Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial

Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial

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Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial

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http://www.wikidata.org/entity/Q57133525

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wetenschappelijk artikel

@nl

наукова стаття, опублікована в червні 2018

@uk

name

Long-Term Clinical Experience ...... evice Exemption Clinical Trial

@en

Long-Term Clinical Experience ...... evice Exemption Clinical Trial

@nl

type

Item

label

Long-Term Clinical Experience ...... evice Exemption Clinical Trial

@en

Long-Term Clinical Experience ...... evice Exemption Clinical Trial

@nl

prefLabel

Long-Term Clinical Experience ...... evice Exemption Clinical Trial

@en

Long-Term Clinical Experience ...... evice Exemption Clinical Trial

@nl

P1476

Long-Term Clinical Experience ...... evice Exemption Clinical Trial

@en

P2093

Alexander Vaccaro

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Andrew Mugglin

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Jacqueline Myer

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Joseph Marzluff

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Kelly J Baker

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Prem S Ramakrishnan

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Walter Peppelman

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William Beutler

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P2860

Determining the clinical importance of treatment benefits for interventions for painful orthopedic conditions

Cost Utility Analysis of the Cervical Artificial Disc vs Fusion for the Treatment of 2-Level Symptomatic Degenerative Disc Disease: 5-Year Follow-up.

Cervical Disc Arthroplasty with Prestige LP Disc Versus Anterior Cervical Discectomy and Fusion: Seven-Year Outcomes

Total disc arthroplasty does not affect the incidence of adjacent segment degeneration in cervical spine: results of 93 patients in three prospective randomized clinical trials.

Results of the prospective, randomized, controlled multicenter Food and Drug Administration investigational device exemption study of the ProDisc-C total disc replacement versus anterior discectomy and fusion for the treatment of 1-level symptomatic

Incidence of adjacent segment degeneration in cervical disc arthroplasty versus anterior cervical decompression and fusion meta-analysis of prospective studies.

Cost-utility analysis modeling at 2-year follow-up for cervical disc arthroplasty versus anterior cervical discectomy and fusion: A single-center contribution to the randomized controlled trial

Prevalence of heterotopic ossification after cervical total disc arthroplasty: a meta-analysis

Cervical total disc replacement, part I: rationale, biomechanics, and implant types.

Early clinical experience with the mobi-C disc prosthesis.

P304

377-387

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scholarly article

P356

10.14444/5044

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P407

English

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2018-06-01T00:00:00Z

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30276095

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6159663

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Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial

about

Long-Term Clinical Experience with Selectively Constrained SECURE-C Cervical Artificial Disc for 1-Level Cervical Disc Disease: Results from Seven-Year Follow-Up of a Prospective, Randomized, Controlled Investigational Device Exemption Clinical Trial

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P932