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Histopathology|August 14, 2008
Paediatric renal tumours: recent developments, new entities and pathological featuresNeil J Sebire, Gordan M VujanicPediatric Blood & Cancer|June 29, 2010
Stromal and epithelial predominant Wilms tumours have an excellent outcome: the SIOP 93 01 experienceArnauld C Verschuur, Gordan M Vujanic, Harm Van Tinteren, et al.Pediatric Blood & Cancer|March 4, 2011
Mesoblastic nephroma: a report of the United Kingdom Children's Cancer and Leukaemia Group (CCLG)Richard J England, Nadeem Haider, Gordan M Vujanic, et al.Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 8, 2013
Bilateral wilms tumor with TP53-related anaplasiaSergey D Popov, Gordan M Vujanic, Neil J Sebire, et al.Journal of Clinical Pathology|October 30, 2007
c-KIT overexpression, without gene amplification and mutation, in paediatric renal tumoursChris Jones, Maria Rodriguez-Pinilla, Maryou Lambros, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 26, 2009
Expression of hepatocyte growth factor and its receptor met in Wilms' tumors and nephrogenic rests reflects their roles in kidney developmentRaisa Vuononvirta, Neil J Sebire, Boo Messahel, et al.Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|September 2, 2017
Anaplastic sarcomas of the kidney are characterized by DICER1 mutationsMona K Wu, Gordan M Vujanic, Somayyeh Fahiminiya, et al.Pediatric Blood & Cancer|December 22, 2022
The varied spectrum of nephroblastomatosis, nephrogenic rests, and Wilms tumors: Review of current definitions and challenges of the fieldElizabeth Fialkowski, Hélène Sudour-Bonnange, Gordan M Vujanic, et al.Pediatric Blood & Cancer|March 16, 2026
Results of the Childhood Cancer and Leukaemia Group's United Kingdom Relapsed Wilms Tumour TrialSucheta J Vaidya, Veronica Moroz, Juliet Hale, et al.Pageof 3