Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

18 results
Display

A Case of Arrhythmogenic Right Ventricular Dysplasia

Kim YK, Han DS, Kweon SH, Lee MI, Lee HJ

Arrhythmogenic right ventricular dysplasia is a rare heart muscle disorder of unknown cause that primarily involves the right ventricle. It is characterized pathologically by fibrofatty replacement of the right ventricular...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Catheter Ablation of Ventricular Tachycardia/Fibrillation in a Patient with Right Ventricular Amyloidosis with Initial Manifestations Mimicking Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

Chung FP, Lin YJ, Kuo L, Chen SA

Differentiating arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) from other cardiomyopathies is clinically important but challenging. Although the modified Task Force Criteria can facilitate diagnosis of ARVD/C according to clinical manifestations, histopathological...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Arrythmogenic Right Ventricular Dysplasia

Choi KJ, Kwon HC, Nam GB, Kim YJ, Kim HS, Sohn DW, Oh BH, Lee MM, Park YB, Choi YS, Seo JD, Lee YW, Hong TJ, Shin YW

Arrhythmogenic right ventricular dysplasia is a rare but important cause of ventricular tachycardia in young patioents, which is of a left bundle branch block configuration, The common abnormality on routine...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A case of arrhythmogenic right ventricular cardiomyopathy/dysplasia involving the left ventricle

Kim YK, Kim JH, Kim DG, Jeong KT, Choi YJ, Lee S, Park SC

  • KMID: 2081657
  • Korean J Med.
  • 2009 Apr;76(Suppl 1):S64-S69.
Arrhythmogenic right ventricular cardiomyopathy (ARVC)/dysplasia is characterized by fibro-fatty replacement of the right ventricular myocardium. A 19-year-old soldier was admitted with sudden cardiac arrest that presented as ventricular fibrillation requiring...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy with Cardiac Arrest in the Emergency Department

Yang HB, Sung WY, Park HW, Lee JY, Hong SY, Yang YM

  • KMID: 2331497
  • J Korean Soc Emerg Med.
  • 2006 Dec;17(6):646-651.
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a heart muscle disorder characterized by patch replacement of right ventricular myocardium by adipose and fibrous tissue and by electrical instability of the right...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Arrhythmogenic Noncompaction Cardiomyopathy: Is There an Echocardiographic Phenotypic Overlap of Two Distinct Cardiomyopathies?

Aras D, Ozeke O, Cay S, Ozcan F, Baser K, Dogan U, Unlu M, Demirkan B, Tufekcioglu O, Topaloglu

The clinical diagnosis of right ventricular (RV) cardiomyopathies is often challenging. It is difficult to differentiate the isolated left ventricular (LV) noncompaction cardiomyopathy (NC) from biventricular NC or from coexisting...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Right Ventricular Cardiomyopathy Meeting the Arrhythmogenic Right Ventricular Dysplasia Revised Criteria? Don't Forget Sarcoidosis!

Vasaturo S, Ploeg DE, Buitrago G, Zeppenfeld K, Veselic-Charvat M, Kroft LJ

A 53-year-old woman was referred for ventricular fibrillation with resuscitation. A CT-angiography showed signs of a right ventricular enlargement without obvious cause. A cardiac MRI demonstrated a dilated and hypokinetic...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Meta-analysis on risk stratification of malignant ventricular tachyarrhythmic events in arrhythmogenic right ventricular cardiomyopathy

Roh YE, Jang HJ, Cho MJ

BACKGROUND: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a cardiomyopathy characterized by predominant right ventricular fibro-fatty replacement, right ventricular dysfunction and ventricular arrhythmias. It is a rare but important cause of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Transvascular Implantation of an Implantable Cardioverter-Defibrillator in a Patient Who has Undergone One-and-a-Half Ventricle Repair

Yang PS, Park JW, Lee YJ, Kim DJ, You SC, Park DH, Uhm JS, Kim NK

Implantable cardioverter-defibrillator (ICD) therapy is acknowledged as a valid treatment method for the effective prevention of sudden cardiac death, which is a major cause of mortality in adult congenital heart...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Catheter Ablation of Ventricular Tachycardia in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

