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Journal Abstract Search

143 related items for PubMed ID: 29436723

  • 21. Upper extremity anomalies in Pfeiffer syndrome and mutational correlations.
    Cerrato FE, Nuzzi LC, Theman TA, Taghinia A, Upton J, Labow BI.
    Plast Reconstr Surg; 2014 May; 133(5):654e-661e. PubMed ID: 24776567
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  • 22. Prenatal diagnosis of Apert syndrome with widely separated cranial sutures.
    Lyu KJ, Ko TM.
    Prenat Diagn; 2000 Mar; 20(3):254-6. PubMed ID: 10719333
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  • 23. Vertebral abnormality without spine-curvature deformity on prenatal ultrasonography: sonographic findings and postnatal radiographic correlations.
    Song MJ, Kim YH.
    J Med Ultrason (2001); 2018 Jan; 45(1):89-95. PubMed ID: 28444475
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  • 24. Outcomes of congenital diaphragmatic hernia: a population-based study in Western Australia.
    Colvin J, Bower C, Dickinson JE, Sokol J.
    Pediatrics; 2005 Sep; 116(3):e356-63. PubMed ID: 16140678
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  • 25. Comparison of ultrasound and magnetic resonance imaging in the prenatal diagnosis of Apert syndrome: report of a case.
    Giancotti A, D'Ambrosio V, De Filippis A, Aliberti C, Pasquali G, Bernardo S, Manganaro L, PECRAM Study Group.
    Childs Nerv Syst; 2014 Aug; 30(8):1445-8. PubMed ID: 24566675
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  • 26. FGFR1 and FGFR2 mutations in Pfeiffer syndrome.
    Chokdeemboon C, Mahatumarat C, Rojvachiranonda N, Tongkobpetch S, Suphapeetiporn K, Shotelersuk V.
    J Craniofac Surg; 2013 Jan; 24(1):150-2. PubMed ID: 23348274
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  • 27. Pfeiffer syndrome.
    Vogels A, Fryns JP.
    Orphanet J Rare Dis; 2006 Jun 01; 1():19. PubMed ID: 16740155
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  • 28. 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 Jun 01; 19(2):165-72. PubMed ID: 18618990
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  • 32. Prenatal diagnosis of Pfeiffer syndrome and role of three-dimensional ultrasound: case report and review of literature.
    Vimercati A, Olivieri C, Dellino M, Gentile M, Tinelli R, Cicinelli E.
    J Matern Fetal Neonatal Med; 2022 Dec 01; 35(25):7840-7843. PubMed ID: 34182859
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  • 35. Ultrasound diagnosis of tracheal cartilaginous sleeve in a patient with Pfeiffer syndrome.
    Wanner MR, Marine MB, Dahl JP.
    Pediatr Radiol; 2018 Nov 01; 48(12):1814-1816. PubMed ID: 30022259
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  • 38. Prenatal diagnosis of Pfeiffer syndrome prior to 20 weeks' gestation.
    Gómez-Gómez JL, Fernández-Alonso AM, Moreno-Ortega I, Mas-Greño L, Berenguel-Martínez J, Fiol-Ruiz G.
    J Obstet Gynaecol; 2013 Apr 01; 33(3):309-310. PubMed ID: 23550868
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  • 39. Apert syndrome: prenatal diagnosis challenge.
    Vieira C, Teixeira N, Cadilhe A, Reis I.
    BMJ Case Rep; 2019 Dec 09; 12(12):. PubMed ID: 31822532
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  • 40. Negative autoregulation of fibroblast growth factor receptor 2 expression characterizing cranial development in cases of Apert (P253R mutation) and Pfeiffer (C278F mutation) syndromes and suggesting a basis for differences in their cranial phenotypes.
    Britto JA, Moore RL, Evans RD, Hayward RD, Jones BM.
    J Neurosurg; 2001 Oct 09; 95(4):660-73. PubMed ID: 11596961
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