Results 181 to 190 of about 4,451 (219)

New Immunohistochemical Findings on Amelogenin and Dentin Sialophosphoprotein in Genetic Tooth Diseases. [PDF]

Int Dent J
Camacho-Escalera C, Ortega-Pinto A, Rojas-Flores S, Pianeta-Alviz R, Urzúa-Orellana B.   +4 more
europepmc   +1 more source

Expert consensus on the diagnosis and management of tooth developmental anomalies. [PDF]

Int J Oral Sci
Zhu J, Wan M, Duan X, Fan Z, Sun Y, Wang X, Zheng S, Zheng L, Zhu Q, Chen D, Dai J, Han D, He M, Huang C, Jiang Y, Jia Z, Pan Y, Pan Y, Wang T, Wang W, Xu B, Yin W, Zhang T, Zhang Y, Zhao Z, Bian Z, Song Y.   +26 more
europepmc   +1 more source

A rare 5'UTR variant in SEC24D reveals translational dysfunction in osteogenesis imperfecta: a roadmap for RNA therapeutic rescue. [PDF]

Sci Rep
Essawi O, Jarayseh T, Tapaneeyaphan P, Bouckaert M, Naessens S, Malfait F, Coppieters F, Coucke PJ.   +7 more
europepmc   +1 more source

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Uninherited dentinogenesis imperfecta

Oral Surgery, Oral Medicine, Oral Pathology, 1975
The rare hereditary disease, dentinogenesis imperfecta, is a disturbance of dentin formation in both the deciduous and permanent dentitions. It may be associated with osteogenesis imperfecta, though it is probably that the two diseases are carried by different genes. This association was recognized in a 19-year-old man.
R M, Orlowski, C M, Reeve
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Hereditary dentinogenesis imperfecta

The Journal of Pediatrics, 1964
Summary A classic case of hereditary dentinogenesis imperfecta with its genealogy has been presented and its possible treatment discussed.
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Dentinogenesis imperfecta. A new perspective

Australian Dental Journal, 1985
Abstract— ‐Recent knowledge of collagen biochemistry has increased dramatically with current concepts of its biosynthesis and structure, strengthening the belief that osteogenesis imperfecta and dentinogenesis imperfecta syndromes are basically molecular collagen defects of Type I collagen.The information presently available from studies on dentine ...
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Dentinogenesis imperfecta: A case report

American Journal of Orthodontics and Dentofacial Orthopedics, 1998
Dentinogenesis imperfecta is a rare structural anomaly that is not frequently encountered in an orthodontic office. This case report of the treatment of a patient with this condition is presented in the hope that it will add to the knowledge of this hereditary condition.
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Hereditary dentinogenesis imperfecta

The Journal of Pediatrics, 1959
O N, JOHNSON, A P, CHAUDHRY, R J, GORLIN, D F, MITCHELL, W L, BARTHOLDI   +4 more
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