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.


PUBMED FOR HANDHELDS

Journal Abstract Search


123 related items for PubMed ID: 297513

  • 1. [A case report of hereditary amelogenesis imperfecta in a family (author's transl)].
    Minegishi H, Irie E, Osaka N, Moriyama K, Sano M, Ito H, Hamamoto Y, Goto H.
    Josai Shika Daigaku Kiyo; 1979; 8(3):413-7. PubMed ID: 297513
    [No Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. [Hereditary type enamel hypoplasia. Clinical and histopathological findings of an observed case].
    Debernardi C, Pirrello D.
    Minerva Stomatol; 1989 Mar; 38(3):321-34. PubMed ID: 2657367
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. [A particular type of dominant hereditary enamel dysplasia?].
    Weyers H.
    Dtsch Zahnarztl Z; 1977 Mar; 32(3):243-7. PubMed ID: 265269
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. [Amelogenesis imperfecta in young patients].
    Roeters FJ, Frankenmolen FW.
    Ned Tijdschr Tandheelkd; 1997 Feb; 104(2):78-80. PubMed ID: 11924374
    [Abstract] [Full Text] [Related]

  • 8. [Genetic defects of the enamel].
    Skrinjarić I.
    Acta Stomatol Croat; 1985 Feb; 19(1):57-67. PubMed ID: 3859996
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. [An enamel disorder in two siblings].
    Créton MA, Cune MS.
    Ned Tijdschr Tandheelkd; 2004 Oct; 111(10):400-2. PubMed ID: 15553370
    [Abstract] [Full Text] [Related]

  • 11. [Clinical report on a case of amelogenesis imperfecta].
    Yoshida T, Minegishi H, Osaka N, Irie E, Kurihara J, Goto H.
    Josai Shika Daigaku Kiyo; 1981 Oct; 10(2):315-21. PubMed ID: 6959664
    [No Abstract] [Full Text] [Related]

  • 12. Hereditary enamel hypoplasia.
    Shokeir MH.
    Clin Genet; 1971 Oct; 2(6):387-91. PubMed ID: 5155316
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. 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 01; 50(1):79-83. PubMed ID: 8160757
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. The effects of acid-etching on enamel from different clinical variants of amelogenesis imperfecta: an SEM study.
    Seow WK, Amaratunge A.
    Pediatr Dent; 1998 Mar 01; 20(1):37-42. PubMed ID: 9524971
    [Abstract] [Full Text] [Related]

  • 19. The surface of genetically determined hypoplastic enamel in human teeth.
    Sauk JJ, Vickers RA, Copeland JS, Lyon HW.
    Oral Surg Oral Med Oral Pathol; 1972 Jul 01; 34(1):60-8. PubMed ID: 4504318
    [No Abstract] [Full Text] [Related]

  • 20. [A critical study of amelogenesis imperfecta].
    Kerebel B, Dubois T.
    Bull Group Int Rech Sci Stomatol Odontol; 1982 Dec 01; 25(4):291-311. PubMed ID: 6961948
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 7.