Results 1 to 10 of about 32,361 (211)

Arrhythmogenic Cardiomyopathy

Zdravniški Vestnik, 2019
Arrhythmogenic cardiomyopathy (AC) is a genetic disease of the myocardium characterized by fibro-fatty replacement of the apoptotic myocardium. It primarily affects the right ventricle, however in advanced stages of the disease the left ventricle can ...
Blaž Podgoršek, Gregor Poglajen, Andraž Cerar, Matjaž Šinkovec, Bojan Vrtovec   +4 more
doaj   +3 more sources

Arrhythmogenic Cardiomyopathy [PDF]

Circulation, 2018
Arrhythmogenic cardiomyopathy (AC) is a genetic disorder characterized by high risk of life-threatening ventricular arrhythmias, sudden cardiac death, and progressive heart failure. Currently, there is evidence that AC includes a spectrum of cardiomyopathy phenotypes, ranging from the classical form of arrhythmogenic right ventricular cardiomyopathy ...
Pilichou K., Basso C., Corrado D., Thiene G.   +3 more
  +9 more sources

Arrhythmogenic Cardiomyopathy [PDF]

European Heart Journal, 2020
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Beffagna, Giorgia, Zorzi, Alessandro, Pilichou, Kalliopi, Perazzolo Marra, Martina, Rigato, Ilaria, Corrado, Domenico, Migliore, Federico, Rampazzo, Alessandra, Bauce, Barbara, Basso, Cristina, Thiene, Gaetano   +10 more
  +7 more sources

Arrhythmogenic Cardiomyopathy [PDF]

Circulation Research, 2017
Arrhythmogenic cardiomyopathy is an inherited heart muscle disorder, predisposing to sudden cardiac death, particularly in young patients and athletes. Pathological features include loss of myocytes and fibrofatty replacement of right ventricular myocardium; biventricular involvement is often observed.
Corrado, Domenico, Basso, Cristina, Judge, Daniel P.   +2 more
  +13 more sources

Multimodality imaging in arrhythmogenic cardiomyopathy [PDF]

Romanian Journal of Cardiology, 2021
Arrhythmogenic cardiomyopathy, as it has been recently redefined, is characterized by progressive myocyte loss with fibrosis and fat infiltration of the myocardium, which finally leads to a broad clinical spectrum ranging from heart failure symptoms to ...
Laura Tapoi, Alexandra Clement, Rodica Radu, Radu Sascau   +3 more
doaj   +1 more source

Arrhythmogenic Cardiomyopathy: Expanding Phenotypic Variability in Different Populations Around the World. [PDF]

JACC Asia
Olivetti N, Sacilotto L, Vieira MLC.
europepmc   +2 more sources

Biventricular arrhythmogenic cardiomyopathy diagnosed in a young patient: A case report with literature review

Radiology Case Reports, 2023
Arrhythmogenic cardiomyopathy is a genetic heart muscle disease that typically affects the right ventricle. However, 2 other phenotypes affecting the left ventricle were recently discovered.
Hajar El Ouartassi, MD, Raid Faraj, MD, Zakariae Laraichi, MD, Rhita Ezzahraoui, MD, Zaineb Bourouhou, MD, Nawal Doghmi, PhD, Mohamed Cherti, PhD   +6 more
doaj   +1 more source

Scarring/arrhythmogenic cardiomyopathy

European Heart Journal Supplements, 2023
Abstract The designation of ‘arrhythmogenic cardiomyopathy’ reflects the evolving concept of a heart muscle disease affecting not only the right ventricle (ARVC) but also the left ventricle (LV), with phenotypic variants characterized by a biventricular (BIV) or predominant LV involvement (ALVC).
Corrado, Domenico, Zorzi, Alessandro, Cipriani, Alberto, Bauce, Barbara, Bariani, Riccardo, Brunetti, Giulia, Graziano, Francesca, De Lazzari, Manuel, Mattesi, Giulia, Migliore, Federico, Pilichou, Kalliopi, Rigato, Ilaria, Rizzo, Stefania, Thiene, Gaetano, Perazzolo Marra, Martina, Basso, Cristina   +15 more
openaire   +2 more sources

Arrhythmogenic Right Ventricular Cardiomyopathy [PDF]

Circulation: Arrhythmia and Electrophysiology, 2011
Arrhythmogenic disorders of genetic origin include structural cardiomyopathies and inherited arrhythmic syndromes.1 Arrhythmogenic right ventricular cardiomyopathy (ARVC) is listed among the former, because it is characterized by structural and functional abnormalities of the right ventricle (RV), ranging from regional wall motion abnormalities and ...
PILICHOU, KALLIOPI, THIENE, GAETANO, Corrado D, BASSO, CRISTINA   +3 more
openaire   +8 more sources

Generation of human iPSC line from an arrhythmogenic cardiomyopathy patient with a DSP protein-truncating variant

Stem Cell Research, 2023
Arrhythmogenic cardiomyopathy is an inheritable heart disease characterized by lethal heart rhythms and abnormal contractile function. Mutations in desmoplakin (DSP), a protein linking the cardiac desmosome with intermediate filaments, are associated ...
Alexander Loiben, Clayton E. Friedman, Wei-Ming Chien, April Stempien-Otero, Shin Lin, Kai-Chun Yang   +5 more
doaj   +1 more source