoglobin gene mutation with left ventricular fibrosis in familial arrhythmogenic right ventricular cardiomyopathy.
Zinkovsky D, Sood MR. Zinkovsky D, et al. J Cardiovasc Electrophysiol. 2023 Oct;34(10):2112-2121. doi: 10.1111/jce.16044. Epub 2023 Sep 17. J Cardiovasc Electrophysiol. 2023. PMID: 37717241
INTRODUCTION: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare inherited disorder usually affecting the right ventricle (RV), characterized by fibro-fatty tissue replacement of the healthy ventricular myocardium. ...During his …
INTRODUCTION: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare inherited disorder usually affecting the …
Arrhythmogenic Right Ventricular Dysplasia: An Under-recognized Form of Inherited Cardiomyopathy.
Adesina GO, Hall SA, Mendez JC, Joseph SM, Gottlieb RL, Kale PP, Bindra AS. Adesina GO, et al. Rev Cardiovasc Med. 2017;18(1):37-43. doi: 10.3909/ricm0855. Rev Cardiovasc Med. 2017. PMID: 28509892 Review.
We report a case of arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVD) in order to evaluate the course of an under-recognized form of cardiomyopathy with a vast array of clinical manifestations. ...Initial work-up for hypoxia was u …
We report a case of arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVD) in order to evaluate the …
Scintigraphic spectrum of a patient population with suspected arrhythmogenic right ventricular dysplasia.
Merabet Y, Bontemps L, Chevalier P, Itti R. Merabet Y, et al. Int J Cardiovasc Imaging. 2012 Jun;28(5):1267-77. doi: 10.1007/s10554-011-9918-y. Epub 2011 Jul 6. Int J Cardiovasc Imaging. 2012. PMID: 21732029
Gated radionuclide ventriculography (RNV), combined with inter- and intraventricular dyssynchrony measurement by phase analysis, is able to evidence right and left ventricular mechanical cardiac disorders and may contribute to the diagnosis of arrhythmogenic …
Gated radionuclide ventriculography (RNV), combined with inter- and intraventricular dyssynchrony measurement by phase analysis, is able to …
Inherited cardiac arrhythmias: diagnosis, treatment, and prevention.
Beckmann BM, Pfeufer A, Kääb S. Beckmann BM, et al. Dtsch Arztebl Int. 2011 Sep;108(37):623-33; quiz 634. doi: 10.3238/arztebl.2011.0623. Epub 2011 Sep 16. Dtsch Arztebl Int. 2011. PMID: 21977220 Free PMC article. Review.
Among such cases, the hereditary arrhythmia syndrome is primary in 70% and caused by an arrhythmogenic structural heart disease in 30%. In addition to autopsy findings, a thorough family history, relevant medical findings obtained during life (if available), the exa …
Among such cases, the hereditary arrhythmia syndrome is primary in 70% and caused by an arrhythmogenic structural heart disease in 30 …
Prophylactic implantable defibrillator in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia and no prior ventricular fibrillation or sustained ventricular tachycardia.
Corrado D, Calkins H, Link MS, Leoni L, Favale S, Bevilacqua M, Basso C, Ward D, Boriani G, Ricci R, Piccini JP, Dalal D, Santini M, Buja G, Iliceto S, Estes NA 3rd, Wichter T, McKenna WJ, Thiene G, Marcus FI. Corrado D, et al. Circulation. 2010 Sep 21;122(12):1144-52. doi: 10.1161/CIRCULATIONAHA.109.913871. Epub 2010 Sep 7. Circulation. 2010. PMID: 20823389
BACKGROUND: The role of implantable cardioverter-defibrillator (ICD) in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia and no prior ventricular fibrillation (VF) or sustained ventricular tachycardia is an unsolved …
BACKGROUND: The role of implantable cardioverter-defibrillator (ICD) in patients with arrhythmogenic right ventricular …
Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene.
Merner ND, Hodgkinson KA, Haywood AF, Connors S, French VM, Drenckhahn JD, Kupprion C, Ramadanova K, Thierfelder L, McKenna W, Gallagher B, Morris-Larkin L, Bassett AS, Parfrey PS, Young TL. Merner ND, et al. Am J Hum Genet. 2008 Apr;82(4):809-21. doi: 10.1016/j.ajhg.2008.01.010. Epub 2008 Feb 28. Am J Hum Genet. 2008. PMID: 18313022 Free PMC article.
Autosomal-dominant arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) causes sudden cardiac death and is characterized by clinical and genetic heterogeneity. Fifteen unrelated ARVC families with a disease-associated haplotype on …
Autosomal-dominant arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) causes sudden cardiac deat …
Follow-up of patients with arrhythmogenic right ventricular cardiomyopathy dysplasia.
Munclinger MJ, Patel JJ, Mitha AS. Munclinger MJ, et al. S Afr Med J. 2000 Jan;90(1):61-8. S Afr Med J. 2000. PMID: 10721396
OBJECTIVE: The enlargement of data on the natural course and management of patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D). ...At the end of follow-up for 3.4 +/- 3.2 years, 7 of them were well and alive on anti- …
OBJECTIVE: The enlargement of data on the natural course and management of patients with arrhythmogenic right ventri …
Cardiac magnetic resonance in patients with ARVC and family members: the potential role of native T1 mapping.
Georgiopoulos G, Zampieri M, Molaro S, Chaloupka A, Aimo A, Barra B, Roberts L, Monje-Garcia L, Evans C, Sheikh N, Bastiaenen R, Cooklin M, Masci PG, Carr-White G, Finocchiaro G, Chiribiri A. Georgiopoulos G, et al. Int J Cardiovasc Imaging. 2021 Jun;37(6):2037-2047. doi: 10.1007/s10554-021-02166-7. Epub 2021 Feb 7. Int J Cardiovasc Imaging. 2021. PMID: 33550486 Free PMC article.
Left ventricular (LV) involvement in patients with arrhythmogenic right ventricular cardiomyopathy (ARVC) is not evaluated in the revised Task Force Criteria, possibly leading to underdiagnosis. ...Thirty ARVC patients (47% males, mean age 45 27 years) …
Left ventricular (LV) involvement in patients with arrhythmogenic right ventricular cardiomyopathy (ARVC) is not …
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