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Journal Abstract Search

241 related items for PubMed ID: 35478319

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  • 3. The overlap between Sotos and Beckwith-Wiedemann syndromes.
    Mussa A, Chiesa N, Porta F, Baldassarre G, Silengo MC, Ferrero GB.
    J Pediatr; 2010 Jun; 156(6):1035-1036. PubMed ID: 20394943
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  • 4. 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; 66(1):e27492. PubMed ID: 30270492
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  • 5. Duplication of exon 2 of the GPC3 gene in a case of Simpson-Golabi-Behmel syndrome.
    Cottereau E, Moizard MP, David A, Raynaud M, Marmin N, Toutain A.
    Am J Med Genet A; 2014 Jan; 164A(1):282-4. PubMed ID: 24214682
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  • 6. Simpson-Golabi-Behmel syndrome type 1 and hepatoblastoma in a patient with a novel exon 2-4 duplication of the GPC3 gene.
    Mateos ME, Beyer K, López-Laso E, Siles JL, Pérez-Navero JL, Peña MJ, Guzmán J, Matas J.
    Am J Med Genet A; 2013 May; 161A(5):1091-5. PubMed ID: 23463737
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  • 7. Somatic CTNNB1 mutation in hepatoblastoma from a patient with Simpson-Golabi-Behmel syndrome and germline GPC3 mutation.
    Kosaki R, Takenouchi T, Takeda N, Kagami M, Nakabayashi K, Hata K, Kosaki K.
    Am J Med Genet A; 2014 Apr; 164A(4):993-7. PubMed ID: 24459012
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  • 8. α-Fetoprotein assay on dried blood spot for hepatoblastoma screening in children with overgrowth-cancer predisposition syndromes.
    Mussa A, Pagliardini S, Pagliardini V, Molinatto C, Baldassarre G, Corrias A, Silengo MC, Ferrero GB.
    Pediatr Res; 2014 Dec; 76(6):544-8. PubMed ID: 25167201
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  • 12. Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?
    Aretz S, Koch A, Uhlhaas S, Friedl W, Propping P, von Schweinitz D, Pietsch T.
    Pediatr Blood Cancer; 2006 Nov; 47(6):811-8. PubMed ID: 16317745
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  • 13. 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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  • 14. The utility of alpha-fetoprotein screening in Beckwith-Wiedemann syndrome.
    Duffy KA, Deardorff MA, Kalish JM.
    Am J Med Genet A; 2017 Mar; 173(3):581-584. PubMed ID: 28160403
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  • 15. The importance of differentiating Simpson-Golabi-Behmel and Beckwith-Wiedemann syndromes.
    Hughes-Benzie R, Allanson J, Hunter A, Cole T.
    J Med Genet; 1992 Dec; 29(12):928. PubMed ID: 1479609
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  • 16. Twenty-one years to the right diagnosis - clinical overlap of Simpson-Golabi-Behmel and Beckwith-Wiedemann syndrome.
    Knopp C, Rudnik-Schöneborn S, Zerres K, Gencik M, Spengler S, Eggermann T.
    Am J Med Genet A; 2015 Jan; 167A(1):151-5. PubMed ID: 25339544
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  • 17. Agenesis of the corpus callosum and hepatoblastoma.
    Luckie TM, Potter SL, Bacino CA, Shah R, Heczey A, Venkatramani R.
    Am J Med Genet A; 2020 Jan; 182(1):224-228. PubMed ID: 31729153
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  • 18. Serum alpha-fetoprotein screening for hepatoblastoma in Beckwith-Wiedemann syndrome.
    Mussa A, Ferrero GB.
    Am J Med Genet A; 2017 Mar; 173(3):585-587. PubMed ID: 28211991
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  • 19. Hepatoblastoma in patients with molecularly proven familial adenomatous polyposis: Clinical characteristics and rationale for surveillance screening.
    Trobaugh-Lotrario AD, López-Terrada D, Li P, Feusner JH.
    Pediatr Blood Cancer; 2018 Aug; 65(8):e27103. PubMed ID: 29719120
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  • 20. Preneoplastic liver colonization by 11p15.5 altered mosaic cells in young children with hepatoblastoma.
    Pilet J, Hirsch TZ, Gupta B, Roehrig A, Morcrette G, Pire A, Letouzé E, Fresneau B, Taque S, Brugières L, Branchereau S, Chardot C, Aerts I, Sarnacki S, Fabre M, Guettier C, Rebouissou S, Zucman-Rossi J.
    Nat Commun; 2023 Nov 06; 14(1):7122. PubMed ID: 37932266
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