Bölüm "İstanbul Medipol Üniversitesi, Diş Hekimliği Fakültesi, Çocuk Diş Hekimliği Ana Bilim Dalı" Scopus İndeksli Yayınlar Koleksiyonu için listeleme
Toplam kayıt 34, listelenen: 1-20
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Alteration of exon definition causes amelogenesis imperfecta
(SAGE Publications Inc., 2020)Amelogenesis imperfecta (AI) is a collection of genetic disorders affecting the quality and/or quantity of tooth enamel. More than 20 genes are, so far, known to be responsible for this condition. In this study, we recruited ... -
Aquaporin 5 interacts with fluoride and possibly protects against caries
(Public Library of Science, 2015)Aquaporins (AQP) are water channel proteins and the genes coding for AQP2, AQP5, and AQP6 are clustered in 12q13. Since AQP5 is expressed in serous acinar cells of salivary glands, we investigated its involvement in caries. ... -
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 ... -
Candidate gene studies in hypodontia suggest role for FGF3
(2013)Introduction The majority of tooth agenesis cases are mild (hypodontia) and typically not associated with the gene mutations linked to oligodontia. From this, we hypothesise that most cases of tooth agenesis fit a polygenic ... -
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 ... -
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, ... -
Comparison of fracture resistance of immature sheep teeth using pozzolan MTA-based sealer
(Publishing House Bulgarian Academy of Sciences, 2021)The aim of this study was to evaluate the influence of pozzolan sealers used for apexification in immature permanent teeth on the root fragility using a performance simulation in sheep teeth in vitro. The fracture ... -
Comparison of root canal length measurement methods in primary teeth
(University Library System, University of Pittsburgh, 2018)Objectves: The purpose of this study was to evaluate the accuracy of conven5onal radiography, intraoral digital radi- ovisiography and electronic apex locator in determining the working length of root canals in primary ... -
Conservative surgical treatment of the jaw cysts in children: Case study of five patients
(Medknow Publications & Media Pvt Ltd, 2017)Aims: Conservative treatment of jaw cysts establishes low surgical complication risk and protects vital anatomical structures such as inferior alveolar nerve, maxillary sinus and permanent tooth germs. Marsupialization and ... -
Dental management of a patient with nager acrofacial dysostosis
(Hindawi Publishing Corporation, 2015)Nager syndrome is a rare syndrome resulting from developmental abnormalities of the first and second branchial arches. Nager syndrome is rare and mostly sporadic. The main clinical features consist of craniofacial, limb, ... -
Dental treatment of a child with pallister-killian syndrome
(Hindawi Ltd, 2016)The Pallister-Killian syndrome (PKS) is an extremely rare genetic disorder with an incidence estimated around 1/25000. PKS is a multiple congenital anomaly deficit syndrome caused by mosaic tissue limited tetrasomy for ... -
Effect of three different remineralizing agents on artificial erosive lesions of primary teeth
(Wiley, 2022)Background This study aimed to investigate the efficacy of three remineralizing agents on dental erosion in primary teeth. Methods Forty primary molars were randomly divided into four groups (n = 10 each): self-assembling ... -
Enamel formation genes influence enamel microhardness before and after cariogenic challenge
(Public Library Science, 2012)There is evidence for a genetic component in caries susceptibility, and studies in humans have suggested that variation in enamel formation genes may contribute to caries. For the present study, we used DNA samples collected ... -
Evaluation of dental age in individuals of different ages with unilateral cleft lip and palate
(AVES, 2020)Objective: This study aimed to evaluate the dental age of unilateral cleft lip and palate (UCLP) patients aged 7-12 and 12-16 years using Demirjian's method and to compare these results with a control group. Methods: We ... -
Evaluation of maxillary sinus findings in children using CBCT
(Edizioni Minerva Medica, 2019)BACKGROUND: Evaluation of the maxillary sinus is usually overlooked in children. The aim of this study was to evaluate incidental findings in the maxillary sinus in a group of children using cone beam computerized tomography ... -
Fine mapping of locus Xq25.1-27-2 for a low caries experience phenotype
(Pergamon-Elsevier Science Ltd., 2014)Objective: The purpose of this study was to fine map the locus Xq25.1-27-2 in order to identify genetic contributors involved in low caries experience. Design: Seventy-two families from the Philippines were studied. Caries ... -
Fine-Mapping of 5q12.1-13.3 unveils new genetic contributors to caries
(Karger, 2013)Caries is a multifactorial disease and little is still known about the host genetic factors influencing susceptibility. Our previous genome-wide linkage scan has identified the interval 5q12.1-5q13.3 as linked to low caries ... -
Gene-environment interaction in molar-incisor hypomineralization
(Public Library of Science, 2021)Molar incisor hypomineralization (MIH) is an enamel condition characterized by lesions ranging in color from white to brown which present rapid caries progression, and mainly affects permanent first molars and incisors. ... -
Genetic influences on dental enamel that impact caries differ between the primary and permanent dentitions
(Wiley, 2015)Clinically, primary and permanent teeth are distinct anatomically and the presentation of caries lesions differs between the two dentitions. Hence, the possibility exists that genetic contributions to tooth formation of ... -
Genetic mapping of high caries experience on human chromosome 13
(BMC, 2013)Background: Our previous genome-wide linkage scan mapped five loci for caries experience. The purpose of this study was to fine map one of these loci, the locus 13q31.1, in order to identify genetic contributors to caries. ...