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385 related items for PubMed ID: 29932284
1. Diagnosis of Beckwith-Wiedemann syndrome in children presenting with Wilms tumor. MacFarland SP, Duffy KA, Bhatti TR, Bagatell R, Balamuth NJ, Brodeur GM, Ganguly A, Mattei PA, Surrey LF, Balis FM, Kalish JM. Pediatr Blood Cancer; 2018 Oct; 65(10):e27296. PubMed ID: 29932284 [Abstract] [Full Text] [Related]
2. 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 [Abstract] [Full Text] [Related]
3. Characteristics and outcome of children with Beckwith-Wiedemann syndrome and Wilms' tumor: a report from the National Wilms Tumor Study Group. Porteus MH, Narkool P, Neuberg D, Guthrie K, Breslow N, Green DM, Diller L. J Clin Oncol; 2000 May 01; 18(10):2026-31. PubMed ID: 10811666 [Abstract] [Full Text] [Related]
4. The effectiveness of Wilms tumor screening in Beckwith-Wiedemann spectrum. Mussa A, Duffy KA, Carli D, Griff JR, Fagiano R, Kupa J, Brodeur GM, Ferrero GB, Kalish JM. J Cancer Res Clin Oncol; 2019 Dec 01; 145(12):3115-3123. PubMed ID: 31583434 [Abstract] [Full Text] [Related]
5. Screening for Wilms tumor in children with Beckwith-Wiedemann syndrome or idiopathic hemihypertrophy. Choyke PL, Siegel MJ, Craft AW, Green DM, DeBaun MR. Med Pediatr Oncol; 1999 Mar 01; 32(3):196-200. PubMed ID: 10064187 [Abstract] [Full Text] [Related]
6. Epigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS). Bliek J, Gicquel C, Maas S, Gaston V, Le Bouc Y, Mannens M. J Pediatr; 2004 Dec 01; 145(6):796-9. PubMed ID: 15580204 [Abstract] [Full Text] [Related]
7. Perlman and Wiedemann-Beckwith syndromes: two distinct conditions associated with Wilms' tumour. Grundy RG, Pritchard J, Baraitser M, Risdon A, Robards M. Eur J Pediatr; 1992 Dec 01; 151(12):895-8. PubMed ID: 1361910 [Abstract] [Full Text] [Related]
8. Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumor. Niemitz EL, Feinberg AP, Brandenburg SA, Grundy PE, DeBaun MR. Am J Hum Genet; 2005 Nov 01; 77(5):887-91. PubMed ID: 16252245 [Abstract] [Full Text] [Related]
9. Screening for Wilms tumor and hepatoblastoma in children with Beckwith-Wiedemann syndromes: a cost-effective model. McNeil DE, Brown M, Ching A, DeBaun MR. Med Pediatr Oncol; 2001 Oct 01; 37(4):349-56. PubMed ID: 11568898 [Abstract] [Full Text] [Related]
10. Wilms tumour in Beckwith-Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelines. Brzezinski J, Shuman C, Choufani S, Ray P, Stavropoulos DJ, Basran R, Steele L, Parkinson N, Grant R, Thorner P, Lorenzo A, Weksberg R. Eur J Hum Genet; 2017 Sep 01; 25(9):1031-1039. PubMed ID: 28699632 [Abstract] [Full Text] [Related]
11. Is Nephron Sparing Surgery Justified in Wilms Tumor With Beckwith-Wiedemann Syndrome or Isolated Hemihypertrophy? Scalabre A, Bergeron C, Brioude F, Dainese L, Cropet C, Coulomb L'hermine A, Pasqualini C, Auber F, Verschuur A, Schleiermacher G, Le Bouc Y, Audry G, Irtan S. Pediatr Blood Cancer; 2016 Sep 01; 63(9):1571-7. PubMed ID: 27228957 [Abstract] [Full Text] [Related]
12. Feasibility of partial nephrectomy for Wilms' tumor in children with Beckwith-Wiedemann syndrome who have been screened with abdominal ultrasonography. McNeil DE, Langer JC, Choyke P, DeBaun MR. J Pediatr Surg; 2002 Jan 01; 37(1):57-60. PubMed ID: 11781987 [Abstract] [Full Text] [Related]
13. Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors. O'Keefe D, Dao D, Zhao L, Sanderson R, Warburton D, Weiss L, Anyane-Yeboa K, Tycko B. Am J Hum Genet; 1997 Aug 01; 61(2):295-303. PubMed ID: 9311733 [Abstract] [Full Text] [Related]
14. A constitutional BWS-related t(11;16) chromosome translocation occurring in the same region of chromosome 16 implicated in Wilms' tumors. Newsham I, Kindler-Röhrborn A, Daub D, Cavenee W. Genes Chromosomes Cancer; 1995 Jan 01; 12(1):1-7. PubMed ID: 7534105 [Abstract] [Full Text] [Related]
15. Misleading leads: Wilms tumor with a metachronous lesion appearing in the remaining kidney. Hilden JM, Brennom WS, Wolpert JJ, Beckwith JB. Med Pediatr Oncol; 1998 Mar 01; 30(3):180-2. PubMed ID: 9434829 [Abstract] [Full Text] [Related]
16. Nephromegaly in infancy and early childhood: a risk factor for Wilms tumor in Beckwith-Wiedemann syndrome. DeBaun MR, Siegel MJ, Choyke PL. J Pediatr; 1998 Mar 01; 132(3 Pt 1):401-4. PubMed ID: 9544890 [Abstract] [Full Text] [Related]
17. Cancer predisposition signaling in Beckwith-Wiedemann Syndrome drives Wilms tumor development. Nirgude S, Naveh NSS, Kavari SL, Traxler EM, Kalish JM. Br J Cancer; 2024 Mar 01; 130(4):638-650. PubMed ID: 38142265 [Abstract] [Full Text] [Related]
18. Beckwith-Wiedemann syndrome with overlapping Perlman syndrome manifestation. Ferianec V, Bartova M. J Matern Fetal Neonatal Med; 2014 Oct 01; 27(15):1607-9. PubMed ID: 24215131 [Abstract] [Full Text] [Related]
19. Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome. Gaston V, Le Bouc Y, Soupre V, Burglen L, Donadieu J, Oro H, Audry G, Vazquez MP, Gicquel C. Eur J Hum Genet; 2001 Jun 01; 9(6):409-18. PubMed ID: 11436121 [Abstract] [Full Text] [Related]
20. Screening for Wilms' tumour in patients with aniridia, Beckwith syndrome, or hemihypertrophy. Craft AW, Parker L, Stiller C, Cole M. Med Pediatr Oncol; 1995 Apr 01; 24(4):231-4. PubMed ID: 7700167 [Abstract] [Full Text] [Related] Page: [Next] [New Search]