Outcomes of endovascular therapy for Stanford type B aortic dissection in patients with Marfan syndrome
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine,Pulmonary and Respiratory Medicine,Surgery
Reference40 articles.
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2. Marfan syndrome: from gene to therapy;Bolar;Curr Opin Pediatr,2012
3. Should aortic arch replacement be performed during initial surgery for aortic root aneurysm in patients with Marfan syndrome?;Schoenhoff;Eur J Cardiothorac Surg,2013
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1. Hybrid approach to achieve secure distal seal zones during endovascular aortic repair in a patient with Marfan syndrome;Journal of Vascular Surgery Cases, Innovations and Techniques;2024-12
2. Endovascular aortic repair in patients with Marfan and Loeys–Dietz syndrome is safe and durable when employed by a multi-disciplinary aortic team;European Journal of Cardio-Thoracic Surgery;2024-03-01
3. Diagnosis and treatment of cardiovascular disease in patients with heritable connective tissue disorders or heritable thoracic aortic diseases;Cardiovascular Intervention and Therapeutics;2024-01-05
4. Outcomes of thoracic aortic interventions in Marfan syndrome in the state of Texas over 11 years;Interdisciplinary CardioVascular and Thoracic Surgery;2023-08-01
5. Endovascular and Hybrid Repair in Patients with Heritable Thoracic Aortic Disease;Annals of Vascular Surgery;2022-11
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