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Journal Abstract Search

425 related items for PubMed ID: 21089741

  • 1. Genetic syndrome suspicion: examples of clinical approach in the neonatal unit.
    Giuffrè M, De Sanctis L.
    Minerva Pediatr; 2010 Jun; 62(3 Suppl 1):199-201. PubMed ID: 21089741
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  • 3. Oesophageal atresia.
    Spitz L.
    Orphanet J Rare Dis; 2007 May 11; 2():24. PubMed ID: 17498283
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  • 5. Patterns of malformation associated with esophageal atresia/tracheoesophageal fistula: A retrospective single center study.
    Galarreta CI, Vaida F, Bird LM.
    Am J Med Genet A; 2020 Jun 11; 182(6):1351-1363. PubMed ID: 32250545
    [Abstract] [Full Text] [Related]

  • 6. VACTERL (vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, cardiac defects, renal and limb anomalies) association: disease spectrum in 25 patients ascertained for their upper limb involvement.
    Carli D, Garagnani L, Lando M, Fairplay T, Bernasconi S, Landi A, Percesepe A.
    J Pediatr; 2014 Mar 11; 164(3):458-62.e1-2. PubMed ID: 24210691
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  • 8. VACTERL/VATER Association.
    Solomon BD.
    Orphanet J Rare Dis; 2011 Aug 16; 6():56. PubMed ID: 21846383
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  • 9. Novel association of VACTERL, neural tube defect and crossed renal ectopia: sonic hedgehog signaling: a point of coherence?
    Vaze D, Mahalik S, Rao KL.
    Congenit Anom (Kyoto); 2012 Dec 16; 52(4):211-5. PubMed ID: 23181497
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  • 10. Spinal dysraphism as a new entity in V.A.C.TE.R.L syndrome, resulting in a novel acronym V.A.C.TE.R.L.S.
    Amelot A, Cretolle C, de Saint Denis T, Sarnacki S, Catala M, Zerah M.
    Eur J Pediatr; 2020 Jul 16; 179(7):1121-1129. PubMed ID: 32055959
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  • 12. VACTERL associations in children undergoing surgery for esophageal atresia and anorectal malformations: Implications for pediatric surgeons.
    Lautz TB, Mandelia A, Radhakrishnan J.
    J Pediatr Surg; 2015 Aug 16; 50(8):1245-50. PubMed ID: 25913268
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  • 13. Clinical and etiological heterogeneity in patients with tracheo-esophageal malformations and associated anomalies.
    Brosens E, Ploeg M, van Bever Y, Koopmans AE, IJsselstijn H, Rottier RJ, Wijnen R, Tibboel D, de Klein A.
    Eur J Med Genet; 2014 Aug 16; 57(8):440-52. PubMed ID: 24931924
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  • 14. Patients with anorectal malformation and upper limb anomalies: genetic evaluation is warranted.
    van den Hondel D, Wijers CH, van Bever Y, de Klein A, Marcelis CL, de Blaauw I, Sloots CE, IJsselstijn H.
    Eur J Pediatr; 2016 Apr 16; 175(4):489-97. PubMed ID: 26498647
    [Abstract] [Full Text] [Related]

  • 15. Second study on the recurrence risk of isolated esophageal atresia with or without trachea-esophageal fistula among first-degree relatives: no evidence for increased risk of recurrence of EA/TEF or for malformations of the VATER/VACTERL association spectrum.
    Choinitzki V, Zwink N, Bartels E, Baudisch F, Boemers TM, Hölscher A, Turial S, Bachour H, Heydweiller A, Kurz R, Bartmann P, Pauly M, Brokmeier U, Leutner A, Nöthen MM, Schumacher J, Jenetzky E, Reutter H.
    Birth Defects Res A Clin Mol Teratol; 2013 Dec 16; 97(12):786-91. PubMed ID: 24307608
    [Abstract] [Full Text] [Related]

  • 16. Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study.
    van de Putte R, van Rooij IALM, Marcelis CLM, Guo M, Brunner HG, Addor MC, Cavero-Carbonell C, Dias CM, Draper ES, Etxebarriarteun L, Gatt M, Haeusler M, Khoshnood B, Klungsoyr K, Kurinczuk JJ, Lanzoni M, Latos-Bielenska A, Luyt K, O'Mahony MT, Miller N, Mullaney C, Nelen V, Neville AJ, Perthus I, Pierini A, Randrianaivo H, Rankin J, Rissmann A, Rouget F, Schaub B, Tucker D, Wellesley D, Wiesel A, Zymak-Zakutnia N, Loane M, Barisic I, de Walle HEK, Roeleveld N, Bergman JEH.
    Pediatr Res; 2020 Feb 16; 87(3):541-549. PubMed ID: 31499513
    [Abstract] [Full Text] [Related]

  • 17. Underlying genetic factors of the VATER/VACTERL association with special emphasis on the "Renal" phenotype.
    Reutter H, Hilger AC, Hildebrandt F, Ludwig M.
    Pediatr Nephrol; 2016 Nov 16; 31(11):2025-33. PubMed ID: 26857713
    [Abstract] [Full Text] [Related]

  • 18. De novo microduplication at 22q11.21 in a patient with VACTERL association.
    Schramm C, Draaken M, Bartels E, Boemers TM, Aretz S, Brockschmidt FF, Nöthen MM, Ludwig M, Reutter H.
    Eur J Med Genet; 2011 Nov 16; 54(1):9-13. PubMed ID: 20849991
    [Abstract] [Full Text] [Related]

  • 19. An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with esophageal atresia, cardiac anomalies, renal anomalies, and limb anomalies) association.
    Solomon BD, Baker LA, Bear KA, Cunningham BK, Giampietro PF, Hadigan C, Hadley DW, Harrison S, Levitt MA, Niforatos N, Paul SM, Raggio C, Reutter H, Warren-Mora N.
    J Pediatr; 2014 Mar 16; 164(3):451-7.e1. PubMed ID: 24332453
    [No Abstract] [Full Text] [Related]

  • 20. Urorectal septum malformation sequence in a newborn with VACTERL association.
    Patra S, Purkait R.
    J Coll Physicians Surg Pak; 2012 Feb 16; 22(2):116-7. PubMed ID: 22313652
    [Abstract] [Full Text] [Related]

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