Single-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study
about
Exome sequencing and complex disease: practical aspects of rare variant association studiesClinical and Mechanistic Insights Into the Genetics of CardiomyopathyShared genetic causes of cardiac hypertrophy in children and adultsFounder mutations in hypertrophic cardiomyopathy patients in the NetherlandsCardiovascular genomics, personalized medicine, and the National Heart, Lung, and Blood Institute: part I: the beginning of an eraRelation of left ventricular mass at age 23 to 35 years to global left ventricular systolic function 20 years later (from the Coronary Artery Risk Development in Young Adults study)Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.Frequency of Fabry disease in male and female haemodialysis patients in Spain.Idiopathic small fiber neuropathy: phenotype, etiologies, and the search for fabry diseaseElectrocardiographic versus echocardiographic left ventricular hypertrophy and sudden cardiac arrest in the communityGenetics of hypertrophic cardiomyopathy.Cardiac fibrosis in mice with hypertrophic cardiomyopathy is mediated by non-myocyte proliferation and requires Tgf-β.Obtaining insurance after DNA diagnostics: a survey among hypertrophic cardiomyopathy mutation carriersGenomic approaches to coronary artery diseaseGenomics of heart failure.Sarcomere gene mutations in hypertrophy and heart failure.Genetics and clinical destiny: improving care in hypertrophic cardiomyopathyStrategic approaches to unraveling genetic causes of cardiovascular diseases.ESCAPE-HCM study: Evaluation of SCreening of Asymptomatic PatiEnts with Hypertrophic CardioMyopathy.Fabry disease: incidence of the common later-onset α-galactosidase A IVS4+919G→A mutation in Taiwanese newborns--superiority of DNA-based to enzyme-based newborn screening for common mutationsResults of comprehensive diagnostic work-up in 'idiopathic' dilated cardiomyopathy.Burden of rare sarcomere gene variants in the Framingham and Jackson Heart Study cohorts.Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing.Screening for Fabry Disease by Urinary Globotriaosylceramide Isoforms Measurement in Patients with Left Ventricular Hypertrophy.Evaluation of the Mayo Clinic Phenotype-Based Genotype Predictor Score in Patients with Clinically Diagnosed Hypertrophic CardiomyopathyHypertrophic cardiomyopathy in 2013: Current speculations and future perspectives.Familial hypertrophic cardiomyopathy associated with a new mutation in gene MYBPC3.Cardiac remodeling at the population level--risk factors, screening, and outcomes.A systematic review on screening for Fabry disease: prevalence of individuals with genetic variants of unknown significance.Genetics of sudden cardiac death in the young.Clinical utility gene card for: hypertrophic cardiomyopathy (type 1-14)Cardiomyopathy-related mutation (A30V) in mouse cardiac troponin T divergently alters the magnitude of stretch activation in α- and β-myosin heavy chain fibers.Short communication: the cardiac myosin binding protein C Arg502Trp mutation: a common cause of hypertrophic cardiomyopathy.Mitochondrial DNA analysis by multiplex denaturing high-performance liquid chromatography and selective sequencing in pediatric patients with cardiomyopathy.Nephropathy in Fabry disease: the importance of early diagnosis and testing in high-risk populations.Three-dimensional echocardiography for the assessment of left ventricular geometry and papillary muscle morphology in hypertrophic cardiomyopathy.Fabry disease mimicking hypertrophic cardiomyopathy: genetic screening needed for establishing the diagnosis in women.A novel mouse model of X-linked cardiac hypertrophy.Left ventricular hypertrophy diagnosed after a stroke: a case report.Ventricular diastolic dimension over maximal myocardial thickness is robust landmark of systolic impairment in patients with hypertrophic cardiomyopathy.
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P2860
Single-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study
description
2006 nî lūn-bûn
@nan
2006 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Single-gene mutations and incr ...... ty: the Framingham Heart Study
@ast
Single-gene mutations and incr ...... ty: the Framingham Heart Study
@en
Single-gene mutations and incr ...... ty: the Framingham Heart Study
@en-gb
Single-gene mutations and incr ...... ty: the Framingham Heart Study
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type
label
Single-gene mutations and incr ...... ty: the Framingham Heart Study
@ast
Single-gene mutations and incr ...... ty: the Framingham Heart Study
@en
Single-gene mutations and incr ...... ty: the Framingham Heart Study
@en-gb
Single-gene mutations and incr ...... ty: the Framingham Heart Study
@nl
prefLabel
Single-gene mutations and incr ...... ty: the Framingham Heart Study
@ast
Single-gene mutations and incr ...... ty: the Framingham Heart Study
@en
Single-gene mutations and incr ...... ty: the Framingham Heart Study
@en-gb
Single-gene mutations and incr ...... ty: the Framingham Heart Study
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Single-gene mutations and incr ...... ty: the Framingham Heart Study
@en
P2093
Christine E Seidman
Christopher J O'Donnell
Daniel Levy
Diane Corey
Hiroyuki Morita
J G Seidman
Joel N Hirschhorn
Scott C Barr
P304
P3181
P356
10.1161/CIRCULATIONAHA.105.593558
P407
P577
2006-06-13T00:00:00Z