Stroek K - Search Results

1

Critical evaluation of the newborn screening for congenital hypothyroidism in the Netherlands.

Stroek K, Heijboer AC, Bouva MJ, van der Ploeg CPB, Heijnen MA, Weijman G, Bosch AM, de Jonge R, Schielen PCJI, van Trotsenburg ASP, Boelen A. Stroek K, et al. Eur J Endocrinol. 2020 Sep;183(3):265-273. doi: 10.1530/EJE-19-1048. Eur J Endocrinol. 2020. PMID: 32580148

2

Recommendations for newborn screening for galactokinase deficiency: A systematic review and evaluation of Dutch newborn screening data.

Stroek K, Bouva MJ, Schielen PCJI, Vaz FM, Heijboer AC, de Jonge R, Boelen A, Bosch AM. Stroek K, et al. Mol Genet Metab. 2018 May;124(1):50-56. doi: 10.1016/j.ymgme.2018.03.008. Epub 2018 Mar 21. Mol Genet Metab. 2018. PMID: 29580649

3

Evaluation of 11 years of newborn screening for maple syrup urine disease in the Netherlands and a systematic review of the literature: Strategies for optimization.

Stroek K, Boelen A, Bouva MJ, De Sain-van der Velden M, Schielen PCJI, Maase R, Engel H, Jakobs B, Kluijtmans LAJ, Mulder MF, Rubio-Gozalbo ME, van Spronsen FJ, Visser G, de Vries MC, Williams M, Heijboer AC, Kemper EA, Bosch AM. Stroek K, et al. JIMD Rep. 2020 May 13;54(1):68-78. doi: 10.1002/jmd2.12124. eCollection 2020 Jul. JIMD Rep. 2020. PMID: 32685353 Free PMC article.

4

Second-tier Testing for 21-Hydroxylase Deficiency in the Netherlands: A Newborn Screening Pilot Study.

Stroek K, Ruiter A, van der Linde A, Ackermans M, Bouva MJ, Engel H, Jakobs B, Kemper EA, van den Akker ELT, van Albada ME, Bocca G, Finken MJJ, Hannema SE, Mieke Houdijk ECA, van der Kamp HJ, van Tellingen V, Paul van Trotsenburg AS, Zwaveling-Soonawala N, Bosch AM, de Jonge R, Heijboer AC, Claahsen-van der Grinten HL, Boelen A. Stroek K, et al. J Clin Endocrinol Metab. 2021 Oct 21;106(11):e4487-e4496. doi: 10.1210/clinem/dgab464. J Clin Endocrinol Metab. 2021. PMID: 34171085

5

Improving the Dutch Newborn Screening for Central Congenital Hypothyroidism by Using 95% Reference Intervals for Thyroxine-Binding Globulin.

Stroek K, Heijboer AC, van Veen-Sijne M, Bosch AM, van der Ploeg CPB, Zwaveling-Soonawala N, de Jonge R, van Trotsenburg ASP, Boelen A. Stroek K, et al. Eur Thyroid J. 2021 Jun;10(3):222-229. doi: 10.1159/000513516. Epub 2021 Mar 5. Eur Thyroid J. 2021. PMID: 34178708 Free PMC article.

6

The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives.

Bosch AM, Stroek K, Abeling NG, Waterham HR, Ijlst L, Wanders RJ. Bosch AM, et al. Among authors: stroek k. Orphanet J Rare Dis. 2012 Oct 29;7:83. doi: 10.1186/1750-1172-7-83. Orphanet J Rare Dis. 2012. PMID: 23107375 Free PMC article. Review.

7

Bahler L, Stroek K, Hoekstra JB, Verberne HJ, Holleman F. Bahler L, et al. Among authors: stroek k. Diabetes Res Clin Pract. 2016 Apr;114:55-63. doi: 10.1016/j.diabres.2016.02.009. Epub 2016 Mar 5. Diabetes Res Clin Pract. 2016. PMID: 27103370

8

Machine learning to improve false-positive results in the Dutch newborn screening for congenital hypothyroidism.

Stroek K, Visser A, van der Ploeg CPB, Zwaveling-Soonawala N, Heijboer AC, Bosch AM, van Trotsenburg ASP, Boelen A, Hoogendoorn M, de Jonge R. Stroek K, et al. Clin Biochem. 2023 Jun;116:7-10. doi: 10.1016/j.clinbiochem.2023.03.001. Epub 2023 Mar 4. Clin Biochem. 2023. PMID: 36878346 Free article.

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