A5083559427- Aortic Disease and Treatment Approaches
- Cardiomyopathy and Myosin Studies
- Cardiac Structural Anomalies and Repair
- Cardiac electrophysiology and arrhythmias
- Cardiovascular Function and Risk Factors
- Aortic aneurysm repair treatments
- Cardiac Valve Diseases and Treatments
- Cardiovascular Issues in Pregnancy
- Cardiovascular Effects of Exercise
- Congenital Heart Disease Studies
- Cardiac Imaging and Diagnostics
- Cerebrovascular and Carotid Artery Diseases
- Connective tissue disorders research
- Cardiac Arrhythmias and Treatments
- Viral Infections and Immunology Research
- Mitochondrial Function and Pathology
- Mechanical Circulatory Support Devices
- COVID-19 and healthcare impacts
- Coronary Interventions and Diagnostics
- Genomics and Rare Diseases
- Atrial Fibrillation Management and Outcomes
- Advanced MRI Techniques and Applications
- Takotsubo Cardiomyopathy and Associated Phenomena
- Cardiovascular and Diving-Related Complications
- Cardiac, Anesthesia and Surgical Outcomes
Cornell University
2016-2024
Presbyterian Hospital
2018-2024
Weill Cornell Medicine
2018-2024
New York Hospital Queens
2018-2023
NewYork–Presbyterian Hospital
2018-2023
Cleveland Clinic
2023
Cleveland Clinic Lerner College of Medicine
2023
Istituti di Ricovero e Cura a Carattere Scientifico
2011-2022
Policlinico San Matteo Fondazione
2011-2020
Mayo Clinic in Arizona
2013-2019
<h3>Objective</h3> To evaluate the prevalence and phenotype of smooth muscle alpha-actin (<i>ACTA2</i>) mutations in non-syndromic thoracic aortic aneurysms dissections (TAAD). <h3>Design</h3> Observational study <i>ACTA2</i> TAAD. <h3>Setting</h3> Centre for Inherited Cardiovascular Diseases. <h3>Patients</h3> A consecutive series 100 patients with Exclusion criteria included genetically confirmed Marfan syndrome, Loeys–Dietz type 2, familial bicuspid valve Ehlers–Danlos IV syndromes....
Background— Atrial dilatation and atrial standstill are etiologically heterogeneous phenotypes with poorly defined nosology. In 1983, we described 8-years follow-up of evolution in 8 patients from 3 families. We later identified 5 additional identical phenotypes: 1 member the largest original family 4 unrelated to All families same geographic area Northeast Italy. Methods Results— followed up 13 for 37 years, extended clinical investigation monitoring living relatives, investigated genetic...
Abdominal aortic aneurysms expand over time and increase the risk of fatal ruptures. To predict expansion, isolated assessment
An aberrant subclavian artery (ASA) (or lusoria) is the most common congenital anomaly of aortic arch (0.5%-2.2%; female-to-male ratio 2:1 to 3:1). ASA can become aneurysmal and result in dissection, involving Kommerell's diverticulum when present aorta. Data its significance genetic arteriopathies are not available. The purpose this study was assess prevalence complications gene-positive -negative nonatherosclerotic arteriopathies. series includes 1,418 consecutive patients with (n = 854)...