Harteveld CL - Search Results

1

Evaluation of the suitability of the World Health Organization International Reference Reagent for Hb A₂ quantitation (89/666) for continued use.

De la Salle B, Stephens AD, Wild BJ, Harteveld CL, Hyde K. De la Salle B, et al. Among authors: harteveld cl. Int J Lab Hematol. 2019 Apr;41(2):262-270. doi: 10.1111/ijlh.12966. Epub 2019 Jan 20. Int J Lab Hematol. 2019. PMID: 30663262

2

Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi-ethnic populations.

Van Delft P, Lenters E, Bakker-Verweij M, de Korte M, Baylan U, Harteveld CL, Giordano PC. Van Delft P, et al. Among authors: harteveld cl. Int J Lab Hematol. 2009 Oct;31(5):484-95. doi: 10.1111/j.1751-553X.2009.01158.x. Epub 2009 Apr 17. Int J Lab Hematol. 2009. PMID: 19486364

3

Occurrence of common and rare δ-globin gene defects in two multiethnic populations: thirteen new mutations and the significance of δ-globin gene defects in β-thalassemia diagnostics.

Phylipsen M, Gallivan MV, Arkesteijn SG, Harteveld CL, Giordano PC. Phylipsen M, et al. Among authors: harteveld cl. Int J Lab Hematol. 2011 Feb;33(1):85-91. doi: 10.1111/j.1751-553X.2010.01255.x. Int J Lab Hematol. 2011. PMID: 20678137

4

Hb Haaglanden: a new nonsickling β7Glu>Val variant. Consequences for basic diagnostics, screening, and risk assessment when dealing with HbS-like variants.

Harteveld CL, Ponjee G, Bakker-Verweij M, Arkesteijn SG, Phylipsen M, Giordano PC. Harteveld CL, et al. Int J Lab Hematol. 2012 Oct;34(5):551-5. doi: 10.1111/j.1751-553X.2012.01424.x. Epub 2012 Apr 11. Int J Lab Hematol. 2012. PMID: 22494447

5

State of the art and new developments in molecular diagnostics for hemoglobinopathies in multiethnic societies.

Harteveld CL. Harteveld CL. Int J Lab Hematol. 2014 Feb;36(1):1-12. doi: 10.1111/ijlh.12108. Epub 2013 May 31. Int J Lab Hematol. 2014. PMID: 23721114 Review.

6

EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.

Traeger-Synodinos J, Harteveld CL, Old JM, Petrou M, Galanello R, Giordano P, Angastioniotis M, De la Salle B, Henderson S, May A; EMQN haemoglobinopathies best practice meeting. Traeger-Synodinos J, et al. Among authors: harteveld cl. Eur J Hum Genet. 2015 Apr;23(4):426-37. doi: 10.1038/ejhg.2014.131. Epub 2014 Jul 23. Eur J Hum Genet. 2015. PMID: 25052315 Free PMC article.

7

The first report of hemoglobin E in combination with the highly unstable alpha-globin variant Hb Adana: The importance of molecular confirmation.

Achour A, de Grouw E, van Erp F, Arkesteijn S, Schaap R, Huurne JT, Bisoen S, Verschuren M, Harteveld CL. Achour A, et al. Among authors: harteveld cl. Int J Lab Hematol. 2019 Jun;41(3):e76-e78. doi: 10.1111/ijlh.12965. Epub 2019 Jan 20. Int J Lab Hematol. 2019. PMID: 30663218 Free PMC article. No abstract available.

8

A Woman with Missing Hb A₂ Due to a Novel (εγ)δβ⁰-Thalassemia and a Novel δ-Globin Variant Hb A₂-Gebenstorf (HBD: c.209G>A).

Saller E, Knijnenburg J, Harteveld CL, Dutly F. Saller E, et al. Among authors: harteveld cl. Hemoglobin. 2020 May;44(3):214-217. doi: 10.1080/03630269.2020.1779739. Epub 2020 Jul 1. Hemoglobin. 2020. PMID: 32605393

9

Further evaluation of the world health organization international reference reagent for Haemoglobin A₂ measurement.

Wild BJ, Chohan DK, Harteveld CL, De la Salle B. Wild BJ, et al. Among authors: harteveld cl. Int J Lab Hematol. 2021 Jun;43(3):494-499. doi: 10.1111/ijlh.13403. Epub 2020 Dec 2. Int J Lab Hematol. 2021. PMID: 33264474

10

Breakpoint characterization of a rare alpha⁰ -thalassemia deletion using targeted locus amplification on genomic DNA.

Hottentot QP, de Meijer E, Buermans HPJ, White SJ, Harteveld CL. Hottentot QP, et al. Among authors: harteveld cl. Int J Lab Hematol. 2021 Dec;43(6):1628-1634. doi: 10.1111/ijlh.13651. Epub 2021 Jul 12. Int J Lab Hematol. 2021. PMID: 34251753 Free PMC article.

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