Publications by authors named "Kevin Stroek"

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Machine learning to improve false-positive results in the Dutch newborn screening for congenital hypothyroidism.
Kevin Stroek, Allerdien Visser, Catharina P B van der Ploeg, Nitash Zwaveling-Soonawala, Annemieke C Heijboer

Clin Biochem· June 2023

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Second-tier Testing for 21-Hydroxylase Deficiency in the Netherlands: A Newborn Screening Pilot Study.
Kevin Stroek, An Ruiter, Annelieke van der Linde, Mariette Ackermans, Marelle J Bouva

J Clin Endocrinol Metab· October 2021

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Improving the Dutch Newborn Screening for Central Congenital Hypothyroidism by Using 95% Reference Intervals for Thyroxine-Binding Globulin.
Kevin Stroek, Annemieke C Heijboer, Marja van Veen-Sijne, Annet M Bosch, Catharina P B van der Ploeg

Eur Thyroid J· June 2021

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Critical evaluation of the newborn screening for congenital hypothyroidism in the Netherlands.
Kevin Stroek, Annemieke C Heijboer, Marelle J Bouva, Catharina P B van der Ploeg, Marie-Louise A Heijnen

Eur J Endocrinol· September 2020

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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.
Kevin Stroek, Anita Boelen, Marelle J Bouva, Monique De Sain-van der Velden, Peter C J I Schielen

JIMD Rep· July 2020

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Recommendations for newborn screening for galactokinase deficiency: A systematic review and evaluation of Dutch newborn screening data.
Kevin Stroek, Marelle J Bouva, Peter C J I Schielen, Frédéric M Vaz, Annemieke C Heijboer

Mol Genet Metab· May 2018

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Metformin-related colonic glucose uptake; potential role for increasing glucose disposal?--A retrospective analysis of (18)F-FDG uptake in the colon on PET-CT.
Lonneke Bahler, Kevin Stroek, Joost B Hoekstra, Hein J Verberne, Frits Holleman

Diabetes Res Clin Pract· April 2016

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The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives.
Annet M Bosch, Kevin Stroek, Nico G Abeling, Hans R Waterham, Lodewijk Ijlst

Orphanet J Rare Dis· October 2012

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