Results 161 to 170 of about 5,937 (217)

Novel Ameloblastin Variants, Contrasting Amelogenesis Imperfecta Phenotypes. [PDF]

J Dent Res
Hany U, Watson CM, Liu L, Nikolopoulos G, Smith CEL, Poulter JA, Brown CJ, Patel A, Rodd HD, Balmer R, Harfoush A, Al-Jawad M, Inglehearn CF, Mighell AJ.   +13 more
europepmc   +1 more source

Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability. [PDF]

J Med Genet
Smith CEL, Laugel-Haushalter V, Hany U, Best S, Taylor RL, Poulter JA, Wortmann SB, Feichtinger RG, Mayr JA, Al Bahlani S, Nikolopoulos G, Rigby A, Black GC, Watson CM, Mansour S, Inglehearn CF, Mighell AJ, Bloch-Zupan A, UK Inherited Retinal Disease Consortium, Genomics England Research Consortium.   +19 more
europepmc   +1 more source

Full-mouth rehabilitation with lithium disilicate ceramic crowns in hypoplastic amelogenesis imperfecta: a case report and review of literature. [PDF]

BMC Oral Health
Chen R, Lin Y, Sun Y, Pan X, Xu Y, Kong X, Zhang L.   +6 more
europepmc   +1 more source

Establishment of a clinical network for children with amelogenesis imperfecta and dentinogenesis imperfecta in the UK: 4-year experience. [PDF]

Eur Arch Paediatr Dent
Monteiro J, Balmer R, Lafferty F, Lyne A, Mighell A, O'Donnell K, Parekh S.   +6 more
europepmc   +1 more source

Navigating Complexity: A Case Report on a Comprehensive Dental Management Approach to Amelogenesis Imperfecta and Gingival Fibromatosis Syndrome. [PDF]

Cureus
Nasrallah H, Berro K.
europepmc   +1 more source

A novel ODAPH mutation causing amelogenesis imperfecta and its expression in human dental tissues. [PDF]

J Dent Sci
Wang SK, Lee ZH, Aref P, Chu KY.
europepmc   +1 more source

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Trichodysplasia and amelogenesis imperfecta

Oral Surgery, Oral Medicine, Oral Pathology, 1993
This paper describes a family in which members of two generations have an X-linked type of enamel dysplasia. All affected persons have symmetric pits in the cuticles of their hair shafts. The observation of these concurrent traits raises questions about the classification of amelogenesis imperfecta and the value of microscopic studies of the hair in ...
G, Angelos, R J, Jorgenson
openaire   +2 more sources

Amelogenesis Imperfecta: Case Study

Operative Dentistry, 2017
SUMMARY Amelogenesis imperfecta (AI) refers to a group of rare genetic disorders that involve tooth development and that are passed down through families as a dominant trait. This condition is characterized by abnormal enamel formation caused by gene mutations that alter the quality and/or quantity of enamel.
C, Leevailoj, S, Lawanrattanakul, K, Mahatumarat   +2 more
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Multidisciplinary treatment of amelogenesis imperfecta

Nederlands Tijdschrift voor Tandheelkunde, 2021
A healthy 13-year-old patient with amelogenesis imperfecta was referred by her orthodontist to the joint consultation hour (Center for Specialised Dentistry and Oral and Maxillofacial Surgery). In addition to her amelogenesis imperfecta, she was diagnosed with a class 2 malocclusion and a mandibular hypoplasia.
G, Mensink, P A L, Mel, B A J A, van Oirschot, J P, Verweij   +3 more
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