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Cardiomyopathies with Mixed and Inapparent Morphological Features in Cardiac Troponin I3 Mutation

Sohn DW, Kim HK, Kim YJ, Oh S, Seong MW, Park SS

The fact that different types of cardiomyopathies can be manifested by the same sarcomere protein gene mutation in a single family is well known. However, mixed features of different types...
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The myocarditis and cardiomyopathy in children

Kil HR

Myocarditis represent an important condition encountered by general pediatricians & general practitioners. Its presentation is varied, and therefore a high index of suspicion must be maintained when the possibility of...
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Ventricular Tachycardia Ablation in Non-ischemic Cardiomyopathy

Bhaskaran , De Silva K, Rao K, Campbell T, Trivic I, Bennett RG, Kizana E, Kumar S

Non-ischemic cardiomyopathies are a heterogeneous group of diseases of the myocardium that have a distinct proclivity to ventricular arrhythmias. Of these, ventricular tachycardias pose significant management challenges with the risk...
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Primary Carnitine Deficiency and Cardiomyopathy

Fu L, Huang M, Chen S

Carnitine is essential for the transfer of long-chain fatty acids from the cytosol into mitochondria for subsequent beta-oxidation. A lack of carnitine results in impaired energy production from long-chain fatty...
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Diverse Phenotypic Expression of Cardiomyopathies in a Family with TNNI3 p.Arg145Trp Mutation

Hwang JW, Jang MA, Jang SY, Seo SH, Seong MW, Park SS, Ki CS, Kim DK

Genetic diagnosis of cardiomyopathies is challenging, due to the marked genetic and allelic heterogeneity and the lack of knowledge of the mutations that lead to clinical phenotypes. Here, we present...
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Sphingolipid Mediators of Myocardial Pathology

Kovilakath A, Cowart LA

Cardiomyopathy is the leading cause of mortality worldwide. While the causes of cardiomyopathy continue to be elucidated, current evidence suggests that aberrant bioactive lipid signaling plays a crucial role as...
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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...
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A Case of Mitochondrial Myopathy With Cardiac Involvement

Son SW, Kim DB, Kwon BJ, Jang SW, Cho EJ, Park CH, Kim DB, Shin JY, Rho TH, Kim JH

Mitochondrial myopathy is a disease caused by structural, biochemical or genetic disturbance of the mitochondria and this affects many organs, and it may also involve the cardiac muscles. We experienced...
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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...
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Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

Cho Y

Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is characterized by rogressive, fibrofatty replacement of the myocardium, ventricular arrhythmia, sudden death, and progressive heart failure. ARVC/D may be an important cause of syncope,...
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Recurrent Catecholamine-Induced Cardiomyopathy in a Patient With a Pheochromocytoma

Jang SY, Yang DH, Lee SH, Kim JH, Park SH, Park HS, Cho Y, Chae SC, Jun JE, Park WH

Pheochromocytomas presents with variable clinical manifestations. Cardiomyopathy caused by a pheochromocytoma is well known. We report the case of a 62-year-old woman with recurrent left ventricular dysfunction, who was subsequently...
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Tachycardia-induced Cardiomyopathy Presenting in a Coma: a Case Report

Cho YK, Choi WY, Kim YO, Ma JS

Tachycardia-induced cardiomyopathy can be defined as a condition characterized by myocardial dysfunction resulting from atrial or ventricular tachyarrhythmia, without underlying structural heart disease. It is a potentially reversible cause of...
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A Novel Approach for Identifying Ischemic Cardiomyopathy

Choi EY

No abstract available.
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A Case of Reflux Nephropathy Associated with Cardiomyopathy

Eom SH, Cha SH, Cho BS, Ahn CI

  • KMID: 1682548
  • J Korean Pediatr Soc.
  • 1988 Feb;31(2):258-262.
No abstract available.
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Heart failure as the first manifestation of renal cell carcinoma

Lee CM, Sim A, Kurugulasigamoney G, Ng LG

We report the rare case of a patient with advanced renal cell carcinoma (RCC) who initially presented to the hospital with symptoms of cardiac failure. Preoperative cardiac studies did not...
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A Case of Congenital Hypothyroidism with Echocardiographic Features Similar to Cardiomyopathy

Choi SM, Kim HD

  • KMID: 1661281
  • J Korean Pediatr Soc.
  • 1995 Oct;38(10):1417-1421.
No abstract available.
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A Case of Congestive Heart Failure in Adolescent with Diabetes Mellitus

Ahn HS, Park SJ, Lee EJ, Kim HJ

  • KMID: 1482022
  • J Korean Soc Pediatr Endocrinol.
  • 2008 Dec;13(2):193-197.
The number of patients with diabetes mellitus continues to increase worldwide. Diabetes is strongly associated with cardiovascular disease including myocardial infarction, hypertension and diabetic cardiomyopathy. The prevalence of heart failure...
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Pediatric Heart Failure: Current State and Future Possibilities

Rossano JW, Jang GY

Heart failure is a complex pathophysiological syndrome that can occur in children from a variety of diseases, including cardiomyopathies, myocarditis, and congenital heart disease. The condition is associated with a...
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Prevalence, Characteristics, and Clinical Significance of Concomitant Cardiomyopathies in Subjects with Bicuspid Aortic Valves

Jeong H, Shim CY, Kim D, Choi JY, Choi KU, Lee SY, Hong GR, Ha JW

PURPOSE: The present study aimed to investigate the prevalence, characteristics, and clinical significance of concomitant specific cardiomyopathies in subjects with bicuspid aortic valves (BAVs). MATERIALS AND METHODS: A total of 1186...
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A case of peripartum cardiomyopathy

Kim CJ, Kwon OS, Kim HK, Cho TI

  • KMID: 2259552
  • Korean J Obstet Gynecol.
  • 1993 Jul;36(7):1620-1623.
No abstract available.
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