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Journal Abstract Search

268 related items for PubMed ID: 19915277

  • 1. Cleidocranial dysplasia: a family report.
    Chelvan HT, Malathi N, Kailasam V, Ponnudurai A.
    J Indian Soc Pedod Prev Dent; 2009; 27(4):249-52. PubMed ID: 19915277
    [Abstract] [Full Text] [Related]

  • 2. Cleidocranial dysplasia: oral features and genetic analysis of 11 patients.
    Bufalino A, Paranaíba LM, Gouvêa AF, Gueiros LA, Martelli-Júnior H, Junior JJ, Lopes MA, Graner E, De Almeida OP, Vargas PA, Coletta RD.
    Oral Dis; 2012 Mar; 18(2):184-90. PubMed ID: 22023169
    [Abstract] [Full Text] [Related]

  • 3. Diversity of supernumerary tooth formation in siblings with cleidocranial dysplasia having identical mutation in RUNX2 : possible involvement of non-genetic or epigenetic regulation.
    Suda N, Hamada T, Hattori M, Torii C, Kosaki K, Moriyama K.
    Orthod Craniofac Res; 2007 Nov; 10(4):222-5. PubMed ID: 17973689
    [Abstract] [Full Text] [Related]

  • 4. RUNX2 mutations in cleidocranial dysplasia patients.
    Ryoo HM, Kang HY, Lee SK, Lee KE, Kim JW.
    Oral Dis; 2010 Jan; 16(1):55-60. PubMed ID: 19744171
    [Abstract] [Full Text] [Related]

  • 5. [Orthodontic and oral surgery therapy in cleidocranial dysplasia].
    Balaton G, Tarján I, Balaton P, Barabási Z, Gyulai Gál S, Nagy K, Vajó Z.
    Fogorv Sz; 2007 Feb; 100(1):17-21. PubMed ID: 17444132
    [Abstract] [Full Text] [Related]

  • 6. Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report.
    Inchingolo AD, Patano A, Coloccia G, Ceci S, Inchingolo AM, Marinelli G, Malcangi G, Montenegro V, Laudadio C, Palmieri G, Bordea IR, Ponzi E, Orsini P, Ficarella R, Scarano A, Lorusso F, Dipalma G, Corsalini M, Gentile M, Venere DD, Inchingolo F.
    Medicina (Kaunas); 2021 Dec 10; 57(12):. PubMed ID: 34946295
    [Abstract] [Full Text] [Related]

  • 7. RUNX2 gene status in a cleidocranial dysplasia patient without supernumerary teeth.
    Anthonappa RP, King NM, Mahmoud Rabie AB.
    J Investig Clin Dent; 2013 May 10; 4(2):124-7. PubMed ID: 23188595
    [Abstract] [Full Text] [Related]

  • 8. Correlation between genotype and supernumerary tooth formation in cleidocranial dysplasia.
    Suda N, Hattori M, Kosaki K, Banshodani A, Kozai K, Tanimoto K, Moriyama K.
    Orthod Craniofac Res; 2010 Nov 10; 13(4):197-202. PubMed ID: 21040462
    [Abstract] [Full Text] [Related]

  • 9. Mutations in the RUNX2 gene in patients with cleidocranial dysplasia.
    Otto F, Kanegane H, Mundlos S.
    Hum Mutat; 2002 Mar 10; 19(3):209-16. PubMed ID: 11857736
    [Abstract] [Full Text] [Related]

  • 10. Delayed tooth eruption and suppressed osteoclast number in the eruption pathway of heterozygous Runx2/Cbfa1 knockout mice.
    Yoda S, Suda N, Kitahara Y, Komori T, Ohyama K.
    Arch Oral Biol; 2004 Jun 10; 49(6):435-42. PubMed ID: 15099800
    [Abstract] [Full Text] [Related]

  • 11. Differing therapeutic approaches to cleidocranial dysplasia (CCD).
    Mortellaro C, Greco Lucchina A, Prota E.
    Minerva Stomatol; 2012 Apr 10; 61(4):155-63. PubMed ID: 22441418
    [Abstract] [Full Text] [Related]

  • 12. Altered gene expression in human cleidocranial dysplasia dental pulp cells.
    Chen S, Santos L, Wu Y, Vuong R, Gay I, Schulze J, Chuang HH, MacDougall M.
    Arch Oral Biol; 2005 Feb 10; 50(2):227-36. PubMed ID: 15721154
    [Abstract] [Full Text] [Related]

  • 13. [Pierre Marie-Sainton cleidocranial dysplasia].
    Diaconescu S, Păduraru G, Vâscu AM, Burlea M.
    Rev Med Chir Soc Med Nat Iasi; 2011 Feb 10; 115(2):341-8. PubMed ID: 21870721
    [Abstract] [Full Text] [Related]

  • 14. Identification of a novel RUNX2 gene mutation in an Italian family with cleidocranial dysplasia.
    Marchisella C, Rolando F, Muscarella LA, Zelante L, Bracco P, Piemontese MR.
    Eur J Orthod; 2011 Oct 10; 33(5):498-502. PubMed ID: 21131390
    [Abstract] [Full Text] [Related]

  • 15. Six novel mutations of the RUNX2 gene in Italian patients with cleidocranial dysplasia.
    Tessa A, Salvi S, Casali C, Garavelli L, Digilio MC, Dotti MT, Di Giandomenico S, Valoppi M, Grieco GS, Comanducci G, Bianchini G, Fortini D, Federico A, Giannotti A, Santorelli FM.
    Hum Mutat; 2003 Jul 10; 22(1):104. PubMed ID: 12815605
    [Abstract] [Full Text] [Related]

  • 16. A novel mutation of gene CBFA1/RUNX2 in cleidocranial dysplasia.
    Lo Muzio L, Tetè S, Mastrangelo F, Cazzolla AP, Lacaita MG, Margaglione M, Campisi G.
    Ann Clin Lab Sci; 2007 Jul 10; 37(2):115-20. PubMed ID: 17522365
    [Abstract] [Full Text] [Related]

  • 17. Cleidocranial dysplasia: etiology and stomatognathic and craniofacial abnormalities.
    D'Alessandro G, Tagariello T, Piana G.
    Minerva Stomatol; 2010 Mar 10; 59(3):117-27. PubMed ID: 20357738
    [Abstract] [Full Text] [Related]

  • 18. Effect of cleidocranial dysplasia-related novel mutation of RUNX2 on characteristics of dental pulp cells and tooth development.
    Xuan D, Sun X, Yan Y, Xie B, Xu P, Zhang J.
    J Cell Biochem; 2010 Dec 15; 111(6):1473-81. PubMed ID: 20872798
    [Abstract] [Full Text] [Related]

  • 19. Cleidocranial dysplasia. Case report.
    Taşar F, Bulut E, Tümer C, Saysel M, Muhtarogullari M.
    Aust Dent J; 1995 Dec 15; 40(6):352-6. PubMed ID: 8615738
    [Abstract] [Full Text] [Related]

  • 20. A RUNX2/PEBP2alpha A/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia.
    Zhang YW, Yasui N, Ito K, Huang G, Fujii M, Hanai J, Nogami H, Ochi T, Miyazono K, Ito Y.
    Proc Natl Acad Sci U S A; 2000 Sep 12; 97(19):10549-54. PubMed ID: 10962029
    [Abstract] [Full Text] [Related]

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