Results 31 to 40 of about 26,419 (210)

Familial screening in case of acute myocarditis reveals inherited arrhythmogenic left ventricular cardiomyopathies

ESC Heart Failure, 2020
Aims Several data suggest that acute myocarditis could be related to genetic variants involved in familial cardiomyopathies, particularly arrhythmogenic cardiomyopathy, but the management of patients with acute myocarditis and their families regarding ...
Nicolas Piriou, Lara Marteau, Florence Kyndt, Jean Michel Serfaty, Claire Toquet, Laurianne Le Gloan, Karine Warin‐Fresse, Damien Guijarro, Thierry Le Tourneau, Emilie Conan, Aurélie Thollet, Vincent Probst, Jean‐Noël Trochu   +12 more
doaj   +1 more source

Arrhythmogenic right ventricular cardiomyopathy in monozygotic twin sisters, and persistent left superior vena cava in one complicating implantation of ICD

Türk Kardiyoloji Derneği Arşivi, 2015
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy characterized histologically by fibro-fatty replacement of heart muscle, and clinically by ventricular arrhythmias and right ventricular dysfunction.
Mehmet Ali Astarcıoğlu, Mehmet Yaymacı, Taner Şen, Celal Kilit, Basri Amasyalı   +4 more
doaj   +1 more source

Emergency department extracorporeal membrane oxygenation as a rescue therapy for ventricular tachycardia electrical storm: a case report

Journal of the American College of Emergency Physicians Open, 2020
Arrhythmogenic right ventricular cardiomyopathy is a cause of sudden cardiac death in often otherwise healthy young adults. Cardiac arrest following an unstable tachydysrhythmia may be the primary presenting symptom.
Andrew Pugh, Joseph E. Tonna, Scott Youngquist, John J. Ryan, Graham Brant‐Zawadzki   +4 more
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
core   +2 more sources

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
core   +2 more sources

Mixed phenotype cardiomyopathy, associated with DSP genetic variant: a case report and literature review.

Российский кардиологический журнал, 2020
We report a case of mixed phenotype cardiomyopathy (non-compaction cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy), associated with DSP genetic variant.  The sudden cardiac death was the first and only symptom.
I. V. Shlyk, A. A. Streltsova, V. M. Teplov, E. G. Gavrilova, A. N. Kulikov, A. N. Krutikov, M. G. Rybakova, I. A. Kuznetsova, S. E. Andreeva, T. G. Bezhanishvili, A. A. Khudiakov, A. A. Kostareva, A. Ya. Gudkova   +12 more
doaj   +1 more source

Sudden Death and Left Ventricular Involvement in Arrhythmogenic Cardiomyopathy [PDF]

, 2019
BACKGROUND: Arrhythmogenic cardiomyopathy (ACM) is an inherited heart muscle disorder characterized by myocardial fibrofatty replacement and an increased risk of sudden cardiac death (SCD).
Asimaki, A, Basu, J, Behr, ER, Cook, SA, Ensam, B, Finocchiaro, G, Gray, B, Malhotra, A, Miles, C, Papadakis, M, Papatheodorou, E, Parry-Williams, G, Paterson, C, Robertus, JL, Sharma, S, Sheppard, MN, Ster, IC, Tome, M, Ware, JS, Westaby, J, Witney, A   +20 more
core   +1 more source

Wide Complex Tachycardia in Arrhythmogenic Right Ventricular Cardiomyopathy: Electrocardiogramand Intracardiac Electrogram Features

Indian Journal of Clinical Cardiology, 2022
Case of an arrhythmogenic right ventricular cardiomyopathy with associated arrhythmias discussing classical electrocardiogram and intracardiac electrogram findings.
Rangadham Nagarakanti, Kavin Raj
doaj   +1 more source

Aetiology of sudden cardiac death in sport: a histopathologist's perspective. [PDF]

, 2012
In the UK, when a young person dies suddenly, the coroner is responsible for establishing the cause of death. They will ask a consultant pathologist to carry out an autopsy in order to ascertain when, where and how that person died.
Sheppard, MN
core   +1 more source

A case of arrhythmogenic right ventricular dysplasia/cardiomyopathy with pneumothorax and degloving injury of the right upper limb

BLDE University Journal of Health Sciences, 2020
Arrhythmogenic right ventricular dysplasia / cardiomyopathy (ARVD / C) is a rare genetic cardiomyopathy characterized by fibro-fatty replacement primarily of the right ventricular myocytes,and can present as any of 'concealed' disease, 'overt arrhythmia'
Varun Suresh
doaj   +1 more source