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Hypertrophic Cardiomyopathy: Assessment with MR Imaging and Multidetector CT

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dc.contributor.authorChun, Eun Ju-
dc.contributor.authorChoi, Sang Il-
dc.contributor.authorJin, Kwang Nam-
dc.contributor.authorKwag, Hyon Joo-
dc.contributor.authorChoi, Byoung Wook-
dc.contributor.authorPark, Jae Hyung-
dc.contributor.authorLee, Whal-
dc.contributor.authorKim, Young Jin-
dc.date.accessioned2012-07-02T02:31:44Z-
dc.date.available2012-07-02T02:31:44Z-
dc.date.issued2010-09-
dc.identifier.citationRADIOGRAPHICS; Vol.30(5); 1309-1328ko_KR
dc.identifier.issn0271-5333-
dc.identifier.urihttps://hdl.handle.net/10371/78062-
dc.description.abstractHypertrophic cardiomyopathy (HCM) is a genetic cardiac disease. Its early detection is important because it is the most common cause of sudden cardiac death among young people. However, HCM is often a dilemma for clinicians because it manifests with diverse phenotypic expressions and clinical courses. With the advances in imaging technology, magnetic resonance (MR) imaging and multidetector computed tomography (CT) serve as suitable modalities for detecting and characterizing HCM and obtaining information for appropriate management of cases of HCM, although echocardiography is currently the most widely used modality. This article is an overview of the definition of HCM, its various phenotypes, risk stratification of HCM, and the potential application of cardiac MR imaging and multidetector CT for the assessment of HCM.ko_KR
dc.language.isoenko_KR
dc.publisherRADIOLOGICAL SOC NORTH AMERICAko_KR
dc.titleHypertrophic Cardiomyopathy: Assessment with MR Imaging and Multidetector CTko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor천은주-
dc.contributor.AlternativeAuthor최상일-
dc.contributor.AlternativeAuthor진광남-
dc.contributor.AlternativeAuthor곽현주-
dc.contributor.AlternativeAuthor김영진-
dc.contributor.AlternativeAuthor최병욱-
dc.contributor.AlternativeAuthor이활-
dc.contributor.AlternativeAuthor박재형-
dc.identifier.doi10.1148/rg.305095074-
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