Results 21 to 30 of about 2,626,293 (190)

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

Analysis of desmoplakin in arrythmogenic right ventricular cardiomyopathy [PDF]

, 2010
Includes bibliographical references (leaves 71-79).It has been shown that all forms of cardiomyopathy, including the dilated, hypertrophic, restrictive, and right ventricular arrhythmogenic forms, are found in African populations.
Fish, Maryam
core   +1 more source

Molecular genetics of arrhythmogenic right ventricular cardiomyopathy in South Africa [PDF]

, 2011
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heritable disorder characterised by progressive degeneration of the right ventricular myocardium, arrhythmias and an increased risk of sudden death at a young age. Fourteen chromosomal loci have
Blanckenberg, Janine
core   +1 more source

The multi-modality cardiac imaging approach to the Athlete's heart: an expert consensus of the European Association of Cardiovascular Imaging [PDF]

, 2015
peer reviewedThe term 'athlete's heart' refers to a clinical picture characterized by a slow heart rate and enlargement of the heart. A multi-modality imaging approach to the athlete's heart aims to differentiate physiological changes due to intensive ...
Galderisi, Maurizio, Popescu, Bogdan A., Cosyns, B, Petersen, SE, Cardim, Nuno, DAVIN, Laurent, Schroeder, S, Kitsiou, Anastasia, Cosyns, Bernard, Lancellotti, Patrizio, Petersen, Steffen E., Habib, G, Kitsiou, A, Edvardsen, T, Davin, L, Cardim, N, Bruder, Oliver, Popescu, Bogdan Alexandru, Burgstahler, C, D'Andrea, Antonello, Donal, E, Bruder, O, Plein, S, Freitas, A, Freitas, Antonio, Burgstahler, Christof, Galderisi, M, Edvardsen, Thor, Donal, Erwan, Lancellotti, P, Plein, Sven, D'Andrea, A, Schroeder, Stephen, Habib, Gilbert, Popescu, BA   +34 more
core   +1 more source

Arrhythmogenic right ventricular cardiomyopathy

Journal of Arrhythmia, 2018
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a progressive cardiomyopathy characterized by fibrofatty infiltration of the myocardium, ventricular arrhythmias, sudden death, and heart failure. ARVC may be an important cause of syncope, sudden
Yongkeun Cho
doaj   +1 more source

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

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

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

, 2017
滋賀医科大学博士（医学）Background: Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an inherited cardiomyopathy mainly caused by desmosomal gene mutation.
WADA, Yuko
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

Arrhythmogenic right ventricular cardiomyopathy/dysplasia

Orphanet Journal of Rare Diseases, 2007
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a heart muscle disease clinically characterized by life-threatening ventricular arrhythmias. Its prevalence has been estimated to vary from 1:2,500 to 1:5,000.
Basso Cristina, Corrado Domenico, Thiene Gaetano   +2 more
doaj   +1 more source