Myocardial structural alteration and systolic dysfunction in preclinical hypertrophic cardiomyopathy mutation carriers

10.1371/journal.pone.0036115

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Main Authors: Yiu K.H., Atsma D.E., Delgado V., Ng A.C.T., Witkowski T.G., Ewe S.H., Auger D., Holman E.R., van Mil A.M., Breuning M.H., Tse H.F., Bax J.J., Schalij M.J., Marsan N.A.
Other Authors: DUKE-NUS MEDICAL SCHOOL
Format: Article
Published: 2019
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Online Access:https://scholarbank.nus.edu.sg/handle/10635/161984
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spelling sg-nus-scholar.10635-1619842023-11-01T07:40:37Z Myocardial structural alteration and systolic dysfunction in preclinical hypertrophic cardiomyopathy mutation carriers Yiu K.H. Atsma D.E. Delgado V. Ng A.C.T. Witkowski T.G. Ewe S.H. Auger D. Holman E.R. van Mil A.M. Breuning M.H. Tse H.F. Bax J.J. Schalij M.J. Marsan N.A. DUKE-NUS MEDICAL SCHOOL angiotensin receptor antagonist beta adrenergic receptor blocking agent calcium channel blocking agent dipeptidyl carboxypeptidase inhibitor diuretic agent myosin binding protein C adult article calibration cardiovascular risk clinical article controlled study coronary artery disease diabetes mellitus electrocardiogram female gene mutation heart ejection fraction heart infarction heart left ventricle heart muscle heart muscle revascularization heart ventricle wall motion heterozygote detection human hyperlipidemia hypertension hypertrophic cardiomyopathy kidney dysfunction male phenotype protein expression reproducibility sensitivity and specificity smoking systolic dysfunction echocardiography echography genetics heterozygote hypertrophic cardiomyopathy middle aged mutation pathology pathophysiology physiology prognosis systole Adult Cardiomyopathy, Hypertrophic Echocardiography Female Heterozygote Humans Male Middle Aged Mutation Myocardium Phenotype Prognosis Reproducibility of Results Systole 10.1371/journal.pone.0036115 PLoS ONE 7 5 e36115 2019-11-11T06:39:48Z 2019-11-11T06:39:48Z 2012 Article Yiu K.H., Atsma D.E., Delgado V., Ng A.C.T., Witkowski T.G., Ewe S.H., Auger D., Holman E.R., van Mil A.M., Breuning M.H., Tse H.F., Bax J.J., Schalij M.J., Marsan N.A. (2012). Myocardial structural alteration and systolic dysfunction in preclinical hypertrophic cardiomyopathy mutation carriers. PLoS ONE 7 (5) : e36115. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0036115 19326203 https://scholarbank.nus.edu.sg/handle/10635/161984 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Unpaywall 20191101
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic angiotensin receptor antagonist
beta adrenergic receptor blocking agent
calcium channel blocking agent
dipeptidyl carboxypeptidase inhibitor
diuretic agent
myosin binding protein C
adult
article
calibration
cardiovascular risk
clinical article
controlled study
coronary artery disease
diabetes mellitus
electrocardiogram
female
gene mutation
heart ejection fraction
heart infarction
heart left ventricle
heart muscle
heart muscle revascularization
heart ventricle wall motion
heterozygote detection
human
hyperlipidemia
hypertension
hypertrophic cardiomyopathy
kidney dysfunction
male
phenotype
protein expression
reproducibility
sensitivity and specificity
smoking
systolic dysfunction
echocardiography
echography
genetics
heterozygote
hypertrophic cardiomyopathy
middle aged
mutation
pathology
pathophysiology
physiology
prognosis
systole
Adult
Cardiomyopathy, Hypertrophic
Echocardiography
Female
Heterozygote
Humans
Male
Middle Aged
Mutation
Myocardium
Phenotype
Prognosis
Reproducibility of Results
Systole
spellingShingle angiotensin receptor antagonist
beta adrenergic receptor blocking agent
calcium channel blocking agent
dipeptidyl carboxypeptidase inhibitor
diuretic agent
myosin binding protein C
adult
article
calibration
cardiovascular risk
clinical article
controlled study
coronary artery disease
diabetes mellitus
electrocardiogram
female
gene mutation
heart ejection fraction
heart infarction
heart left ventricle
heart muscle
heart muscle revascularization
heart ventricle wall motion
heterozygote detection
human
hyperlipidemia
hypertension
hypertrophic cardiomyopathy
kidney dysfunction
male
phenotype
protein expression
reproducibility
sensitivity and specificity
smoking
systolic dysfunction
echocardiography
echography
genetics
heterozygote
hypertrophic cardiomyopathy
middle aged
mutation
pathology
pathophysiology
physiology
prognosis
systole
Adult
Cardiomyopathy, Hypertrophic
Echocardiography
Female
Heterozygote
Humans
Male
Middle Aged
Mutation
Myocardium
Phenotype
Prognosis
Reproducibility of Results
Systole
Yiu K.H.
Atsma D.E.
Delgado V.
Ng A.C.T.
Witkowski T.G.
Ewe S.H.
Auger D.
Holman E.R.
van Mil A.M.
Breuning M.H.
Tse H.F.
Bax J.J.
Schalij M.J.
Marsan N.A.
Myocardial structural alteration and systolic dysfunction in preclinical hypertrophic cardiomyopathy mutation carriers
description 10.1371/journal.pone.0036115
author2 DUKE-NUS MEDICAL SCHOOL
author_facet DUKE-NUS MEDICAL SCHOOL
Yiu K.H.
Atsma D.E.
Delgado V.
Ng A.C.T.
Witkowski T.G.
Ewe S.H.
Auger D.
Holman E.R.
van Mil A.M.
Breuning M.H.
Tse H.F.
Bax J.J.
Schalij M.J.
Marsan N.A.
format Article
author Yiu K.H.
Atsma D.E.
Delgado V.
Ng A.C.T.
Witkowski T.G.
Ewe S.H.
Auger D.
Holman E.R.
van Mil A.M.
Breuning M.H.
Tse H.F.
Bax J.J.
Schalij M.J.
Marsan N.A.
author_sort Yiu K.H.
title Myocardial structural alteration and systolic dysfunction in preclinical hypertrophic cardiomyopathy mutation carriers
title_short Myocardial structural alteration and systolic dysfunction in preclinical hypertrophic cardiomyopathy mutation carriers
title_full Myocardial structural alteration and systolic dysfunction in preclinical hypertrophic cardiomyopathy mutation carriers
title_fullStr Myocardial structural alteration and systolic dysfunction in preclinical hypertrophic cardiomyopathy mutation carriers
title_full_unstemmed Myocardial structural alteration and systolic dysfunction in preclinical hypertrophic cardiomyopathy mutation carriers
title_sort myocardial structural alteration and systolic dysfunction in preclinical hypertrophic cardiomyopathy mutation carriers
publishDate 2019
url https://scholarbank.nus.edu.sg/handle/10635/161984
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