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Bulletin Du Cancer|January 19, 2010
[Rhadboid tumours: hSNF/INI1 deficient cancers of early childhood with aggressive behaviour]F Bourdeaut, C Dufour, O DelattreOncogene|December 12, 2007
In neuroblastic tumours, Schwann cells do not harbour the genetic alterations of neuroblasts but may nevertheless share the same clonal originF Bourdeaut, A Ribeiro, R Paris, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 2, 2010
[The alliance of the parent, child and the nurse to challenge medical error]D Davous, E Seigneur, A Auvrignon, et al.The Journal of Pathology|December 8, 2006
hSNF5/INI1-deficient tumours and rhabdoid tumours are convergent but not fully overlapping entitiesF Bourdeaut, P Fréneaux, B Thuille, et al.AJNR. American Journal of Neuroradiology|August 21, 2020
Focal Areas of High Signal Intensity in Children with Neurofibromatosis Type 1: Expected Evolution on MRIS Calvez, R Levy, R Calvez, et al.AJNR. American Journal of Neuroradiology|December 10, 2021
Imaging Features with Histopathologic Correlation of CNS High-Grade Neuroepithelial Tumors with a <i>BCOR</i> Internal Tandem DuplicationL Cardoen, A Tauziède-Espariat, V Dangouloff-Ros, et al.Pediatric Blood & Cancer|August 24, 2013
Malformations, genetic abnormalities, and Wilms tumorS Dumoucel, M Gauthier-Villars, D Stoppa-Lyonnet, et al.Pediatric Blood & Cancer|February 13, 2019
Indications and results of diagnostic biopsy in pediatric renal tumors: A retrospective analysis of 317 patients with critical review of SIOP guidelinesYvan de la Monneraye, J Michon, H Pacquement, et al.Journal of Medical Genetics|February 22, 2014
Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium "Care for CMMR-D" (C4CMMR-D)H F A Vasen, Z Ghorbanoghli, F Bourdeaut, et al.Pageof 2