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Journal of Chromatography. A|September 6, 2011
A sensitive and simple ultra-high-performance-liquid chromatography-tandem mass spectrometry based method for the quantification of D-amino acids in body fluidsWouter F Visser, Nanda M Verhoeven-Duif, Roel Ophoff, et al.
BMJ Open|November 17, 2022
Autonomy-supportive decision-making in maternity care during prenatal consultations: a qualitative interaction analysisJoyce Kors, Anne de la Croix, Linda Martin, et al.
Pharmacopsychiatry|March 10, 1999
Stress and self-injurious behavior; hormonal and serotonergic parameters in mentally retarded subjectsW M Verhoeven, S Tuinier, Y W van den Berg, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|August 12, 2009
Validation of models that predict Cesarean section after induction of laborC J M Verhoeven, A Oudenaarden, M A A Hermus, et al.
Reproduction in Domestic Animals = Zuchthygiene|October 13, 2011
Split-weaning before altrenogest synchronization of multiparous sows alters follicular development and reduces embryo survivalJ J J van Leeuwen, M Verhoeven, I van der Heden-van Noort, et al.
Journal of Inherited Metabolic Disease|May 15, 2021
Inborn disorders of the malate aspartate shuttleMelissa H Broeks, Clara D M van Karnebeek, Ronald J A Wanders, et al.
Molecular Genetics and Metabolism|July 6, 2004
Creatine and guanidinoacetate: diagnostic markers for inborn errors in creatine biosynthesis and transportLígia S Almeida, Nanda M Verhoeven, Birthe Roos, et al.
Journal of Biomedical Materials Research|February 1, 1995
Blood-biomaterial interactions in a flow system in the presence of bacteria: effect of protein adsorptionS Sapatnekar, K M Kieswetter, K Merritt, et al.
European Journal of Pediatrics|March 29, 2001
Carnitine-acylcarnitine translocase deficiency: phenotype, residual enzyme activity and outcomeE Lopriore, R J Gemke, N M Verhoeven, et al.
JIMD Reports|February 23, 2013
A Patient with Congenital Generalized Lipodystrophy Due To a Novel Mutation in BSCL2: Indications for Secondary Mitochondrial DysfunctionEllen H Jeninga, Monique de Vroede, Nicole Hamers, et al.
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