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Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome.
Jongmans MC, Kuiper RP, Carmichael CL, Wilkins EJ, Dors N, Carmagnac A, Schouten-van Meeteren AY, Li X, Stankovic M, Kamping E, Bengtsson H, Schoenmakers EF, van Kessel AG, Hoogerbrugge PM, Hahn CN, Brons PP, Scott HS, Hoogerbrugge N. Jongmans MC, et al. Among authors: dors n. Leukemia. 2010 Jan;24(1):242-6. doi: 10.1038/leu.2009.210. Epub 2009 Oct 15. Leukemia. 2010. PMID: 19946261 No abstract available.
Variation in baseline factor VIII concentration in a retrospective cohort of mild/moderate hemophilia A patients carrying identical F8 mutations.
Loomans JI, van Velzen AS, Eckhardt CL, Peters M, Mäkipernaa A, Holmstrom M, Brons PP, Dors N, Haya S, Voorberg J, van der Bom JG, Fijnvandraat K. Loomans JI, et al. Among authors: dors n. J Thromb Haemost. 2017 Feb;15(2):246-254. doi: 10.1111/jth.13581. Epub 2017 Feb 3. J Thromb Haemost. 2017. PMID: 27943580 Free article.
Causes of early death and treatment-related death in newly diagnosed pediatric acute myeloid leukemia: Recent experiences of the Dutch Childhood Oncology Group.
Klein K, van Litsenburg RRL, de Haas V, Dors N, van den Heuvel-Eibrink MM, Knops RRG, Tissing WJE, Versluys BA, Zwaan CM, Kaspers GJL. Klein K, et al. Among authors: dors n. Pediatr Blood Cancer. 2020 Apr;67(4):e28099. doi: 10.1002/pbc.28099. Epub 2019 Dec 23. Pediatr Blood Cancer. 2020. PMID: 31872548
Thrombotic thrombocytopenic purpura in childhood.
Bouw MC, Dors N, van Ommen H, Ramakers-van Woerden NL. Bouw MC, et al. Among authors: dors n. Pediatr Blood Cancer. 2009 Oct;53(4):537-42. doi: 10.1002/pbc.22094. Pediatr Blood Cancer. 2009. PMID: 19544391 Review.
37 results