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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 4
2003 4
2004 8
2005 8
2006 7
2007 6
2008 3
2009 8
2010 12
2011 6
2012 8
2013 5
2014 7
2015 6
2016 4
2017 4
2018 4
2019 4
2020 6
2021 4
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107 results
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Page 1
Molecular basis of α-thalassemia.
Farashi S, Harteveld CL. Farashi S, et al. Among authors: harteveld cl. Blood Cells Mol Dis. 2018 May;70:43-53. doi: 10.1016/j.bcmd.2017.09.004. Epub 2017 Sep 21. Blood Cells Mol Dis. 2018. PMID: 29032940 Free article. Review.
Alpha-thalassaemia.
Harteveld CL, Higgs DR. Harteveld CL, et al. Orphanet J Rare Dis. 2010 May 28;5:13. doi: 10.1186/1750-1172-5-13. Orphanet J Rare Dis. 2010. PMID: 20507641 Free PMC article. Review.
A roadmap for the standardization of hemoglobin A2.
Mosca A, Paleari R, Harteveld CL; IFCC ICSH Joint Working Group for standardization of HbA2. Mosca A, et al. Among authors: harteveld cl. Clin Chim Acta. 2021 Jan;512:185-190. doi: 10.1016/j.cca.2020.11.008. Epub 2020 Nov 10. Clin Chim Acta. 2021. PMID: 33181152
ATR-16 syndrome: mechanisms linking monosomy to phenotype.
Babbs C, Brown J, Horsley SW, Slater J, Maifoshie E, Kumar S, Ooijevaar P, Kriek M, Dixon-McIver A, Harteveld CL, Traeger-Synodinos J, Wilkie AOM, Higgs DR, Buckle VJ. Babbs C, et al. Among authors: harteveld cl. J Med Genet. 2020 Jun;57(6):414-421. doi: 10.1136/jmedgenet-2019-106528. Epub 2020 Jan 31. J Med Genet. 2020. PMID: 32005695 Free PMC article.
A new gene associated with a β-thalassemia phenotype: the observation of variants in SUPT5H.
Achour A, Koopmann T, Castel R, Santen GWE, den Hollander N, Knijnenburg J, Ruivenkamp CAL, Arkesteijn SGJ, Ter Huurne J, Bisoen S, Verschuren M, Vijfhuizen L, Schaap R, Grimbergen A, Slomp J, Traeger-Synodinos J, Vrettou C, Pissard S, Galacteros F, Baas F, Harteveld CL. Achour A, et al. Among authors: harteveld cl. Blood. 2020 Oct 8;136(15):1789-1793. doi: 10.1182/blood.2020005934. Blood. 2020. PMID: 32589702 No abstract available.
107 results
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