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Von Willebrand disease type 2M: Correlation between genotype and phenotype.
Maas DPMSM, Atiq F, Blijlevens NMA, Brons PPT, Krouwel S, Laros-van Gorkom BAP, Leebeek FWG, Nieuwenhuizen L, Schoormans SCM, Simons A, Meijer D, van Heerde WL, Schols SEM. Maas DPMSM, et al. Among authors: simons a. J Thromb Haemost. 2022 Feb;20(2):316-327. doi: 10.1111/jth.15586. Epub 2021 Nov 21. J Thromb Haemost. 2022. PMID: 34758185 Free PMC article.
Platelet CD34 expression in a patient with a partial deletion of transcription factor subunit CBFB.
van Bergen MGJM, Saes JL, Simons A, Hebeda KM, Henskens YMC, Barteling W, Huys E, Laros-van Gorkom BAP, Schols SEM, Preijers FW, Jongmans MCJ, Jansen JH, van der Reijden BA. van Bergen MGJM, et al. Among authors: simons a. Am J Hematol. 2020 Jun;95(6):E136-E139. doi: 10.1002/ajh.25770. Epub 2020 Apr 8. Am J Hematol. 2020. PMID: 32124467 Free PMC article. No abstract available.
Platelet CD34 expression and α/δ-granule abnormalities in GFI1B- and RUNX1-related familial bleeding disorders.
Marneth AE, van Heerde WL, Hebeda KM, Laros-van Gorkom BA, Barteling W, Willemsen B, de Graaf AO, Simons A, Jansen JH, Preijers F, Jongmans MC, van der Reijden BA. Marneth AE, et al. Among authors: simons a. Blood. 2017 Mar 23;129(12):1733-1736. doi: 10.1182/blood-2016-11-749366. Epub 2017 Jan 17. Blood. 2017. PMID: 28096094 Free article. No abstract available.
Specific proteome changes in platelets from individuals with GATA1-, GFI1B-, and RUNX1-linked bleeding disorders.
Van Bergen MGJM, Marneth AE, Hoogendijk AJ, Van Alphen FPJ, Van den Akker E, Laros-Van Gorkom BAP, Hoeks M, Simons A, De Munnik SA, Janssen JJWM, Martens JHA, Jansen JH, Meijer AB, Van der Reijden BA. Van Bergen MGJM, et al. Among authors: simons a. Blood. 2021 Jul 8;138(1):86-90. doi: 10.1182/blood.2020008118. Blood. 2021. PMID: 33690840 Free article.
ALK activation by the CLTC-ALK fusion is a recurrent event in large B-cell lymphoma.
De Paepe P, Baens M, van Krieken H, Verhasselt B, Stul M, Simons A, Poppe B, Laureys G, Brons P, Vandenberghe P, Speleman F, Praet M, De Wolf-Peeters C, Marynen P, Wlodarska I. De Paepe P, et al. Among authors: simons a. Blood. 2003 Oct 1;102(7):2638-41. doi: 10.1182/blood-2003-04-1050. Epub 2003 May 15. Blood. 2003. PMID: 12750159 Free article.
Therapy-related, donor-derived AML responding to a second allogeneic BMT.
Jacobs JF, Brons PP, Simons A, van der Reijden BA, Hoogerbrugge PM. Jacobs JF, et al. Among authors: simons a. Bone Marrow Transplant. 2007 Sep;40(5):499-500. doi: 10.1038/sj.bmt.1705750. Epub 2007 Jun 25. Bone Marrow Transplant. 2007. PMID: 17589531 No abstract available.
Implementation of Early Next-Generation Sequencing for Inborn Errors of Immunity: A Prospective Observational Cohort Study of Diagnostic Yield and Clinical Implications in Dutch Genome Diagnostic Centers.
Elsink K, Huibers MMH, Hollink IHIM, Simons A, Zonneveld-Huijssoon E, van der Veken LT, Leavis HL, Henriet SSV, van Deuren M, van de Veerdonk FL, Potjewijd J, Berghuis D, Dalm VASH, Vermont CL, van de Ven AAJM, Lambeck AJA, Abbott KM, van Hagen PM, de Bree GJ, Kuijpers TW, Frederix GWJ, van Gijn ME, van Montfrans JM; Genetics First for Primary Immunodeficiency Disorders Consortium. Elsink K, et al. Among authors: simons a. Front Immunol. 2021 Dec 21;12:780134. doi: 10.3389/fimmu.2021.780134. eCollection 2021. Front Immunol. 2021. PMID: 34992599 Free PMC article.
National external quality assessment for next-generation sequencing-based diagnostics of primary immunodeficiencies.
Elsink K, Huibers MMH, Hollink IHIM, van der Veken LT, Ernst RF, Simons A, Zonneveld-Huijssoon E, van der Hout AH, Abbott KM, Hoischen A, Pieterse M, Kuijpers TW, van Montfrans JM, van Gijn ME. Elsink K, et al. Among authors: simons a. Eur J Hum Genet. 2021 Jan;29(1):20-28. doi: 10.1038/s41431-020-0702-0. Epub 2020 Jul 30. Eur J Hum Genet. 2021. PMID: 32733070 Free PMC article.
530 results