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Journal Abstract Search

282 related items for PubMed ID: 31927149

  • 1. Associated syndromes in patients with Pierre Robin Sequence.
    Karempelis P, Hagen M, Morrell N, Roby BB.
    Int J Pediatr Otorhinolaryngol; 2020 Apr; 131():109842. PubMed ID: 31927149
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  • 2. Nager syndrome and Pierre Robin sequence.
    Rosa RF, Guimarães VB, Beltrão LA, Trombetta JS, Lliguin KL, de Mattos VF, Zen PR.
    Pediatr Int; 2015 Apr; 57(2):e69-72. PubMed ID: 25808856
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  • 3. Stickler syndrome: a possible presentation of Pierre Robin sequence.
    Briosa F, Oliveira S, Sousa R, Oom P.
    BMJ Case Rep; 2019 Jan 31; 12(1):. PubMed ID: 30709837
    [No Abstract] [Full Text] [Related]

  • 4. Fast and early mandibular osteodistraction (FEMOD) in severe Pierre Robin Sequence.
    Cascone P, Papoff P, Arangio P, Vellone V, Calafati V, Silvestri A.
    J Craniomaxillofac Surg; 2014 Oct 31; 42(7):1364-70. PubMed ID: 24787079
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  • 8. Clinical, cytogenetic, and molecular outcomes in a series of 66 patients with Pierre Robin sequence and literature review: 22q11.2 deletion is less common than other chromosomal anomalies.
    Gomez-Ospina N, Bernstein JA.
    Am J Med Genet A; 2016 Apr 31; 170A(4):870-80. PubMed ID: 26756138
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  • 9. Importance of early diagnosis of Stickler syndrome in newborns.
    Antunes RB, Alonso N, Paula RG.
    J Plast Reconstr Aesthet Surg; 2012 Aug 31; 65(8):1029-34. PubMed ID: 22424767
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  • 10. Pierre Robin sequence: Management of respiratory and feeding complications during the first year of life in a tertiary referral centre.
    Rathé M, Rayyan M, Schoenaers J, Dormaar JT, Breuls M, Verdonck A, Devriendt K, Poorten VV, Hens G.
    Int J Pediatr Otorhinolaryngol; 2015 Aug 31; 79(8):1206-12. PubMed ID: 26092549
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  • 15. Management of cleft palate among patients with Pierre Robin sequence.
    Wang C, Shi B, Li J.
    Br J Oral Maxillofac Surg; 2023 Sep 31; 61(7):475-481. PubMed ID: 37453893
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  • 17. Cleft palate morphology, genetic etiology, and risk of mortality in infants with Robin sequence.
    Wenger TL, Perkins J, Parish-Morris J, Hing AV, Chen ML, Cielo CM, Li D, Bhoj EJ, Hakonarson H, Zackai E, McDonald-McGinn DM, Taylor JA, Jackson O, Sie K, Bly R, Dahl J, Evans KN.
    Am J Med Genet A; 2021 Dec 31; 185(12):3694-3700. PubMed ID: 34291880
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