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Integrated use of minimal residual disease classification and IKZF1 alteration status accurately predicts 79% of relapses in pediatric acute lymphoblastic leukemia.
Waanders E, van der Velden VH, van der Schoot CE, van Leeuwen FN, van Reijmersdal SV, de Haas V, Veerman AJ, van Kessel AG, Hoogerbrugge PM, Kuiper RP, van Dongen JJ. Waanders E, et al. Among authors: hoogerbrugge pm. Leukemia. 2011 Feb;25(2):254-8. doi: 10.1038/leu.2010.275. Epub 2010 Nov 19. Leukemia. 2011. PMID: 21102428
Cryptococcal meningitis in a child with acute lymphoblastic leukemia.
Mavinkurve-Groothuis AM, Bokkerink JP, Verweij PE, Veerman AJ, Hoogerbrugge PM. Mavinkurve-Groothuis AM, et al. Among authors: hoogerbrugge pm. Pediatr Infect Dis J. 2003 Jun;22(6):576. doi: 10.1097/01.inf.0000069793.03027.8f. Pediatr Infect Dis J. 2003. PMID: 12799518 No abstract available.
Role of 5'-nucleotidase in thiopurine metabolism: enzyme kinetic profile and association with thio-GMP levels in patients with acute lymphoblastic leukemia during 6-mercaptopurine treatment.
Brouwer C, Vogels-Mentink TM, Keizer-Garritsen JJ, Trijbels FJ, Bökkerink JP, Hoogerbrugge PM, van Wering ER, Veerman AJ, De Abreu RA. Brouwer C, et al. Among authors: hoogerbrugge pm. Clin Chim Acta. 2005 Nov;361(1-2):95-103. doi: 10.1016/j.cccn.2005.05.006. Clin Chim Acta. 2005. PMID: 15990089
High-resolution genomic profiling of pediatric lymphoblastic lymphomas reveals subtle differences with pediatric acute lymphoblastic leukemias in the B-lineage.
Schraders M, van Reijmersdal SV, Kamping EJ, van Krieken JH, van Kessel AG, Groenen PJ, Hoogerbrugge PM, Kuiper RP. Schraders M, et al. Among authors: hoogerbrugge pm. Cancer Genet Cytogenet. 2009 May;191(1):27-33. doi: 10.1016/j.cancergencyto.2009.01.002. Cancer Genet Cytogenet. 2009. PMID: 19389505
Regulation of MYCN expression in human neuroblastoma cells.
Jacobs JF, van Bokhoven H, van Leeuwen FN, Hulsbergen-van de Kaa CA, de Vries IJ, Adema GJ, Hoogerbrugge PM, de Brouwer AP. Jacobs JF, et al. Among authors: hoogerbrugge pm. BMC Cancer. 2009 Jul 18;9:239. doi: 10.1186/1471-2407-9-239. BMC Cancer. 2009. PMID: 19615087 Free PMC article.
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: hoogerbrugge pm, hoogerbrugge 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.
163 results