Buijs A - Search Results

1

Identification of chromosomal abnormalities relevant to prognosis in chronic lymphocytic leukemia using multiplex ligation-dependent probe amplification.

Stevens-Kroef M, Simons A, Gorissen H, Feuth T, Weghuis DO, Buijs A, Raymakers R, Geurts van Kessel A. Stevens-Kroef M, et al. Among authors: buijs a. Cancer Genet Cytogenet. 2009 Dec;195(2):97-104. doi: 10.1016/j.cancergencyto.2009.06.020. Cancer Genet Cytogenet. 2009. PMID: 19963108

2

Outcome of allogeneic transplantation in newly diagnosed and relapsed/refractory multiple myeloma: long-term follow-up in a single institution.

Franssen LE, Raymakers RA, Buijs A, Schmitz MF, van Dorp S, Mutis T, Lokhorst HM, van de Donk NW. Franssen LE, et al. Among authors: buijs a. Eur J Haematol. 2016 Nov;97(5):479-488. doi: 10.1111/ejh.12758. Epub 2016 May 3. Eur J Haematol. 2016. PMID: 27028304

3

Translocation (12;22) (p13;q11) in myeloproliferative disorders results in fusion of the ETS-like TEL gene on 12p13 to the MN1 gene on 22q11.

Buijs A, Sherr S, van Baal S, van Bezouw S, van der Plas D, Geurts van Kessel A, Riegman P, Lekanne Deprez R, Zwarthoff E, Hagemeijer A, et al. Buijs A, et al. Oncogene. 1995 Apr 20;10(8):1511-9. Oncogene. 1995. PMID: 7731705

4

A new subtype of MLL-SEPT2 fusion transcript in therapy-related acute myeloid leukemia with t(2;11)(q37;q23): a case report and literature review.

van Binsbergen E, de Weerdt O, Buijs A. van Binsbergen E, et al. Among authors: buijs a. Cancer Genet Cytogenet. 2007 Jul 1;176(1):72-5. doi: 10.1016/j.cancergencyto.2007.04.001. Cancer Genet Cytogenet. 2007. PMID: 17574968 Review.

5

Gene expression profiling for molecular classification of multiple myeloma in newly diagnosed patients.

Broyl A, Hose D, Lokhorst H, de Knegt Y, Peeters J, Jauch A, Bertsch U, Buijs A, Stevens-Kroef M, Beverloo HB, Vellenga E, Zweegman S, Kersten MJ, van der Holt B, el Jarari L, Mulligan G, Goldschmidt H, van Duin M, Sonneveld P. Broyl A, et al. Among authors: buijs a. Blood. 2010 Oct 7;116(14):2543-53. doi: 10.1182/blood-2009-12-261032. Epub 2010 Jun 23. Blood. 2010. PMID: 20574050 Free article.

6

A survey of undetected, clinically relevant chromosome abnormalities when replacing postnatal karyotyping by Whole Genome Sequencing.

Hochstenbach R, van Binsbergen E, Schuring-Blom H, Buijs A, Ploos van Amstel HK. Hochstenbach R, et al. Among authors: buijs a. Eur J Med Genet. 2019 Sep;62(9):103543. doi: 10.1016/j.ejmg.2018.09.010. Epub 2018 Sep 22. Eur J Med Genet. 2019. PMID: 30248410

7

A ZMYM2-FGFR1 8p11 myeloproliferative neoplasm with a novel nonsense RUNX1 mutation and tumor lysis upon imatinib treatment.

Buijs A, van Wijnen M, van den Blink D, van Gijn M, Klein SK. Buijs A, et al. Cancer Genet. 2013 Apr;206(4):140-4. doi: 10.1016/j.cancergen.2013.04.001. Cancer Genet. 2013. PMID: 23751892

8

Detection of risk-identifying chromosomal abnormalities and genomic profiling by multiplex ligation-dependent probe amplification in chronic lymphocytic leukemia.

Buijs A, Krijtenburg PJ, Meijer E. Buijs A, et al. Haematologica. 2006 Oct;91(10):1434-5. Haematologica. 2006. PMID: 17018399

9

Philadelphia chromosome of a constitutional der(22)t(Y;22)(q11.2;p11) with a variant t(1;9;22)(p36;q34;q11) in a case of chronic myelogenous leukemia.

Buijs A, Terhal PA, Thunnissen PL. Buijs A, et al. Cancer Genet Cytogenet. 2006 Jul 1;168(1):80-2. doi: 10.1016/j.cancergencyto.2005.11.009. Cancer Genet Cytogenet. 2006. PMID: 16772126 No abstract available.

10

Cytogenetic aberrations in neuropathy associated with IgM monoclonal gammopathy.

Eurelings M, Lokhorst HM, Notermans NC, Krijtenburg PJ, Kessel Bv, Eleveld MJ, Bloem A, Wokke JH, Poot M, Buijs A. Eurelings M, et al. Among authors: buijs a. J Neurol Sci. 2007 Sep 15;260(1-2):124-31. doi: 10.1016/j.jns.2007.04.022. Epub 2007 Jun 1. J Neurol Sci. 2007. PMID: 17543994

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