SCOTT LEMAIRE to Young Adult
This is a "connection" page, showing publications SCOTT LEMAIRE has written about Young Adult.
Connection Strength
0.383
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Single-Cell Analysis of Aneurysmal Aortic Tissue in Patients with Marfan Syndrome Reveals Dysfunctional TGF-? Signaling. Genes (Basel). 2021 12 30; 13(1).
Score: 0.072
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Valve-sparing aortic root replacement: early and midterm outcomes in 83 patients. Ann Thorac Surg. 2014 Apr; 97(4):1267-73; discussion 1273-4.
Score: 0.042
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Thoracic or thoracoabdominal approaches to endovascular device removal and open aortic repair. Ann Thorac Surg. 2012 Mar; 93(3):726-32; discussion 733.
Score: 0.037
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Aortic root replacement with stentless porcine xenografts: early and late outcomes in 132 patients. Ann Thorac Surg. 2009 Feb; 87(2):503-12; discussion 512-3.
Score: 0.030
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Clinical Characteristics and Long-Term Outcomes of Midaortic Syndrome. Ann Vasc Surg. 2020 Jul; 66:318-325.
Score: 0.016
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Thoracic Aortic, Aortic Valve, and Mitral Valve Surgery in Pediatric and Young Adult Patients With Marfan Syndrome: Characteristics and Outcomes. Semin Thorac Cardiovasc Surg. 2019; 31(4):818-825.
Score: 0.015
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Endovascular thoracic aortic repair in confirmed or suspected genetically triggered thoracic aortic dissection. J Vasc Surg. 2018 08; 68(2):364-371.
Score: 0.014
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Aortic Dilatation Associated With Bicuspid Aortic Valve: Relation to Sex, Hemodynamics, and Valve Morphology (the National Heart Lung and Blood Institute-Sponsored National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions). Am J Cardiol. 2017 Oct 01; 120(7):1171-1175.
Score: 0.013
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Associations of Age and Sex With Marfan Phenotype: The National Heart, Lung, and Blood Institute GenTAC (Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions) Registry. Circ Cardiovasc Genet. 2017 Jun; 10(3).
Score: 0.013
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Aortic Complications Associated With Pregnancy in Marfan Syndrome: The NHLBI National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC). J Am Heart Assoc. 2016 08 11; 5(8).
Score: 0.012
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Midterm Survival and Quality of Life After Extent II Thoracoabdominal Aortic Repair in Marfan Syndrome. Ann Thorac Surg. 2016 Apr; 101(4):1402-9; discussion 1409.
Score: 0.012
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Aortic Disease Presentation and Outcome Associated With ACTA2 Mutations. Circ Cardiovasc Genet. 2015 Jun; 8(3):457-64.
Score: 0.011
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Valve-sparing aortic root replacement in patients with Marfan syndrome enrolled in the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions. J Heart Valve Dis. 2014 May; 23(3):292-8.
Score: 0.011
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Early and 1-year outcomes of aortic root surgery in patients with Marfan syndrome: a prospective, multicenter, comparative study. J Thorac Cardiovasc Surg. 2014 Jun; 147(6):1758-66, 1767.e1-4.
Score: 0.010
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Emergent pectus excavatum repair after aortic root replacement in Marfan patient. J Card Surg. 2012 Mar; 27(2):222-4.
Score: 0.009
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Long-term implications of emergency versus elective proximal aortic surgery in patients with Marfan syndrome in the Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions Consortium Registry. J Thorac Cardiovasc Surg. 2012 Feb; 143(2):282-6.
Score: 0.009
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The National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC): results from phase I and scientific opportunities in phase II. Am Heart J. 2011 Oct; 162(4):627-632.e1.
Score: 0.009
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Open repair of thoracoabdominal aortic aneurysm in the modern surgical era: contemporary outcomes in 509 patients. J Am Coll Surg. 2011 Apr; 212(4):569-79; discussion 579-81.
Score: 0.009
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Intraoperative conversion after surgical failure: an overlooked complication of aortic root replacement in Marfan patients? Tex Heart Inst J. 2011; 38(6):684-6.
Score: 0.008
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Aortic valve replacement: mortality predictions of surgeons versus risk model. J Surg Res. 2010 Sep; 163(1):1-6.
Score: 0.008
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Surgical treatment of patients enrolled in the national registry of genetically triggered thoracic aortic conditions. Ann Thorac Surg. 2009 Sep; 88(3):781-7; discussion 787-8.
Score: 0.008
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Valve-sparing and valve-replacing techniques for aortic root replacement in patients with Marfan syndrome: Analysis of early outcome. J Thorac Cardiovasc Surg. 2009 May; 137(5):1124-32.
Score: 0.008
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Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease. Am J Hum Genet. 2009 May; 84(5):617-27.
Score: 0.008