Results 101 to 110 of about 14,453 (188)

DIAGNOSIS OF DENTINOGENESIS IMPERFECTA

open access: yesInternational Seven Journal of Multidisciplinary
Dentinogenesis Imperfecta (DI) is a rare hereditary disorder that compromises dentine formation, resulting in structural fragility, early wear and functional and aesthetic impairment of the teeth. The present study aimed to review recent scientific evidence related to the diagnosis and management of DI. This is a narrative literature review carried out
Margareth Pandolfi   +2 more
openaire   +1 more source

Dentinogenesis imperfecta: A review and case report of a family over four generations

open access: yesIndian Journal of Dental Research, 2008
Dentinogenesis imperfecta (DGI) is one of the most common hereditary disorders of dentin formation. It follows an autosomal dominant pattern of transmission, affecting both the formation and mineralization of dentin.
Bhandari Sudhir, Pannu Karneev
doaj  

Mouse Dspp frameshift model of human dentinogenesis imperfecta. [PDF]

open access: yesSci Rep, 2021
Liang T   +11 more
europepmc   +1 more source

Non-Syndromic Dentinogenesis Imperfecta Caused by Mild Mutations in COL1A2. [PDF]

open access: yesJ Pers Med, 2021
Lee Y   +5 more
europepmc   +1 more source

Phenotype and molecular characterizations of a family with dentinogenesis imperfecta shields type II with a novel DSPP mutation. [PDF]

open access: yesAnn Transl Med, 2021
Du Q   +11 more
europepmc   +1 more source

Dentinogenesis imperfecta: An update [PDF]

open access: yesJournal of Research and Practice on the Musculoskeletal System, 2022
Efthimia Tsoukala   +3 more
openaire   +1 more source

[The pedodontist and dentinogenesis imperfecta].

open access: yesAvances en odontoestomatologia, 1991
The purpose of this article is to present a treatment of dentinogenesis imperfecta in a 3 years old child. We reviewed some of the aspects to consider in the treatments of this alteration in primary dentition.
M J, De Nova García   +3 more
openaire   +1 more source

SEM-morphology in dentinogenesis imperfecta type II: microscopic anatomy and efficacy of a dentine bonding system

open access: yes, 2006
AIM: Dentinogenesis Imperfecta is a hereditary defect consisting of opalescent teeth composed of irregularly formed and undermineralised dentin that obliterates the coronal and root pulpal chambers.
Campanella, V   +3 more
core   +1 more source

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