Chung FP, Lin CY, Lin YJ, Chang SL, Lo LW, Hu YF, Tuan TC, Chao TF, Liao JN, Chang TY, Chen SA

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 outflow tract, and RV...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Value of Cardiac MR Imaging for the Diagnosis of Arrhythmogenic Right Ventricular Dysplasia:Comparison of Clinical and MR Imaging Diagnostic Grades

Lee IS, Kim HY, Choi SI, Noh HN, Hwang JH, Lim TH

PURPOSE: To evaluate the usefulness of cardiac MRI in the diagnosis of clinically suspected arrhythmogenic right ventricular dysplasia (ARVD). MATERIALS AND METHODS: Between February 1991 and January 1999, 15 patients...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Arrhythmogenic Right Ventricular Cardiomyopathy as a Cause of Sudden Unexplained Death

Park TI, Kim DJ, Sohn YK, Chae JM, Kwak JS, Park HS, Cho Y, Chae SC, Chun JE, Park EH

OBJECTIVE: Arrhythmogenic right ventricular cardiomyopathy(ARVC) is a progressive cardiac muscle disease characterized as progressive fibrofatty replacement of the right ventricle, severe ventricular arrhythmia, and sudden death. However, there is no...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Endomyocardial Biopsy: One Center's Report About Its Role

Oh SS, Youn HJ, Park JH, Lee DH, Choi YS, Park CS, Oh YS, Chung WS, Hong SJ

BACKGROUND AND OBJECTIVES: Cardiomyopathy is a common cause of heart failure, yet it is sometimes difficult to determine its exact etiology. Endomyocardial biopsy (EMBx) has been considered to be one...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Patients with Isolated Focal Right Ventricular Dyskinetic Segments: Toward a Better Understanding of This Cohort

Mansour MJ, Hamoui O, Asmar J, Chammas E, Ayoub W, Daher J, AlJaroudi

BACKGROUND: The 2010 revised Task Force criteria for the diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC) provided guidance for the classification of patients as definitive, borderline or possible ARVC. However,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Unusual form of Cardiomyopathy

Youn HJ

  • KMID: 2204313
  • J Korean Soc Echocardiogr.
  • 2005 Jun;13(2):51-65.
The cardiomyopathies constitute a group of diseases in which the dominant feature is direct involvement of the heart muscle itself. They are distinctive because they are not the result of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Usefulness of Immunohistochemistry in Various Types of Sudden Cardiac Death

Kim JS, Lee SH, Kwak JS, Chae JM

  • KMID: 2250522
  • Korean J Leg Med.
  • 2005 May;29(1):21-32.
Postmortem diagnosis of early myocardial infarction is still a puzzling problem in forensic pathology practice, especially in sudden cardiac death. This study was undertaken to evaluate the distribution patterns of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Recent Update of Advanced Imaging for Diagnosis of Cardiac Sarcoidosis: Based on the Findings of Cardiac Magnetic Resonance Imaging and Positron Emission Tomography

Chang S, Lee WW, Chun EJ

Sarcoidosis is a multisystem disease characterized by noncaseating granulomas. Cardiac involvement is known to have poor prognosis because it can manifest as a serious condition such as the conduction abnormality,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Masked inherited primary arrhythmia syndromes in sudden cardiac death patients accompanied by coronary vasospasm

Lee KH, Park HW, Eun JN, Cho JG, Yoon NS, Kim MR, Ku YH, Park H, Lee SH, Kim JH, Kim MC, Kim WJ, Kim HK, Cho JY, Park KH, Sim DS, Yoon HJ, Kim KH, Hong YJ, Kim JH, Ahn Y, Jeong MH, Park JC

BACKGROUND/AIMS: Coronary vasospasms are one of the important causes of sudden cardiac death (SCD). Provocation of coronary vasospasms can be useful, though some results may lead to false positives, with...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr