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Journal Abstract Search

238 related items for PubMed ID: 11826361

  • 1. Association of alveolar rhabdomyosarcoma with the Beckwith-Wiedemann syndrome.
    Smith AC, Squire JA, Thorner P, Zielenska M, Shuman C, Grant R, Chitayat D, Nishikawa JL, Weksberg R.
    Pediatr Dev Pathol; 2001; 4(6):550-8. PubMed ID: 11826361
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  • 4. Detection of PAX3-FKHR and PAX7-FKHR fusion transcripts in rhabdomyosarcoma by reverse transcriptase-polymerase chain reaction using paraffin-embedded tissue.
    Chen BF, Chen ML, Liang DC, Huang YW, Liu HC, Chen SH.
    Zhonghua Yi Xue Za Zhi (Taipei); 1999 Feb; 62(2):86-91. PubMed ID: 10063718
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  • 5. Sclerosing rhabdomyosarcoma in adults: report of four cases of a hyalinizing, matrix-rich variant of rhabdomyosarcoma that may be confused with osteosarcoma, chondrosarcoma, or angiosarcoma.
    Folpe AL, McKenney JK, Bridge JA, Weiss SW.
    Am J Surg Pathol; 2002 Sep; 26(9):1175-83. PubMed ID: 12218574
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  • 6. PAX3-FKHR and PAX7-FKHR gene fusions are prognostic indicators in alveolar rhabdomyosarcoma: a report from the children's oncology group.
    Sorensen PH, Lynch JC, Qualman SJ, Tirabosco R, Lim JF, Maurer HM, Bridge JA, Crist WM, Triche TJ, Barr FG.
    J Clin Oncol; 2002 Jun 01; 20(11):2672-9. PubMed ID: 12039929
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  • 7. The clinical course of an overgrowth syndrome, from diagnosis in infancy through adulthood: the case of Beckwith-Wiedemann syndrome.
    Pappas JG.
    Curr Probl Pediatr Adolesc Health Care; 2015 Apr 01; 45(4):112-7. PubMed ID: 25861997
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  • 8. (Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome.
    Mussa A, Russo S, De Crescenzo A, Freschi A, Calzari L, Maitz S, Macchiaiolo M, Molinatto C, Baldassarre G, Mariani M, Tarani L, Bedeschi MF, Milani D, Melis D, Bartuli A, Cubellis MV, Selicorni A, Cirillo Silengo M, Larizza L, Riccio A, Ferrero GB.
    Eur J Hum Genet; 2016 Feb 01; 24(2):183-90. PubMed ID: 25898929
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  • 9. Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.
    Slatter RE, Elliott M, Welham K, Carrera M, Schofield PN, Barton DE, Maher ER.
    J Med Genet; 1994 Oct 01; 31(10):749-53. PubMed ID: 7837249
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  • 10. 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
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  • 11. 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 01; 65(10):e27296. PubMed ID: 29932284
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  • 12. The significance of molecular studies in the long-term follow-up of children with beckwith- wiedemann syndrome.
    Gizewska M, Wilk M, Patalan M, Mackay D, Peregud-Pegorzelski J, Gawrych E, Walczak M, Petriczko E, Brodkiewicz A.
    Turk J Pediatr; 2014 Oct 01; 56(2):177-82. PubMed ID: 24911853
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  • 13. 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
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  • 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
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  • 15. Novel deletion in 11p15.5 imprinting center region 1 in a patient with Beckwith-Wiedemann syndrome provides insight into distal enhancer regulation and tumorigenesis.
    Bachmann N, Crazzolara R, Bohne F, Kotzot D, Maurer K, Enklaar T, Prawitt D, Bergmann C.
    Pediatr Blood Cancer; 2017 Mar 01; 64(3):. PubMed ID: 27650505
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  • 16. Beckwith-Wiedemann syndrome-associated hepatoblastoma: wnt signal activation occurs later in tumorigenesis in patients with 11p15.5 uniparental disomy.
    Fukuzawa R, Hata J, Hayashi Y, Ikeda H, Reeve AE.
    Pediatr Dev Pathol; 2003 Mar 01; 6(4):299-306. PubMed ID: 14692643
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  • 17. Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome.
    Little MH, Thomson DB, Hayward NK, Smith PJ.
    Hum Genet; 1988 Jun 01; 79(2):186-9. PubMed ID: 2839410
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  • 19. Mixed embryonal/alveolar rhabdomyosarcoma of the prostate: report of a case with molecular genetic studies and literature review.
    Treetipsatit J, Kittikowit W, Zielenska M, Chaipipat M, Thorner PS, Shuangshoti S.
    Pediatr Dev Pathol; 2009 Jun 01; 12(5):383-9. PubMed ID: 19175284
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  • 20. Use of a novel FISH assay on paraffin-embedded tissues as an adjunct to diagnosis of alveolar rhabdomyosarcoma.
    Nishio J, Althof PA, Bailey JM, Zhou M, Neff JR, Barr FG, Parham DM, Teot L, Qualman SJ, Bridge JA.
    Lab Invest; 2006 Jun 01; 86(6):547-56. PubMed ID: 16607381
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