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Page 1
Absence of SBDS mutations in sporadic paediatric acute myeloid leukaemia.
Aalbers AM, Calado RT, Young NS, Zwaan CM, Kajigaya S, Baruchel A, Geleijns K, de Haas V, Kaspers GJ, Reinhardt D, Trka J, Kuijpers TW, Pieters R, van der Velden VH, van den Heuvel-Eibrink MM. Aalbers AM, et al. Among authors: van der velden vh, van den heuvel eibrink mm. Br J Haematol. 2013 Feb;160(4):559-61. doi: 10.1111/bjh.12134. Epub 2012 Nov 28. Br J Haematol. 2013. PMID: 23189942 Free PMC article. No abstract available.
Is there a relationship between in vitro drug resistance and level of minimal residual disease as detected by polymerase chain reaction at the end of induction therapy in childhood acute lymphoblastic leukaemia?
De Haas V, Kaspers GJ, Oosten L, Bresters D, Pieters R, Van Der Velden VH, Van Wering ER, Van Den Berg H, Van Der Schoot CE. De Haas V, et al. Among authors: van der velden vh, van den berg h, van der schoot ce, van wering er. Br J Haematol. 2002 Sep;118(4):1190-1. doi: 10.1046/j.1365-2141.2002.36211.x. Br J Haematol. 2002. PMID: 12199807 Free article. No abstract available.
Standardization of WT1 mRNA quantitation for minimal residual disease monitoring in childhood AML and implications of WT1 gene mutations: a European multicenter study.
Willasch AM, Gruhn B, Coliva T, Kalinova M, Schneider G, Kreyenberg H, Steinbach D, Weber G, Hollink IH, Zwaan CM, Biondi A, van der Velden VH, Reinhardt D, Cazzaniga G, Bader P, Trka J; European Study Group on WT1 Expression in Childhood AML. Willasch AM, et al. Among authors: van der velden vh. Leukemia. 2009 Aug;23(8):1472-9. doi: 10.1038/leu.2009.51. Epub 2009 Mar 26. Leukemia. 2009. PMID: 19322206
Long-term survival after significant treatment reduction in a patient with CBF-AML.
Driessen EM, van der Velden VH, Catsman-Berrevoets CE, van den Heuvel-Eibrink MM, Beishuizen A. Driessen EM, et al. Among authors: van der velden vh, van den heuvel eibrink mm. Pediatr Blood Cancer. 2011 Feb;56(2):325-6. doi: 10.1002/pbc.22854. Epub 2010 Nov 11. Pediatr Blood Cancer. 2011. PMID: 21157900 No abstract available.
Human telomere disease due to disruption of the CCAAT box of the TERC promoter.
Aalbers AM, Kajigaya S, van den Heuvel-Eibrink MM, van der Velden VH, Calado RT, Young NS. Aalbers AM, et al. Among authors: van den heuvel eibrink mm, van der velden vh. Blood. 2012 Mar 29;119(13):3060-3. doi: 10.1182/blood-2011-10-383182. Epub 2012 Feb 8. Blood. 2012. PMID: 22323451 Free PMC article.
High frequency of copy number alterations in myeloid leukaemia of Down syndrome.
Blink M, van den Heuvel-Eibrink MM, Aalbers AM, Balgobind BV, Hollink IH, Meijerink JP, van der Velden VH, Beverloo BH, de Haas V, Hasle H, Reinhardt D, Klusmann JH, Pieters R, Calado RT, Zwaan CM. Blink M, et al. Among authors: van den heuvel eibrink mm, van der velden vh. Br J Haematol. 2012 Sep;158(6):800-3. doi: 10.1111/j.1365-2141.2012.09224.x. Epub 2012 Jul 7. Br J Haematol. 2012. PMID: 22775985 Free article. No abstract available.
High GATA2 expression is a poor prognostic marker in pediatric acute myeloid leukemia.
Luesink M, Hollink IH, van der Velden VH, Knops RH, Boezeman JB, de Haas V, Trka J, Baruchel A, Reinhardt D, van der Reijden BA, van den Heuvel-Eibrink MM, Zwaan CM, Jansen JH. Luesink M, et al. Among authors: van der velden vh, van den heuvel eibrink mm, van der reijden ba. Blood. 2012 Sep 6;120(10):2064-75. doi: 10.1182/blood-2011-12-397083. Epub 2012 Jul 11. Blood. 2012. PMID: 22786876 Free article.
Improved flow cytometric detection of minimal residual disease in childhood acute lymphoblastic leukemia.
Denys B, van der Sluijs-Gelling AJ, Homburg C, van der Schoot CE, de Haas V, Philippé J, Pieters R, van Dongen JJ, van der Velden VH. Denys B, et al. Among authors: van der velden vh, van dongen jj, van der schoot ce, van der sluijs gelling aj. Leukemia. 2013 Mar;27(3):635-41. doi: 10.1038/leu.2012.231. Epub 2012 Aug 16. Leukemia. 2013. PMID: 22945774
246 results