Results 81 to 90 of about 14,453 (188)
Three Decades of Enamel Matrix Derivative: From Dental Innovation to Extra‐Oral Applications
International Journal of Dentistry, Volume 2026, Issue 1, 2026.Introduction Enamel matrix derivative (EMD; Emdogain) has been deployed for three decades as a biologically active material in periodontal regeneration. Widely adopted in periodontology, its indications are expanding into endodontics, ridge preservation, implantology, dermatology and oncology‐related indication.
Faustino Mercado +5 more
wiley +1 more source
Dentinogenesis Imperfecta - Clinical Presentation and Management
, 2010 Dentinogenesis imperfecta (DI) is a hereditary condition which affects the development of dentine in both the primary and permanent dentitions. Three types of DI have been described in the literature. The presentation of DI is variable, depending on the
Harmeet Dhaliwal, Sarah McKaig
core +1 more source
Oral rehabilitation of a child with dentinogenesis imperfecta – case report [PDF]
, 2016 eport the clinic case of a 5-yearold boy with presenting yellow-gray teeth and generalized severe tooth crown wear. Case report: After clinical and radiographic examination, he was diagnosed with dentinogenesis imperfecta.
Rayen Milanao Drugowick +4 more
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Dentinogenesis imperfecta type II: case report.
, 1996 A case of dentinogenesis imperfecta type II is described. The authors also present a brief literature review and focus on the difficulty in treating such cases.\ud ...
Modesto, A +3 more
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TYPE II DENTINOGENESIS IMPERFECTA : CASE REPORT
, 2001 Dentinogenesis imperfecta is an example of an inheritable dentinal defect originating during the histodifferentiation stage of tooth development, with involvement of the primary and permanent teeth.
이제호, 최병재
core
Early Rehabilitation of Incisors with Dentinogenesis Imperfecta Type II – Case Report
, 2017 Dentinogenesis imperfecta is an phenotypic alteration in the formation of the organic matrix. It causes the rapid and progressive wear of tooth structure, which may compromise tooth function and aesthetics.
Maíra Mery Rosa +3 more
core +1 more source
A Novel Mutation in the DSPP Gene Associated with Dentinogenesis Imperfecta Type II
, 2009 Hereditary dentin defects are divided into dentinogenesis imperfecta and dentin dysplasia. We identified a family segregating severe dentinogenesis imperfecta.
Jeon, D. +9 more
core +1 more source
Dentinogenesis imperfecta Type II. Case report
, 2014 La Dentinogénesis Imperfecta (DI) es una alteración hereditaria originada en la etapa de histodiferenciación de la odontogénesis. Existen dos tipos de Dentinogénesis Imperfecta, la tipo I, asociada a osteogénesis imperfecta, y la tipo II en la cual los ...
Guevara, Carlos +3 more
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, 2005 The follow-up history and oral findings in two brothers from consanguineous parents suggest that the association of dentinogenesis imperfecta (DI), delayed tooth eruption, mild mental retardation, proportionate short stature, sensorineural hearing loss ...
De Coster, Peter +4 more
core +1 more source
THE CONTRIBUTION OF KINETIC THERAPY IN LOBSTEIN’S DISEASE [PDF]
Annals of the “Ştefan cel Mare” University: Physical Education and Sport Section - The Science and Art of Movement, 2018 Osteogenesis imperfecta is a genetic disease of the connective tissue whose main clinical sign is increased bone fragility, manifested especially through fractures of the long limbs. OI presents major clinical signs and minor clinical signs.
Sergiu Danail, Danelciuc Francisc Tadeus
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