Results 81 to 90 of about 7,984 (209)

Diagnostic and prognostic roles of echocardiography and cardiac magnetic resonance [PDF]

, 2016
Cardiolog
Chiara Bucciarelli-Ducci, Jeroen J. Bax, Victoria Delgado   +2 more
core   +2 more sources

[Arrhythmogenic right ventricular dysplasia].

Arquivos brasileiros de cardiologia, 1992
To evaluate the clinical findings and complementary investigation to support the diagnosis of arrhythmogenic right ventricular dysplasia.Six males with a mean age of 40 years old with episodes of sustained ventricular tachycardia with left bundle branch block pattern.
I G, Maia, R, Sá, R, Bassan, P, Alves, J C, Ribeiros, L H, Loyola, F E, Cruz Filho, A, Valverde, L, Belém   +8 more
openaire   +2 more sources

Arrhythmogenic Right Ventricular Cardiomyopathy in Children: A Systematic Review

Diagnostics
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited disease characterized by the progressive replacement of the normal myocardium by fibroadipocytic tissue.
Stefana Maria Moisa, Elena Lia Spoiala, Eliza Cinteza, Radu Vatasescu, Lacramioara Ionela Butnariu, Crischentian Brinza, Alexandru Burlacu   +6 more
doaj   +1 more source

Naxos disease: from the origin to today

Orphanet Journal of Rare Diseases, 2018
Naxos disease, first described by Dr. Nikos Protonotarios and colleagues on the island of Naxos, Greece, is a special form of arrhythmogenic right ventricular dysplasia (ARVD).
Guo-Liang Li, Ardan M. Saguner, Guy H. Fontaine   +2 more
doaj   +1 more source

Heart MRI Images Analysis in Case of Arrythmogenic Right Ventricular Cardiomyopathy (ARVC) [PDF]

, 2018
Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is a cause of sudden cardiac death in otherwise healthy young adults. (ARVD/C) is an inherited cardiomyopathy characterized by life-threatening ventricular arrhythmias and slowly progressive ...
Apriantoro, N. H. (Nursama), Sari, G. (Gando), Sriyatun, S. (Sriyatun)   +2 more
core  

Abnormal ECG Findings in Athletes: Clinical Evaluation and Considerations. [PDF]

, 2019
PURPOSE OF REVIEW: Pre-participation cardiovascular evaluation with electrocardiography is normal practice for most sporting bodies. Awareness about sudden cardiac death in athletes and recognizing how screening can help identify vulnerable athletes have
A Biffi, A Biffi, A D’Silva, A D’Silva, A Magalski, A Malhotra, A Malhotra, A Malhotra, A Merghani, A Morshedi-Meibodi, A Pelliccia, A Pelliccia, A Zaidi, A Zaidi, A Zorzi, A Zorzi, A Zorzi, AD Desai, AL Aro, AL Rao, AO Usoro, BJ Maron, BJ Maron, C Antzelevitch, C Calore, C Daubert, C Miles, D Corrado, D Corrado, D Corrado, D Corrado, F D’Ascenzi, F Migliore, F Schnell, FI Marcus, G Finocchiaro, G Malfatto, G Mcclean, GJ Klein, GJ Klein, H Dhutia, H Morita, HUH Virk, J Basu, J Ehtisham, J Marek, J Novak, J Pei, J Steinfurt, JA Drezner, JA Drezner, KG Harmon, KM Park, L Calò, L Verdile, M Brosnan, M Papadakis, M Papadakis, M Sadron Blaye-Felice, MAE Haukilahti, Mark Abela, MG Wilson, MI Cohen, MJ Ackerman, MJ Brosnan, N Chandra, N Panhuyzen-goedkoop, N Sheikh, P Banankhah, PG Postema, PT Matusik, RE Bent, RE Eckart, S Gati, S Kapa, S Masrur, S Peters, S Sharma, S Viskin, Sanjay Sharma, SEE Page, T Senturk, X Li, YH Lee   +83 more
core   +1 more source

An atypical case report of an arrhythmogenic cardiomyopathy in a 70-years-old patient with suggestive left ventricular signs

Radiology Case Reports
Arrhythmogenic dysplasia of the right ventricule (ARVC), actually known as arrhythmogenic cardiomyopathy (ACM) is a rare genetic condition caused by the replacement of the normal right ventricular myocardium with fibrofatty tissue.
ikram Tahani, MD, oumayma Hattab, MD, Nabila ismaili, PhD, Noha el ouafi, PhD   +3 more
doaj   +1 more source

Varied Presentation of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C): A Case Series. [PDF]

Cureus, 2023
Mishra D, Shankar O, Aggarwal V.
europepmc   +1 more source

Sudden cardiac death in inherited cardiomyopathy [PDF]

, 2017
Cardiomyopathy is an important cause of sudden cardiac death particularly in adolescents and young adults. The risk of sudden cardiac death varies between individual cardiomyopathies and is dependent on the severity of disease, age and gender.
Collis, R, Elliott, PM
core   +1 more source

Arrhythmogenic Right Ventricular Dysplasia (ARVD) With Protein Plakophilin-2 Mutation. [PDF]

Cureus, 2022
Riasat M, Khan A, Meghrajani V, Gaikwad M, Gill R.   +4 more
europepmc   +1 more source