Results 101 to 110 of about 7,984 (209)

Role of cardiovascular magnetic resonance imaging in arrhythmogenic right ventricular dysplasia

Journal of Cardiovascular Magnetic Resonance, 2008
Arrhythmogenic right ventricular dysplasia (ARVD) is a genetic cardiomyopathy characterized clinically by ventricular arrhythmias and progressive right ventricular (RV) dysfunction. The histopathologic hallmark is fibro-fatty replacement of RV myocardium.
Bluemke David A, Calkins Hugh, Tandri Harikrishna, Jain Aditya   +3 more
doaj   +1 more source

Ventricular Tachycardia in the Absence of Structural Heart Disease [PDF]

In up to 10% of patients who present with ventricular tachycardia (VT), obvious structural heart disease is not identified. In such patients, causes of ventricular arrhythmia include right ventricular outflow tract (RVOT) VT, extrasystoles, idiopathic ...
Srivathsan, Komandoor, Lester, Steven J, Appleton, Christopher P, Scott, Luis R P, Munger, Thomas M   +4 more
core  

Prognostic value of right atrial strains in arrhythmogenic right ventricular cardiomyopathy

Insights into Imaging
Objectives Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy characterized by progressive fibrofatty infiltration of atrial and ventricular myocardium resulting in adverse cardiac events.
Jin-Yu Zheng, Bing-Hua Chen, Rui Wu, Dong-Aolei An, Ruo-Yang Shi, Chong-Wen Wu, Lang-Lang Tang, Lei Zhao, Lian-Ming Wu   +8 more
doaj   +1 more source

First International Symposium on Arrhythmogenic Right Ventricular Dysplasia on Internet: April, 1st to 15th 2005

Indian Pacing and Electrophysiology Journal, 2005
The Symposium will consist of a series of lectures on the web. The program will have the participation of several faculty members, the most distinguished international specialists in the topic. The registration is totally free of charge.
ARVD Symposium Scientific Committee
doaj  

Sudden cardiac death in congenital arrhythmogenic syndromes: Risk stratification and management

Heart Vessels and Transplantation
In young individuals, sudden cardiac death (SCD) is often caused by genetic heart diseases, which are usually classified into inherited cardiomyopathies and primary electrical heart diseases.
Samir Morcos Rafla, Moustafa Eissa Nawar, Mohamed Ibrahim Sanhoury, Moustafa Ali Dawood, Ashraf Abdelaziz Elamin, Aly Aboelhoda Ahmed, Moataz Ahmed Zaki, Hany Samir Assaad   +7 more
doaj   +1 more source

Epicardial access facilitated by carbon dioxide insufflation for redo ventricular tachycardia ablation in a patient with arrhythmogenic right ventricular dysplasia and dense adhesions. [PDF]

HeartRhythm Case Rep, 2021
Leyton-Mange JS, Sze EY, Conley C, Vasaiwala SC, Sesselberg HW.   +4 more
europepmc   +1 more source

Genetics of Inherited Arrhythmias in Children

Indian Pacing and Electrophysiology Journal, 2008
Over the past two decades, breakthroughs in basic science have revealed the genetic etiology for several inherited arrhythmias. Onset of arrhythmias often commences in childhood and adolescence.
Maully J. Shah
doaj  

Arrhythmogenic Right Ventricular Dysplasia

Journal of the American College of Cardiology, 2009
Barrios, Vivencio, Escobar, Carlos, Calderon, Alberto   +2 more
openaire   +2 more sources

Transesophageal and intracardiac ultrasound in arrhythmogenic right ventricular dysplasia/cardiomyopathy: Two case reports. [PDF]

Medicine (Baltimore), 2020
Cismaru G, Grosu A, Istratoaie S, Mada L, Ilea M, Gusetu G, Zdrenghea D, Pop D, Rosu R.   +8 more
europepmc   +1 more source

Anesthetic management of a parturient with Behcet's disease and suspected arrhythmogenic right ventricular dysplasia. [PDF]

Korean J Anesthesiol, 2020
Giuri PP, Gonnella GL, Catarci S, Ciancia M, Draisci G.   +4 more
europepmc   +1 more source