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Journal Abstract Search

206 related items for PubMed ID: 34133757

  • 1. Complex Airway Management in Patients with Tracheal Cartilaginous Sleeves.
    Noble AR, Cunningham ML, Lam A, Wenger TL, Sie KC, Perkins JA, Dahl JP.
    Laryngoscope; 2022 Jan; 132(1):215-221. PubMed ID: 34133757
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  • 2. [Tracheal cartilaginous sleeve in craniosynostosis].
    Nakano T, Aiba T, Kubo T, Kusuki M, Hirano A, Matsushita N.
    Nihon Jibiinkoka Gakkai Kaiho; 2008 Sep; 111(9):623-7. PubMed ID: 18939407
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  • 3. Tracheal Cartilaginous Sleeve in Syndromic Craniosynostosis: An Underrecognized Source of Significant Morbidity and Mortality.
    Pickrell BB, Meaike JD, Cañadas KT, Chandy BM, Buchanan EP.
    J Craniofac Surg; 2017 May; 28(3):696-699. PubMed ID: 28468151
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  • 4. Genotype-Phenotype Correlation of Tracheal Cartilaginous Sleeves and Fgfr2 Mutations in Mice.
    Lam AS, Liu CC, Deutsch GH, Rivera J, Perkins JA, Holmes G, Jabs EW, Cunningham ML, Dahl JP.
    Laryngoscope; 2021 Apr; 131(4):E1349-E1356. PubMed ID: 32886384
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  • 6. Tracheal cartilaginous sleeves in children with syndromic craniosynostosis.
    Wenger TL, Dahl J, Bhoj EJ, Rosen A, McDonald-McGinn D, Zackai E, Jacobs I, Heike CL, Hing A, Santani A, Inglis AF, Sie KC, Cunningham M, Perkins J.
    Genet Med; 2017 Jan; 19(1):62-68. PubMed ID: 27228464
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  • 7. Beare-Stevenson syndrome: two new patients, including a novel finding of tracheal cartilaginous sleeve.
    Wenger TL, Bhoj EJ, Wetmore RF, Mennuti MT, Bartlett SP, Mollen TJ, McDonald-McGinn DM, Zackai EH.
    Am J Med Genet A; 2015 Apr; 167A(4):852-7. PubMed ID: 25706251
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  • 8. Tracheal cartilaginous sleeve in Pfeiffer syndrome: lesson learnt from its rarity.
    Mahmud N, Abdul Latif H, Mohd Zaki F, Goh BS.
    BMJ Case Rep; 2021 Apr 02; 14(4):. PubMed ID: 33811090
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  • 9. Laryngotracheal anomalies in children with syndromic craniosynostosis undergoing tracheostomy.
    Alli A, Gupta S, Elloy MD, Wyatt M.
    J Craniofac Surg; 2013 Jul 02; 24(4):1423-7. PubMed ID: 23851823
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  • 10. Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation.
    Chen CP, Lin SP, Su YN, Chien SC, Tsai FJ, Wang W.
    Genet Couns; 2008 Jul 02; 19(2):165-72. PubMed ID: 18618990
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  • 11. Tracheal cartilaginous sleeve in Crouzon syndrome.
    Scheid SC, Spector AR, Luft JD.
    Int J Pediatr Otorhinolaryngol; 2002 Sep 02; 65(2):147-52. PubMed ID: 12176186
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  • 12. A Delayed Finding of a Tracheal Cartilaginous Sleeve in a Patient with Pfeiffer Syndrome Type 2 and a Complex Airway History.
    Colomb C, Hippard HK, Canadas K, Watcha M.
    A A Case Rep; 2015 Aug 01; 5(3):36-9. PubMed ID: 26230305
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  • 16. 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 01; 50(5):482-90. PubMed ID: 24656465
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  • 19. Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis.
    Kan SH, Elanko N, Johnson D, Cornejo-Roldan L, Cook J, Reich EW, Tomkins S, Verloes A, Twigg SR, Rannan-Eliya S, McDonald-McGinn DM, Zackai EH, Wall SA, Muenke M, Wilkie AO.
    Am J Hum Genet; 2002 Feb 01; 70(2):472-86. PubMed ID: 11781872
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  • 20. Management of congenital cartilaginous sleeve trachea in children.
    Hamilton J, Clement WA, Kubba H.
    Int J Pediatr Otorhinolaryngol; 2014 Nov 01; 78(11):2011-4. PubMed ID: 25200602
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