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International Journal of Neonatal Screening|October 19, 2020
Newborn Screening for Sickle Cell Disease in EuropeYvonne Daniel, Jacques Elion, Bichr Allaf, et al.Hemoglobin|July 21, 2010
Codon 24 (TAT>TAG) and codon 32 (ATG>AGG) (Hb Rotterdam): two novel alpha2 gene mutations associated with mild alpha-thalassemia found in the same family after newborn screeningPiero C Giordano, Marjon H Cnossen, Annemarie M S Joosten, et al.European Journal of Endocrinology|June 25, 2020
Critical evaluation of the newborn screening for congenital hypothyroidism in the NetherlandsKevin Stroek, Annemieke C Heijboer, Marelle J Bouva, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|December 18, 2022
Newborn screening for Cerebrotendinous Xanthomatosis: A retrospective biomarker study using both flow-injection and UPLC-MS/MS analysis in 20,000 newbornsFrédéric M Vaz, Youssra Jamal, Rob Barto, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 28, 2018
Newborn blood spot screening for cystic fibrosis with a four-step screening strategy in the NetherlandsJeannette E Dankert-Roelse, Marelle J Bouva, Bernadette S Jakobs, et al.European Thyroid Journal|October 19, 2023
Optimizing the Dutch newborn screening for congenital hypothyroidism by incorporating amino acids and acylcarnitines in a machine learning-based modelHeleen I Jansen, Marije van Haeringen, Marelle J Bouva, et al.JIMD Reports|July 21, 2020
Evaluation of 11 years of newborn screening for maple syrup urine disease in the Netherlands and a systematic review of the literature: Strategies for optimizationKevin Stroek, Anita Boelen, Marelle J Bouva, et al.Frontiers in Cell and Developmental Biology|February 15, 2021
Corrigendum: Adrenoleukodystrophy Newborn Screening in the Netherlands (SCAN Study): The X-FactorRinse W Barendsen, Inge M E Dijkstra, Wouter F Visser, et al.Frontiers in Cell and Developmental Biology|July 7, 2020
Adrenoleukodystrophy Newborn Screening in the Netherlands (SCAN Study): The X-FactorRinse W Barendsen, Inge M E Dijkstra, Wouter F Visser, et al.The Journal of Clinical Endocrinology and Metabolism|June 25, 2021
Second-tier Testing for 21-Hydroxylase Deficiency in the Netherlands: A Newborn Screening Pilot StudyKevin Stroek, An Ruiter, Annelieke van der Linde, et al.Pageof 3