Results 11 to 20 of about 4,606 (191)

Left Ventricular Involvement in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Predicts Adverse Clinical Outcomes: A Cardiovascular Magnetic Resonance Feature Tracking Study. [PDF]

Sci Rep, 2019
The aim of this study was to investigate left ventricular (LV) global myocardial strain and LV involvement characteristics in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and to evaluate their predictive value of ...
Shen MT, Yang ZG, Diao KY, Jiang L, Zhang Y, Liu X, Gao Y, Hu BY, Huang S, Guo YK.   +9 more
europepmc   +2 more sources

Right atrial pathology in arrhythmogenic right ventricular dysplasia. [PDF]

Cardiol J, 2019
Background Atrial fibrillation (AF) is the most common atrial arrhythmia in arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVD). Considering the histologic changes known in the right ventricular (RV) in ARVD, the aim of the present study was
Li G, Fontaine GH, Fan S, Yan Y, Bode PK, Duru F, Frank R, Saguner AM.   +7 more
europepmc   +2 more sources

Epicardial Fat Distribution Assessed with Cardiac CT in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy. [PDF]

Radiology, 2018
Purpose To compare epicardial fat in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) with that in healthy subjects. Materials and Methods In this retrospective study, cardiac CT scans in 44 patients with ARVD/C (mean age,
Aliyari Ghasabeh M, Te Riele ASJM, James CA, Chen HSV, Tichnell C, Murray B, Eng J, Kral BG, Tandri H, Calkins H, Kamel IR, Zimmerman SL.   +11 more
europepmc   +2 more sources

Arrhythmogenic Right Ventricular Dysplasia

Current Problems in Cardiology, 2013
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD) is a genetic cardiomyopathy characterized by ventricular arrhythmias and structural abnormalities of the right ventricle (RV). The discovery of desmosomal mutations associated with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) has led researchers to hypothesize equal ...
Wojciech Mazur, Marilyn J. Siegel, Tomasz Miszalski-Jamka, Robert Pelberg   +3 more
semanticscholar   +6 more sources

TMEM43-S358L mutation enhances NF-κB-TGFβ signal cascade in arrhythmogenic right ventricular dysplasia/cardiomyopathy. [PDF]

Protein Cell, 2019
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a genetic cardiac muscle disease that accounts for approximately 30% sudden cardiac death in young adults.
Zheng G, Jiang C, Li Y, Yang D, Ma Y, Zhang B, Li X, Zhang P, Hu X, Zhao X, Du J, Lin X.   +11 more
europepmc   +2 more sources

Catheter Ablation of Ventricular Tachycardia in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy. [PDF]

Korean Circ J, 2018
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is predominantly an inherited cardiomyopathy with typical histopathological characteristics of fibro-fatty infiltration mainly involving the right ventricular (RV) inflow tract, RV ...
Chung FP, Lin CY, Lin YJ, Chang SL, Lo LW, Hu YF, Tuan TC, Chao TF, Liao JN, Chang TY, Chen SA.   +10 more
europepmc   +2 more sources

Feature tracking CMR reveals abnormal strain in preclinical arrhythmogenic right ventricular dysplasia/ cardiomyopathy: a multisoftware feasibility and clinical implementation study. [PDF]

J Cardiovasc Magn Reson, 2017
BackgroundRegional right ventricular (RV) dysfunction is the hallmark of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C), but is currently only qualitatively evaluated in the clinical setting.
Bourfiss M, Vigneault DM, Aliyari Ghasebeh M, Murray B, James CA, Tichnell C, Mohamed Hoesein FA, Zimmerman SL, Kamel IR, Calkins H, Tandri H, Velthuis BK, Bluemke DA, Te Riele ASJM.   +13 more
europepmc   +2 more sources

Unique genetic background and outcome of non-Caucasian Japanese probands with arrhythmogenic right ventricular dysplasia/cardiomyopathy. [PDF]

Mol Genet Genomic Med, 2017
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an inherited cardiomyopathy mainly caused by desmosomal gene mutation. More than half of Caucasian probands have desmosomal mutations, which lead to earlier onset of ventricular ...
Wada Y, Ohno S, Aiba T, Horie M.
europepmc   +2 more sources

Exercise-related sudden cardiac death of an American football player with arrhythmogenic right ventricular dysplasia/cardiomyopathy AND sarcoidosis. [PDF]

Clin Case Rep, 2019
This case emphasizes the value of cardiac MRI and genetic testing in the early phase of ARVD/C. It also emphasizes the increased risk of SCD for patients with ARVD/C participating in competitive sports, even with immediate cardiopulmonary resuscitation.
Müssigbrodt A, Knopp H, Czimbalmos C, Jahnke C, Richter S, Husser D, Gradistanac T, Hindricks G.   +7 more
europepmc   +2 more sources

Cardiac sarcoidosis mimicking arrhythmogenic right ventricular dysplasia in a patient presenting with monomorphic ventricular tachycardia. [PDF]

HeartRhythm Case Rep, 2017
Key Teaching Points • After coronary ischemia is ruled out, in the setting of new-onset ventricular arrhythmias, it is essential to consider all etiologies of ventricular arrhythmias. • Cardiac fluorodeoxyglucose–positron emission tomography computed
Biggs R, Patel B, Martinez MW, McCambridge M, Kim S, Marcus N.   +5 more
europepmc   +2 more sources