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Journal Abstract Search

357 related items for PubMed ID: 27226847

  • 1. Genetic Syndromes Associated with Craniosynostosis.
    Ko JM.
    J Korean Neurosurg Soc; 2016 May; 59(3):187-91. PubMed ID: 27226847
    [Abstract] [Full Text] [Related]

  • 2. Genetic Analysis of Syndromic and Nonsyndromic Patients With Craniosynostosis Identifies Novel Mutations in the TWIST1 and EFNB1 Genes.
    Apostolopoulou D, Kaxira OS, Hatzaki A, Panagopoulos KP, Alexandrou K, Stratoudakis A, Kollia P, Aleporou V.
    Cleft Palate Craniofac J; 2018 Sep; 55(8):1092-1102. PubMed ID: 29561715
    [Abstract] [Full Text] [Related]

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  • 4. Syndromic Craniosynostosis: A Comprehensive Review.
    Katouni K, Nikolaou A, Mariolis T, Protogerou V, Chrysikos D, Theofilopoulou S, Filippou D.
    Cureus; 2023 Dec; 15(12):e50448. PubMed ID: 38222144
    [Abstract] [Full Text] [Related]

  • 5. Identical Twins Discordant for Metopic Craniosynostosis: Evidence of Epigenetic Influences.
    Magge SN, Snyder K, Sajja A, DeFreitas TA, Hofherr SE, Broth RE, Keating RF, Rogers GF.
    J Craniofac Surg; 2017 Jan; 28(1):14-16. PubMed ID: 28060197
    [Abstract] [Full Text] [Related]

  • 6. Clinical and genetic characteristics of craniosynostosis in Hungary.
    Bessenyei B, Nagy A, Szakszon K, Mokánszki A, Balogh E, Ujfalusi A, Tihanyi M, Novák L, Bognár L, Oláh É.
    Am J Med Genet A; 2015 Dec; 167A(12):2985-91. PubMed ID: 26289989
    [Abstract] [Full Text] [Related]

  • 7. Molecular Mechanisms Involved in Craniosynostosis.
    Yapijakis C, Pachis N, Sotiriadou T, Vaila C, Michopoulou V, Vassiliou S.
    In Vivo; 2023 Dec; 37(1):36-46. PubMed ID: 36593018
    [Abstract] [Full Text] [Related]

  • 8. Syndromic Craniosynostosis.
    Sawh-Martinez R, Steinbacher DM.
    Clin Plast Surg; 2019 Apr; 46(2):141-155. PubMed ID: 30851747
    [Abstract] [Full Text] [Related]

  • 9. Clinicogenetic study of Turkish patients with syndromic craniosynostosis and literature review.
    Nur BG, Pehlivanoğlu S, Mıhçı E, Calışkan M, Demir D, Alper OM, Kayserili H, Lüleci G.
    Pediatr Neurol; 2014 May; 50(5):482-90. PubMed ID: 24656465
    [Abstract] [Full Text] [Related]

  • 10. Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses.
    Heuzé Y, Holmes G, Peter I, Richtsmeier JT, Jabs EW.
    Curr Genet Med Rep; 2014 Sep 01; 2(3):135-145. PubMed ID: 26146596
    [Abstract] [Full Text] [Related]

  • 11. Syndromic craniosynostosis: from history to hydrogen bonds.
    Cunningham ML, Seto ML, Ratisoontorn C, Heike CL, Hing AV.
    Orthod Craniofac Res; 2007 May 01; 10(2):67-81. PubMed ID: 17552943
    [Abstract] [Full Text] [Related]

  • 12. Molecular and cellular bases of syndromic craniosynostoses.
    Bonaventure J, El Ghouzzi V.
    Expert Rev Mol Med; 2003 Jan 29; 5(4):1-17. PubMed ID: 14987407
    [Abstract] [Full Text] [Related]

  • 13. Genome-Wide Association Study in Craniosynostosis Condition Using Innovative Systematic Bioinformatic Analysis Tools and Techniques: Future Prospective and Clinical Practice.
    Barik M, Bajpai M, Malhotra A, Samantaray JC, Dwivedi S, Das S.
    J Pediatr Neurosci; 2018 Jan 29; 13(2):170-175. PubMed ID: 30090130
    [Abstract] [Full Text] [Related]

  • 14. Clinical study and some molecular features of Mexican patients with syndromic craniosynostosis.
    Ibarra-Arce A, Almaraz-Salinas M, Martínez-Rosas V, Ortiz de Zárate-Alarcón G, Flores-Peña L, Romero-Valdovinos M, Olivo-Díaz A.
    Mol Genet Genomic Med; 2020 Aug 29; 8(8):e1266. PubMed ID: 32510873
    [Abstract] [Full Text] [Related]

  • 15. Fibroblast Growth Factor Receptor 2 (FGFR2) Mutation Related Syndromic Craniosynostosis.
    Azoury SC, Reddy S, Shukla V, Deng CX.
    Int J Biol Sci; 2017 Aug 29; 13(12):1479-1488. PubMed ID: 29230096
    [Abstract] [Full Text] [Related]

  • 16. Early mandibular morphological differences in patients with FGFR2 and FGFR3-related syndromic craniosynostoses: A 3D comparative study.
    Morice A, Cornette R, Giudice A, Collet C, Paternoster G, Arnaud É, Galliani E, Picard A, Legeai-Mallet L, Khonsari RH.
    Bone; 2020 Dec 29; 141():115600. PubMed ID: 32822871
    [Abstract] [Full Text] [Related]

  • 17. Somatic FGFR and TWIST mutations are not a common cause of isolated nonsyndromic single suture craniosynostosis.
    Anderson PJ, Cox TC, Roscioli T, Elakis G, Smithers L, David DJ, Powell B.
    J Craniofac Surg; 2007 Mar 29; 18(2):312-4. PubMed ID: 17414280
    [Abstract] [Full Text] [Related]

  • 18. Syndromic Craniosynostosis.
    Wang JC, Nagy L, Demke JC.
    Facial Plast Surg Clin North Am; 2016 Nov 29; 24(4):531-543. PubMed ID: 27712819
    [Abstract] [Full Text] [Related]

  • 19. Molecular genetic analysis of TWIST1 and FGFR3 genes in Korean patients with coronal synostosis: identification of three novel TWIST1 mutations.
    Ko JM, Jeong SY, Yang JA, Park DH, Yoon SH.
    Plast Reconstr Surg; 2012 May 29; 129(5):814e-821e. PubMed ID: 22544111
    [Abstract] [Full Text] [Related]

  • 20. Reduced Intercarotid Artery Distance in Syndromic and Isolated Brachycephaly.
    Assadsangabi R, Hajmomenian M, Nabavizadeh SA, Schmitt JE, Vossough A.
    Pediatr Neurol; 2018 Feb 29; 79():3-7. PubMed ID: 29290519
    [Abstract] [Full Text] [Related]

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