Results 101 to 110 of about 4,451 (219)
Dental discoloration, particularly due to fluorosis, presents a significant aesthetic challenge for many patients. This article explores the combined use of dental bleaching and enamel microabrasion as effective treatments for managing fluorosis‐induced discoloration. Dental bleaching, a widely used method for lightening extrinsic and intrinsic stains,
Priyanka Bhojwani +8 more
wiley +1 more source
The Importance of Serine Phosphorylation of Ameloblastin on Enamel Formation [PDF]
FAM20C is a newly identified kinase on the secretory pathway responsible for the phosphorylation of serine residues in the Ser-x-Glu/pSer motifs in several enamel matrix proteins. Fam20C-knockout mice showed severe enamel defects very similar to those in
Brookes, SJ +5 more
core +1 more source
Dentinogenesis imperfecta type II
Dentinogenesis imperfecta (DI) is a hereditary developmental disorder of dentin formation that can occur associated with osteogenesis imperfecta (type I), isolated (type II), or in a specific isolated resident group of Brandywine, in southern Maryland (type III).
Paulo Nelson Filho +7 more
openaire +1 more source
Target gene analyses of 39 amelogenesis imperfecta kindreds [PDF]
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/90297/1/EOS_857_sm_FigsS1-S3.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/90297/2/j.1600-0722.2011.00857.x ...
Al-Hashimi +85 more
core +1 more source
Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations [PDF]
Amelogenesis imperfecta (AI) is a genetically and clinically heterogeneous group of inherited dental enamel defects. Commonly described as an isolated trait, it may be observed concomitantly with other orodental and/or systemic features such as ...
Acevedo, A-C +8 more
core +1 more source
A novel DSPP mutation causes dentinogenesis imperfecta type II in a large Mongolian family [PDF]
Background Several studies have shown that the clinical phenotypes of dentinogenesis imperfecta type II (DGI-II) may be caused by mutations in dentin sialophosphoprotein (DSPP).
AC Acevedo +28 more
core +3 more sources
Dental Manifestations of Ehlers-Danlos Syndromes: A Systematic Review
Ehlers-Danlos syndromes (EDS) are a group of inherited connective tissue disorders characterized by joint hypermobility, skin hyperextensibility, and variable tissue fragility. However, there are limited published data on the dental manifestations of EDS.
Ines Kapferer-Seebacher +3 more
doaj +1 more source
Guideline on therapeutic dentistry for the 5-th term [PDF]
РУКОВОДСТВАСТОМАТОЛОГИЯ ЛЕЧЕБНО-ВОССТАНОВИТЕЛЬНАЯСТОМАТОЛОГИЯ ТЕРАПЕВТИЧЕСКАЯИНОСТРАННЫЕ СТУДЕНТЫУЧЕБНО-МЕТОДИЧЕСКИЕ ПОСОБИЯПособие составлено в соответствии с учебной программой для медицинских вузов по терапевтической стоматологии.
Korenevskaya, N. A. +2 more
core
PENGARUH PEMBERIAN JUS BUAH TOMAT (Lycopersicon esculentum Mill.) TERHADAP PERUBAHAN WARNA GIGI PADA PROSES PEMUTIHAN GIGI SECARA IN VITRO [PDF]
Latar belakang : Lycopersicon esculentum Mill. merupakan tanaman yang sering digunakan sebagai bahan tambahan masakan dan dikenal sebagai tomat. Tomat mengandung beberapa bahan aktif yang diduga dapat memutihkan gigi.
Pratiwi, Septiva Asih
core
THE CONTRIBUTION OF KINETIC THERAPY IN LOBSTEIN’S DISEASE [PDF]
Osteogenesis imperfecta is a genetic disease of the connective tissue whose main clinical sign is increased bone fragility, manifested especially through fractures of the long limbs. OI presents major clinical signs and minor clinical signs.
Sergiu Danail, Danelciuc Francisc Tadeus
doaj

