Ara
Toplam kayıt 19, listelenen: 11-19
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 ...
Assessment of dehiscence and fenestration in children and adolescents using cone beam computed tomography
(University Library System, University of Pittsburgh, 2021)
Objective: To define the prevalence of dehiscence and fenestration and classify them in terms of the localization of fenestrations in a random sampled group of children and adolescent patients using cone-beam computed ...
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). ...
Influence of COVID-19 pandemic on paediatric dental attendance
(Springer Heidelberg, 2021)
Objectives: This retrospective study aimed to evaluate the effect of COVID-19 pandemic on dental attendance and emergency/non-emergency visits of children during the outbreak, compared to the same period of 2019. Materials ...
Clinical and oral findings of a patient with Simpson-Golabi-Behmel syndrome
(Springer, 2015)
Background The Simpson-Golabi-Behmel syndrome (SGBS) is an overgrowth condition characterised by macrosomia, mental deficiency, large head, prominent skull sutures, midface deficiency, hypertelorism, broad nose, wide mouth, ...
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 ...
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 ...
Children's dental treatment requirements of first permanent molars with poor prognosis
(Springer Heidelberg, 2022)
Objectives This retrospective study aimed to (i) survey the correlation between decayed, missing, filled teeth (DMFT), and presence of first permanent molars (FPMs) with poor prognosis and (ii) evaluate the treatment ...
Characterizing infraocclusion in primary molars: prevalence, accompanying findings, and infraocclusion severity and treatment implications
(2024)
Background: This manuscript investigates the prevalence, classification, accompanying findings, and treatment modalities associated with infraoccluded primary molars. The aim of this study categorizing primary molars based ...