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Journal Abstract Search


160 related items for PubMed ID: 34100307

  • 1. Comprehensive management of Crouzon syndrome: A case report with three-year follow-up.
    Tripathi T, Srivastava D, Bhutiani N, Rai P.
    J Orthod; 2022 Mar; 49(1):71-78. PubMed ID: 34100307
    [Abstract] [Full Text] [Related]

  • 2. Correcting Exorbitism by Monobloc Frontofacial Advancement in Crouzon-Pfeiffer Syndrome: An Age-Specific, Time-Related, Controlled Study.
    Way BLM, Khonsari RH, Karunakaran T, Nysjö J, Nyström I, Dunaway DJ, Evans RD, Hayward RD, Britto JA.
    Plast Reconstr Surg; 2019 Jan; 143(1):121e-132e. PubMed ID: 30589795
    [Abstract] [Full Text] [Related]

  • 3. Circummaxillary Sutures in Patients With Apert, Crouzon, and Pfeiffer Syndromes Compared to Nonsyndromic Children: Growth, Orthodontic, and Surgical Implications.
    Meazzini MC, Corradi F, Mazzoleni F, De Ponti E, Maccagni M, Novelli G, Bozzetti A.
    Cleft Palate Craniofac J; 2021 Mar; 58(3):299-305. PubMed ID: 32772851
    [Abstract] [Full Text] [Related]

  • 4. 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; 37(7):2391-2397. PubMed ID: 33404724
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. 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; 141():115600. PubMed ID: 32822871
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Crouzon syndrome and the eye: An overview.
    Bhattacharjee K, Rehman O, Venkatraman V, Kikkawa D, Bhattacharjee H, Gogoi R, Grewal AM, Bhattacharjee P.
    Indian J Ophthalmol; 2022 Jul; 70(7):2346-2354. PubMed ID: 35791116
    [Abstract] [Full Text] [Related]

  • 9. Midface correction in patients with Crouzon syndrome is Le Fort III distraction osteogenesis with a rigid external distraction device the gold standard?
    Engel M, Berger M, Hoffmann J, Kühle R, Rückschloss T, Ristow O, Freudlsperger C, Kansy K.
    J Craniomaxillofac Surg; 2019 Mar; 47(3):420-430. PubMed ID: 30642732
    [Abstract] [Full Text] [Related]

  • 10. A newborn with acanthosis nigricans: can it be Crouzon syndrome with acanthosis nigricans?
    Sharda S, Panigrahi I, Gupta K, Singhi S, Kumar R.
    Pediatr Dermatol; 2010 Mar; 27(1):43-7. PubMed ID: 20199409
    [Abstract] [Full Text] [Related]

  • 11. Classification of Subtypes of Crouzon Syndrome Based on the Type of Vault Suture Synostosis.
    Lu X, Sawh-Martinez R, Forte AJ, Wu R, Cabrejo R, Wilson A, Steinbacher DM, Alperovich M, Alonso N, Persing JA.
    J Craniofac Surg; 2020 Mar; 31(3):678-684. PubMed ID: 32068731
    [Abstract] [Full Text] [Related]

  • 12. Early orthodontic management of Crouzon Syndrome: a case report.
    Hlongwa P.
    J Maxillofac Oral Surg; 2009 Mar; 8(1):74-6. PubMed ID: 23139476
    [Abstract] [Full Text] [Related]

  • 13. Growth patterns of the airway in Crouzon syndrome patients with different types of cranial vault suture synostosis.
    Lu X, Forte AJ, Wilson A, Park KE, Allam O, Alperovich M, Steinbacher DM, Tonello C, Alonso N, Persing JA.
    Int J Oral Maxillofac Surg; 2021 Jul; 50(7):924-932. PubMed ID: 33384236
    [Abstract] [Full Text] [Related]

  • 14. An inherited FGFR2 mutation increased osteogenesis gene expression and result in Crouzon syndrome.
    Fan J, Li Y, Jia R, Fan X.
    BMC Med Genet; 2018 May 30; 19(1):91. PubMed ID: 29848297
    [Abstract] [Full Text] [Related]

  • 15. The value of the maxillo-malar osteotomy in the treatment of Crouzon syndrome with exorbitism.
    Taglialatela Scafati C, Aliberti F, Taglialatela Scafati S, Mangone GM, Taglialatela Scafati M.
    Ann Plast Surg; 2008 Sep 30; 61(3):285-9. PubMed ID: 18724129
    [Abstract] [Full Text] [Related]

  • 16. Influence of Nonsyndromic Bicoronal Synostosis and Syndromic Influences on Orbit and Periorbital Malformation.
    Lu X, Forte AJ, Dinis J, Junn A, Alperovich M, Alonso N, Persing JA.
    Plast Reconstr Surg; 2022 May 01; 149(5):930e-942e. PubMed ID: 35286288
    [Abstract] [Full Text] [Related]

  • 17. [Acanthosis nigricans in children and Crouzon syndrome].
    Lagaude M, Barreau M, Jokic M, Gerard M, DiRocco F, Hadj-Rabia S, Dompmartin A, Verneuil L.
    Ann Dermatol Venereol; 2014 Nov 01; 141(11):685-8. PubMed ID: 25442473
    [Abstract] [Full Text] [Related]

  • 18. Long-term stability of LeFort III distraction osteogenesis with a rigid external distraction device in a patient with Crouzon syndrome.
    Kuroda S, Watanabe K, Ishimoto K, Nakanishi H, Moriyama K, Tanaka E.
    Am J Orthod Dentofacial Orthop; 2011 Oct 01; 140(4):550-61. PubMed ID: 21967944
    [Abstract] [Full Text] [Related]

  • 19. Fronto-facial advancement and bipartition in Crouzon-Pfeiffer and Apert syndromes: Impact of fronto-facial surgery upon orbital and airway parameters in FGFR2 syndromes.
    Khonsari RH, Way B, Nysjö J, Odri GA, Olszewski R, Evans RD, Dunaway DJ, Nyström I, Britto JA.
    J Craniomaxillofac Surg; 2016 Oct 01; 44(10):1567-1575. PubMed ID: 27639780
    [Abstract] [Full Text] [Related]

  • 20. Syndromic Craniosynostosis.
    Wang JC, Nagy L, Demke JC.
    Facial Plast Surg Clin North Am; 2016 Nov 01; 24(4):531-543. PubMed ID: 27712819
    [Abstract] [Full Text] [Related]


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