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Nature Reviews. Urology|November 2, 2017
Position paper: Rationale for the treatment of Wilms tumour in the UMBRELLA SIOP-RTSG 2016 protocolMarry M van den Heuvel-Eibrink, Janna A Hol, Kathy Pritchard-Jones, et al.Cancer|November 4, 2020
Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30-year SIOP-RTSG experienceJanna A Hol, Marjolijn C J Jongmans, Hélène Sudour-Bonnange, et al.Human Molecular Genetics|October 21, 2022
Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetranceJaël S Copier, Marianne Bootsma, Chai A Ng, et al.Journal of Clinical Medicine|December 10, 2021
Bilateral Renal Tumors in Children: The First 5 Years' Experience of National Centralization in The Netherlands and a Narrative Review of the LiteratureSophie E van Peer, Janna A Hol, Alida F W van der Steeg, et al.JAMA Network Open|February 3, 2023
Assessment of Cancer Predisposition Syndromes in a National Cohort of Children With a NeoplasmJette J Bakhuizen, Saskia M J Hopman, Machteld I Bosscha, et al.Familial Cancer|March 9, 2021
Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS): a prospective, observational, multi-center studyFloor A M Postema, Saskia M J Hopman, Corianne A J M de Borgie, et al.Plos One|January 13, 2022
Characteristics and outcome of children with renal tumors in the Netherlands: The first five-year's experience of national centralizationPrakriti Roy, Sophie E van Peer, Martin M de Witte, et al.International Journal of Cancer|January 18, 2021
Characteristics and outcome of pediatric renal cell carcinoma patients registered in the International Society of Pediatric Oncology (SIOP) 93-01, 2001 and UK-IMPORT database: A report of the SIOP-Renal Tumor Study GroupJustine N van der Beek, Janna A Hol, Aurore Coulomb-l'Hermine, et al.European Journal of Human Genetics : EJHG|July 29, 2025
Clinical utility of DNA-methylation signatures in routine diagnostics for neurodevelopmental disordersDaphne J Smits, Christophe Debuy, Alice S Brooks, et al.American Journal of Human Genetics|July 16, 2024
Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndromeDmitrijs Rots, Arianne Bouman, Ayumi Yamada, et al.Pageof 2