Search Results - "Nakano, Stephanie"
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Heart failure in single right ventricle congenital heart disease: physiological and molecular considerations
Published in American journal of physiology. Heart and circulatory physiology (01-04-2020)“…Because of remarkable surgical and medical advances over the past several decades, there are growing numbers of infants and children living with single…”
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A PDE3A Promoter Polymorphism Regulates cAMP-Induced Transcriptional Activity in Failing Human Myocardium
Published in Journal of the American College of Cardiology (19-03-2019)“…The phosphodiesterase 3A (PDE3A) gene encodes a PDE that regulates cardiac myocyte cyclic adenosine monophosphate (cAMP) levels and myocardial contractile…”
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Pediatric Heart Failure: An Evolving Public Health Concern
Published in The Journal of pediatrics (01-03-2020)Get full text
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Elevated serum vascular endothelial growth factor and development of cardiac allograft vasculopathy in children
Published in The Journal of heart and lung transplantation (01-09-2018)“…Cardiac allograft vasculopathy (CAV) is a leading cause of retransplantation and death in pediatric heart transplant recipients. Our aim was to evaluate the…”
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Cardiac Adenylyl Cyclase and Phosphodiesterase Expression Profiles Vary by Age, Disease, and Chronic Phosphodiesterase Inhibitor Treatment
Published in Journal of cardiac failure (01-01-2017)“…Abstract Background Pediatric heart failure (HF) patients have a suboptimal response to traditional HF medications, although phosphodiesterase-3 inhibition…”
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Myocardial Response to Milrinone in Single Right Ventricle Heart Disease
Published in The Journal of pediatrics (01-07-2016)“…Objectives Empiric treatment with milrinone, a phosphodiesterase (PDE) 3 inhibitor, has become increasingly common in patients with single ventricle heart…”
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Risk factors for lethal arrhythmic events in children and adolescents with hypertrophic cardiomyopathy and an implantable defibrillator: An international multicenter study
Published in Heart rhythm (01-10-2019)“…Predictors of risk of lethal arrhythmic events (LAE) is poorly understood and may differ from adults in children with hypertrophic cardiomyopathy (HCM). The…”
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A novel GNAS variant presents with disorders of GNAS inactivation and cardiomyopathy
Published in American journal of medical genetics. Part A (01-07-2022)“…The GNAS gene (OMIM#139320), located on chromosome 20q13.2, encodes for the alpha‐subunit of the stimulatory signaling protein, Gsα protein. GNAS variants with…”
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General pediatric care for a patient after heart transplant: what the practitioner needs to know
Published in Current opinion in pediatrics (01-10-2019)“…The scope of this review is to discuss aspects of general pediatric care which significantly impact the outcome of children after heart transplant. The general…”
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Risk of Sudden Death in Patients With RASopathy Hypertrophic Cardiomyopathy
Published in Journal of the American College of Cardiology (21-03-2023)“…Genetic defects in the RAS/mitogen-activated protein kinase pathway are an important cause of hypertrophic cardiomyopathy (RAS-HCM). Unlike primary HCM…”
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Increased myocyte calcium sensitivity in end-stage pediatric dilated cardiomyopathy
Published in American journal of physiology. Heart and circulatory physiology (01-12-2019)“…Dilated cardiomyopathy (DCM) is the most common cause of heart failure (HF) in children, resulting in high mortality and need for heart transplantation. The…”
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Phosphodiesterase-5 Is Elevated in Failing Single Ventricle Myocardium and Affects Cardiomyocyte Remodeling In Vitro
Published in Circulation. Heart failure (01-09-2018)“…Background Single ventricle (SV) congenital heart disease is fatal without intervention, and eventual heart failure is a major cause of morbidity and…”
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Age-related differences in phosphodiesterase activity and effects of chronic phosphodiesterase inhibition in idiopathic dilated cardiomyopathy
Published in Circulation. Heart failure (01-01-2015)“…Despite the application of proven adult heart failure therapies to children with idiopathic dilated cardiomyopathy (IDC), prognosis remains poor. Clinical…”
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Ex vivo Methods for Measuring Cardiac Muscle Mechanical Properties
Published in Frontiers in physiology (08-01-2021)“…Cardiovascular disease continues to be the leading cause of morbidity and mortality in the United States and thousands of manuscripts each year are aimed at…”
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Patterns of Electrocardiographic Abnormalities in Children with Hypertrophic Cardiomyopathy
Published in Pediatric cardiology (01-12-2024)“…Hypertrophic cardiomyopathy (HCM), a common cardiomyopathy in children, is an important cause of morbidity and mortality. Early recognition and appropriate…”
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Fibrosis-Related Gene Expression in Single Ventricle Heart Disease
Published in The Journal of pediatrics (01-12-2017)“…To evaluate fibrosis and fibrosis-related gene expression in the myocardium of pediatric subjects with single ventricle with right ventricular failure…”
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Risk stratification in pediatric hypertrophic cardiomyopathy: Insights for bridging the evidence gap?
Published in Progress in pediatric cardiology (01-06-2018)“…Identification of children with hypertrophic cardiomyopathy (HCM) who are at high risk for sudden cardiac death (SCD) remains challenging. Although a large…”
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Circulating cyclic adenosine monophosphate concentrations in milrinone treated paediatric patients after congenital heart surgery
Published in Cardiology in the young (01-09-2021)“…Milrinone is a phosphodiesterase type 3 inhibitor that results in a positive inotropic effect in the heart through an increase in cyclic adenosine…”
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Educational and learning morbidity in pediatric heart transplant recipients: A pediatric heart transplant society study
Published in Pediatric transplantation (01-06-2020)“…Educational development is an important component of quality of life for children with heart transplant. Aims include determining prevalence of and risk…”
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