Results 31 to 40 of about 7,984 (209)

Atrial tachycardia in a patient with arrhythmogenic right ventricular cardiomyopathy/dysplasia

Journal of Arrhythmia, 2013
We describe a 49-year-old woman with atrial tachycardia (AT) and arrhythmogenic right ventricular cardiomyopathy/dysplasia. Cardiac magnetic resonance images showed a markedly dilated right atrium and right ventricle.
Hiroaki Mano, Ichiro Watanabe, Yasuo Okumura, Kazumasa Sonoda, Koichi Nagashima, Toshiko Nakai, Kimie Ohkubo, Tatsuya Kofune, Hironori Haruta, Masayoshi Kofune, Satoshi Kunimoto, Atsushi Hirayama   +11 more
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Evolution of diagnostic criteria for arrhythmogenic right ventricular cardiomyopathy and their application in clinical practice

Российский кардиологический журнал, 2021
This article describes evolution of criteria for arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C). The novel diagnostic criteria for ARVD/C published in 2020 are analyzed in detail, among which biventricular and leftdominant ...
Yu. A. Lutokhina, O. B. Blagova, A. G. Shestak, E. V. Zaklyazminskaya, S. A. Alexandrova, A. V. Nedostup   +5 more
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Novel compound mutations in the mitochondrial translation elongation factor (TSFM) gene cause severe cardiomyopathy with myocardial fibro-adipose replacement [PDF]

, 2019
Primary mitochondrial dysfunction is an under-appreciated cause of cardiomyopathy, especially when cardiac symptoms are the unique or prevalent manifestation of disease.
Bonnen, Penelope E, Carbo, Miriam, Cerbelli, Bruna, D'Amati, Giulia, Della Monica, Paola Lilla, Falkous, Gavin, Giordano, Carla, Glasgow, Ruth I C, Hardy, Steven A, He, Langping, Morea, Veronica, Perli, Elena, Pignataro, Maria Gemma, Pisano, Annalinda, Re, Federica, Taylor, Robert W, Zacara, Elisabetta   +16 more
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Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice [PDF]

, 2017
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an inherited myocardial disease characterized by fibro-fatty replacement of the right ventricular myocardium, and associated with paroxysmal ventricular arrhythmias and sudden cardiac ...
Antoniades, Aquaro, Avella, Bai, Bao, Battipaglia, Beffagna, Bhonsale, Bhonsale, Breithardt, Broch, Burghouwt, Calkins, Camm, Carvajal-Huerta, Chung, Corrado, D'Ascenzi, Dawson, Dechering, Erkapic, Ermakov, Ermakov, Femia, Fontaine, Gerull, Hamid, Hengel, Hoffmayer, Iriyama, Iyer, James, Jiang, Kataoka, Khaji, Kimura, Kirubakaran, Klauke, Leren, Lewis, Li, Liao, Lin, Lopez-Moreno, Mano, Marcus, Maron, Maron, Mayosi, McKenna, McKoy, Merner, Mussigbrodt, Mussigbrodt, Ohno, Opbergen, Peters, Peters, Peters, Philips, Pilichou, Platonov, Protonotarios, Protonotarios, Quarta, Rampazzo, Riele, Riele, Romero, Romero, Ruwald, Saffitz, Santangeli, Saprungruang, Schinkel, Sen-Chowdhry, Sen-Chowdhry, Sen-Chowdhry, Severini, Silvano, Souissi, Steckman, Sultan, Suzuki, Syrris, Taylor, Te Riele, Tiso, Tse, Tse, Tse, Tse, Vite, Wang, Ward, Wei, Weiner, Wichter, Wlodarska, Wu, Xu, Zhurinsky, Zwaag   +102 more
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Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Diagnostic Task Force Criteria Impact of New Task Force Criteria [PDF]

, 2010
Background-Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C) Diagnostic Task Force Criteria (TFC) proposed in 1994 are highly specific but lack sensitivity. A new international task force modified criteria to improve diagnostic yield.
Arens, Y., Atsma, D.E., Cox, M.G.P.J., Cramer, M.J., Doevendans, P.A., Dooijes, D., Hauer, R.N.W., Houweling, A.C., Jordaens, L., Langen, I.M. van, Loh, P., Noorman, M., Smagt, J.J. van der, Tintelen, P. van, Volders, P.G.A., Wiesfeld, A.C., Wilde, A.A.M.   +16 more
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Treatment of arrhythmogenic right ventricular cardiomyopathy (dysplasia) [PDF]

Кардіохірургія та інтервенційна кардіологія, 2016
Arrhythmogenic right ventricular cardiomyopathy (dysplasia) is an inheritable heart muscle disease predisposing to ventricular arrhythmias and increasing risk of sudden cardiac death.
M.Т. Vatutin, G.S. Smyrnova, Y.V. Yeshchenko, G.E. Degtiarova, V.S. Kolesnikov, Y.P. Gritsenko   +5 more
doaj  

Arrhythmogenic right ventricular cardiomyopathy: From pathophysiology to diagnosis and advances in management [PDF]

, 2017
Our understanding of arrhythmogenic right ventricular cardiomyopathy (ARVC) has advanced considerably over the past 30- 40 years. This is an inherited cardiomyopathy with complicated genetic inheritance and variable penetrance.
Bastiaenen, R, Deyell, MW, Krahn, AD
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First Reported Case of Arrhythmogenic Right Ventricular Cardiomyopathy in Oman

Oman Medical Journal, 2017
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare genetic disorder characterized by fatty degeneration of the right ventricular myocardium with variable involvement of the left ventricle.
Hatim Al Lawati, Humoud Al Dhuhli
doaj   +1 more source

Association of tricuspid annular plane systolic excursion (TAPSE) with survival time in Boxer dogs with ventricular arrhythmias [PDF]

, 2015
BACKGROUND: Tricuspid annular plane systolic excursion (TAPSE) is a useful estimate of right ventricular function in humans. Reference intervals for dogs have been generated, but the value of measuring TAPSE in other diseases, or investigating the ...
Basso, Baumwart, Baumwart, Boon, Bussadori, Dini, Finocchiaro, Forfia, Gupta, Haddad, Hansson, Harpster, Lobo, López-Candales, Marcus, Mercer-Rosa, Meurs, Meurs, Mõtsküla, Oxford, Palermo, Pariaut, Saguner, Sahn, Smets, Spier, Spier, Stern, Thomas, Ueti, Vizzardi   +30 more
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Electrocardiographic Patterns of Ventricular Arrhythmias in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

Frontiers in Physiology, 2012
Ventricular arrhythmias in patients with ARVD/C are common. Differentiation between idiopathic ventricular tachycardia and arrhythmogenic right ventricular dysplasia is of utmost importance.
Kurt eHoffmayer, Melvin M Scheinman
doaj   +1 more source