These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
24. Aetiology of developmental enamel defects not related to fluorosis. Pindborg JJ Int Dent J; 1982 Jun; 32(2):123-34. PubMed ID: 6749692 [TBL] [Abstract][Full Text] [Related]
26. A conservative treatment for amelogenesis imperfecta with direct resin composite restorations: a case report. Sabatini C; Guzmán-Armstrong S J Esthet Restor Dent; 2009; 21(3):161-9; discussion 170. PubMed ID: 19508258 [TBL] [Abstract][Full Text] [Related]
27. Diagnosis of enamel defects. Sarnat H; Moss SJ N Y State Dent J; 1985 Feb; 51(2):103-4, 106. PubMed ID: 3856783 [No Abstract] [Full Text] [Related]
28. [Organic sealing materials--use in practice]. Ulvestad H Nor Tannlaegeforen Tid; 1973 Jun; 83(6):238-41. PubMed ID: 4518474 [No Abstract] [Full Text] [Related]
29. [Histological examination of teeth in hereditary bullous epidermolysis]. Szafraniec I; Jakób-Dolezal K; Knycharska-Karwan Z; Pasykowa K Czas Stomatol; 1972 Dec; 25(12):1169-75. PubMed ID: 4509455 [No Abstract] [Full Text] [Related]
31. A novel autosomal-recessive mutation, whitish chalk-like teeth, resembling amelogenesis imperfecta, maps to rat chromosome 14 corresponding to human 4q21. Masuyama T; Miyajima K; Ohshima H; Osawa M; Yokoi N; Oikawa T; Taniguchi K Eur J Oral Sci; 2005 Dec; 113(6):451-6. PubMed ID: 16324133 [TBL] [Abstract][Full Text] [Related]
32. Ataxia, mental deterioration, epilepsy in a family with dominant enamel hypoplasia: a variant of Kohlschütter-Tönz syndrome? Guazzi G; Palmeri S; Malandrini A; Ciacci G; Di Perri R; Mancini G; Messina C; Salvadori C Am J Med Genet; 1994 Mar; 50(1):79-83. PubMed ID: 8160757 [TBL] [Abstract][Full Text] [Related]
33. Hereditary amelogenesis imperfecta. An epidemiological, genetic and clinical study in a Swedish child population. Sundell S Swed Dent J Suppl; 1986; 31():1-38. PubMed ID: 3460191 [TBL] [Abstract][Full Text] [Related]
34. Hypoplastic-hypomaturation amelogenesis imperfecta with taurodontism: report of case. Parker JL; Regattieri LR; Thomas JP ASDC J Dent Child; 1975; 42(5):379-83. PubMed ID: 1100695 [No Abstract] [Full Text] [Related]
36. Restoring function and esthetics in a patient with amelogenesis imperfecta: a case report. Sengun A; Ozer F Quintessence Int; 2002 Mar; 33(3):199-204. PubMed ID: 11921768 [TBL] [Abstract][Full Text] [Related]
37. [Clinical management of a case of epidermolysis bullosa]. Campos de Freitas A; Mussolino Ribeiro Z; Tambasco de Oliveira MC; Assed S Rev Fac Odontol Ribeiro Preto; 1986; 23(2):71-8. PubMed ID: 2976514 [No Abstract] [Full Text] [Related]
38. Rat wct mutation induces a hypo-mineralization form of amelogenesis imperfecta and cyst formation in molar teeth. Osawa M; Kenmotsu S; Masuyama T; Taniguchi K; Uchida T; Saito C; Ohshima H Cell Tissue Res; 2007 Oct; 330(1):97-109. PubMed ID: 17710440 [TBL] [Abstract][Full Text] [Related]