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Toplam kayıt 15, listelenen: 11-15
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 ...
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 ...
Erken çocukluk döneminde travmatik diş yaralanmalarının, maloklüzyonların ve diş çürüğünün ağız sağlığı ile ilişkili yaşam kalitesi üzerine etkisi
(Selcuk University, 2021)
Amaç: Bu çalışmanın amacı, travmatik diş yaralanmalarının (TDY) ve diş çürüğünün okul öncesi çocukların Ağız Sağlığı ile İlişkili Yaşam Kalitesi (OHRQoL) üzerindeki etkisini değerlendirmektir. Gereç ve Yöntemler: Ağız ...