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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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [No Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]