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A prospective, randomized, multicenter Food and Drug Administration investigational device exemptions study of lumbar total disc replacement with the CHARITE artificial disc versus lumbar fusion: part I: evaluation of clinical outcomes.
Blumenthal S, McAfee PC, Guyer RD, Hochschuler SH, Geisler FH, Holt RT, Garcia R Jr, Regan JJ, Ohnmeiss DD. Blumenthal S, et al. Among authors: geisler fh. Spine (Phila Pa 1976). 2005 Jul 15;30(14):1565-75; discussion E387-91. doi: 10.1097/01.brs.0000170587.32676.0e. Spine (Phila Pa 1976). 2005. PMID: 16025024 Clinical Trial.
Revisability of the CHARITE artificial disc replacement: analysis of 688 patients enrolled in the U.S. IDE study of the CHARITE Artificial Disc.
McAfee PC, Geisler FH, Saiedy SS, Moore SV, Regan JJ, Guyer RD, Blumenthal SL, Fedder IL, Tortolani PJ, Cunningham B. McAfee PC, et al. Among authors: geisler fh. Spine (Phila Pa 1976). 2006 May 15;31(11):1217-26. doi: 10.1097/01.brs.0000217689.08487.a8. Spine (Phila Pa 1976). 2006. PMID: 16688035 Clinical Trial.
Prospective, randomized, multicenter Food and Drug Administration investigational device exemption study of lumbar total disc replacement with the CHARITE artificial disc versus lumbar fusion: five-year follow-up.
Guyer RD, McAfee PC, Banco RJ, Bitan FD, Cappuccino A, Geisler FH, Hochschuler SH, Holt RT, Jenis LG, Majd ME, Regan JJ, Tromanhauser SG, Wong DC, Blumenthal SL. Guyer RD, et al. Among authors: geisler fh. Spine J. 2009 May;9(5):374-86. doi: 10.1016/j.spinee.2008.08.007. Epub 2008 Sep 19. Spine J. 2009. PMID: 18805066 Clinical Trial.
102 results