Area of research
Pulmonary and Respiratory Medicine · Genetics
Research interest
Research interests include Connective tissue disorders research, Aortic Disease and Treatment Approaches, Cardiac Valve Diseases and Treatments, and Aortic aneurysm repair treatments.
Early Mortality in Type A Acute Aortic Dissection
Comparative Risks of Initial Aortic Events Associated With Genetic Thoracic Aortic Disease
Clinical Features and Outcomes of Pregnancy-Related Acute Aortic Dissection
Features of Marfan syndrome not listed in the Ghent nosology – the dark side of the disease
Patient re-contact after revision of genomic test results: points to consider—a statement of the American College of Medical Genetics and Genomics (ACMG)
Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations
Health-Related Quality of Life in Children and Young Adults with Marfan Syndrome
Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review
Influence of Aortic Stiffness on Aortic-Root Growth Rate and Outcome in Patients With the Marfan Syndrome
Predictors of Rapid Aortic Root Dilation and Referral for Aortic Surgery in Marfan Syndrome
Associations of Age and Sex With Marfan Phenotype
Aortic Complications Associated With Pregnancy in Marfan Syndrome: The NHLBI National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC)
Aortic Dissection in Patients With Genetically Mediated Aneurysms
Effect of Topical Intranasal Therapy on Epistaxis Frequency in Patients With Hereditary Hemorrhagic Telangiectasia
Chronobiology of Acute Aortic Dissection in the Marfan Syndrome (from the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions and the International Registry of Acute Aortic Dissection)
Aortic Disease Presentation and Outcome Associated With <i>ACTA2</i> Mutations
Atenolol versus Losartan in Children and Young Adults with Marfan's Syndrome
<i>RASA1</i>Mutations and Associated Phenotypes in 68 Families with Capillary Malformation-Arteriovenous Malformation
Acute Aortic Dissection in Blacks: Insights from the International Registry of Acute Aortic Dissection
Clinical presentation, management, and short-term outcome of patients with type A acute dissection complicated by mesenteric malperfusion: Observations from the International Registry of Acute Aortic Dissection