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Three-year randomized clinical evaluation of a low-shrinkage silorane-based resin composite in non-carious cervical lesions

dc.contributor.authorDogruer, Isil
dc.contributor.authorEfes, Begum Guray
dc.contributor.authorGumustas, Burak
dc.contributor.authorYAMAN, BATU CAN
dc.date.accessioned2021-03-03T12:03:20Z
dc.date.available2021-03-03T12:03:20Z
dc.date.issued2014
dc.identifier.citationYAMAN B. C. , Dogruer I., Gumustas B., Efes B. G. , "Three-year randomized clinical evaluation of a low-shrinkage silorane-based resin composite in non-carious cervical lesions", CLINICAL ORAL INVESTIGATIONS, cilt.18, sa.4, ss.1071-1079, 2014
dc.identifier.issn1432-6981
dc.identifier.otherav_2b93d3c4-7871-4ffc-b016-b85bceeaeade
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/34045
dc.identifier.urihttps://doi.org/10.1007/s00784-013-1079-z
dc.description.abstractThe clinical suitability of low-shrinkage resin composites for class V cavities has not been investigated in vivo. The purpose of this double-blind randomized clinical trial was to compare the clinical performances of low-shrinkage resin composite Filtek silorane and nanoceramic resin composite Ceram X mono in non-carious cervical lesions (NCCLs) over 36 months.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.subjectDİŞ HEKİMLİĞİ, ORAL CERRAHİ VE TIP
dc.subjectKlinik Tıp
dc.subjectTıp
dc.subjectDiş Hekimliği
dc.titleThree-year randomized clinical evaluation of a low-shrinkage silorane-based resin composite in non-carious cervical lesions
dc.typeMakale
dc.relation.journalCLINICAL ORAL INVESTIGATIONS
dc.contributor.departmentEskişehir Osmangazi Üniversitesi , ,
dc.identifier.volume18
dc.identifier.issue4
dc.identifier.startpage1071
dc.identifier.endpage1079
dc.contributor.firstauthorID214318


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