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Source:
Enable® Aortic Sutureless Bioprosthesis Evaluation: A Post-market Release Non-interventional StudyMartens S, Sadowski J, Eckstein FS, Bartus K, Kapelak B, Sievers
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Evaluation of the Clinical Outcomes of CoreValve in Degenerative Surgical Aortic Bioprosthesis. A Prospective, Observational Post-market Study.Kornowski R,
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Post-Approval Study for the MOSAIC® Bioprostheses: A Long Term Follow Up Study.Riess FC, Cramer E, Hansen L, Schiffelers S, Wahl G, Wallrath J, Winkel S, Kremer P. Clinical results of the
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Feasibility Study of Percutaneous Aortic Valve Implantation With the Medtronic CoreValve System for Percutaneous Aortic Valve Replacement (PAVR) in Patients With a Failing Previously Surgically
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The Engager ALIGN Study. To Characterize the Safety and Clinical Benefit of the Engager Transcatheter Aortic Valve Implantation System in a Real World Environment.
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Enable I Long-term Follow-up StudyMartens S, Sadowski J, Eckstein FS, Bartus K, Kapelak B, Sievers HH, Schlensak C, Carrel T. Clinical experience with the ATS 3f Enable(R) Sutureless
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Mosaic Ultra Porcine Bioprosthesis - Hemodynamic Study
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Source:
CoreValve Advance-II Study: Best Practices Investigation of Patients Implanted With the Medtronic CoreValve Bioprosthesis.Petronio AS, Sinning JM, Van Mieghem N,
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