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Surviving Takayasu's Arteritis—A Young Girl with Long Segment Stenosis of the Descending Thoracic Aorta and Myocarditis

Abas SI, Ramli KA, Tiong KG, Mohammed Y

We report the case of a 12-year-old girl who presented with heart failure symptoms that were treated as dilated cardiomyopathy. The echocardiogram showed a dilated left ventricle, poor ejection fraction,...
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Dilated Cardiomyopathy in Acromegaly: a Case Report with Cardiac MR Findings

Kim MS, Choi HW, Seo YS, Lee W, Park EA

Acromegaly is a rare endocrine disorder caused by excessive secretion of the growth hormone. There is a wide range of clinical manifestations from somatic symptoms to respiratory or cardiac failure....
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How small is enough for the left heart decompression cannula during extracorporeal membrane oxygenation?

Kim S, Kim JS, Shin JS, Shin HJ

BACKGROUND: Left ventricular (LV) distension is a recognizable problem accompanied by subsequent complications during venoarterial extracorporeal membrane oxygenation (VA-ECMO). However, no gold standard for LV decompression has been established, and...
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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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Erector spinae plane block combined with a novel technique for selective brachial plexus block in breast cancer surgery: a case report

De Cassai , Bonvicini , Ruol M, Correale C, Furnari M

BACKGROUND: The breast is innervated by the intercostal nerves and the brachial plexus. We propose a technique to perform breast surgery without general anesthesia using the erector spinae plane (ESP)...
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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,...
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Long-term cardiac composite risk following adjuvant treatment in breast cancer patients

Choi HB, Yun S, Cho SW, Lee MH, Lee J, Park S

PURPOSE: Cardiotoxicity is a serious late complication of breast cancer treatment. Individual treatment risk of specific drugs has been investigated. However, studies on the evaluation of the composite risk of...
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Successful Endovascular Therapy for Bilateral Popliteal Thrombotic Occlusions

Park SH, Jang WY, Hyun HJ, Choi SJ, Kim MJ, Rha SW

The popliteal artery is a relatively short vascular structure, but acute occlusion can decrease blood flow into the lower extremities and cause subsequent critical limb ischemia, amputation, and even mortality....
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2018 KHRS Guidelines for Catheter Ablation of Ventricular Arrhythmias: Part 3

Cho Y, Kim SH, Kim YR, Kim YN, Kim JY, Kim TH, Nam GB, Roh SY, Park KM, Park HS, Pak HN, Bae EJ, Oh S, Yoon N, Lee MY, Cho Y, Jin ES, Cha TJ, Choi JI, Kim J

Treatment of ventricular arrhythmias (VA) usually involves managing the underlying cardiac conditions that cause the arrhythmia. However, managing the underlying disease is often challenging, and catheter ablation, or treatment targeting...
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Reversal of Left Ventricular Function by PVC Ablation in Dilated Cardiomyopathy Patient

Jun SJ, Lee KH

Premature ventricular complex (PVC) usually follows a benign course and shows good response to medical therapy. However, high burden of PVC deteriorates cardiac function and is often associated with progression...
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Left Ventricular Noncompaction in Adults: Imaging and Clinical Findings in 63 Patients

Cho SJ, Yang DH, Kang JW, Lim TH

PURPOSE: To describe imaging and clinical findings for a left ventricular noncompaction (LVNC) in the adult. MATERIALS AND METHODS: From 2000 to 2014, 63 patients were diagnosed with LVNC by echocardiography,...
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Application of Multigene Panel Sequencing in Patients with Prolonged Rate-corrected QT Interval and No Pathogenic Variants Detected in KCNQ1, KCNH2, and SCN5A

Seo SH, Kim SY, Cho SI, Park H, Lee S, Choi JM, Kim MJ, Lee JS, Ahn KJ, Song MK, Bae EJ, Park SS, Seong MW

Long QT syndrome (LQTS) is an inherited cardiac disease characterized by a prolonged heart rate-corrected QT (QTc) interval. We investigated the genetic causes in patients with prolonged QTc intervals who...
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Implantable Cardioverter-Defibrillator of Korean Patients in a Single Center Registry

Hwang JK, Gwag HB, Park SJ, Park KM, Kim JS, On YK

BACKGROUND AND OBJECTIVES: The safety and efficacy of implantable cardioverter-defibrillator (ICD) for Korean is unclear. We investigated the clinical characteristics and outcomes of Korean patients undergoing ICD for primary or...
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Zebrafish Larvae Model of Dilated Cardiomyopathy Induced by Terfenadine

Gu G, Na Y, Chung H, Seok SH, Lee HY

BACKGROUND AND OBJECTIVES: Dilated cardiomyopathy can be the end-stage of severe cardiac disorders and directly affects the cardiac muscle, inducing cardiomegaly and heart failure (HF). Although a wide variety of...
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Initial Report of the Korean Organ Transplant Registry (KOTRY): Heart Transplantation

Lee HY, Jeon ES, Kang SM, Kim JJ

BACKGROUND AND OBJECTIVES: The Korean Organ Transplant Registry (KOTRY), which was the first national transplant registry in Korea, was founded by the Korean Society for Transplantation and the Korean Center...
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Rapid and Potent Antiarrhythmic Effect of Cardiac Resynchronization Therapy in a Patient with Advanced Dilated Cardiomyopathy and a Large Ventricular Arrhythmia Burden

Jeon DS, Park JS

We report a case demonstrating a rapid and potent antiarrhythmic effect of biventricular pacing. A 67-year-old male patient with dilated cardiomyopathy was admitted for heart failure. The initial surface electrocardiogram...
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2q37 Deletion syndrome confirmed by high-resolution cytogenetic analysis

Cho EK, Kim J, Yang A, Cho SY, Jin DK

Chromosome 2q37 deletion syndrome is a rare chromosomal disorder characterized by mild to moderate developmental delay, brachydactyly of the third to fifth digits or toes, short stature, obesity, hypotonia, a...
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Hereditary Dilated Cardiomyopathy: Recent Advances in Genetic Diagnostics

Park HY

Dilated cardiomyopathy (DCM) is the most common cause of heart failure in young adults and up to 50% of idiopathic DCM is thought to be caused by genetic mutations in...
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Transaxillary Subpectoral Placement of Cardiac Implantable Electronic Devices in Young Female Patients

Oh JH, Kim CM, Song SY, Uhm JS, Lew DH, Lee DW

BACKGROUND: The current indications of cardiac implantable electronic devices (CIEDs) have expanded to include young patients with serious cardiac risk factors, but CIED placement has the disadvantage of involving unsightly...
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A novel c.563 T>G, p.L189R lamin A/C mutation in identical twins with dilated cardiomyopathy

Lee E, Park KT, Kang J, Park H, Park JJ, Oh IY, Yoon YE

No abstract available.
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