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Comparison of Two-Level versus One-Level Total Disc Replacement: Results from a Prospective FDA-Regulated Trial August 2008
Jack E. Zigler, Donna D. Ohnmeiss
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The First 18 Months Following Food and Drug Administration Approval of Lumbar Total Disc Replacement in the United States: Reported Adverse Events Outside an Investigational Device Exemption Study Environment January 2008
Scott L. Blumenthal, Richard D. Guyer, F. Geisler, Paul C. McAfee, J. Regan
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Two- to Three-Year Follow-Up of ProDisc-L: Results from a Prospective Randomized Trial of Arthroplasty versus Fusion October 2007
Jack E. Zigler, Barton L. Sachs, Ralph F. Rashbaum, Donna D. Ohnmeiss
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An Economic Model of One-Level Lumbar Arthroplasty versus Fusion October 2007
Richard D. Guyer, Scott G. Tromanhauser, John J. Regan
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Complications of Lumbar Artificial Disc Replacement Compared to Fusion: Results from the Prospective, Randomized, Multicenter U.S. Food and Drug Administration Investigational Device Exemption Study of the Charité Artificial Disc April 2007
R. T. Holt, M. E. Majd, J. E. Isaza, Scott L. Blumenthal, Paul C. McAfee, Richard D. Guyer, et al.
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Lumbar Spine Arthroplasty Using the ProDisc II November 2004
Jack E. Zigler
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Prospective Randomized Study of the Charité Artificial Disc: Data from Two Investigational Centers November 2004
Richard D. Guyer, Paul C. McAfee, Stephen H. Hochschuler, Scott L. Blumenthal, Ira L. Fedder, Donna D. Ohnmeiss, Bryan W. Cunningham
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Artificial Intervertebral Discs and Beyond: A North American Spine Society Annual Meeting Symposium December 2002
Scott L. Blumenthal, Donna D. Ohnmeiss, Richard D. Guyer, Stephen Hochschuler, Paul McAfee, Rolando Garcia, Richard Salib, Hansen Yuan, Casey Lee, Rudolph Bertagnoli, Vincent Bryan, Robert Winter
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