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Journal Abstract Search

133 related items for PubMed ID: 18561808

  • 21. Hyperplastic dental follicle - review of literature and report of two cases in one family.
    Sun CX, Ririe C, Henkin JM.
    Chin J Dent Res; 2010; 13(1):71-5. PubMed ID: 20936196
    [Abstract] [Full Text] [Related]

  • 22. Multiple calcifying hyperplastic dental follicles: comparison with hyperplastic dental follicles.
    Cho YA, Yoon HJ, Hong SP, Lee JI, Hong SD.
    J Oral Pathol Med; 2011 Mar; 40(3):243-9. PubMed ID: 21059105
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  • 24. Ultrastructural study of tooth enamel with amelogenesis imperfecta in AI-nephrocalcinosis syndrome.
    Phakey P, Palamara J, Hall RK, McCredie DA.
    Connect Tissue Res; 1995 Mar; 32(1-4):253-9. PubMed ID: 7554924
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  • 25. A Rare Co-occurrence of Amelogenesis Imperfecta (AI) and Various Non-Enamel Manifestations In Siblings-Report of Two Cases.
    Sankar AJ, Samatha Y, Suneela S, Ankineedu Babu D.
    J Clin Diagn Res; 2014 Jan; 8(1):282-4. PubMed ID: 24596797
    [Abstract] [Full Text] [Related]

  • 26. Oral characteristics of a patient with Ekman-Westborg-Julin trait: a case history.
    Komatsu T, Kurihara T, Ito Y, Lee MC, Miyagi A, Ikeda M.
    Spec Care Dentist; 2012 Mar; 32(2):70-4. PubMed ID: 22416990
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  • 29. Infantile refsum disease with enamel defects: a case report.
    Tran D, Greenhill W, Wilson S.
    Pediatr Dent; 2011 Mar; 33(3):266-70. PubMed ID: 21703082
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  • 30. Asymmetrical tooth defects observed in hypoplastic primary teeth and amelogenesis imperfecta: case reports.
    Symons AL, Gage JP.
    Pediatr Dent; 1987 Jun; 9(2):152-7. PubMed ID: 3475684
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  • 31. Kissing molars: report of three cases and new prospective on aetiopathogenetic theories.
    Menditti D, Laino L, Cicciù M, Mezzogiorno A, Perillo L, Menditti M, Cervino G, Lo Muzio L, Baldi A.
    Int J Clin Exp Pathol; 2015 Jun; 8(12):15708-18. PubMed ID: 26884840
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  • 32. Four novel mutations of FAM20A in amelogenesis imperfecta type IG and review of literature for its genotype and phenotype spectra.
    Nitayavardhana I, Theerapanon T, Srichomthong C, Piwluang S, Wichadakul D, Porntaveetus T, Shotelersuk V.
    Mol Genet Genomics; 2020 Jul; 295(4):923-931. PubMed ID: 32246227
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  • 34. Otodental syndrome: a case report and genetic considerations.
    Sedano HO, Moreira LC, de Souza RA, Moleri AB.
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2001 Sep; 92(3):312-7. PubMed ID: 11552150
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  • 35. Amelogenesis imperfecta: multiple impactions associated with odontogenic fibromas (WHO) type.
    van Heerden WF, Raubenheimer EJ, Dreyer AF, Benn AM.
    J Dent Assoc S Afr; 1990 Nov; 45(11):467-71. PubMed ID: 2098937
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  • 36. Novel dental anomalies associated with congenital contractural arachnodactyly: a case report.
    Ayers KM, Drummond BK.
    Pediatr Dent; 2003 Nov; 25(5):501-4. PubMed ID: 14649616
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  • 37. Enamel renal syndrome: a rare case report.
    Kala Vani SV, Varsha M, Sankar YU.
    J Indian Soc Pedod Prev Dent; 2012 Nov; 30(2):169-72. PubMed ID: 22918105
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  • 39. Pathological study of the hyperplastic dental follicle.
    Fukuta Y, Totsuka M, Takeda Y, Yamamoto H.
    J Nihon Univ Sch Dent; 1991 Sep; 33(3):166-73. PubMed ID: 1748887
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