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Aortic Root Replacement in 372 Marfan Patients: Evolution of Operative Repair Over 30 Years

The Annals of thoracic surgery, 2009-05, Vol.87 (5), p.1344-1350

2009

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Aortic Root Operations for Marfan Syndrome: A Comparison of the Bentall and Valve-Sparing Procedures

The Annals of thoracic surgery, 2008-06, Vol.85 (6), p.2003-2011

2008

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American society of echocardiography guidelines and standards for performance of the fetal echocardiogram

Journal of the American Society of Echocardiography, 2004-07, Vol.17 (7), p.803-810

2004

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Early Surgical Experience With Loeys-Dietz: A New Syndrome of Aggressive Thoracic Aortic Aneurysm Disease

The Annals of thoracic surgery, 2007-02, Vol.83 (2), p.S757-S763

2007

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Familial thoracic aortic dilation and bicommissural aortic valve: A prospective analysis of natural history and inheritance

American journal of medical genetics. Part A, 2007-09, Vol.143A (17), p.1960-1967

2007

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Progressive Dilation of the Ascending Aorta in Children With Isolated Bicuspid Aortic Valve

The American journal of cardiology, 2007-04, Vol.99 (7), p.978-983

2007

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Ventricular arrhythmia risk prediction in repaired Tetralogy of Fallot using personalized computational cardiac models

Heart rhythm, 2020-03, Vol.17 (3), p.408-414

2020

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Tetralogy of Fallot and Aortic Root Dilation: A Long-Term Outlook

Pediatric cardiology, 2013-04, Vol.34 (4), p.809-816

2013

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A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

Nature genetics, 2005-03, Vol.37 (3), p.275-281

2005

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Placement of implantable cardioverter‐defibrillators in paediatric and congenital heart defect patients: a pipeline for model generation and simulation prediction of optimal configurations

The Journal of physiology, 2013-09, Vol.591 (17), p.4321-4334

2013

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Arrhythmogenic right ventricular dysplasia : A United States experience

Circulation (New York, N.Y.), 2005-12, Vol.112 (25), p.3823-3832

2005

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Computational Identification of Ventricular Arrhythmia Risk in Pediatric Myocarditis

Pediatric cardiology, 2019-04, Vol.40 (4), p.857-864

2019

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Hepatic venous blood and the development of pulmonary arteriovenous malformations in congenital heart disease

Circulation (New York, N.Y.), 1995-09, Vol.92 (5), p.1217-1222

1995

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Clinical features of arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in plakophilin-2

Circulation (New York, N.Y.), 2006-04, Vol.113 (13), p.1641-1649

2006

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Implantable Cardioverter-Defibrillators in patients with arrhythmogenic right ventricular Dysplasia/Cardiomyopathy

Journal of the American College of Cardiology, 2004-05, Vol.43 (10), p.1843-1852

2004

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Surgically corrected congenital heart disease: utility of 64-MDCT

American journal of roentgenology (1976), 2008-09, Vol.191 (3), p.854

2008

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Penetrance of Mutations in Plakophilin-2 Among Families With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

Journal of the American College of Cardiology, 2006-10, Vol.48 (7), p.1416-1424

2006

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Utility of a High-Resolution 3D MRI Sequence (3D-SPACE) for Evaluation of Congenital Heart Disease

Pediatric cardiology, 2015-10, Vol.36 (7), p.1510-1514

2015

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Cardiac valve assessment with MR imaging and 64-section multi-detector row CT

Radiographics, 2006-11, Vol.26 (6), p.1769

2006

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Cardiovascular pathologies in mucopolysaccharidosis type VII (Sly Syndrome)

Cardiovascular pathology, 2015-09, Vol.24 (5), p.322-326

2015

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Recessive arrhythmogenic right ventricular dysplasia due to novel cryptic splice mutation in PKP2

Human mutation, 2006-11, Vol.27 (11), p.1157-1157

2006

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Results of aortic valve-sparing operations: Experience with remodeling and reimplantation procedures in 65 patients

The Annals of thoracic surgery, 2004-09, Vol.78 (3), p.767-772

2004

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Valve-Sparing Aortic Root Replacement: Early Experience With the De Paulis Valsalva Graft in 51 Patients

The Annals of thoracic surgery, 2006-08, Vol.82 (2), p.548-553

2006

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Abnormal myocardial mechanics in Kawasaki disease: Rapid response to γ-globulin

The American heart journal, 2000-02, Vol.139 (2), p.217-223

2000

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Left heart obstructive lesions and left ventricular growth in the midtrimester fetus : a longitudinal study

Circulation (New York, N.Y.), 1995-09, Vol.92 (6), p.1531-1538

1995

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Aortic Root Replacement in 372 Marfan Patients: Evolution of Operative Repair Over 30 Years

Aortic Root Operations for Marfan Syndrome: A Comparison of the Bentall and Valve-Sparing Procedures

American society of echocardiography guidelines and standards for performance of the fetal echocardiogram

Early Surgical Experience With Loeys-Dietz: A New Syndrome of Aggressive Thoracic Aortic Aneurysm Disease

Familial thoracic aortic dilation and bicommissural aortic valve: A prospective analysis of natural history and inheritance

Progressive Dilation of the Ascending Aorta in Children With Isolated Bicuspid Aortic Valve

Ventricular arrhythmia risk prediction in repaired Tetralogy of Fallot using personalized computational cardiac models

Tetralogy of Fallot and Aortic Root Dilation: A Long-Term Outlook

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

Placement of implantable cardioverter‐defibrillators in paediatric and congenital heart defect patients: a pipeline for model generation and simulation prediction of optimal configurations

Arrhythmogenic right ventricular dysplasia : A United States experience

Computational Identification of Ventricular Arrhythmia Risk in Pediatric Myocarditis

Hepatic venous blood and the development of pulmonary arteriovenous malformations in congenital heart disease

Clinical features of arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in plakophilin-2

Implantable Cardioverter-Defibrillators in patients with arrhythmogenic right ventricular Dysplasia/Cardiomyopathy

Surgically corrected congenital heart disease: utility of 64-MDCT

Penetrance of Mutations in Plakophilin-2 Among Families With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

Utility of a High-Resolution 3D MRI Sequence (3D-SPACE) for Evaluation of Congenital Heart Disease

Cardiac valve assessment with MR imaging and 64-section multi-detector row CT

Cardiovascular pathologies in mucopolysaccharidosis type VII (Sly Syndrome)

Recessive arrhythmogenic right ventricular dysplasia due to novel cryptic splice mutation in PKP2

Results of aortic valve-sparing operations: Experience with remodeling and reimplantation procedures in 65 patients

Valve-Sparing Aortic Root Replacement: Early Experience With the De Paulis Valsalva Graft in 51 Patients

Abnormal myocardial mechanics in Kawasaki disease: Rapid response to γ-globulin

Left heart obstructive lesions and left ventricular growth in the midtrimester fetus : a longitudinal study

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