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ProDisc-C and anterior cervical discectomy and fusion as surgical treatment for single-level cervical symptomatic degenerative disc disease: five-year results of a Food and Drug Administration study

Spine (Philadelphia, Pa. 1976), 2013-02, Vol.38 (3), p.203-209

2013

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Segmental Motion of Cervical Arthroplasty Leads to Decreased Adjacent-Level Degeneration: Analysis of the 7-Year Postoperative Results of a Multicenter Randomized Controlled Trial

International journal of spine surgery, 2022-02, Vol.16 (1), p.186-193

2022

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ProDisc-C Total Disc Replacement Versus Anterior Cervical Discectomy and Fusion for Single-Level Symptomatic Cervical Disc Disease: Seven-Year Follow-up of the Prospective Randomized U.S. Food and Drug Administration Investigational Device Exemption Study

Journal of bone and joint surgery. American volume, 2015-11, Vol.97 (21), p.1738

2015

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Comparison of 1-Level Versus 2-Level Anterior Cervical Discectomy and Fusion: Clinical and Radiographic Follow-Up at 60 Months

Spine (Philadelphia, Pa. 1976), 2016-03, Vol.41 (6), p.463-469

2016

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Clinical results with ProDisc: European experience and U.S. investigation device exemption study

Spine (Philadelphia, Pa. 1976), 2003-10, Vol.28 (20), p.S163-S166

Zigler, Jack E

2003

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Lumbar Total Disk Replacement Device Removals and Revisions Performed During a 20-Year Experience with 2141 Patients

Spine (Philadelphia, Pa. 1976), 2024-05, Vol.49 (10), p.671

2024

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Impact of previous lumbar spine surgery on the outcome of lumbar total disc replacement: analysis of prospective 5-year follow-up study data

European spine journal, 2023-03, Vol.32 (3), p.797-802

2023

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Prosthesis design and likelihood of achieving physiological range of motion after cervical disc arthroplasty: Analysis of range of motion data from 1,173 patients from 7 IDE clinical trials

The spine journal, 2024-06, Vol.24 (6), p.969-978

2024

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Seven-year cost-effectiveness of ProDisc-C total disc replacement: results from investigational device exemption and post-approval studies

Journal of neurosurgery. Spine, 2016-05, Vol.24 (5), p.760

2016

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Analysis of re-operations after cervical total disc replacement in a consecutive series of 535 patients receiving the ProDisc-C device

European spine journal, 2020-11, Vol.29 (11), p.2683-2687

2020

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Effect of Adverse Events on Low Back Surgery Outcome: Twenty-Four-Month Follow-up Results From a Food and Drug Administration Investigational Device ExemptionTrial

Spine (Philadelphia, Pa. 1976), 2010-04, Vol.35 (7), p.835-838

2010

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In which cases do surgeons specializing in total disc replacement perform fusion in patients with symptomatic lumbar disc degeneration?

European spine journal, 2022-10, Vol.31 (10), p.2607-2611

2022

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Cervical Disc Arthroplasty: Rationale and History

International journal of spine surgery, 2020-08, Vol.14 (s2), p.S5-S13

2020

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Screw-Related Complications After Instrumentation of the Osteoporotic Spine: A Systematic Literature Review With Meta-Analysis

Global Spine Journal, 2020-02, Vol.10 (1), p.69-88

2020

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In which cases do surgeons specializing in total disc replacement perform fusion in patients with cervical spine symptoms?

European spine journal, 2020-11, Vol.29 (11), p.2665-2669

2020

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Letter to the editor regarding, "Long-term results of the NECK trial-implanting a disc prosthesis after cervical anterior discectomy cannot prevent adjacent segment disease: five-year clinical follow-up of a double-blinded randomised controlled trial" by Goedmakers et al

The spine journal, 2024-02, Vol.24 (2), p.387-388

2024

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Prospective, Randomized Comparison of One-level Mobi-C Cervical Total Disc Replacement vs. Anterior Cervical Discectomy and Fusion: Results at 5-year Follow-up

International journal of spine surgery, 2016-01, Vol.10, p.10-10

2016

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The 5-year cost-effectiveness of anterior cervical discectomy and fusion and cervical disc replacement: a Markov analysis

Spine (Philadelphia, Pa. 1976), 2014-11, Vol.39 (23), p.1924-1933

2014

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Reoperations in Cervical Total Disc Replacement Compared With Anterior Cervical Fusion: Results Compiled From Multiple Prospective Food and Drug Administration Investigational Device Exemption Trials Conducted at a Single Site

Spine (Philadelphia, Pa. 1976), 2013-06, Vol.38 (14), p.1177-1182

2013

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Comparison of Results of Total Disc Replacement in Postdiscectomy Patients Versus Patients With No Previous Lumbar Surgery

Spine (Philadelphia, Pa. 1976), 2008-07, Vol.33 (15), p.1690-1695

2008

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Prospective, randomized, multicenter Food and Drug Administration investigational device exemption study of the ProDisc-L total disc replacement compared with circumferential arthrodesis for the treatment of two-level lumbar degenerative disc disease: results at twenty-four months

Journal of bone and joint surgery. American volume, 2011-04, Vol.93 (8), p.705

2011

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Progression of Adjacent-level Degeneration After Lumbar Total Disc Replacement: Results of a Post-hoc Analysis of Patients with Available Radiographs from a Prospective Study with 5-year Follow-up

Spine (Philadelphia, Pa. 1976), 2018-10, Vol.43 (20), p.1395-1400

2018

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Lumbar spine arthroplasty using the ProDisc II

The spine journal, 2004-11, Vol.4 (6), p.S260-S267

Zigler, Jack E.

