Results 71 to 80 of about 508 (131)

Amelogenesis imperfecta [PDF]

, 2020
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amelogenesis imperfecta

Citation: 'amelogenesis imperfecta' in the IUPAC Compendium of Chemical Terminology, 5th ed.; International Union of Pure and Applied Chemistry; 2025. Online version 5.0.0, 2025. 10.1351/goldbook.10364 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
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Disruption of Steroid Axis, a New Paradigm for Molar Incisor Hypomineralization (MIH)

Frontiers in Physiology, 2017
Sylvie Babajko, Sylvie Babajko, Katia Jedeon, Katia Jedeon, Sophia Houari, Sophia Houari, Sophia Loiodice, Sophia Loiodice, Ariane Berdal, Ariane Berdal, Ariane Berdal   +10 more
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Enamel Research: Priorities and Future Directions

Frontiers in Physiology, 2017
Jennifer Kirkham, Steven J. Brookes, Thomas G. H. Diekwisch, Henry C. Margolis, Ariane Berdal, Michael J. Hubbard   +5 more
doaj   +1 more source

[Amelogenesis imperfecta].

Revista de odontologia da UNESP, 1971
R, Luberti, G, Moize
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[AMELOGENESIS IMPERFECTA].

Revista de la Asociacion Odontologica Argentina, 1996
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[Amelogenesis imperfecta].

Nihon Koku Geka Gakkai zasshi, 1972
T, Ito, Y, Matuse, T, Imai, M, Yo, T, Tsuboguchi   +4 more
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Amelogénesis imperfecta en una familia

Revista Cubana de Estomatología
Paula Hurtado-Villa, Fabián Tobar-Tosse, Julio Osorio, Freddy Moreno   +3 more
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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
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Amelogenesis imperfecta with taurodontism

Oral Surgery, Oral Medicine, Oral Pathology, 1979
Reports of families having a combination of amelogenesis imperfecta and taurodontism are limited. This study of members of three families shows that the combination is inherited as an autosomal dominant trait. In each of the patients examined, neither condition was seen without the other.
J, Congleton, E J, Burkes
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