pubmed-article:20192625 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20192625 | lifeskim:mentions | umls-concept:C0543467 | lld:lifeskim |
pubmed-article:20192625 | lifeskim:mentions | umls-concept:C1305533 | lld:lifeskim |
pubmed-article:20192625 | lifeskim:mentions | umls-concept:C1522577 | lld:lifeskim |
pubmed-article:20192625 | lifeskim:mentions | umls-concept:C0175649 | lld:lifeskim |
pubmed-article:20192625 | lifeskim:mentions | umls-concept:C1274040 | lld:lifeskim |
pubmed-article:20192625 | lifeskim:mentions | umls-concept:C0559956 | lld:lifeskim |
pubmed-article:20192625 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
pubmed-article:20192625 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
pubmed-article:20192625 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:20192625 | pubmed:dateCreated | 2010-3-2 | lld:pubmed |
pubmed-article:20192625 | pubmed:abstractText | In this study, long-term results are presented from clinical studies of the Bryan Cervical Disc Prosthesis at University Hospital Gasthuisberg in Leuven, Belgium. A total of 98 patients (89 with 1-level and 9 with 2-level implantations) agreed to participate in follow-up studies for up to 10 years postoperatively. This article focuses on the 4- and 6-year results. Patients in one of the clinical studies had either radiculopathy or myelopathy associated with spondylosis and/or disc herniations that did not respond to conservative treatment. Patients from the other clinical study received commercially available Bryan devices and the study protocol did not have specific inclusion/exclusion criteria. More than 90% of the patients were considered to have radiculopathy. | lld:pubmed |
pubmed-article:20192625 | pubmed:language | eng | lld:pubmed |
pubmed-article:20192625 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20192625 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:20192625 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20192625 | pubmed:month | Mar | lld:pubmed |
pubmed-article:20192625 | pubmed:issn | 1547-5646 | lld:pubmed |
pubmed-article:20192625 | pubmed:author | pubmed-author:Van... | lld:pubmed |
pubmed-article:20192625 | pubmed:author | pubmed-author:GoffinJanJ | lld:pubmed |
pubmed-article:20192625 | pubmed:author | pubmed-author:van... | lld:pubmed |
pubmed-article:20192625 | pubmed:author | pubmed-author:LipscombBaile... | lld:pubmed |
pubmed-article:20192625 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20192625 | pubmed:volume | 12 | lld:pubmed |
pubmed-article:20192625 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20192625 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20192625 | pubmed:pagination | 261-9 | lld:pubmed |
pubmed-article:20192625 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
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pubmed-article:20192625 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:20192625 | pubmed:articleTitle | A clinical analysis of 4- and 6-year follow-up results after cervical disc replacement surgery using the Bryan Cervical Disc Prosthesis. | lld:pubmed |
pubmed-article:20192625 | pubmed:affiliation | Department of Neurosurgery, Catholic University of Leuven, Belgium. neurochirurgie@uzleuven.be | lld:pubmed |
pubmed-article:20192625 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:20192625 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:20192625 | pubmed:publicationType | Clinical Trial, Phase II | lld:pubmed |
pubmed-article:20192625 | pubmed:publicationType | Clinical Trial, Phase I | lld:pubmed |