375 related articles for article (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
[TBL] [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; 45(4):e525-e529. PubMed ID: 36730589
[TBL] [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; 18(10):2026-31. PubMed ID: 10811666
[TBL] [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; 145(12):3115-3123. PubMed ID: 31583434
[TBL] [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; 32(3):196-200. PubMed ID: 10064187
[TBL] [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; 145(6):796-9. PubMed ID: 15580204
[TBL] [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; 151(12):895-8. PubMed ID: 1361910
[TBL] [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; 77(5):887-91. PubMed ID: 16252245
[TBL] [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; 37(4):349-56. PubMed ID: 11568898
[TBL] [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; 25(9):1031-1039. PubMed ID: 28699632
[TBL] [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; 63(9):1571-7. PubMed ID: 27228957
[TBL] [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; 37(1):57-60. PubMed ID: 11781987
[TBL] [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; 61(2):295-303. PubMed ID: 9311733
[TBL] [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; 12(1):1-7. PubMed ID: 7534105
[TBL] [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; 30(3):180-2. PubMed ID: 9434829
[TBL] [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; 132(3 Pt 1):401-4. PubMed ID: 9544890
[TBL] [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; 130(4):638-650. PubMed ID: 38142265
[TBL] [Abstract][Full Text] [Related]
18. Beckwith-Wiedemann syndrome with overlapping Perlman syndrome manifestation.
Ferianec V; Bartova M
J Matern Fetal Neonatal Med; 2014 Oct; 27(15):1607-9. PubMed ID: 24215131
[TBL] [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; 9(6):409-18. PubMed ID: 11436121
[TBL] [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; 24(4):231-4. PubMed ID: 7700167
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