2004

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Ten-Year Follow-Up of Patients Enrolled in the FDA-Regulated Trial for Single-Level Lumbar Total Disc Replacement: One Site's Experience

The spine journal, 2016-10, Vol.16 (10), p.S284-S284

2016

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Does 360° lumbar spinal fusion improve long-term clinical outcomes after failure of conservative treatment in patients with functionally disabling single-level degenerative lumbar disc disease? Results of 5-year follow-up in 75 postoperative patients

International journal of spine surgery, 2013, Vol.7 (1), p.e1-e7

2013

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ProDisc-C and anterior cervical discectomy and fusion as surgical treatment for single-level cervical symptomatic degenerative disc disease: five-year results of a Food and Drug Administration study

Segmental Motion of Cervical Arthroplasty Leads to Decreased Adjacent-Level Degeneration: Analysis of the 7-Year Postoperative Results of a Multicenter Randomized Controlled Trial

ProDisc-C Total Disc Replacement Versus Anterior Cervical Discectomy and Fusion for Single-Level Symptomatic Cervical Disc Disease: Seven-Year Follow-up of the Prospective Randomized U.S. Food and Drug Administration Investigational Device Exemption Study

Comparison of 1-Level Versus 2-Level Anterior Cervical Discectomy and Fusion: Clinical and Radiographic Follow-Up at 60 Months

Clinical results with ProDisc: European experience and U.S. investigation device exemption study

Lumbar Total Disk Replacement Device Removals and Revisions Performed During a 20-Year Experience with 2141 Patients

Impact of previous lumbar spine surgery on the outcome of lumbar total disc replacement: analysis of prospective 5-year follow-up study data

Prosthesis design and likelihood of achieving physiological range of motion after cervical disc arthroplasty: Analysis of range of motion data from 1,173 patients from 7 IDE clinical trials

Seven-year cost-effectiveness of ProDisc-C total disc replacement: results from investigational device exemption and post-approval studies

Analysis of re-operations after cervical total disc replacement in a consecutive series of 535 patients receiving the ProDisc-C device

Effect of Adverse Events on Low Back Surgery Outcome: Twenty-Four-Month Follow-up Results From a Food and Drug Administration Investigational Device ExemptionTrial

In which cases do surgeons specializing in total disc replacement perform fusion in patients with symptomatic lumbar disc degeneration?

Cervical Disc Arthroplasty: Rationale and History

Screw-Related Complications After Instrumentation of the Osteoporotic Spine: A Systematic Literature Review With Meta-Analysis

In which cases do surgeons specializing in total disc replacement perform fusion in patients with cervical spine symptoms?

Letter to the editor regarding, "Long-term results of the NECK trial-implanting a disc prosthesis after cervical anterior discectomy cannot prevent adjacent segment disease: five-year clinical follow-up of a double-blinded randomised controlled trial" by Goedmakers et al

Prospective, Randomized Comparison of One-level Mobi-C Cervical Total Disc Replacement vs. Anterior Cervical Discectomy and Fusion: Results at 5-year Follow-up

The 5-year cost-effectiveness of anterior cervical discectomy and fusion and cervical disc replacement: a Markov analysis

Reoperations in Cervical Total Disc Replacement Compared With Anterior Cervical Fusion: Results Compiled From Multiple Prospective Food and Drug Administration Investigational Device Exemption Trials Conducted at a Single Site

Comparison of Results of Total Disc Replacement in Postdiscectomy Patients Versus Patients With No Previous Lumbar Surgery

Prospective, randomized, multicenter Food and Drug Administration investigational device exemption study of the ProDisc-L total disc replacement compared with circumferential arthrodesis for the treatment of two-level lumbar degenerative disc disease: results at twenty-four months

Progression of Adjacent-level Degeneration After Lumbar Total Disc Replacement: Results of a Post-hoc Analysis of Patients with Available Radiographs from a Prospective Study with 5-year Follow-up

Lumbar spine arthroplasty using the ProDisc II

Ten-Year Follow-Up of Patients Enrolled in the FDA-Regulated Trial for Single-Level Lumbar Total Disc Replacement: One Site's Experience

Does 360° lumbar spinal fusion improve long-term clinical outcomes after failure of conservative treatment in patients with functionally disabling single-level degenerative lumbar disc disease? Results of 5-year follow-up in 75 postoperative patients

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