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Journal Abstract Search

191 related items for PubMed ID: 21448630

  • 1. Neonatal hepatoblastoma in a newborn with severe phenotype of Beckwith-Wiedemann syndrome.
    Mussa A, Ferrero GB, Ceoloni B, Basso E, Chiesa N, De Crescenzo A, Pepe E, Silengo M, de Sanctis L.
    Eur J Pediatr; 2011 Nov; 170(11):1407-11. PubMed ID: 21448630
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  • 5. Serum alpha-fetoprotein screening for hepatoblastoma in children with Beckwith-Wiedemann syndrome or isolated hemihyperplasia.
    Clericuzio CL, Chen E, McNeil DE, O'Connor T, Zackai EH, Medne L, Tomlinson G, DeBaun M.
    J Pediatr; 2003 Aug; 143(2):270-2. PubMed ID: 12970646
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  • 7. Concurrent Hepatoblastoma and Wilms Tumor Leading to Diagnosis of Beckwith-Wiedemann Syndrome.
    Wolfe DM, Webster Carrion A, Masukhani MM, Oberg JA, Pavisic J, El-Ali A, Gupta M, Weng K, Glasser CL.
    J Pediatr Hematol Oncol; 2023 May 01; 45(4):e525-e529. PubMed ID: 36730589
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  • 9. Severe presentation of Beckwith-Wiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15.
    Smith AC, Shuman C, Chitayat D, Steele L, Ray PN, Bourgeois J, Weksberg R.
    Am J Med Genet A; 2007 Dec 15; 143A(24):3010-5. PubMed ID: 18000906
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  • 10. Serum alpha-fetoprotein screening for hepatoblastoma in Beckwith-Wiedemann syndrome.
    Mussa A, Ferrero GB.
    Am J Med Genet A; 2017 Mar 15; 173(3):585-587. PubMed ID: 28211991
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  • 11. Defining an optimal time window to screen for hepatoblastoma in children with Beckwith-Wiedemann syndrome.
    Mussa A, Duffy KA, Carli D, Ferrero GB, Kalish JM.
    Pediatr Blood Cancer; 2019 Jan 15; 66(1):e27492. PubMed ID: 30270492
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  • 12. Decreased CDKN1C Expression in Congenital Alveolar Rhabdomyosarcoma Associated with Beckwith-Wiedemann Syndrome.
    Piersigilli F, Auriti C, Mondì V, Francalanci P, Salvatori G, Danhaive O.
    Indian J Pediatr; 2016 Nov 15; 83(12-13):1476-1478. PubMed ID: 27345568
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  • 14. Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith-Wiedemann syndrome.
    Lin HY, Chuang CK, Tu RY, Fang YY, Su YN, Chen CP, Chang CY, Liu HC, Chu TH, Niu DM, Lin SP.
    Mol Genet Metab; 2016 Sep 15; 119(1-2):8-13. PubMed ID: 27436784
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  • 16. The placenta in Beckwith-Wiedemann syndrome: genotype-phenotype associations, excessive extravillous trophoblast and placental mesenchymal dysplasia.
    Armes JE, McGown I, Williams M, Broomfield A, Gough K, Lehane F, Lourie R.
    Pathology; 2012 Oct 15; 44(6):519-27. PubMed ID: 22772341
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  • 17. Epigenotype and phenotype correlations in patients with Beckwith-Wiedemann syndrome.
    Bilgin B, Kabaçam S, Taşkıran E, Şimşek-Kiper PÖ, Alanay Y, Boduroğlu K, Utine GE.
    Turk J Pediatr; 2018 Oct 15; 60(5):506-513. PubMed ID: 30968633
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  • 18. Hepatoblastoma in molecularly defined, congenital diseases.
    Nussbaumer G, Benesch M.
    Am J Med Genet A; 2022 Sep 15; 188(9):2527-2535. PubMed ID: 35478319
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  • 20. Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders.
    Soejima H, Higashimoto K.
    J Hum Genet; 2013 Jul 15; 58(7):402-9. PubMed ID: 23719190
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