K. Stroek MSc publications

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Publications MSc K. Stroek

Position
PhD Candidate
Main activities
Research
Specialisation
Endocrinology & Metabolism, Pediatrics
Focus of research

- Introduction of a newborn screening method for Galactokinase Deficiency

- Improvement of existing newborn screening methods for Congenital Adrenal Hyperplasia, Congenital Hypothyroidism and Maple Syrup Urine disease

- ETHIC-trial: Dose finding pilot study for the optimal dose of Protirelin (TRH) to restore the HPT-axis in critically-ill patients admitted to the ICU

2020

  • Stroek Kevin, Heijboer Annemieke C., Bouva Marelle J., van der Ploeg Catharina P. B., Heijnen Marie-Louise A., Weijman Gert, Bosch Annet M., de Jonge Robert, Schielen Peter C. J. I., van Trotsenburg A. S. Paul, Boelen Anita Critical evaluation of the newborn screening for congenital hypothyroidism in the Netherlands European journal of endocrinology / European Federation of Endocrine Societies 2020;183 (3):265-273 [PubMed]
  • Stroek Kevin, Boelen Anita, Bouva Marelle J., de Sain-van der Velden Monique, Schielen Peter C. J. I., Maase Rose, Engel Henk, Jakobs Bernadette, Kluijtmans Leo A. J., Mulder Margot F., Rubio-Gozalbo M. E., van Spronsen Francjan J., Visser Gepke, de Vries Maaike C., Williams Monique, Heijboer Annemieke C., Kemper Evelien A., Bosch Annet M. 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 JIMD reports 2020;54 (1):68-78 [PubMed]

2018

  • Stroek Kevin, Bouva Marelle J., Schielen Peter C. J. I., Vaz Frédéric M., Heijboer Annemieke C., de Jonge Robert, Boelen Anita, Bosch Annet M. Recommendations for newborn screening for galactokinase deficiency: A systematic review and evaluation of Dutch newborn screening data Molecular genetics and metabolism 2018;124 (1):50-56 [PubMed]