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Loss of Function Mutations in NNT Are Associated With Left Ventricular NoncompactionLeft ventricular non-compaction cardiomyopathy associated with epidermolysis bullosa simplex with muscular dystrophy and PLEC1 mutationTwo-dimensional speckle strain imaging: in the management of paraganglioma, acute junctional tachycardia, and myocardial dysfunction in a child.Imaging for cardiotoxicity in cancer patients.Left ventricular non-compaction cardiomyopathy in children: characterisation of clinical status using tissue Doppler-derived indices of left ventricular diastolic relaxation.The Twiddling AndersenConduction abnormalities in pediatric patients with restrictive cardiomyopathy.Recovery of echocardiographic function in children with idiopathic dilated cardiomyopathy: results from the pediatric cardiomyopathy registry.Chest pain and diaphragmatic pacing after pacemaker implantation.Viral epidemiologic shift in inflammatory heart disease: the increasing involvement of parvovirus B19 in the myocardium of pediatric cardiac transplant patientsMortality and sudden death in pediatric left ventricular noncompaction in a tertiary referral center.Peritoneal dialysis does not adversely affect kidney function recovery after congenital heart surgeryEplerenone for early cardiomyopathy in Duchenne muscular dystrophy: a randomised, double-blind, placebo-controlled trialLeft ventricular noncompaction in a family with lamin A/C gene mutationCompeting risks for death and cardiac transplantation in children with dilated cardiomyopathy: results from the pediatric cardiomyopathy registry.Effects of steroids and angiotensin converting enzyme inhibition on circumferential strain in boys with Duchenne muscular dystrophy: a cross-sectional and longitudinal study utilizing cardiovascular magnetic resonance.Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities.Incidence of and risk factors for sudden cardiac death in children with dilated cardiomyopathy: a report from the Pediatric Cardiomyopathy Registry.Kawasaki disease in the adult: a case report and review of the literature.Prevalence and predictors of aortic dilation as a novel cardiovascular complication in children with end-stage renal diseaseThe neurohormonal axis and biochemical markers of heart failure.Prevalence, predictors, and outcomes of cardiorenal syndrome in children with dilated cardiomyopathy: a report from the Pediatric Cardiomyopathy Registry.Cardiomyopathy Phenotypes and Outcomes for Children With Left Ventricular Myocardial Noncompaction: Results From the Pediatric Cardiomyopathy Registry.Leukocyte suppression is associated with improved clinical outcomes in children's status after orthotopic heart transplantation.Administration of a large nesiritide bolus dose in a pediatric patient: case report and review of nesiritide use in pediatrics.Arrhythmia as a cardiac manifestation in MELAS syndrome.Hospital Charges for Pediatric Heart Failure-Related Hospitalizations from 2000 to 2009Abnormal circumferential strain measured by echocardiography is present in patients with Shwachman-Diamond syndrome despite normal shortening fractionAmbulatory Monitoring and Arrhythmic Outcomes in Pediatric and Adolescent Patients With Duchenne Muscular Dystrophy.Cardiovascular findings in duplication 17p11.2 syndrome.First use of cryoplasty to treat in-stent renal artery restenosis.Disorders of left ventricular trabeculation/compaction or right ventricular wall formation.MCTP2 is a dosage-sensitive gene required for cardiac outflow tract development.Prevalence and distribution of late gadolinium enhancement in a large population of patients with Duchenne muscular dystrophy: effect of age and left ventricular systolic function.Ventricular Tachycardia in Fabry Disease Detected in a 50-Year-Old Woman during 14-Day Continuous Cardiac Monitoring.Risk factors and mode of death in isolated hypertrophic cardiomyopathy in children.The PPAR pan-agonist bezafibrate ameliorates cardiomyopathy in a mouse model of Barth syndromeElectrocardiographic abnormalities and arrhythmias are strongly associated with the development of cardiomyopathy in muscular dystrophy.Restrictive physiology is associated with poor outcomes in children with hypertrophic cardiomyopathy.Mechanical circulatory support in children: bridge to transplant versus recovery.
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name
John L Jefferies
@en
type
label
John L Jefferies
@en
prefLabel
John L Jefferies
@en