Bölüm "İstanbul Medipol Üniversitesi, Diş Hekimliği Fakültesi, Çocuk Diş Hekimliği Ana Bilim Dalı" WoS İndeksli Yayınlar Koleksiyonu için listeleme
Toplam kayıt 30, listelenen: 21-30
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In vitro acid-mediated initial dental enamel loss is associated with genetic variants previously linked to caries experience
(Frontiers Media S.A., 2017)We have previously shown that AQP5 and BTF3 genetic variation and expression in whole saliva are associated with caries experience suggesting that these genes may have a functional role in protecting against caries. To ... -
In vitro comparison of the effectiveness of conventional hand excavation and rotary instrument in caries removal in primary teeth
(Academic Publishing House, 2021)This study aims to evaluate microhardness of remaining dentin after caries removal and to determine whether sufficient preparation is realised with hand excavation. Twenty-six extracted primary molar teeth with occlusal/proximal ... -
Longevity of posterior composite restorations in children suffering from early childhood caries-results from a retrospective study
(Springer Heidelberg, 2021)Objectives This retrospective study aimed to evaluate health status as a new patient risk factor and analyze its influence on the survival of posterior composite restorations in patients with early childhood caries (ECC). ... -
Mutations in RELT cause autosomal recessive amelogenesis imperfecta
(Wiley, 2019)Amelogenesis imperfecta (AI) is a collection of isolated (non-syndromic) inherited diseases affecting dental enamel formation or a clinical phenotype in syndromic conditions. We characterized three consanguineous AI families ... -
Reducing anxiety in children with molar incisor hypomineralization using virtual reality - A randomized crossover study
(Bulgarian Academy of Sciences, 2020)The aim of this study was to evaluate the effects of virtual reality (VR) video games on anxiety levels during dental treatments in children with molar incisor hypomineralization (MIH)-affected teeth. The incidence of MIH, ... -
Rethinking isolated cleft lip and palate as a syndrome
(Elsevier Science Inc, 2018)Objective. The goal of the present work was to use dental conditions that have been independently associated with cleft lip and palate (CL/P) as a tool to identify a broader collection of individuals to be used for gene ... -
Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay
(BMC, 2014)Background: Congenital forms of hearing impairment can be caused by mutations in the estrogen related receptor beta (ESRRB) gene. Our initial linkage studies suggested the ESRRB locus is linked to high caries experience ... -
Role of TRAV locus in low caries experience
(Springer, 2013)Caries is the most common chronic, multifactorial disease in the world today; and little is still known about the genetic factors influencing susceptibility. Our previous genome-wide linkage scan has identified five loci ... -
Rubinstein-taybi syndrome: A case report
(Hindawi Publishing Corporation, 2012)Rubinstein-Taybi syndrome or Broad Thumb-Hallux syndrome is a genetic disorder characterized by facial dysmorphism, growth retardation, and mental deficiency. A seven-year-old girl had come to the Department of Pedodontics, ... -
Saliva profiles in children with congenital heart disease
(Istanbul University Press, 2020)Purpose The low salivary pH and buffering capacity are caused by using heart failure medications. For this reason oral health should be supported in cardiac patients, it is necessary that they attend dental clinics for ...