A5031746220- Congenital Heart Disease Studies
- Cardiovascular Effects of Exercise
- Cardiomyopathy and Myosin Studies
- Cardiac Arrhythmias and Treatments
- Cardiovascular Function and Risk Factors
- Coronary Artery Anomalies
- Pulmonary Hypertension Research and Treatments
- Vascular anomalies and interventions
- Cardiac electrophysiology and arrhythmias
- Cardiac Structural Anomalies and Repair
- Tracheal and airway disorders
- Cardiovascular Issues in Pregnancy
- Heart Failure Treatment and Management
- Nursing Roles and Practices
- Congenital heart defects research
- Viral Infections and Immunology Research
- Physical Activity and Health
- Ultrasound in Clinical Applications
- Trypanosoma species research and implications
- Cutaneous Melanoma Detection and Management
- Cardiac Arrest and Resuscitation
- Aortic Disease and Treatment Approaches
- Medicine and Dermatology Studies History
- Photodynamic Therapy Research Studies
- Magnetic and transport properties of perovskites and related materials
Children's Hospital of Philadelphia
2013-2024
University of Pennsylvania
2003-2023
Philadelphia University
2019-2023
Stephens College
2023
Stoke Mandeville Hospital
2012
Cambridge University Press
2009-2010
University of Memphis
1998
Persistent patent ductus arteriosus (PDA) often produces hemodynamic and respiratory derangement necessitating use of inotropic drugs escalating ventilatory support in premature infants. When medical therapy fails, surgical ligation is indicated. Because the risks transferring unstable neonates to operating room, ductal routinely performed at neonatal intensive care unit (NICU) bedside. Some patients, however, require transfer from hospitals without pediatric cardiac teams. In an attempt...
To evaluate the impact of a pediatric emergency department (ED) chest pain clinical pathway on resource utilization.Motivated by perceived overuse cardiology consultation for non-cardiac in ED, clinicians from Divisions Cardiology and Emergency Medicine collaboratively developed pathway, educated staff, implemented March 1, 2014. We reviewed records children aged 3 to 18 years without prior diagnoses heart disease who presented ED with between 2013, April 22, 2015. compared diagnostic...
We evaluated the presentation, treatment, and outcome of infants who present with ventricular tachycardia in first year life. Seventy-six were admitted to our institution a diagnosis between January, 1987 May, 2006. Forty-five excluded from study because additional confounding diagnoses including accelerated idioventricular rhythm, Wolff-Parkinson-White syndrome, supraventricular aberrancy, long QT cardiac rhabdomyoma, myocarditis, congenital lesions, or incomplete data. The remaining 31...
Journal Article Arterial Pressure in CBA Mice As Related to Age Get access James P. Henry, M.D., M.D. Visiting Professor 2Department of Physiology, School Medicine, University Southern CaliforniaLos Angeles, California 90007, Colonel, USAF, (M.C.) Assigned Headquarters Aerospace Medical Division, Brooks Air Force Base, Texas, with Permanent Duty Station at the Search for other works by this author on: Oxford Academic PubMed Google Scholar John Meehan, Patricia Stephens, Stephens George A....
Exercise stress testing (EST) in pediatric hypertrophic cardiomyopathy (HCM) patients has not well described a large heterogenous cohort. The objective of the study was to determine clinical utility EST HCM. This retrospective single-center analysis HCM younger than 21 years who had between January 1, 2000, and 2019. Clinical, demographic characteristics, data were analyzed, using last during or prior event subjects with primary outcome. composite endpoint included cardiac death, transplant,...
Fontan survivors have depressed cardiac index that worsens over time. Serum biomarker measurement is minimally invasive, rapid, widely available, and may be useful for serial monitoring. The purpose of this study was to identify biomarkers correlate with lower in patients. Methods results This a multi-centre case series assessing the correlations between magnetic resonance-derived patients ⩾6 years age biochemical haematopoietic obtained ±12 months from resonance. Medical history values were...
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a familial form of cardiomyopathy typically caused by mutations in genes that encode an element the cardiac desmosome. Branchio-oculo-facial syndrome (BOFS) craniofacial disorder TFAP2A mutations. In family segregating ARVD/C, some members also had features BOFS. Genetic testing for ARVD/C identified mutation PKP2, encoding plakophilin-2, component Evaluation dysmorphology chromosome microarray (CMA) 4.4 Mb deletion at...
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