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A histological continuum between dentinogenesis imperfecta and dentin dysplasia: A case report with literature review.
Gulati N, Juneja S, Singh A, Singh I.
Indian J Dent Res. 2019 Jul-Aug;30(4):643-646. doi: 10.4103/ijdr.IJDR_318_18. Review.
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A multidisciplinary approach to the functional and esthetic rehabilitation of dentinogenesis imperfecta type II: A clinical report.
Fan F, Li N, Huang S, Ma J.
J Prosthet Dent. 2019 Aug;122(2):95-103. doi: 10.1016/j.prosdent.2018.10.028. Epub 2019 Apr 9.
Dentinogenesis Imperfecta Type II in Children: A Scoping Review.
Garrocho-Rangel A, Dávila-Zapata I, Martínez-Rider R, Ruiz-Rodríguez S, Pozos-Guillén A.
J Clin Pediatr Dent. 2019;43(3):147-154. doi: 10.17796/1053-4625-43.3.1. Epub 2019 Apr 9. Review.
Challenges of delivery of dental care and dental pathologies in children and young people with osteogenesis imperfecta.
Clark R, Burren CP, John R.
Eur Arch Paediatr Dent. 2019 Oct;20(5):473-480. doi: 10.1007/s40368-019-00424-w. Epub 2019 Mar 13.
Indirect adhesive rehabilitation by cementation under pressure of a case of Dentinogenesis Imperfecta type II: follow-up after 13 years.
Campanella V, Di Taranto V, Libonati A, Marzo G, Nardi R, Angotti V, Gallusi G.
Eur J Paediatr Dent. 2018 Dec;19(4):303-306. doi: 10.23804/ejpd.2018.19.04.10.
The dental perspective on osteogenesis imperfecta in a Danish adult population.
Thuesen KJ, Gjørup H, Hald JD, Schmidt M, Harsløf T, Langdahl B, Haubek D.
BMC Oral Health. 2018 Oct 24;18(1):175. doi: 10.1186/s12903-018-0639-7.
Treatment of an Adolescent Patient with Dentinogenesis Imperfecta Using Indirect Composite Restorations - A Case Report and Literature Review.
Soliman S, Meyer-Marcotty P, Hahn B, Halbleib K, Krastl G.
J Adhes Dent. 2018;20(4):345-354. doi: 10.3290/j.jad.a40991. Review.
Isolated dentinogenesis imperfecta with glass-like enamel caused by COL1A2 mutation.
Kantaputra PN, Chinadet W, Intachai W, Ngamphiw C, Ketudat Cairns JR, Tongsima S.
Am J Med Genet A. 2018 Dec;176(12):2919-2923. doi: 10.1002/ajmg.a.40501. Epub 2018 Aug 27. No abstract available.
Osteogenesis imperfecta and the teeth, eyes, and ears-a study of non-skeletal phenotypes in adults.
Hald JD, Folkestad L, Swan CZ, Wanscher J, Schmidt M, Gjørup H, Haubek D, Leonhard CH, Larsen DA, Hjortdal JØ, Harsløf T, Duno M, Lund AM, Jensen JB, Brixen K, Langdahl B.
Osteoporos Int. 2018 Dec;29(12):2781-2789. doi: 10.1007/s00198-018-4663-x. Epub 2018 Aug 24.
Dentinogenesis imperfecta type II in Swedish children and adolescents.
Andersson K, Malmgren B, Åström E, Dahllöf G.
Orphanet J Rare Dis. 2018 Aug 22;13(1):145. doi: 10.1186/s13023-018-0887-2.
Complete overdenture fabrication for a 12-year-old child with dentinogenesis imperfecta type 2.
Garces S, Shipman B, Barbosa A, Newman RM, Benjamin P.
Gen Dent. 2018 Jul-Aug;66(4):62-65.
Compromised alveolar bone cells in a patient with dentinogenesis imperfecta caused by DSPP mutation.
Porntaveetus T, Nowwarote N, Osathanon T, Theerapanon T, Pavasant P, Boonprakong L, Sanon K, Srisawasdi S, Suphapeetiporn K, Shotelersuk V.
Clin Oral Investig. 2019 Jan;23(1):303-313. doi: 10.1007/s00784-018-2437-7. Epub 2018 Apr 20.
Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and a COL1A2 mutation.
Kantaputra PN, Sirirungruangsarn Y, Intachai W, Ngamphiw C, Tongsima S, Dejkhamron P.
J Hum Genet. 2018 Jul;63(7):811-820. doi: 10.1038/s10038-018-0448-5. Epub 2018 Apr 10.
Dentin dysplasia type I-A dental disease with genetic heterogeneity.
Chen D, Li X, Lu F, Wang Y, Xiong F, Li Q.
Oral Dis. 2019 Mar;25(2):439-446. doi: 10.1111/odi.12861. Epub 2018 Apr 10. Review.
Dentinogenesis imperfecta type II- genotype and phenotype analyses in three Danish families.
Taleb K, Lauridsen E, Daugaard-Jensen J, Nieminen P, Kreiborg S.
Mol Genet Genomic Med. 2018 May;6(3):339-349. doi: 10.1002/mgg3.375. Epub 2018 Mar 6.
Dental properties, ultrastructure, and pulp cells associated with a novel DSPP mutation.
Porntaveetus T, Osathanon T, Nowwarote N, Pavasant P, Srichomthong C, Suphapeetiporn K, Shotelersuk V.
Oral Dis. 2018 May;24(4):619-627. doi: 10.1111/odi.12801. Epub 2018 Mar 13.
Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta - A retrospective cohort study.
Andersson K, Dahllöf G, Lindahl K, Kindmark A, Grigelioniene G, Åström E, Malmgren B.
PLoS One. 2017 May 12;12(5):e0176466. doi: 10.1371/journal.pone.0176466. eCollection 2017.
Early Rehabilitation of Incisors with Dentinogenesis Imperfecta Type II - Case Report.
Beltrame AP, Rosa MM, Noschang RA, Almeida IC.
J Clin Pediatr Dent. 2017;41(2):112-115. doi: 10.17796/1053-4628-41.2.112.
Phenotype and genotype analyses in seven families with dentinogenesis imperfecta or dentin dysplasia.
Li F, Liu Y, Liu H, Yang J, Zhang F, Feng H.
Oral Dis. 2017 Apr;23(3):360-366. doi: 10.1111/odi.12621. Epub 2017 Jan 24.
Hereditary dentine dysplasias: terminology in the context of osteogenesis imperfecta.
Chetty M, Roberts T, Stephen LX, Beighton P.
Br Dent J. 2016 Dec 9;221(11):727-730. doi: 10.1038/sj.bdj.2016.915.
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