Results 101 to 110 of about 2,550 (192)

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

J Pers Med, 2021
Lee Y, Kim YJ, Hyun HK, Lee JC, Lee ZH, Kim JW.   +5 more
europepmc   +1 more source

Dentinal Ultrastructure In Osteogenesis Imperfecta and Dentinogenesis Imperfecta [PDF]

, 2013
Osteogenesis Imperfecta (OI) associated with Dentinogenesis Imperfecta, type I (DI) is a rare genetic condition, where mutations of COL1A1 and COL1A2 genes result in variations of the collagen α-chains.
Harith, NSB
core  

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

Ann Transl Med, 2021
Du Q, Cao L, Liu Y, Pang C, Wu S, Zheng L, Jiang W, Na X, Yu J, Wang S, Zhu X, Yang J.   +11 more
europepmc   +1 more source

[The pedodontist and dentinogenesis imperfecta].

Avances 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, P, Planells del Pozo, F, Costa Ferrer, E, Barbería Leache   +3 more
openaire   +1 more source

Dentinogenesis imperfecta: An update [PDF]

Journal of Research and Practice on the Musculoskeletal System, 2022
Efthimia Tsoukala, Georgia Chochtoula, Iosifina Theodorou, George I. Lambrou   +3 more
openaire   +1 more source

Embarazada con osteogénesis imperfecta tipo IV, un caso

Revista de Ciencias Médicas de Pinar del Río, 2016
La Osteogénesis Imperfecta –OI– o Huesos de Cristal enfermedad genética, de transmisión autosómica dominante; en específico la tipo IV, las pacientes nacen con fracturas y curvaturas de los huesos largos de los miembros inferiores, muestran ...
Amado Antonio García Odio
doaj  

<i>Dentinogenesis Imperfecta</i> in Primary Dentition: Case Report. [PDF]

Reports (MDPI)
Petrova L, Ustiča J, Čēma I.
europepmc   +1 more source

Diagnosis complexity of dentinogenesis imperfecta involving <i>DSPP</i> genetic variants. [PDF]

J Med Genet
Caravello G, Jiménez-Armijo A, Kawczynski M, Rey T, O-Rares Consortium, Antin M, Roth A, Lamouche JB, Gouronc A, Alioua A, Schluth-Bolard C, Bloch-Zupan A.   +11 more
europepmc   +1 more source

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

, 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, CAMPANELLA, VINCENZO, Libonati, A, Gallusi, G   +3 more
core  

Beyond the diagnosis: Unraveling <i>DSPP</i> genotype-phenotype correlations in dentin dysplasia and dentinogenesis imperfecta. [PDF]

Jpn Dent Sci Rev
Boonyakanog A, Sriwangyang K, Eamtanaporn T, Krasaesin A, Fakhruddin KS, Chantarangsu S, Cho SD, Rokny HA, Porntaveetus T.   +8 more
europepmc   +1 more source