Author pages are created from data sourced from our academic publisher partnerships and public sources.
Endothelial pulse amplitude testing: feasibility and reproducibility in adolescents.
- E. S. Selamet Tierney, J. Newburger, +4 authors S. D. de Ferranti
- The Journal of pediatrics
- 1 June 2009
OBJECTIVES To test prospectively the reproducibility and feasibility of endothelial pulse amplitude testing (Endo-PAT), a novel Food and Drug Administration-approved technology, in healthy… Expand
Atenolol versus losartan in children and young adults with Marfan's syndrome.
- R. Lacro, H. Dietz, +30 authors L. Mahony
- The New England journal of medicine
- 26 November 2014
BACKGROUND Aortic-root dissection is the leading cause of death in Marfan's syndrome. Studies suggest that with regard to slowing aortic-root enlargement, losartan may be more effective than… Expand
Mitral valve replacement in infants and children 5 years of age or younger: evolution in practice and outcome over three decades with a focus on supra-annular prosthesis implantation.
- E. S. Selamet Tierney, F. Pigula, C. Berul, J. Lock, P. D. del Nido, D. McElhinney
- The Journal of thoracic and cardiovascular…
- 1 October 2008
OBJECTIVE Successful mitral valve replacement in young children is limited by the lack of small prosthetic valves. Supra-annular prosthesis implantation can facilitate mitral valve replacement with a… Expand
Changes in left heart hemodynamics after technically successful in‐utero aortic valvuloplasty
- E. S. Selamet Tierney, R. Wald, +9 authors W. Tworetzky
- Ultrasound in obstetrics & gynecology : the…
- 1 October 2007
Severe aortic stenosis in the mid‐gestation fetus can progress to hypoplastic left heart syndrome (HLHS). @ In‐utero aortic valvuloplasty is an innovative therapy to promote left ventricular growth… Expand
The ventricular volume variability study of the Pediatric Heart Network: study design and impact of beat averaging and variable type on the reproducibility of echocardiographic measurements in…
- S. Colan, G. Shirali, +14 authors L. Sleeper
- Journal of the American Society of…
- 1 August 2012
BACKGROUND Clinical trials often rely on echocardiographic measures of left ventricular size and function as surrogate end points. However, the quantitative impact of factors that affect the… Expand
Characteristics of children and young adults with Marfan syndrome and aortic root dilation in a randomized trial comparing atenolol and losartan therapy.
BACKGROUND The Pediatric Heart Network designed a clinical trial to compare aortic root growth and other short-term cardiovascular outcomes in children and young adults with Marfan syndrome… Expand
Mutations in ZIC3 and ACVR2B are a common cause of heterotaxy and associated cardiovascular anomalies.
- L. Ma, E. S. Selamet Tierney, T. Lee, P. Lanzano, W. Chung
- Cardiology in the young
- 1 April 2012
BACKGROUND Heterotaxy syndrome is caused by left-right asymmetry disturbances and is associated with abnormal lateralisation of the abdominal and thoracic organs. The heart is frequently involved and… Expand
Arterial applanation tonometry: feasibility and reproducibility in children and adolescents.
- A. Lowenthal, Jasmine M A Evans, +4 authors E. S. Selamet Tierney
- American journal of hypertension
- 1 September 2014
BACKGROUND Aortic pulse wave velocity (PWV) and augmentation index (AIx) are markers of vascular health and have recently been used in pediatric clinical trials. However, there are limited data on… Expand
Assessment of Progressive Pathophysiology After Early Prenatal Diagnosis of the Ebstein Anomaly or Tricuspid Valve Dysplasia.
- E. S. Selamet Tierney, D. McElhinney, +11 authors A. Moon-Grady
- The American journal of cardiology
In fetuses with Ebstein anomaly or tricuspid valve dysplasia (EA/TVD), poor hemodynamic status is associated with worse neonatal outcome. It is not known whether EA/TVD fetuses with more favorable… Expand
Comparison of impact of prenatal versus postnatal diagnosis of congenitally corrected transposition of the great arteries.
- A. Wan, Alexandra Jevremovic, +7 authors L. Nield
- The American journal of cardiology
- 1 November 2009
Congenitally corrected transposition of the great arteries (CCTGA) in the absence of major cardiac anomalies is thought to have a good outcome, although this has not been well documented. The… Expand