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Unmasked Obstructive Hypertrophic Cardiomyopathy after Mitral Valve Repair for Severe Mitral Regurgitation

Kim D, Shim CY, Hong GR, Chang BC

No abstract available.
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A comprehensive review of hypertrophic cardiomyopathy and arterial thromboembolism in cats

Han D, Jung DI

The number of cats requiring treatment for hypertrophic cardiomyopathy (HCM) and arterial thromboembolism (ATE) continues to increase, and the knowledge regarding its management is constantly evolving. The pathological lesions of...
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Sigmoid Septum and Aberrant Calcified Papillary Muscle in the Setting of Advanced Hypertrophic Cardiomyopathy: An Unusual Life-threatening Coalescence

Hallo C, Kottiech S, Castillo J

No abstract available.
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Fabry Disease that Phenocopies Hypertrophic Cardiomyopathy: a thorough Genetic ‘Detective’ Identifies the ‘Rogue’ Hidden in the GLA Gene

Kwon S, Lee SP, Park SS, Kim BJ, Kim HK, Cho HJ, Seong MW, Sohn DW

No abstract available.
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Biventricular Hypertrophic Cardiomyopathy with Severe Right Ventricular Outflow Track Obstruction

Lim DS, Lee CH

Hypertrophic cardiomyopathy (HCM) has diverse pathophysiological and clinical features, according to the extent and severity of the hypertrophy development. Hypertrophy mostly involves the left ventricle and sometimes causes a left...
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Left Ventricular Noncompaction Associated with Hypertrophic Cardiomyopathy: Morphologic and Functional Evaluation with Multidetector CT

Lee H, Lee JW, Meinel FG, Schoepf UJ

Hypertrophic cardiomyopathy and left ventricular (LV) noncompaction are American Heart Association-recognized cardiomyopathies with distinct clinical and pathoanatomical features that are presumed to have different etiologies. We present two cases with...
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The association between T wave inversion and apical hypertrophic cardiomyopathy

Chae CB, Ha JH, Kim JH, Lee JJ, Choi HI, Park KB, Kim JH, Choi JH

OBJECTIVES: Electrocardiograhy (ECG) is the first step in hypertrophic cardiomyopathy (HCMP) diagnosis. For various reasons, the T wave inversion (TWI) and ECG change with time and HCMP is not easy...
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Identification of LAMP2 mutations in early-onset hypertrophic cardiomyopathy by targeted exome sequencing

Gill I, Kim JH, Moon JH, Kim YJ, Kim NS

X-linked dominant mutations in lysosome-associated membrane protein 2 (LAMP2) gene have been shown to be the cause of Danon disease, which is a rare disease associated with clinical triad of...
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Hypertrophic obstructive cardiomyopathy in a Yorkshire Terrier

Hwang T, Park J, Jung D, Lee HC

An 11-year-old, castrated male dog presented with a 3-month history of cough and depression. Auscultation revealed systolic murmur and thoracic radiographs showing enlargement of both the atrium and left ventricle....
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Tips for Successful Septal Myectomy in Patients with Hypertrophic Cardiomyopathy

Kim JH

Septal myectomy is the gold-standard treatment of hypertrophic cardiomyopathy. However, it involves the risk of incomplete resection of septal muscles or iatrogenic septal perforation depending on the surgeon's practice. Herein,...
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Fabry Disease Presenting with Hypertrophic Cardiomyopathy and Tricuspid Regurgitation

Cho SC, Yoo HW, Lee JW, Jang JY, Heo R, Song JM

A 71-year-old female who was diagnosed with nonobstructive hypertrophic cardiomyopathy since 1999 presented with dyspnea and severe edema on both legs. For the management of her symptom, cardiac surgery including...
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Findings of Cardiac Magnetic Resonance Imaging in Hypertrophic Cardiomyopathy after 16 Years

