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Genes, Chromosomes & Cancer|November 7, 2015
The clinical phenotype of YWHAE-NUTM2B/E positive pediatric clear cell sarcoma of the kidneySaskia L Gooskens, Colin Kenny, Antonio Lazaro, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 10, 2010
TP53 mutation is frequently associated with CTNNB1 mutation or MYCN amplification and is compatible with long-term survival in medulloblastomaElke Pfaff, Marc Remke, Dominik Sturm, et al.Cancers|March 3, 2021
Outcome of Stage IV Completely Necrotic Wilms Tumour and Local Stage III Treated According to the SIOP 2001 ProtocolRaquel Dávila Fajardo, Rhoikos Furtwängler, Martine van Grotel, et al.Pediatric Blood & Cancer|April 20, 2026
Characteristics and Survival of Patients With Wilms Tumor and Bone Metastases: A SIOP-RTSG 93-01, SIOP 2001, and UK-IMPORT StudyArianna Tagarelli, Rana Dandis, Harm Van Tinteren, et al.Expert Review of Anticancer Therapy|August 3, 2011
Management of adults with Wilms' tumor: recommendations based on international consensusHeidi Segers, Marry M van den Heuvel-Eibrink, Kathy Pritchard-Jones, et al.Cancer Medicine|August 5, 2024
Targeted therapies in children with renal cell carcinoma (RCC): An International Society of Pediatric Oncology-Renal Tumor Study Group (SIOP-RTSG)-related retrospective descriptive studyJulia Sprokkerieft, Justine N van der Beek, Filippo Spreafico, et al.Clinical Pharmacology and Therapeutics|February 6, 2025
Model-Based Prediction of Clinically Relevant Thrombocytopenia after Allogeneic Hematopoietic Stem Cell TransplantationKatharina M Götz, Amin T Turki, Katharina Och, et al.Cancer Medicine|May 27, 2016
Improved 6-year overall survival in AT/RT - results of the registry study Rhabdoid 2007Kerstin Bartelheim, Karolina Nemes, Angela Seeringer, et al.Der Pathologe|December 1, 2020
[Diagnosis and therapy of tumors with NTRK gene fusion]Albrecht Stenzinger, Cornelis M van Tilburg, Ghazaleh Tabatabai, et al.Pediatric Blood & Cancer|October 19, 2019
Is radiotherapy required in first-line treatment of stage I diffuse anaplastic Wilms tumor? A report of SIOP-RTSG, AIEOP, JWiTS, and UKCCSGRaquel Dávila Fajardo, Marry M van den Heuvel-Eibrink, Harm van Tinteren, et al.Pageof 38