- Dentinogenesis imperfecta type II: A case report with 17 years of follow-up
-
Gama FJ, Corrêa IS, Valerio CS, Ferreira E, Manzi FR
- KMID: 2389894
- Imaging Sci Dent.
- 2017 Jun;47(2):129-133.
- doi: 10.5624/isd.2017.47.2.129
Dentinogenesis imperfecta is a dominant autosomal hereditary disorder of dentin formation that affects the deciduous and permanent teeth. Its etiology is characterized by inadequate cell differentiation during odontogenesis. The clinical... -
- CITED
-
- Close
- SHARE
-
- Close
- Clinical predictors of potentially impacted canines in low-risk patients: A retrospective study in mixed dentition
-
Barros SE, Heck B, Chiqueto K, Ferreira E
- KMID: 2540950
- Korean J Orthod.
- 2023 Mar;53(2):106-115.
- doi: 10.4041/kjod22.179
Objective: To evaluate the null hypothesis that there is no difference in a set of clinical predictors of potentially impacted canines between low-risk patients with and without displaced canines. Methods:... -
- CITED
-
- Close
- SHARE
-
- Close
