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

PUBMED FOR HANDHELDS

Journal Abstract Search

246 related items for PubMed ID: 27891566

  • 1. Sudden death associated with syndromic craniosynostosis.
    Ginelliová A, Farkaš D, Iannaccone SF, Vyhnálková V, Vasovčák P.
    Forensic Sci Med Pathol; 2016 Dec; 12(4):506-509. PubMed ID: 27891566
    [Abstract] [Full Text] [Related]

  • 2. Further analysis of the Crouzon mouse: effects of the FGFR2(C342Y) mutation are cranial bone-dependent.
    Liu J, Nam HK, Wang E, Hatch NE.
    Calcif Tissue Int; 2013 May; 92(5):451-66. PubMed ID: 23358860
    [Abstract] [Full Text] [Related]

  • 3. Dura in the pathogenesis of syndromic craniosynostosis: fibroblast growth factor receptor 2 mutations in dural cells promote osteogenic proliferation and differentiation of osteoblasts.
    Ang BU, Spivak RM, Nah HD, Kirschner RE.
    J Craniofac Surg; 2010 Mar; 21(2):462-7. PubMed ID: 20489451
    [Abstract] [Full Text] [Related]

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

  • 5. The craniofacial phenotype of the Crouzon mouse: analysis of a model for syndromic craniosynostosis using three-dimensional MicroCT.
    Perlyn CA, DeLeon VB, Babbs C, Govier D, Burell L, Darvann T, Kreiborg S, Morriss-Kay G.
    Cleft Palate Craniofac J; 2006 Nov; 43(6):740-8. PubMed ID: 17105336
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Overexpression of Fgfr2c causes craniofacial bone hypoplasia and ameliorates craniosynostosis in the Crouzon mouse.
    Lee KKL, Peskett E, Quinn CM, Aiello R, Adeeva L, Moulding DA, Stanier P, Pauws E.
    Dis Model Mech; 2018 Nov 09; 11(11):. PubMed ID: 30266836
    [Abstract] [Full Text] [Related]

  • 8. Severe craniolacunae and upper and lower extremity anomalies resulting from Crouzon syndrome, FGFR2 mutation, and Ser347Cys variant.
    Raposo-Amaral CE, Oliveira YM, Denadai R, Raposo-Amaral CA, Ghizoni E.
    Childs Nerv Syst; 2021 Jul 09; 37(7):2391-2397. PubMed ID: 33404724
    [Abstract] [Full Text] [Related]

  • 9. S267P mutation in FGFR2: first report in a patient with Crouzon syndrome.
    Ke R, Yang X, Ge M, Cai T, Lei J, Mu X.
    J Craniofac Surg; 2015 Mar 09; 26(2):592-4. PubMed ID: 25759927
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Synchondrosis fusion contributes to the progression of postnatal craniofacial dysmorphology in syndromic craniosynostosis.
    Hoshino Y, Takechi M, Moazen M, Steacy M, Koyabu D, Furutera T, Ninomiya Y, Nuri T, Pauws E, Iseki S.
    J Anat; 2023 Mar 09; 242(3):387-401. PubMed ID: 36394990
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 14. Extremely severe scoliosis, heterotopic ossification, and osteoarthritis in a three-generation family with Crouzon syndrome carrying a mutant c.799T>C FGFR2.
    Lin M, Lu Y, Sui Y, Zhao N, Jin Y, Yi D, Jiang M.
    Mol Genet Genomic Med; 2019 Sep 09; 7(9):e843. PubMed ID: 31318164
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Minor Suture Fusion in Syndromic Craniosynostosis.
    Runyan CM, Xu M D W, Alperovich M, Massie M D JP, Paek G, Cohen BA, Staffenberg DA, Flores RL, Taylor JA.
    Plast Reconstr Surg; 2017 Sep 09; 140(3):434e-445e. PubMed ID: 28574949
    [Abstract] [Full Text] [Related]

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

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Attenuation of signaling pathways stimulated by pathologically activated FGF-receptor 2 mutants prevents craniosynostosis.
    Eswarakumar VP, Ozcan F, Lew ED, Bae JH, Tomé F, Booth CJ, Adams DJ, Lax I, Schlessinger J.
    Proc Natl Acad Sci U S A; 2006 Dec 05; 103(49):18603-8. PubMed ID: 17132737
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.