Echocardiographic measurements in normal subjects from infancy to old age.
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Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the alpha cardiac myosin heavy chain gene.TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathyHomozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathyMarfan's syndromeArrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 geneIdiopathic dilated cardiomyopathy: lack of association with hepatitis C virus infectionSystematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathyAlcoholic cardiomyopathy : The result of dosage and individual predispositionArrhythmogenic Phenotype in Dilated Cardiomyopathy: Natural History and Predictors of Life-Threatening Arrhythmias.Cardiac involvement in congenital myotonic dystrophyConcentrations of plasma atrial natriuretic factor during and after reversion of ventricular tachycardiaFamilial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 families.Familial dilated cardiomyopathy.Similar prevalence of enteroviral genome within the myocardium from patients with idiopathic dilated cardiomyopathy and controls by the polymerase chain reaction.Cardiac abnormalities in end stage renal failure and anaemia.Mitral valve prolapse syndrome and MASS phenotype: Stability of aortic dilatation but progression of mitral valve prolapse.Model of the distribution of diastolic left ventricular posterior wall thickness in healthy adults and its impact on the behavior of a string of virtual cardiomyocytes.Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.Familial spontaneous complete heart block in hypertrophic cardiomyopathy.Inheritance of hypertrophic cardiomyopathy: a cross sectional and M mode echocardiographic study of 50 families.Patterns of diastolic dysfunction in left ventricular hypertrophyAthlete"s heart and hypertrophic cardiomyopathy.Hypertrophic cardiomyopathy in three generations of a large Norwegian family. A clinical, echocardiographic, and genetic study.Dexrazoxane for preventing anthracycline cardiotoxicity in children with solid tumors.Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22.Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase.The three integrated phases of left atrial macrophysiology and their interactions.Cineangiographic aortic dimensions in normal children.Brain natriuretic peptide is not predictive of dilated cardiomyopathy in Becker and Duchenne muscular dystrophy patients and carriers.GENETIC CAUSES OF DILATED CARDIOMYOPATHY.Cardiomyopathy, familial dilated.Whole exome sequencing identifies a troponin T mutation hot spot in familial dilated cardiomyopathy.Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionalsβ-Blockers and angiotensin converting enzyme inhibitors: comparison of effects on aortic growth in pediatric patients with Marfan syndromeThe impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5)Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genesMarfan syndrome in children and adolescents: an adjusted nomogram for screening aortic root dilatation.Marfan syndrome in children and adolescents: predictive and prognostic value of aortic root growth for screening for aortic complications.Absence of viral nucleic acids in early and late dilated cardiomyopathy.Abnormal cardiopulmonary exercise variables in asymptomatic relatives of patients with dilated cardiomyopathy who have left ventricular enlargement
P2860
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P2860
Echocardiographic measurements in normal subjects from infancy to old age.
description
1980 nî lūn-bûn
@nan
1980年の論文
@ja
1980年学术文章
@wuu
1980年学术文章
@zh
1980年学术文章
@zh-cn
1980年学术文章
@zh-hans
1980年学术文章
@zh-my
1980年学术文章
@zh-sg
1980年學術文章
@yue
1980年學術文章
@zh-hant
name
Echocardiographic measurements in normal subjects from infancy to old age.
@en
Echocardiographic measurements in normal subjects from infancy to old age.
@nl
type
label
Echocardiographic measurements in normal subjects from infancy to old age.
@en
Echocardiographic measurements in normal subjects from infancy to old age.
@nl
prefLabel
Echocardiographic measurements in normal subjects from infancy to old age.
@en
Echocardiographic measurements in normal subjects from infancy to old age.
@nl
P2093
P356
P1433
P1476
Echocardiographic measurements in normal subjects from infancy to old age.
@en
P2093
P304
P356
10.1161/01.CIR.62.5.1054
P407
P577
1980-11-01T00:00:00Z