Results 141 to 150 of about 7,940 (235)

Dental Management of a Child with Dentinogenesis Imperfecta: A Case Report

open access: yesFrontiers in Dentistry, 2016
Dentinogenesis imperfecta (DI) is a hereditary dentin defect caused by an autosomal dominant mutation in dentin sialophosphoprotein gene. Defective dentin development results in discolored teeth that are prone to wear and fracture.
Najmeh Akhlaghi   +2 more
doaj  

Case of the Month #171: Osteogenesis Imperfecta of the Temporal Bone [PDF]

open access: yes, 2011
Aviv, Richard I.   +6 more
core   +1 more source

Osteogenesis imperfecta and dentinogenesis imperfecta

open access: diamond, 2022
Chetna Grover   +3 more
openalex   +1 more source

Unravelling the Genetic Basis of Dentinogenesis Imperfecta

open access: gold, 2023
Dr Maleeha Gilani   +1 more
openalex   +1 more source

Oral health in prevalent types of Ehlers-Danlos syndromes [PDF]

open access: yes, 2005
Ainamo J   +47 more
core   +2 more sources

The role of transforming growth factor beta in tertiary dentinogenesis

open access: gold, 2008
Tetiana Haniastuti   +2 more
openalex   +2 more sources

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