Kim GH, Kim CM, Jang BH, Lee HH, Hong S, Eum SH, Jeon H, Moon D

A 58-year-old man had been diagnosed with non-obstructive hypertrophic cardiomyopathy (HCMP) according to echocardiography findings 16 years ago. Echocardiography showed ischemic cardiomyopathy (CMP)-like features with decreased systolic function but a...
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Pregnancy in Hypertrophic Cardiomyopathy with Severe Left Ventricular Outflow Tract Obstruction

Shin J, Kim M, Lee J, Kim S, Kim M, Hwang H, Moon J, Shin MS, Chung WJ

Hypertrophic obstructive cardiomyopathy (HOCM) patients with severe left ventricular outflow tract (LVOT) obstruction (those with a gradient of > 100 mm Hg) are at the highest risk of hemodynamic deterioration...
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A Totally Occluded Long Segment Myocardial Bridge: 10-year Follow-up after Percutaneous Coronary Intervention in a Patient with Hypertrophic Cardiomyopathy

Kim HK, Jeong MH, Kim M, Ahn Y, Cho JG, Park JC

Intracoronary stent implantation can improve coronary hemodynamics and myocardial ischemia in patients with symptomatic bridging. However, percutaneous coronary intervention for this lesion is limited due to the high prevalence of...
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Minimally Invasive Trans-Mitral Septal Myectomy to Treat Hypertrophic Obstructive Cardiomyopathy

Kim HR, Yoo JS, Lee JW

A 43-year-old man with symptomatic hypertrophic obstructive cardiomyopathy (HOCM) was admitted to our hospital with aggravated exertional dyspnea and successfully treated with robotic transmitral septal myectomy. Minimally invasive transmitral septal...
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Characteristic Clinical Features and Survival in Cats with Symptomatic Hypertrophic Cardiomyopathy

Kang MH, Min SH, Kim SG, Lee CM, Park HM

Hypertrophic cardiomyopathy (HCM) is recognized as the most common feline cardiac disease. Several studies have evaluated the population characteristics and survival time of cats with HCM; however, these reports included...
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Hypertrophic cardiomyopathy secondary to severe right and left ventricular outflow tract obstruction in a Maltese dog

Yoon WK, Suh SI, Oh YS, Hyun C

An 8-year-old spayed female Maltese (2.5 kg of body weight) presented with the primary complaint of loud heart murmur and exercise intolerance. Diagnostic imaging revealed severe pulmonic stenosis (peak velocity...
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Coexistent Coronary Artery Disease or Myocardial Bridging in Patients with Hypertrophic Cardiomyopathy Using Coronary CT Angiography

Lee JH, Chun EJ, Kim YK, Yoo JY, Choi SI, Choi DJ

PURPOSE: To evaluate the prevalence of coexistent coronary artery disease (CAD) or myocardial bridging (MB) in patients with hypertrophic cardiomyopathy (HCM) using coronary CT angiography (CCTA) and assess the role...
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Survival and Clinical Behavior of Hypertrophic Cardiomyopathy in a Latin American Cohort in Contrast to Cohorts from the Developed World

Espinola-Zavaleta N, Vega A, Basto DM, Alcantar-Fernandez AC, Guarner Lans V, Soto ME

BACKGROUND: Hypertrophic cardiomyopathy (HCM) is the most common hereditary heart disease with diverse phenotipyc, genetic expession and clinical presentations. The evolution of patients with HCM in Latin America has not...
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Impact of Coronary Artery Anatomy on Clinical Course and Prognosis in Apical Hypertrophic Cardiomyopathy: Analysis of Coronary Angiography and Computed Tomography

Shin DG, Son JW, Park JY, Choi JW, Ryu SK

BACKGROUND AND OBJECTIVES: Apical hypertrophic cardiomyopathy (AHCM) is an uncommon variant of hypertrophic cardiomyopathy with a relatively benign course. However, the prognostic factors of AHCM-particularly those associated with coronary artery...
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